Front. Cell. Infect. Microbiol. Frontiers in Cellular and Infection Microbiology Front. Cell. Infect. Microbiol. 2235-2988 Frontiers Media S.A. 10.3389/fcimb.2025.1604259 Cellular and Infection Microbiology Original Research TLR3 rs3775291 C/T polymorphism is associated with elevated IFN-α level in asymptomatic HTLV-1 infection Ferreira Fabiane dos Santos 1 2 Brito Wandrey Roberto dos Santos 1 2 Santana Emmanuelle Giuliana Mendes 1 Oliveira Aline Kelly Alves 1 Lima Aline Cecy Rocha de 1 2 Amoras Ednelza da Silva Graça 1 da Costa Carlos Araujo 3 Souza Maísa Silva 3 Lima Sandra Souza 1 Ishak Ricardo 1 Cayres-Vallinoto Izaura Maria Vieira 1 2 Vallinoto Antonio Carlos Rosário 1 2 Queiroz Maria Alice Freitas 1 2 * 1 Laboratory of Virology, Institute of Biological Sciences, Federal University of Pará, Belém, Brazil 2 Graduate Program in Biology of Infectious and Parasitic Agents, Institute of Biological Sciences, Federal University of Pará, Belém, Brazil 3 Laboratory of Cellular and Molecular Biology, Tropical Medicine Center, Federal University of Pará, Belém, Brazil

Edited by: Henry Puerta-Guardo, Universidad Autónoma de Yucatán, Mexico

Reviewed by: Maria Grazia Romanelli, University of Verona, Italy

Tomoko Hanawa, Kyorin University, Japan

Beatrice Macchi, University of Rome Tor Vergata, Italy

*Correspondence: Maria Alice Freitas Queiroz, alicefarma@hotmail.com/alicefreitas@ufpa.br

04 08 2025 2025 15 1604259 01 04 2025 03 07 2025 Copyright © 2025 Ferreira, Brito, Santana, Oliveira, Lima, Amoras, da Costa, Souza, Lima, Ishak, Cayres-Vallinoto, Vallinoto and Queiroz. 2025 Ferreira, Brito, Santana, Oliveira, Lima, Amoras, da Costa, Souza, Lima, Ishak, Cayres-Vallinoto, Vallinoto and Queiroz

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 Introduction

Alterations in the immune response may influence the development of HTLV-1-associated diseases. TLR3 detects viral nucleic acids, including HTLV-1, and triggers the production of IFN-I and other cytokines. Genetic variations in TLR3 may alter the antiviral and inflammatory responses and contribute to the progression of HTLV-1 infection. The present study investigated the association of polymorphisms in the TLR3 gene (rs5743305 T/A and rs3775291 C/T) with HTLV-1 infection status and their relationship with infection-associated diseases, receptor expression levels, proviral load, and inflammatory and antiviral cytokines.

 Methods

Blood samples were collected from 179 individuals with HTLV-1 infection (82 with inflammatory diseases and 97 asymptomatic individuals) and 179 controls. Genotyping of polymorphisms, analysis of TLR3 gene expression, and quantification of proviral load were performed by real-time PCR, and cytokine levels were measured by enzyme-linked immunosorbent assay (ELISA).

 Results

The polymorphisms showed no correlation with susceptibility to HTLV-1 infection, or the occurrence of disease symptoms linked to the infection. The presence of disease symptoms was associated with higher TNF-α levels and proviral load. TLR3 rs5743305 T/A polymorphism was not associated with variations in TLR3 and IFN-α levels. For the TLR3 rs3775291 C/T polymorphism, asymptomatic individuals carrying the TT polymorphic genotype presented significantly higher IFN-α levels and lower proviral load. The profile of asymptomatic individuals carrying the polymorphic genotypes for TLR3 rs3775291 C/T was characterized by higher levels of TLR3 and IFN-α and lower levels of proviral load, TNF-α and IL-6 compared to those with the wild-type genotype.

 Conclusion

Although polymorphisms in the TLR3 gene have not been associated with the presence of symptoms of HTLV-1-related inflammatory diseases, the TLR3 rs3775291 C/T polymorphism appears to contribute to a better evolution of the HTLV-1 infection status and inflammatory process among asymptomatic individuals.

 HTLV-I infection inflammatory diseases toll-like receptor 3 polymorphism genetic cytokines section-in-acceptance Virus and Host Introduction

The majority of human T-lymphotropic virus 1 (HTLV-1) infections are asymptomatic. However, 5 to 10% of infected individuals may develop different types of diseases, including adult T-cell leukemia (ATL) and inflammatory diseases such as HTLV-1-associated myelopathy (HAM), which causes demyelination of neurons, as well as dermatitis, uveitis, and rheumatic diseases (Schierhout et al., 2020; Kalyanaraman et al., 1982; Osame et al., 1986; Kamoi and Mochizuki, 2012). Factors that may contribute to the development of diseases associated with HTLV-1 are being investigated, such as high levels of proviral load (Nagai et al., 1998; Taylor et al., 1999; Pineda et al., 2019) and changes in the immune response against the virus, which are associated with an increased risk of progression to diseases (Yamauchi et al., 2021; Brites et al., 2021; Clauze et al., 2022).

Genetic variations in components of the immune response have been the focus of several studies in the search for biomarkers that may justify differences in the evolution of infection among individuals with HTLV-1, since some people develop pathological conditions, while others remain in an asymptomatic state (Queiroz et al., 2020; Rafatpanah et al., 2021; Santana et al., 2024). Among the various components of innate immunity, Toll-like receptors (TLRs) stand out for their diversity and for initiating the activation of one of the main intracellular signaling pathways, responsible for promoting an antiviral and inflammatory state during various types of viral infections (Akira and Takeda, 2004). The TLR3 receptor, located in the endosome, detects double-stranded RNA (dsRNA). dsRNA is characterized as a byproduct resulting from the replication and transcription process of several viruses, including HTLV (Van montfoort et al., 2014; Mohanty and Harhaj, 2023).

TLR3 activation results in the synthesis of type I IFNs (IFN-I) and pro-inflammatory cytokines (Vercammen et al., 2008; Mcgettrick and O’neill, 2010). FN-I (IFN-α and IFN-β) have potent antiviral properties, as they interfere with virus replication and act in the immunomodulation of adaptive immunity (Biron, 2001; Xagorari and Chlichlia, 2008; Uematsu and Akira, 2007; Carty et al., 2021). Kinpara et al. (2009) showed that both IFN-α and IFN-β are capable of directly suppressing HTLV-1 expression in HTLV-1-infected cell lines and primary ATL cells (Kinpara et al., 2009).

Alterations in the structure or function of TLR3 may play a crucial role in the progression of viral infections and the potential development of symptoms associated with different clinical conditions linked to HTLV-1. The TLR3 gene is located on chromosome 4 (4q35.1), where some polymorphisms are found (Fischer et al., 2018; Habibabadi et al., 2020; Redondo et al., 2022). The TLR3 rs3775291 C/T genetic variant is located in exon four of the TLR3 gene, generating an amino acid change from leucine to phenylalanine at position 412 of the protein (L412F) (Ranjith-kumar et al., 2007). This alteration may change the binding capacity of dsRNA and influence intracellular signaling when compared to the wild type (Ranjith-kumar et al., 2007; Brown and Razonable, 2010; Zhou et al., 2011). The presence of the rs3775291 C/T polymorphism in the TLR3 gene can generate functional alterations and impact the activation of TLR3-mediated immune responses, influencing the intensity of the inflammatory response. The TLR3 rs3775291 C/T polymorphism has been studied in relation to different viral infections, such as HIV-1 (Sironi et al., 2012), cytomegalovirus (Redondo et al., 2022), tick-borne encephalitis (Kindberg et al., 2011) and hepatitis B virus (HBV) (Chen et al., 2017).

The TLR3 rs5743305 T/A polymorphism is situated in the promoter region of the TLR3 gene and can affect its transcriptional activity, thereby modifying gene expression compared to the wild type. Alteration in TLR3 transcriptional activity may influence receptor functionality and the development of viral diseases. The TLR3 rs5743305 T/A polymorphism has been studied in relation to various viral infections, including HBV (Fischer et al., 2018), hepatitis C virus (HCV) (Askar et al., 2009), and tick-borne encephalitis (Grygorczuk et al., 2017).

In HTLV-1 infection, a single study examined polymorphisms in the TLR3 gene, identifying TLR3 rs3775296 as a potential protective factor against infection (Habibabadi et al., 2020). The absence of comprehensive studies analyzing polymorphisms in the TLR3 gene constitutes a significant limitation in understanding the impact of genetic variations in this receptor on HTLV-1 infection. The present study investigated the association of polymorphisms in the TLR3 gene (rs5743305 T/A and rs3775291 C/T) with HTLV-1 infection and infection status (related to the presence or absence of symptoms of inflammatory disease). The influence of polymorphisms in the TLR3 gene on the levels of proviral load and inflammatory and antiviral cytokines according to the HTLV-1 infection status was also analyzed. The TLR3 rs5743305 T/A and TLR3 rs3775291 C/T polymorphisms were selected for this study because they had not yet been evaluated in HTLV-1 infection, although they were associated with other viral infections.

