Many polymers are engineered as nanoparticle-based vaccine delivery platforms because of their biodegradability, biocompatibility, durability, and low toxicity. Polymers are extremely modifiable, hence their physiochemical properties can be readily modified to enhance their immunomodulatory effects (Bose et al., 2019). Polymeric nanoparticles enhance prolonged antigen delivery due to their increased stability in vivo (Thorp et al., 2020). This category can be further divided into two groups: natural and synthetic polymeric nanoparticles. Natural polymeric nanoparticles are further divided into poly glutamic acid-based nanoparticles and polysaccharide-based nanoparticles including chitosan, starch, alginate, and cellulose (Han et al., 2018). Chitosan-based nanoparticle vaccines, alginate-based nanoparticle vaccines, and their derivatives are the most studied polymeric materials as delivery platforms for vaccines against STIs, as well as other infectious diseases (Han et al., 2018; Bose et al., 2019). Many of these preclinical studies have shown the immunomodulatory effects of such nanoparticle-based vaccines against STIs. For example, several chitosan-based nanoparticle vaccines and therapies known for their intrinsic bio-adhesive properties have been shown to prolong interaction and contact duration with immune cells, which enhances their immunomodulatory effects (Prego et al., 2010; Zhao et al., 2013; Pradines et al., 2015; Rose et al., 2018). Synthetic polymeric nanoparticles include polyphosphazene, poly (glycolic acid) (PGA), poly (lactic acid) (PLA) and poly (DL-lactide-co-glycolic) acid (PLGA), poly (allymines)s, cell-penetrating poly (disulfide)s, and copolymer-based nanoformulations (Bose et al., 2019). Of all the synthetic polymeric nanoparticles, PLGA, a copolymer synthesized by the random polymerization of PLA and PGA, has been the extensively researched for vaccine delivery applications (Aikins et al., 2017).

Protein‐based nanoparticles are highly biodegradable and possess other properties including biocompatibility, biofunctionality, the ability to interact with other molecules for recognition, and their adaptive potential for genetic engineering for specific cell targeting and targeted protein delivery. They are known to exit the vasculature, enter the lymphatic system and permeate tissues through passive diffusion, making them highly beneficial as antigen delivery platforms. Protein-based nanoparticles are made by self‐assembly and desolvation. Examples of proteins that can be used for the fabrication of nanoparticles include collagen, albumin, elastin, gelatin, casein, whey proteins, silk proteins, soy proteins, and lectins (Young Kim et al., 2015; Qin et al., 2019). Some structurally complex and defined protein‐based nanoparticles include virus-like nanoparticles (VLPs), protein cages, and protein-based complexes (Diaz et al., 2018; Nguyen and Tolia, 2021). VLPs are derived from plant, microbial, insect, and mammalian viruses, without the viral genome itself, and are easily internalized by cells (Zeltins, 2013). VLPs are formed from the autonomous oligomerization or self-assembly of monomeric protein building blocks. These protein building blocks assemble into larger, stable and highly ordered structures that can be engineered to have a diameter ranging from 20 to 100 nm and possess unique physical properties (López-Sagaseta et al., 2016). Protein cages on the other hand include viral capsids, ferritins, and heat shock proteins, while protein-based complexes include Cry3Aa fusion protein platform (well known for the delivery of reporter proteins such as GFP in mammalian cells), silk proteins, and bovine serum albumin (Nair et al., 2015; Qin et al., 2019).

In cancer vaccine studies, peptide and protein-based vaccines typically fail to induce efficient immune responses against tumors. However, delivery of the peptides and proteins encapsulated in protein nanoparticles has shown promising improvements in vaccine efficacy characterized by increased immunogenicity of the tumor microenvironment. The highly organized structures and symmetry of protein nanoparticles as well as their ability to have specific functions inside or outside or in between subunits of the protein cage allows for the co-delivery of adjuvants and antigens that promotes antigen-specific immune responses against tumors (Neek et al., 2019). A ferritin nanoparticle vaccine was investigated for its ability to present N. gonorrhoeae peptide antigens on its surface. The N. gonorrhoeae peptides were inserted at the N terminus or in a surface-exposed ferritin loop between helices αA and αB. While crystal structures of the chimeric proteins from this study showed that the proteins were assembled correctly into a 24-mer nanocage structure, the inserted N. gonorrhoeae peptides were disordered on the nanocage surface showing multiple conformations (Wang et al., 2017). Protein nanoparticles have been utilized in many preclinical vaccine studies for hepatitis B, HPV and HIV with promising outcomes including the induction of antigen specific antibodies and viral clearance in animal models (Kirnbauer et al., 1992; Oh et al., 2004; Slupetzky et al., 2007; Paz De la Rosa et al., 2009; Tyler et al., 2014; Sliepen et al., 2015; Motevalli et al., 2018; Tokatlian et al., 2019; Wang et al., 2020; Ximba et al., 2020). These studies confirm the need for more extensive research to harness the potential of protein nanoparticles for vaccines against bacterial STIs that will allow for effective delivery of antigenic peptides and adjuvants.

Most lipid‐based nanoparticles are derived from dietary oils or fats and are sometimes referred to as solid lipid nanoparticles based on their inclusion of lipids that exist as a solid phase at physiological temperatures. They include nanoemulsions, micelles, bicelles (bilayered discoidal micelles) and liposomes made from natural, semi‐synthetic or synthetic lipids, such as fatty acids, fatty alcohols, phospholipids, and medium and long chain mono-, di- and triglycerides. Lipid‐based nanoparticles are regarded as promising delivery platforms due to their ability to bypass multiple biological barriers, low toxicity, biocompatibility, and biodegradability (Niu et al., 2016; Qin et al., 2019).