 Materials and methods Study characterization

This cross-sectional study included 179 individuals infected with HTLV-1. Among them, 82 patients had a clinical diagnosis of inflammatory diseases such as HAM, rheumatological manifestations, dermatitis, pulmonary complications, and uveitis, while 97 individuals were asymptomatic. All individuals infected with HTLV-1 were categorized as people living with HTLV-1. The symptomatic group consisted of those who had a clinical diagnosis of any inflammatory disease assessed in the study. Conversely, the asymptomatic group comprised individuals with HTLV-1 who exhibited no clinical symptoms of disease. The primary clinical symptoms observed in HAM patients included lower back pain, urinary urgency, erectile dysfunction, fatigue, falls, leg pain, changes in gait, with one patient requiring a wheelchair.

Specialist physicians conducted the clinical diagnosis of inflammatory diseases linked to HTLV-1 according to a standard protocol. No patients with HTLV-2 were included in the study. Individuals of both sexes and over 18 years old, who were treated at the outpatient clinic of the Center for Tropical Medicine and the Service for Assistance to People Living with HTLV (SAPEVH) at the Federal University of Pará, were included. The samples were collected in Belém, Pará, Northern region of Brazil, from January 2023 to November 2024.

In Brazil, the highest infection rates are observed in the North and Northeast regions of the country (Legrand et al., 2022). Our study focuses on the population of the city of Belém, located in the state of Pará, which is within the North region of Brazil. HTLV-1/2 infections are endemic to the state of Pará (Silva et al., 2018; Lopes et al., 2022).

Individuals receiving glucocorticoid treatment, those co-infected with HTLV-2, HIV-1/2, HCV and HBV, and those with autoimmune disease were excluded from the study.

A sample containing 10 mL of blood was collected by intravenous puncture using a vacuum collection system containing ethylenediaminetetraacetic acid (EDTA) as an anticoagulant. The samples were centrifuged and separated into aliquots of plasma and leukocytes. An aliquot of the leukocyte samples was used for genomic DNA extraction to perform genotyping of polymorphisms in the TLR3 gene (rs5743305 T/A and rs3775291 C/T) and to quantify proviral load. Another aliquot of the leukocyte samples was used for RNA extraction to quantify TLR3 gene expression. Plasma samples were used to measure plasma cytokines.

A comparison cohort was constituted from 179 blood samples provided by individuals who voluntarily sought testing for HTLV-1 infection at SAPEVH and received a negative diagnosis. All participants were over 18 years of age. Individuals with other infections, including HTLV-2, HIV-1/2, HCV, and HBV, as well as those with autoimmune diseases, were excluded from the cohort. The individuals were selected from Jan/2023 to Nov/2024. The control group samples were utilized to compare the frequencies of polymorphisms, as they represented the same population group as the individuals with HTLV-1. Consequently, there were no interethnic differences observed. Control group samples were matched in age (mean: 49.5; median: 50; IIQ: 22) and sex with the HTLV-1 group.

 DNA extraction

DNA extraction from whole blood leukocytes used the Puregene™ kit (Gentra Systems, Inc., Minneapolis, Minnesota, USA), following the manufacturer’s protocol, which consisted of the steps of cell lysis, protein precipitation, DNA precipitation and hydration. After extraction, the DNA obtained was quantified by spectrophotometric reading on the BioDrop™ equipment (Bio-Rad, Hercules, California, USA), following the protocol recommended by the manufacturer.

 Genotyping of <italic>TLR3</italic> rs5743305 T/A and <italic>TLR3</italic> rs3775291 C/T

The genotypes of the investigated polymorphisms were identified by the real-time PCR technique, using the StepOnePLUS™ Real-Time PCR System (Thermo Fisher, Carlsbad, Califórnia, EUA). Commercial assays containing TaqMan™ hydrolysis probes with the identification C::393058_10 and C:_1731425_10 were used for genotyping the TLR3 rs5743305 and TLR3 rs3775291 polymorphisms, respectively (Thermo Fisher, Carlsbad, California, USA). These assays contained specific primers and probes for amplification of the target sequence. For each reaction, Mastermix (1x) (Thermo Fisher, Carlsbad, California, USA), H2O, assay C::393058_10 or C:_1731425_10 (20X), and DNA (50 ng) were used. The following cycling conditions were used: 10 minutes at 95°C and 40 cycles of 15 seconds at 95°C and 1 minute at 60°C.

 RNA extraction

Total RNA was extracted from peripheral blood leukocytes using the TRIzol™ Plus RNA Purification Kit (Thermo Fisher Scientific, Waltham, Massachusetts, USA). The steps followed the protocol recommended by the manufacturer. The concentration of the extracted RNA was determined using a BioDrop™ (Bio-Rad, Hercules, California, USA) according to the manufacturer’s instructions. All total RNA samples had concentrations equal to 50 ng/µL for the synthesis of complementary DNA (cDNA).

 Reverse transcription

The synthesis of cDNA from RNA was performed using the High-Capacity cDNA Reverse Transcription® with RNAse Inhibitor Kit (Applied Biosystems, Foster City, CA, USA). For each reaction, a mixture with a final volume of 20.0 µL was prepared, contained 2 µL of 10X RT Buffer, 0.8 µL of 25X dNTP Mix (100 nM), 2 µL of random primer, 1 µL of MultiScribe™ Reverse Transcriptase, 1 µL of RNaseOUT™ and 3.2 µL of ultrapure water supplied in the kit and 10.0 µL of extracted RNA. Subsequently, the mixture was placed in a Mastercycler personal thermal cycler (Eppendorf, Hamburg, Germany) and subjected to cycles of 25°C for 10 minutes, 37°C for 120 minutes and 85°C for 5 minutes.

 Quantification of gene expression

Gene expression was measured by quantifying mRNA using real-time PCR. First, the standardization of the quantitative PCRs (qPCRs) with the cDNAs and probes (endogenous and target genes) was performed to calculate the efficiency of the amplification reactions. In the standardization reactions, different concentrations of cDNA were tested (pure and in 4 dilutions with a factor of 2 - 1:2, 1:4, 1:8 and 1:16). All reactions were conducted on plates and performed in triplicate. The same cDNA, at various dilutions, was analyzed with different probes to construct an efficiency curve and validate the 2-ΔΔCt analysis method. All tests showed efficiency as expected (100% ± 10) (Livak and Schmittgen, 2001).

The relative quantification of gene expression consisted of the amplification of the target gene with the endogenous gene (normalizer) using TaqMan™ assays (Applied Biosystems, Foster City, CA, USA) and the StepOnePLUS™ Real-Time PCR System (Thermo Fisher Scientific, Waltham, MA, USA). The reactions were performed in the singleplex format according to the manufacturer’s protocol. The assay used for TLR3 was Hs01551078_m1, and glyceraldehyde-3-phosphate dehydrogenase (GAPDH) was used as the endogenous control (Hs02786624_g1). All assays were obtained commercially (Thermo Fisher Scientific, Waltham, MA, USA). For the reaction, 5 µL of 2X TaqMan® Universal PCR Master Mix, 0.5 µL of 20X TaqMan Gene Expression Assay, 1 µL of cDNA and 10.5 µL of RNAse-free water were used, along with the following thermocycling conditions: 2 minutes at 50°C, followed by 10 minutes at 95°C and 1 minute at 60°C.

The relative quantification (RQ) of target gene expression was determined using the comparative CT method (ΔΔCt) with the formula 2-ΔΔCT, where ΔΔCt = ΔCt sample- ΔCt reference (Life Technologies, Carlsbad, CA, USA).

 Plasma measurement of cytokine levels

The quantification of cytokines FN-α, IL-6, and TNF-α in plasma was conducted utilizing the Read y-SET-Go® enzyme-linked immunosorbent assay (ELISA, eBioscience, California, San Diego, USA), which uses specific monoclonal antibodies to detect each cytokine and measure its level. The test was performed according to the manufacturer’s instructions.

 Quantification of the HTLV-1 proviral load

The proviral load was quantified by qPCR using a TaqMan® system (Applied Biosystems, Foster City, CA) with two target sequences (the albumin gene as an endogenous control and the nonhomologous region of the HTLV-1 pol gene), according to a previously described protocol (Tamegão-Lopes et al., 2006), which starts with the extraction of DNA from leukocytes, followed by relative quantification via real-time PCR. The result is further adjusted to an absolute proviral quantification considering the leukocyte count per mm3, and the result is expressed as the number of proviral DNA copies/mm3.

 Statistical analysis

The genotypic and allelic frequencies of the polymorphisms were estimated by direct counting, and the significance of the differences between the studied groups was calculated using the chi-square (χ2) test and the G test. The Hardy-Weinberg equilibrium calculation was performed to evaluate whether the observed genotypic frequency distributions were in accordance with expectations. Analyses of the normality of the distribution of TLR3 expression levels, the proviral load and cytokine levels were performed using the Shapiro−Wilk test. The TLR3 expression levels, proviral load levels and cytokine levels among the investigated groups were evaluated using the nonparametric Mann−Whitney test. The multiple logistic regression test evaluated the associations of the investigated variables with the presence of disease symptoms. Multiple linear regression analysis was performed to evaluate the association between the gene expression of INF-α in relation to the proviral load of the virus, expression of TLR3, TNF-α, IL-6, TLR3 rs5743305 polymorphism and TLR3 rs3775291 polymorphism. The significance level adopted was 0.05. All tests will be performed using the R program and GraphPad Prism 5.0.

 Ethical aspects

This study was submitted to and approved by the Ethics Committee for Research with Human Beings of the Institute of Health Sciences of the Federal University of Pará (CAAE no. 63427822.3.0000.0018). All individuals included in the study signed an informed consent form.

 Results

Among the 179 individuals diagnosed with HTLV-1 who were evaluated in the study, 126 (70.3%) were female, with a mean age of 49.9 years (19–80 years; median: 50; IQR: 20). Most participants were female: 73.1% (n=60) in the symptomatic group and 67% (n=66) in the asymptomatic group (p= 0.2549). The mean age of the symptomatic group was 52.1 years (median 53.5; IQR: 19.2) and that of the asymptomatic group was 48.8 years (median: 49; IQR: 20).

Genotypic and allele frequency of <italic>TLR3</italic> rs5743305 T/A and <italic>TLR3</italic> rs3775291 C/T

The evaluation of genotypic and allelic frequencies for the TLR3 rs5743305 T/A and TLR3 rs3775291 C/T variations between the group of people living with HTLV-1 and the control group showed no statistically significant difference ( Table 1 ). However, the comparison of genotypic and allelic frequencies for TLR3 rs3775291 C/T among individuals with HTLV-1 according to the presence and absence of symptoms associated with infection showed that asymptomatic individuals had a higher frequency of the polymorphic genotype (p= 0.0206; OR= 0.24) and allele (p= 0.0044; OR= 0.48) (TT and T, respectively; Table 2 ).

Comparison of the genotypic and allelic frequency of polymorphisms in the TLR3 gene between the groups with HTLV-1 and control.

Genotypic and allelic profile HTLV-1 n= 179 n (%) Control n= 179 n (%) px
TLR3 rs5743305 T/A-926
TT 96 (53.63) 88 (49.16) 0.6770
AT 70 (39.10) 78 (43.57)
AA 13 (7.30) 13 (7.30)
*T 0.73 0.71 0.5599
*A 0.27 0.29
TLR3 rs3775291 C/T1234
CC 100 (55.87) 80 (44.69) 0.1068
CT 61 (34.08) 76 (42.46)
TT 18 (10.05) 23 (12.85)
*C 0.73 0.66 0.0516
*T 0.27 0.34

n, number of individuals; *allele; xchi-square test.

Comparison of the genotypic and allelic frequency of polymorphisms in the TLR3 gene between individuals with the presence and absence of symptoms of diseases associated with HTLV-1 infection.

Genotypic and allelic profile Symptomatic n= 82 n (%) Asymptomatic n= 97 n (%) p OR (IC 95%)
TLR3 rs5743305 T/A-926
TT 47 (57.32) 49 (50.51) 0.2126g
AT 27 (32.93) 43 (44.34)
AA 8 (9.75) 5 (5.15)
*T 0.74 0.73 0.9089x
*A 0.26 0.27
TLR3 rs3775291 C/T1234
CC 54 (65.85) 46 (47.43) 0.0206g 0.24a (0.07-0.79)
CT 24 (29.27) 37 (38.14)
TT 4 (4.88) 14 (14.43)
*C 0.80 0.66 0.0044x 0.48 (0.29-0.78)
*T 0.20 0.34

n, number of individuals; *allele; gteste G; xteste qui-quadrado; aTT vs. CC.

 <italic>TLR3</italic> gene expression, plasma cytokines, and HTLV-1 proviral load among symptomatic and asymptomatic individuals for infection-associated diseases

The levels of TLR3 expression, IFN-α, and IL-6 were not statistically different between the group with symptoms of HTLV-1-associated diseases and the group of asymptomatic individuals (p> 0.05; Figures 1A, B, D ). However, plasma TNF-α (p= 0.0044; Figure 1C ) and HTLV-1 proviral load (p= 0.0141; Figure 1E ) levels were significantly higher in the symptomatic group.

Comparison of the levels of (A) TLR3 gene expression, (B) IFN-α, (C) TNF-α, (D) IL-6 and (E) proviral load between symptomatic and asymptomatic individuals for HTLV-1-associated diseases. Mann-Whitney test.

Violin plots comparing symptomatic and asymptomatic groups across five panels: A) TLR3 (p = 0.1217), B) IFN-α (p = 0.6363), C) TNF-α (p = 0.0044), D) IL-6 (p = 0.4159), and E) Proviral load (p = 0.0141). Each plot depicts data distribution and median line for the respective proteins or variables. <italic>TLR3</italic> gene expression, plasma cytokines and HTLV-1 proviral load among individuals with different genotypes of <italic>TLR3</italic> rs5743305 T/A and <italic>TLR3</italic> rs3775291 C/T polymorphisms

TLR3 expression levels were lower in HTLV-1 individuals carrying the AA polymorphic genotype for the TLR3 rs5743305 T/A variation in the HTLV-1, symptomatic and asymptomatic groups ( Figures 2A-C ) and higher in carriers of the TT polymorphic genotype for TLR3 rs3775291 C/T in the HTLV-1, symptomatic and asymptomatic groups ( Figures 2C-F ), but no statistically significant difference was observed, regardless of the presence or absence of symptoms.

Evaluation of TLR3 gene expression levels among individuals with different genotypes for TLR3 rs5743305 T/A in the group (A) with HTLV-1, (B) symptomatic and (C) asymptomatic; among individuals with different genotypes for TLR3 rs3775291 C/T in the group (D) with HTLV-1, (E) symptomatic and (F) asymptomatic. Kruskal-Wallis test.

Violin plots display TLR3 expression in different genotypes. Panels A-C show TLR3 rs5743305T/A with HTLV-1, symptomatic, and asymptomatic groups, respectively. Panels D-F show TLR3 rs3775291C/T with the same groups. Each panel indicates varying expression levels with p-values provided, comparing TT, AT, AA genotypes in the first set, and CC, CT, TT in the second.

No significant difference in IFN-α levels was found between TLR3 rs5743305 T/A genotypes in individuals with HTLV-1 ( Figure 3A ), nor when considering the presence ( Figure 3B ) or absence ( Figure 3C ) of related symptoms. Similarly, no difference in IFN-α concentrations was observed for TLR3 rs3775291 C/T variation in the HTLV group ( Figure 3D ) or the symptomatic group ( Figure 3E ). However, in the asymptomatic group, IFN-α levels were significantly higher in individuals carrying the polymorphic TT genotype compared to those carrying the CC genotype (p= 0.0116; Figure 3F ) for the TLR3 rs3775291 C/T polymorphism.

Evaluation of plasma IFN-α levels among individuals with different genotypes for TLR3 rs5743305 T/A in the group (A) with HTLV-1, (B) symptomatic and (C) asymptomatic; among individuals with different genotypes for TLR3 rs3775291 C/T in the group (D) with HTLV-1, (E) symptomatic and (F) asymptomatic. Kruskal-Wallis test.

Violin plots display IFN-alpha levels (pg/mL) across different TLR3 genotypes. Panels A-C show HTLV-1, symptomatic, and asymptomatic groups for rs5743305T/A. Panels D-F depict the same for rs3775291C/T. Significant differences are noted in panel F with p = 0.0116.

Analyses of TNF-α levels showed no statistical difference between individuals carrying the genotypes for the TLR3 rs5743305 T/A variation ( Figures 4A-C ). Although carriers of the TT polymorphic genotype for TLR3 rs3775291 C/T presented lower levels of TNF-α ( Figures 4D, E ), there was no significant difference between individuals carrying the different genotypes for TLR3 rs3775291 C/T ( Figures 4D-F ).

Evaluation of plasma TNF-α levels among individuals with different genotypes for TLR3 rs5743305 T/A in the group (A) with HTLV-1, (B) symptomatic and (C) asymptomatic; among individuals with different genotypes for TLR3 rs3775291 C/T in the group (D) with HTLV-1, (E) symptomatic and (F) asymptomatic. Kruskal-Wallis test.

Violin plots illustrating TNF-alpha levels (pg/mL) across different genotypes for TLR3 polymorphisms. Panels A to C show data for TLR3 rs5743305T/A, while D to F display TLR3 rs3775291C/T. Each panel represents various clinical states: HTLV-1, Symptomatic, and Asymptomatic. P-values indicate statistical significance levels for differences among genotypes.

IL-6 levels did not show a statistically significant difference between individuals carrying the different genotypes for TLR3 rs5743305 T/A and TLR3 rs3775291 C/T in the HTLV-1, symptomatic, and asymptomatic groups ( Figures 5A-F ).

Evaluation of plasma IL-6 levels among individuals with different genotypes for TLR3 rs5743305 T/A in the group (A) with HTLV-1, (B) symptomatic and (C) asymptomatic; among individuals with different genotypes for TLR3 rs3775291 C/T in the group (D) with HTLV-1, (E) symptomatic and (F) asymptomatic. Kruskal-Wallis test.

Violin plots showing IL-6 levels (picograms per milliliter) across different genotypes: TT, AT, AA in graphs A, B, C for TLR3 rs5743305 and CC, CT, TT in graphs D, E, F for TLR3 rs3775291. Each plot represents different groups: HTLV-1, Symptomatic, and Asymptomatic, with corresponding p-values provided for each. Blue, yellow, and purple colors distinguish the genotypes.

The concentration of HTLV-1 proviral load was not different between individuals carrying the different genotypes for TLR3 rs5743305 T/A in the HTLV-1, symptomatic and asymptomatic groups ( Figures 6A-C ). Regarding the TLR3 rs3775291 C/T variation, there was no difference in the viral load concentration between the genotypes in the HTLV-1 ( Figure 6D ) and symptomatic ( Figure 6E ) groups. However, in the asymptomatic group, carriers of the polymorphic TT genotype had a lower proviral load than those with the CC genotype (p= 0.0434; Figure 6F ) for TLR3 rs3775291 C/T.

Assessment of proviral load levels among individuals carrying different genotypes for TLR3 rs5743305 T/A in the group (A) with HTLV-1, (B) symptomatic and (C) asymptomatic; among individuals carrying different genotypes for TLR3 rs3775291 C/T in the group (D) with HTLV-1, (E) symptomatic and (F) asymptomatic. Kruskal-Wallis test.

Six violin plots display proviral load (DNA copies per mm³) for different genotypes at two genetic loci (TLR3 rs5743305 T/A and TLR3 rs3775291 C/T) among HTLV-1, symptomatic, and asymptomatic groups. Panels A to C show the first locus, with p-values indicating statistical significance. Panels D to F show the second locus, also with p-values. The plots use colors for different genotypes: yellow (TT or CC), red (AT or CT), and green (AA or TT), illustrating the distribution and variability of proviral load within each group.

Expression levels of TLR3, IFN-α, TNF-α, IL-6, and proviral load were compared across different genotypes of the TLR3 rs5743305 T/A and TLR3 rs3775291 C/T polymorphisms, categorized by sex. No significant differences were found in these analyses (see Supplementary Figures 1 , 2 ).

 Multiple evaluations of variables

In the multiple logistic regression analysis, an association was observed between the presence of symptoms and an increase in proviral load (p= 0.0287) and plasma levels of TNF-α (p= 0.0351) ( Table 3 ). Multiple linear regression analysis assessed the association of IFN-α levels with variables among all HTLV-1-infected individuals, including both symptomatic and asymptomatic. In the group with HTLV-1 and symptomatic, no association was observed between any of the variables investigated and IFN-α levels. In the group of asymptomatic individuals, an association was observed between IFN-α levels and TNF-α (β: 1.091; 95% CI: 0.150 – 2.031; p= 0.0225) and IFN-α levels with the TT polymorphic genotype for TLR3 rs3775291 C/T (β: 25.537; 95% CI: 11.611 – 39.463; p= 0.0035) ( Table 4 ).

Multiple logistic regression of variables associated with individuals with symptoms of HTLV-1-related diseases.

Variables OR CI 95% p
Symptoms
Proviral load 1.002 1.000 – 1.003 0.02875
TNF-α 1.104 1.007 – 1.211 0.03511

Multiple linear regression analysis of plasma IFN-α levels in relation to the variables investigated in the group of people living with HTLV-1 and according to the presence and absence of symptoms.

IFN-α
Variables Estimate CI 95% P
HTLV-1
Proviral load 0.001 -0.010 – 0.013 0.8325
TLR3 expression 10.391 -3.448 – 24.231 0.1310
TNF-α 0.354 -0.529 – 1.237 0.4081
IL-6 0.365 -0.634 1.364 0.4500
TLR3 rs5743305 T/A
TT Ref
AT -1.062 -18.937 – 16.812 0.9013
AA -14.975 -44.974 – 15.023 0.3057
TLR3 rs3775291 C/T
CC Ref
CT -2.849 -20.777 – 15.078 0.7405
TT -6.274 -25.884 – 13.335 0.5073
Symptomatic
Proviral load 0.001 -0.010 – 0.013 0.8325
TLR3 expression 10.391 -3.448 – 24.231 0.1310
TNF-α 0.354 -0.529 – 1.237 0.4081
IL-6 0.365 -0.634 – 1.364 0.4500
TLR3 rs5743305 T/A
TT Ref
AT -1.062 -20.777 – 15.078 0.9013
AA -14.975 -25.884 – 13.335 0.3057
TLR3 rs3775291 C/T
CC Ref
CT -2.849 -44.974 – 15.023 0.7405
TT -6.274 -18.937 – 16.812 0.5073
Asymptomatic
Proviral load 0.019 -0.008 – 0.040 0.1624
TLR3 expression 2.934 -5.421 – 11.188 0.4598
TNF-α 1.137 0.150 – 2.031 0. 0217
IL-6 0.176 -0.806 – 0.723 0.6885
TLR3 rs5743305 T/A
TT Ref
AT 1.206 -10.532 – 11.209 0.8255
AA -4.699 -21.047 – 10.214 0.5406
TLR3 rs3775291 C/T
CC Ref
CT 3.404 -8.414 – 13.236 0.5492
TT 27.612 11.611 – 39.463 0.0035

Based on the results observed in the group of asymptomatic individuals, the values of all investigated variables were normalized to construct and evaluate a profile of carriers of the wild genotype (CC) and the polymorphic genotype (TT) for the TLR3 rs3775291 C/T variation. The profile of carriers of the polymorphism was characterized by elevated levels of TLR3 and IFN-α and lower levels of proviral load, TNF-α and IL-6 compared to the profile of those with the wild-type genotype ( Figure 7 ).

Assessment of the profile of the investigated variables of carriers of the wild (CC) and polymorphic (TT) genotype for the TLR3 rs3775291 C/T variation in the group of asymptomatic individuals.

Line graph showing normalized concentration of five indicators: Proviral load, TLR3, INF-α, TNF-α, and IL-6, comparing groups CC (blue line) and TT (red line) in asymptomatic patients. TT has notably higher peaks at TLR3 and TNF-α compared to CC. Discussion

TLR3 recognizes dsRNA (Kawai and Akira, 2010), which is characterized by being an intermediate product during the replication and transcription of most viruses (Alexopoulou et al., 2001; Rathinam and Fitzgerald, 2011). Upon recognizing dsRNA, the production of type I IFN and pro-inflammatory cytokines is induced (Takeda and Akira, 2005; Blasius and Beutler, 2010). The mechanisms by which TLR3 recognizes HTLV-1 are not yet fully understood. Studies suggest that when the retroviral genome dimerizes and forms a secondary structure, a double-stranded RNA is possibly generated, which can be recognized by TLR3 (Russell et al., 2004; Greatorex, 2004; Watts et al., 2009). HTLV-1 generates several forms of nucleic acid during its replication cycle, such as RNA, RNA/DNA intermediates, ssDNA, and dsDNA. This allows different immunological sensors to detect the presence of the virus and activate immune responses, including TLR3 (Van montfoort et al., 2014; Mohanty and Harhaj, 2023).

HTLV-1 infection status can be affected by various immunological factors and the genetic variability of the host (Yamauchi et al., 2021). The onset of the diseases associated with the HTLV-1 infection can be complexly affected by these factors. Therefore, the present study investigated the association of polymorphisms in the TLR3 gene with susceptibility to HTLV-1 infection, as well as its influence on the development of symptoms of inflammatory diseases associated with the virus and on the levels of inflammatory and antiviral cytokines, seeking to identify possible factors that may affect the heterogeneity of the immune response.

This study represents the first evaluation of the TLR3 rs5743305 T/A polymorphism concerning HTLV-1 infection. The genotypic and allelic frequencies between individuals with HTLV-1 and the control group showed no significant differences, indicating that this polymorphism is likely unrelated to HTLV-1 infection susceptibility.

Some studies have found an association between the TLR3 rs5743305 T/A polymorphism and viral infections. In HBV infection, the AA for the TLR3 rs5743305 T/A variation was more frequent in the group with chronic hepatitis B compared to the control group. Furthermore, the A allele was associated with a decrease in spontaneous HBsAg seroclearance in Caucasian patients, suggesting that it may represent an important factor in the immunological control of HBV infection (Fischer et al., 2018). In contrast, in tick-borne encephalitis viral infection, the TT genotype for the TLR3 rs5743305 T/A variant was more frequent in the infected group compared to the control, which was considered a risk genotype (Grygorczuk et al., 2017).

Variations in study results may be attributed to factors such as ethnic diversity among the populations examined, which can affect the prevalence of polymorphisms and their impact on disease progression. The studies that identified an association between the TLR3 rs5743305 T/A polymorphism and viral infections largely involved Caucasian populations (Grygorczuk et al., 2017; Fischer et al., 2018) and, consequently, genetically more homogeneous, while studies carried out in different population groups presented divergent results, as observed in the present study that evaluated a mixed-race population. The study assessed a population from the Brazilian Amazon, which has genetic contributions from Europeans, indigenous peoples, and Africans, resulting in notable genetic diversity (Santos et al., 2010).

Evaluation of the TLR3 rs3775291 C/T polymorphism showed that the genotypic and allelic frequencies did not differ between the HTLV-1 and control groups, suggesting that the polymorphism possibly does not influence susceptibility to HTLV-1 infection. In the context of dengue virus infection, research has suggested that the presence of the polymorphic TT genotype for TLR3 rs3775291 C/T was observed with greater frequency in the infected cohort compared to the control group (Singh et al., 2021). This genotype has been identified as a risk factor for susceptibility to dengue virus infection. The CT genotype for the TLR3 rs3775291 C/T variant was more frequent in the group of patients with an advanced stage of HIV-1 infection when compared to the control group, which may influence the risk of infection progression (Singh and Samani, 2022). In HBV infection, Rong et al. (2013) and Fischer et al. (2018) reported that the polymorphic T allele for the TLR3 rs3775291 C/T variation increased the risk of HBV infection. In contrast, Mickienė et al. (2002) evaluated the TLR3 rs3775291 C/T polymorphism in tick-borne viral encephalitis and identified a lower frequency of the TLR3 rs3775291 C/T polymorphic genotype TT in infected individuals. The frequency of the polymorphism in the infected group was nearly half that observed in the healthy group, indicating that it may serve as a protective factor against infection.

These contradictory studies on the role of TLR3 rs3775291 C/T genetic variation in susceptibility to viral infection show that the mechanism by which TLR3 rs3775291 C/T affects susceptibility/resistance to viral infections is not yet fully understood. The different results observed in these studies may suggest that the effect of the TLR3 rs3775291 C/T polymorphism may depend on the type of virus causing the infection, since some viruses have different pathogenic components.

Comparison of allelic and genotypic frequencies of the TLR3 rs5743305 T/A polymorphism between groups with and without symptoms of HTLV-1-associated diseases showed no statistically significant difference. Polymorphic variants for TLR3 rs5743305 T/A were associated with a low humoral and cellular response to measles vaccination, presenting lower levels of measles-specific antibodies and showing a lower lymphoproliferative response compared to wild type (Dhiman et al., 2008). In HBV infection, no association was observed between the polymorphism and the development of hepatocellular carcinoma in patients with the viral infection (Li and Zheng, 2013). These data suggest that in HTLV-1 infection, the TLR3 rs5743305 T/A polymorphism does not appear to alter TLR3 expression and does not influence the HTLV-1 infection status, since the polymorphism was not associated with the presence of clinically established diseases related to the virus.

In our study, bivariate analysis showed that the frequency of the TLR3 rs3775291 C/T polymorphism was higher in the group of asymptomatic individuals compared to individuals with the presence of symptoms of HTLV-1-associated diseases. Nevertheless, an analysis using multiple logistic regression of the variables examined in relation to HTLV-1-associated disease symptoms indicated that the TLR3 rs3775291 C/T polymorphism was not linked to clinical manifestations resulting from viral infection. The results suggest a probable influence of the TLR3 rs3775291 C/T polymorphism on the HTLV-1 infection status, possibly associated with a lower chance of developing symptoms, but it is not a direct predictor of clinical manifestations when other variables are considered.

The TLR3 rs3775291 C/T polymorphism affects the protein’s ability to bind dsRNA, resulting in a reduced signaling cascade compared to the wild-type form (Ranjith-Kumar et al., 2007; Zhou et al., 2011). Although this functional alteration may impact the activation of TLR3-mediated immune responses, influencing the intensity of the inflammatory response during viral infections, it did not demonstrate a direct relationship with the manifestation of various symptoms of diseases associated with HTLV-1. This suggests that other viral and immunological factors may have more relevant roles in the development of HTLV-1-associated diseases, such as proviral load and the inflammatory cytokine TNF-α (Starling et al., 2013; Neco et al., 2017).

Although the association of the TLR3 rs3775291 C/T polymorphism with the presence of symptoms or clinical outcomes has been identified in other studies evaluating different types of infections, none of these studies performed a multiple analysis that included the immunological variables involved in TLR3 signaling. For example, polymorphism was associated with protection against HIV-1 infection (Sironi et al., 2012), with lower viremia in cytomegalovirus infection (Redondo et al., 2022) and with a lower chance of developing hepatocellular carcinoma in individuals younger than 40 years of age infected with HBV (Chen et al., 2017). The lack of results from analyses of the TLR3 rs3775291 C/T polymorphism in relation to multiple immunological factors resulting from TLR3 signaling makes it difficult to compare with our findings resulting from multiple analyses, which are considered a more detailed evaluation.

The comparison of cytokine levels between patients with and without symptoms of HTLV-1-associated diseases indicated that individuals with symptoms had higher levels of TNF-α. The results found corroborate other studies that report that the increase in the frequency of cells expressing TNF-α is directly associated with the pathogenesis of HTLV-1 infection, contributing to the exacerbated inflammatory environment observed in conditions such as HAM (Santos et al., 2004; Nakamura et al., 1993; Neco et al., 2017). In the cerebrospinal fluid (CSF) of patients with MAH, it is possible to find elevated levels of IFN-γ and TNF-α (Quaresma et al., 2015). The most widely accepted hypothesis for the development of HAM is that neuronal damage occurs due to inflammation in the central nervous system (CNS), triggered by cytokines secreted by infected CD4+ T cells. The main cytokines involved in this process are IFN-γ and TNF-α, which contribute to the neurodegeneration associated with the disease (Osame, 2002; Araujo and Silva, 2006).

The assessment of HTLV-1 proviral load levels indicated that individuals presenting with symptoms exhibited higher levels compared to those without symptoms associated with inflammatory diseases. Multiple logistic regression analysis confirmed that higher proviral loads were linked to clinical symptoms of HTLV-1 infection. This suggests that proviral load is a robust marker that is independent of the presence of other immunological and genetic factors. High levels of proviral load may be directly linked to the risk of developing inflammatory diseases, probably due to active viral replication and persistent inflammatory response (Grassi et al., 2011; Olindo et al., 2006).

In our study, TLR3 gene expression levels did not show significant differences between individuals with different genotypes for the TLR3 rs5743305 T/A and TLR3 rs3775291 C/T polymorphisms. In cases of HCV infection, TLR3 expression levels were also unaffected by the TLR3 rs5743305 T/A polymorphism. However, the TLR3 rs3775291 C/T polymorphism was linked to higher TLR3 expression levels and the absence of infection by the HCV1a viral genotype, which is associated with severe prognosis (Askar et al., 2009). These findings indicate that, in certain viral infections, the TLR3 rs3775291 C/T polymorphism may be related to increased TLR3 levels and the progression of these infections.

In multiple linear regression analysis, higher IFN-α levels were associated with the rs3775291 C/T polymorphism. Since this polymorphism promotes amino acid changes in the protein (Leu412Fen), it may likely influence the functionality of the TLR3 receptor, promoting a more efficient activation of the signaling pathway and, consequently, inducing greater IFN-α production. IFN-α induces control of different types of viral infections (Levy et al., 2011). This cytokine acts by repressing the HTLV-1 viral cycle during infection (Cachat et al., 2013). Furthermore, the use of IFN-α as therapy in patients with HAM has been shown to reduce the percentage of inflammatory cells in the cerebrospinal fluid and blood, contributing to the clinical improvement of the patient (Feng et al., 2004). Therefore, the TLR3 rs3775291/T polymorphism may potentially enhance the efficiency of the antiviral response and mitigate the progression of HTLV-1 infection in asymptomatic individuals.

There are limited studies in literature examining the genetic variations TLR3 rs5743305 T/A and TLR3 rs3775291 C/T in relation to IFN-α levels. Our study is one of the first to perform this evaluation, which makes it difficult to establish the role of these polymorphisms in relation to cytokine levels in viral infections. IFN-I induces the expression of several IFN-stimulated genes (ISGs) in host cells, which act at different stages of viral replication, inhibiting the replication and transcription processes of different viruses (Schoggins et al., 2011; Hoffmann et al., 2015). Thus, the production of more adequate levels of the cytokine could aid in the immunological control of HTLV-1 infection, influencing the maintenance of the asymptomatic state of the infection.

While the study provides valuable insights into the HTLV-1 infection status, it is limited by the inability to assess more specific components of the TLR3 signaling pathway, such as IP-10/CXCL10 and ISGs. Changes in the synthesis of IP-10/CXCL10 are known to affect the inflammatory response (Harvey et al., 2003; Zhang et al., 2014). Therefore, identifying ISGs may help determine differences in antiviral response among individuals with or without the TLR3 rs3775291 C/T polymorphism, particularly among asymptomatic individuals.

Since the TLR3 rs3775291 C/T polymorphism has been associated with the severity of COVID-19, mainly in men, influencing the autophagy process and affecting TNF production and susceptibility to SARS-CoV-2 infection (Croci et al., 2022), we evaluated the influence of the TLR3 rs5743305 T/A and rs3775291 C/T polymorphisms on HTLV-1 infection according to sex. However, there was no significant difference in the levels of TLR3 expression, cytokines, and proviral load in the male and female groups. HTLV-1 infection is more common in women, likely because men transmit the infection more effectively to women. The frequency of transmission of HTLV-1 infection from men to women is approximately 60%, while the frequency of transmission from women to men is 0.4% (Kajiyama et al., 1986; Paiva and Casseb, 2014). Therefore, it is probable that the epidemiological characteristics of HTLV-1 transmission have impacted the analyses with respect to sex.

It is important to highlight that among the studies carried out on polymorphisms in the TLR3 gene, none performed analyses of the TLR3 rs5743305 T/A and TLR3 rs3775291 C/T polymorphisms together with the quantification of the proviral load, antiviral and inflammatory cytokines, which were evaluated in the present study, which allowed a more consistent analysis of these polymorphisms in HTLV-1 infection status. The identification of polymorphisms that influence the HTLV-1 infection status can assist in personalized medicine, through studies of personalized approaches in clinical management, helping to predict which individuals are at greater risk of developing complications. However, we consider a more comprehensive investigation necessary, through analyses with larger population samples, from different ethnicities, and the inclusion of other polymorphisms in the TLR3 gene to provide a greater understanding of the real impact of the genetic variations studied in the context of HTLV-1 infection.

 Conclusion

In summary, the polymorphisms were not linked to susceptibility to HTLV-1 infection or the infection status. Disease symptoms correlated with increased TNF-α levels and proviral load. The TLR3 rs5743305 T/A polymorphism was not connected with changes in TLR3 and IFN-α levels. For the TLR3 rs3775291 C/T polymorphism, asymptomatic individuals with the TT polymorphic genotype exhibited significantly higher IFN-α levels and lower proviral load. Asymptomatic individuals carrying the TT polymorphic genotype for TLR3 rs3775291 C/T demonstrated elevated levels of TLR3 and IFN-α, and reduced levels of proviral load, TNF-α, and IL-6 compared to those with the wild-type genotype. Although polymorphisms in the TLR3 gene have not been associated with the presence of symptoms related to HTLV-1 inflammatory diseases, the TLR3 rs3775291 C/T polymorphism seems to contribute to improved control of the infection and inflammatory process among asymptomatic individuals.

 Data availability statement

The original contributions presented in the study are included in the article/ Supplementary Material . Further inquiries can be directed to the corresponding author.

 Ethics statement

The studies involving humans were approved by Institute of Health Sciences of the Federal University of Pará (CAAE no. 63427822.3.0000.0018). The studies were conducted in accordance with the local legislation and institutional requirements. The participants provided their written informed consent to participate in this study.

 Author contributions

FF: Formal analysis, Investigation, Methodology, Writing – original draft. WB: Methodology, Writing – original draft. EM: Methodology, Writing – original draft. AO: Methodology, Writing – original draft. AL: Methodology, Writing – original draft. EA: Investigation, Methodology, Writing – original draft. CC: Methodology, Writing – original draft. MS: Methodology, Writing – original draft. SL: Formal analysis, Writing – original draft. RI: Investigation, Writing – review & editing. IC-V: Investigation, Writing – review & editing. AV: Funding acquisition, Investigation, Writing – review & editing. MQ: Conceptualization, Formal analysis, Funding acquisition, Project administration, Supervision, Writing – original draft, Writing – review & editing.

 Funding

The author(s) declare that financial support was received for the research and/or publication of this article. This study was supported by the National Council for Scientific and Technological Development (CNPq #304835/2022-6, #401569/2023-3. #302935/2021-5 and #303837/2023-3), INCT Theranostics and Nanobiotechnology (CNPq Process No. 403193/2022-2 and Fapemig: CBB -APQ-03613-17) and the National Institute of Science and Technology in Emerging and Reemerging Viruses (INCT-VER No. 406360/2022-7).

 Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

 Generative AI statement

The author(s) declare that no Generative AI was used in the creation of this manuscript.

 Publisher’s note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

 Supplementary material

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fcimb.2025.1604259/full#supplementary-material

References Akira S. Takeda K. (2004). Toll-like receptor signalling. Nat. Rev. Immunol. 4, 499–511. doi: 10.1038/nri1391, PMID: 15229469 Alexopoulou L. Holt A. C. Medzhitov R. Flavell R. A. (2001). Recognition of double-stranded RNA and activation of NF-kappaB by Toll-like receptor 3. Nature 413, 732–738. doi: 10.1038/35099560, PMID: 11607032 Araujo A. Q. Silva M. T. (2006). The HTLV-1 neurological complex. Lancet Neurol. 5, 1068–1076. doi: 10.1016/S1474-4422(06)70628-7, PMID: 17110288 Askar E. Bregadze R. Mertens J. Schweyer S. Rosenberger A. Ramadori G. . (2009). TLR3 gene polymorphisms and liver disease manifestations in chronic hepatitis C. J. Med. Virol. 81, 1204–1211. doi: 10.1002/jmv.21491, PMID: 19475618 Biron C. A. (2001). Interferons alpha and beta as immune regulators–a new look. Immunity 14, 661–664. doi: 10.1016/s1074-7613(01)00154-6, PMID: 11420036 Blasius A. L. Beutler B. (2010). Intracellular toll-like receptors. Immunity 32, 305–315. doi: 10.1016/j.immuni.2010.03.012, PMID: 20346772 Brites C. Grassi M. F. Quaresma J. A. S. Ishak R. Vallinoto A. C. R. (2021). Pathogenesis of HTLV-1 infection and progression biomarkers: An overview. Braz. J. Infect. Dis. 25, 101594. doi: 10.1016/j.bjid.2021.101594, PMID: 34256025 Brown R. A. Razonable R. R. (2010). A real-time PCR assay for the simultaneous detection of functional N284I and L412F polymorphisms in the human Toll-like receptor 3 gene. J. Mol. Diagn. 12, 493–497. doi: 10.2353/jmoldx.2010.090122, PMID: 20413676 Cachat A. Chevalier S. A. Alais S. Ko N. L. Ratner L. Journo C. . (2013). Alpha interferon restricts human T-lymphotropic virus type 1 and 2 de novo infection through PKR activation. J. Virol. 87, 13386–13396. doi: 10.1128/JVI.02758-13, PMID: 24089560 Carty M. Guy C. Bowie A. G. (2021). Detection of viral infections by innate immunity. Biochem. Pharmacol. 183, 114316. doi: 10.1016/j.bcp.2020.114316, PMID: 33152343 Chen D. Xie W. Lu Y. Su S. Nong L. Jia Y. . (2017). Gene polymorphisms of TLR2 and TLR3 in HBV clearance and HBV-related hepatocellular carcinoma in a Chinese male population. Int. J. Biol. Markers 32, e195–e201. doi: 10.5301/jbm.5000238, PMID: 28009434 Clauze A. Enose-Akahata Y. Jacobson S. (2022). T cell receptor repertoire analysis in HTLV-1-associated diseases. Front. Immunol. 13. doi: 10.3389/fimmu.2022.984274, PMID: 36189294 Croci S. Venneri M. A. Mantovani S. Fallerini C. Benetti E. Picchiotti N. . (2022). he L412F polymorphism in TLR3 inhibits autophagy and is a marker of severe COVID-19 in men. Autophagy. 18, 1662–1672. doi: 10.1080/15548627.2021.1995152, PMID: 34964709 Dhiman N. Ovsyannikova I. G. Vierkant R. A. Ryan J. E. Pankratz V. S. Jacobson R. M. . (2008). Associations between SNPs in toll-like receptors and related intracellular signaling molecules and immune responses to measles vaccine: preliminary results. Vaccine 26, 1731–1736. doi: 10.1016/j.vaccine.2008.01.017, PMID: 18325643 Feng J. Misu T. Fujihara K. Misawa N. Koyanagi Y. Shiga Y. . (2004). Th1/Th2 balance and HTLV-I proviral load in HAM/TSP patients treated with interferon-alpha. J. Neuroimmunol. 151, 189–194. doi: 10.1016/j.jneuroim.2004.02.007, PMID: 15145617 Fischer J. Koukoulioti E. Schott E. Fülöp B. Heyne R. Berg T. . (2018). Polymorphisms in the Toll-like receptor 3 (TLR3) gene are associated with the natural course of hepatitis B virus infection in Caucasian population. Sci. Rep. 8, 12737. doi: 10.1038/s41598-018-31065-6, PMID: 30143709 Grassi M. F. Olavarria V. N. Kruschewsky R. A. Mascarenhas R. E. Dourado I. Correia L. C. . (2011). Human T cell lymphotropic virus type 1 (HTLV-1) proviral load of HTLV-associated myelopathy/tropical spastic paraparesis (HAM/TSP) patients according to new diagnostic criteria of HAM/TSP. J. Med. Virol. 83, 1269–1274. doi: 10.1002/jmv.22087, PMID: 21567429 Greatorex J. (2004). The retroviral RNA dimer linkage: different structures may reflect different roles. Retrovirology 1, 22. doi: 10.1186/1742-4690-1-22, PMID: 15317659 Grygorczuk S. Parczewski M. Świerzbińska R. Czupryna P. Moniuszko A. Dunaj J. . (2017). The increased concentration of macrophage migration inhibitory factor in serum and cerebrospinal fluid of patients with tick-borne encephalitis. J. Neuroinflammation 14, 126. doi: 10.1186/s12974-017-0898-2, PMID: 28646884 Habibabadi H. M. Parsania M. Pourfathollah A. A. Haghighat S. Sharifi Z. (2020). Association of TLR3 single nucleotide polymorphisms with susceptibility to HTLV-1 infection in Iranian asymptomatic blood donors. Rev. Soc. Bras. Med. Trop. 53, e20200026. doi: 10.1590/0037-8682-0026-2020, PMID: 32578708 Harvey C. E. Post J. J. Palladinetti P. Freeman A. J. Ffrench R. A. Kumar R. K. . (2003). Expression of the chemokine IP-10 (CXCL10) by hepatocytes in chronic hepatitis C virus infection correlates with histological severity and lobular inflammation. J. Leukoc. Biol. 74, 360–369. doi: 10.1189/jlb.0303093, PMID: 12949239 Hoffmann H. H. Schneider W. M. Rice C. M. (2015). Interferons and viruses: an evolutionary arms race of molecular interactions. Trends Immunol. 36, 124–138. doi: 10.1016/j.it.2015.01.004, PMID: 25704559 Kajiyama W. Kashiwagi S. Ikematsu H. Hayashi J. Nomura H. Okochi K. (1986). Intrafamilial transmission of adult T cell leukemia virus. J. Infect. Dis. 15, 851–857. doi: 10.1093/infdis/154.5.851, PMID: 2877031 Kalyanaraman V. S. Sarngadharan M. G. Nakao Y. Ito Y. Aoki T. Gallo R. C. (1982). Natural antibodies to the structural core protein (p24) of the human T-cell leukemia (lymphoma) retrovirus found in sera of leukemia patients in Japan. Proc. Natl. Acad. Sci. U.S.A. 79, 1653–1657. doi: 10.1073/pnas.79.5.1653, PMID: 6951204 Kamoi K. Mochizuki M. (2012). HTLV infection and the eye. Curr. Opin. Ophthalmol. 23, 557–561. doi: 10.1097/ICU.0b013e328358b9ec, PMID: 23047174 Kawai T. Akira S. (2010). The role of pattern-recognition receptors in innate immunity: update on Toll-like receptors. Nat. Immunol. 11, 373–384. doi: 10.1038/ni.1863, PMID: 20404851 Kindberg E. Vene S. Mickiene A. Lundkvist Å. Lindquist L. Svensson L. (2011). A functional Toll-like receptor 3 gene (TLR3) may be a risk factor for tick-borne encephalitis virus (TBEV) infection. J. Infect. Dis. 203, 523–528. doi: 10.1093/infdis/jiq082, PMID: 21216866 Kinpara S. Hasegawa A. Utsunomiya A. Nishitsuji H. Furukawa H. Masuda T. . (2009). Stromal cell-mediated suppression of human T-cell leukemia virus type 1 expression in vitro and in vivo by type I interferon. J. Virol. 83, 5101–5108. doi: 10.1128/JVI.02564-08, PMID: 19264779 Legrand N. McGregor S. Bull R. Bajis S. Valencia B. M. Ronnachit A. . (2022). Clinical and public health implications of human T-lymphotropic virus type 1 infection. Clin. Microbiol. Rev. 35, e0007821. doi: 10.1128/cmr.00078-21, PMID: 35195446 Levy D. E. Marié I. J. Durbin J. E. (2011). Induction and function of type I and III interferon in response to viral infection. Curr. Opin. Virol. 1, 476–486. doi: 10.1016/j.coviro.2011.11.001, PMID: 22323926 Li G. Zheng Z. (2013). Toll-like receptor 3 genetic variants and susceptibility to hepatocellular carcinoma and HBV-related hepatocellular carcinoma. Tumour Biol. 34, 1589–1594. doi: 10.1007/s13277-013-0689-z, PMID: 23404408 Livak K. J. Schmittgen T. D. (2001). Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) Method. Methods 25, 402–408. doi: 10.1006/meth.2001.1262, PMID: 11846609 Lopes F. T. de Sousa R. S. Carvalho Gomes J. L. Vallinoto M. C. de Lima A. C. R. Lima S. S. . (2022). The relevance of a diagnostic and counseling service for people living with HTLV-1/2 in a metropolis of the Brazilian amazon. Front. Public Health 10. doi: 10.3389/fpubh.2022.864861, PMID: 35419336 McGettrick A. F. O’Neill L. A. (2010). Localisation and trafficking of Toll-like receptors: an important mode of regulation. Curr. Opin. Immunol. 22, 20–27. doi: 10.1016/j.coi.2009.12.002, PMID: 20060278 Mickiene A. Laiskonis A. Günther G. Vene S. Lundkvist A. Lindquist L. (2002). Tickborne encephalitis in an area of high endemicity in Lithuania: disease severity and long-term prognosis. Clin. Infect. Dis. 35, 650–658. doi: 10.1086/342059, PMID: 12203160 Mohanty S. Harhaj E. W. (2023). Mechanisms of innate immune sensing of HTLV-1 and viral immune evasion. Pathogens 12, 735. doi: 10.3390/pathogens12050735, PMID: 37242405 Nagai M. Usuku K. Matsumoto W. Kodama D. Takenouchi N. Moritoyo T. . (1998). Analysis of HTLV-I proviral load in 202 HAM/TSP patients and 243 asymptomatic HTLV-I carriers: high proviral load strongly predisposes to HAM/TSP. J. Neurovirol. 4, 586–593. doi: 10.3109/13550289809114225, PMID: 10065900 Nakamura S. Nagano I. Yoshioka M. Shimazaki S. Onodera J. Kogure K. (1993). Detection of tumor necrosis factor-alpha-positive cells in cerebrospinal fluid of patients with HTLV-I-associated myelopathy. J. Neuroimmunol. 