Lipid-based nanoparticles have been used for the delivery of antigens including nucleic acids and proteins of infectious agents as well as cancer therapeutic agents to induce humoral immune responses (Aldosari et al., 2021; Lee et al., 2021; Park et al., 2021). These lipid-based nanocarriers pass through the cell membrane for cellular uptake by macropinocytosis, a type of endocytosis where they must escape from the endosomal lumen to deliver their enclosed antigens into the cytosol (Guevara et al., 2020; Lee et al., 2021). While ionizable lipid pK _a was thought to be the main factor involved in driving lipid nanoparticle potency and tolerability due to its effects on opsonization of the particles, cellular uptake and endosomal escape efficiency, it has been shown that other factors play a role in the immunogenicity of lipid nanoparticles (Hassett et al., 2019). Hence, a better understanding of mechanisms that regulate the biodistribution of antigen-loaded lipid nanoparticles will guide research outcomes for optimizing lipid nanoparticles as delivery systems.

Hybrid nanoparticles incorporate key constituents from at least two different nanoparticle classes, leveraging the beneficial attributes of each to enhance their functionality. Hybrid nanoparticles include lipid-polymer hybrid nanoparticles, protein-dendrimer hybrid nanoparticles and high-density lipoprotein (HDL) mimetics (Qin et al., 2019). Lipid–polymer hybrid nanoparticles are core–shell nanoparticle structures made of polymer cores and lipid/lipid–PEG shells that show complementary properties in their biocompatibility and physical stability from both polymeric nanoparticles and liposomes (Hadinoto et al., 2013). Lipid–polymer hybrid nanoparticles exhibit higher in vivo cellular delivery when compared to either polymeric nanoparticles or liposomes. The formulation of lipid–polymer hybrid nanoparticles with chitosan has been shown to significantly increase mucosal immune responses against some STIs (Hadinoto et al., 2013; Rose et al., 2018).

In recent years newly engineered nanoparticles known as nanolipoproteins (NLPs), which are HDL mimetics consisting of discoidal lipid bilayer stabilized by apolipoproteins have been in development with desirable attributes for vaccine delivery. NLPs also known as nanodiscs are effective antigen carriers and supporting adjuvants that improve vaccine performance against infectious diseases. We have previously demonstrated that the use of NLPs enhances immune responses to both antigen and adjuvants in vivo (Fischer et al., 2013; Weilhammer et al., 2013; Weilhammer et al., 2017; Weilhammer et al., 2020). We have demonstrated that NLPs provide a membrane-like environment, which facilitate the embedding of functional membrane-bound proteins in their native conformations (He et al., 2017; Tifrea et al., 2021). The versatility of this type of nanoparticle underscores its potential for vaccines targeting bacterial and viral STIs.

Inorganic nanoparticles include silica nanoparticles, metal nanoparticles (gold, silver, magnetic, metal organic framework-based nanoparticles), carbon-based nanomaterials (carbon nanotubes, nano-diamonds), and superparamagnetic nanoparticles (iron oxide nanoparticles). These nanoparticles are usually coated with organic molecules to make them biologically suitable as well as prevent particle aggregation. Commonly used inorganic nanoparticles for vaccine formulations include silver and gold nanoparticles. Gold nanoparticles are easily internalized by APCs and can facilitate their activation and elicit downstream immune responses, making them suitable platforms for antigen delivery (Bastús et al., 2009; Wang et al., 2018; Al-Halifa et al., 2019). A wide range of antigens and adjuvants can be conjugated on gold nanoparticles at high densities to prolong antigen delivery, improve immunogenicity as well as antigen presentation (Marques Neto et al., 2017). Although gold nanoparticles are a great platform for antigen conjugation, their ability to accumulate in organs such as the liver for long periods could ultimately result in toxicity (Arvizo et al., 2010). Coating with biocompatible materials has been shown to reduce their toxicity, although there is risk of alterations to their physicochemical and biological properties (Zhu et al., 2014).

C. trachomatis is significant to human health worldwide (Paavonen and Eggert-Kruse, 1999; Dean, 2009; World Health Organization, 2018) as it remains the most diagnosed STI in developed countries despite the availability of effective and affordable therapy. Chlamydia exists either as an extracellular elementary body (EB), which is the non-replicating, infectious form or as a reticulate body (RB), the noninfectious form that replicates intracellularly (Nans et al., 2015; Elwell et al., 2016; Fischer and Rudel, 2018). The infection is mostly asymptomatic but can induce inflammatory responses at the site of infection, causing immunopathological sequelae such as pelvic inflammatory disease (PID), ectopic pregnancy, tubal infertility, miscarriage, and trachoma (an ocular disease) (Stamm, 1999; Vasilevsky et al., 2016; Lijek et al., 2018; Murthy et al., 2018). This has led to over 70 years of research dedicated to the development of vaccines that will provide adequate protection against C. trachomatis infection (Phillips et al., 2019). Chlamydial vaccines have utilized numerous approaches to improve vaccine immunogenicity, including the use of plasmid DNA, recombinant proteins, and subunit antigenic determinants, with or without adjuvants, yet the need for effective preventive measures remains unmet (Brunham and Rey-Ladino, 2005; Vasilevsky et al., 2014). Studies have indicated a critical role for chlamydia-specific CD4⁺