42, 127–130. doi: 10.1016/0165-5728(93)90001-f, PMID: 8429097 Neco H. V. P. D. C. Teixeira V. G. D. S. da Trindade A. C. L. Magalhães P. M. R. de Lorena V. M. B. Castellano L. R. C. . (2017). Mediators go together: high production of CXCL9, CXCL10, IFN-γ, and TNF-α in HTLV-1-associated myelopathy/tropical spastic paraparesis. AIDS Res. Hum. Retroviruses 33, 1134–1139. doi: 10.1089/AID.2016.0296, PMID: 28648091 Olindo S. Cabre P. Lézin A. Merle H. Saint-Vil M. Signate A. . (2006). Natural history of human T-lymphotropic virus 1-associated myelopathy: a 14-year follow-up study. Arch. Neurol. 63, 1560–1566. doi: 10.1001/archneur.63.11.1560, PMID: 17101824 Osame M. (2002). Pathological mechanisms of human T-cell lymphotropic virus type I-associated myelopathy (HAM/TSP). J. Neurovirol. 8, 359–364. doi: 10.1080/13550280260422668, PMID: 12402162 Osame M. Usuku K. Izumo S. Ijichi N. Amitani H. Igata A. . (1986). HTLV-I associated myelopathy, a new clinical entity. Lancet 1, 1031–1032. doi: 10.1016/s0140-6736(86)91298-5, PMID: 2871307 Paiva A. Casseb J. (2014). Sexual transmission of human T-cell lymphotropic virus type 1. Rev. Soc. Bras. Med. Trop. 47, 265–274. doi: 10.1590/0037-8682-0232-2013, PMID: 25075475 Pineda M. V. Bouzas M. B. Remesar M. Fridman A. Remondegui C. Mammana L. . (2019). Relevance of HTLV-1 proviral load in asymptomatic and symptomatic patients living in endemic and non-endemic areas of Argentina. PloS One 14, e0225596. doi: 10.1371/journal.pone.0225596, PMID: 31756234 Quaresma J. A. Yoshikawa G. T. Koyama R. V. Dias G. A. Fujihara S. Fuzii H. T. (2015). HTLV-1, immune response and autoimmunity. Viruses 8, 5. doi: 10.3390/v8010005, PMID: 26712781 Queiroz M. A. F. Amoras E. D. S. G. Moura T. C. F. da Costa C. A. de Sousa M. S. Lima S. S. . (2020). The SAMHD1 rs6029941 (A/G) polymorphism seems to influence the HTLV-1 proviral load and IFN-alpha levels. Front. Cell Infect. Microbiol. 10. doi: 10.3389/fcimb.2020.00246, PMID: 32656092 Rafatpanah H. Poursina Z. Boostani R. Marzouni H. Z. Atabaki M. Hosseini R. F. . (2021). A significant association between CXCL10–1447 A > G and IL18–607 C > A gene polymorphism with human T-cell lymphotropic virus type 1 associated myelopathy/tropical spastic paraparesis (HAM-TSP), a case-control report from city of Mashhad, Iran. J. Neurovirol. 27, 249–259. doi: 10.1007/s13365-021-00946-4, PMID: 33651323 Ranjith-Kumar C. T. Miller W. Sun J. Xiong J. Santos J. Yarbrough I. . (2007). Effects of single nucleotide polymorphisms on Toll-like receptor 3 activity and expression in cultured cells. J. Biol. Chem. 282, 17696–17705. doi: 10.1074/jbc.M700209200, PMID: 17434873 Rathinam V. A. Fitzgerald K. A. (2011). Innate immune sensing of DNA viruses. Virology 411, 153–162. doi: 10.1016/j.virol.2011.02.003, PMID: 21334037 Redondo N. Rodríguez-Goncer I. Parra P. Ruiz-Merlo T. López-Medrano F. González E. . (2022). Influence of single-nucleotide polymorphisms in TLR3 (rs3775291) and TLR9 (rs352139) on the risk of CMV infection in kidney transplant recipients. Front. Immunol. 13. doi: 10.3389/fimmu.2022.929995, PMID: 35967300 Rong Y. Song H. You S. Zhu B. Zang H. Zhao Y. . (2013). Association of Toll-like receptor 3 polymorphisms with chronic hepatitis B and hepatitis B-related acute-on-chronic liver failure. Inflammation 36, 413–418. doi: 10.1007/s10753-012-9560-4, PMID: 23076446 Russell R. S. Liang C. Wainberg M. A. (2004). Is HIV-1 RNA dimerization a prerequisite for packaging? Yes, no, probably? Retrovirology 1, 23. doi: 10.1186/1742-4690-1-23, PMID: 15345057 Santana E. G. M. Ferreira F. D. S. Brito W. R. D. S. Lopes F. T. de Lima A. C. R. Neto G. D. S. P. . (2024). TLR7 rs179008 (A/T) and TLR7 rs3853839 (C/G) polymorphisms are associated with variations in IFN-α levels in HTLV-1 infection. Front. Immunol. 15. doi: 10.3389/fimmu.2024.1462352, PMID: 39650644 Santos S. B. Porto A. F. Muniz A. L. de Jesus A. R. Magalhães E. Melo A. . (2004). Exacerbated inflammatory cellular immune response characteristics of HAM/TSP is observed in a large proportion of HTLV-I asymptomatic carriers. BMC Infect. Dis. 4, 7. doi: 10.1186/1471-2334-4-7, PMID: 15070424 Santos N. P. Ribeiro-Rodrigues E. M. Ribeiro-Dos-Santos A. K. Pereira R. Gusmão L. Amorim A. . (2010). Assessing individual interethnic admixture and population substructure using a 48-insertion-deletion (INSEL) ancestry-informative marker (AIM) panel. Hum. Mutat. 31, 184–190. doi: 10.1002/humu.21159, PMID: 19953531 Schierhout G. McGregor S. Gessain A. Einsiedel L. Martinello M. Kaldor J. (2020). Association between HTLV-1 infection and adverse health outcomes: a systematic review and meta-analysis of epidemiological studies. Lancet Infect. Dis. 20, 133–143. doi: 10.1016/S1473-3099(19)30402-5, PMID: 31648940 Schoggins J. W. Wilson S. J. Panis M. Murphy M. Y. Jones C. T. Bieniasz P. . (2011). A diverse range of gene products are effectors of the type I interferon antiviral response. Nature 472, 481–485. doi: 10.1038/nature09907, PMID: 21478870 Silva I. C. Pinheiro B. T. Nobre A. F. S. Coelho J. L. Pereira C. C. C. Ferreira L. S. C. . (2018). Moderate endemicity of the human T-lymphotropic virus infection in the metropolitan region of Belém, Pará, Brazil. Rev. Bras. Epidemiol. 21, e180018. doi: 10.1590/1980-549720180018, PMID: 30328937 Singh A. K. Prakash S. Garg R. K. Jain P. Kumar R. Jain A. (2021). Study of single nucleotide polymorphisms in endosomal toll-like receptors-3, 7, and 9 genes in patients with dengue: A case-control study. Cureus 13, e14883. doi: 10.7759/cureus.14883, PMID: 34113509 Singh H. Samani D. (2022). TLR3 polymorphisms in HIV infected individuals naïve to ART. Curr. HIV Res 20, 397–407. doi: 10.2174/1570162X20666220908105434, PMID: 36089778 Sironi M. Biasin M. Cagliani R. Forni D. De Luca M. Saulle I. . (2012). A common polymorphism in TLR3 confers natural resistance to HIV-1 infection. J. Immunol. 188, 818–823. doi: 10.4049/jimmunol.1102179, PMID: 22174453 Starling A. L. Martins-Filho O. A. Lambertucci J. R. Labanca L. de Souza Pereira S. R. Teixeira-Carvalho A. . (2013). Proviral load and the balance of serum cytokines in HTLV-1-asymptomatic infection and in HTLV-1-associated myelopathy/tropical spastic paraparesis (HAM/TSP). Acta tropica. 125, 75–81. doi: 10.1016/j.actatropica.2012.09.012, PMID: 23022356 Takeda K. Akira S. (2005). Toll-like receptors in innate immunity. Int. Immunol. 17, 1–14. doi: 10.1093/intimm/dxh186, PMID: 15585605 Tamegão-Lopes B. P. Rezende P. R. Maradei-Pereira L. M. de Lemos J. A. (2006). HTLV-1 and HTLV-2 proviral load: a simple method using quantitative real-time PCR. Rev. Soc. Bras. Med. Trop. 39, 548–552. doi: 10.1590/s0037-86822006000600007, PMID: 17308700 Taylor G. P. Tosswill J. H. Matutes E. Daenke S. Hall S. Bain B. J. . (1999). Prospective study of HTLV-I infection in an initially asymptomatic cohort. J. Acquir. Immune Defic. Syndr. 22, 92–100. doi: 10.1097/00042560-199909010-00012, PMID: 10534152 Uematsu S. Akira S. (2007). Toll-like receptors and Type I interferons. J. Biol. Chem. 282, 15319–15323. doi: 10.1074/jbc.R700009200, PMID: 17395581 van Montfoort N. Olagnier D. Hiscott J. (2014). Unmasking immune sensing of retroviruses: interplay between innate sensors and host effectors. Cytokine Growth Factor Rev. 25, 657–668. doi: 10.1016/j.cytogfr.2014.08.006, PMID: 25240798 Vercammen E. Staal J. Beyaert R. (2008). Sensing of viral infection and activation of innate immunity by toll-like receptor 3. Clin. Microbiol. Rev. 21, 13–25. doi: 10.1128/CMR.00022-07, PMID: 18202435 Watts J. M. Dang K. K. Gorelick R. J. Leonard C. W. Bess J. W. Jr. Swanstrom R. . (2009). Architecture and secondary structure of an entire HIV-1 RNA genome. Nature 460, 711–716. doi: 10.1038/nature08237, PMID: 19661910 Xagorari A. Chlichlia K. (2008). Toll-like receptors and viruses: induction of innate antiviral immune responses. Open Microbiol. J. 2, 49–59. doi: 10.2174/1874285800802010049, PMID: 19088911 Yamauchi J. Araya N. Yagishita N. Sato T. Yamano Y. (2021). An update on human T-cell leukemia virus type I (HTLV-1)-associated myelopathy/tropical spastic paraparesis (HAM/TSP) focusing on clinical and laboratory biomarkers. Pharmacol. Ther. 218, 107669. doi: 10.1016/j.pharmthera.2020.107669, PMID: 32835825 Zhang Y. Liu B. Ma Y. Yi J. Zhang C. Zhang Y. . (2014). Hantaan virus infection induces CXCL10 expression through TLR3, RIG-I, and MDA-5 pathways correlated with the disease severity. Mediators Inflamm. 2014, 697837. doi: 10.1155/2014/697837, PMID: 24701034 Zhou P. Fan L. Yu K. D. Zhao M. W. Li X. X. (2011). Toll-like receptor 3 C1234T may protect against geographic atrophy through decreased dsRNA binding capacity. FASEB J. 25, 3489–3495. doi: 10.1096/fj.11-189258, PMID: 21712495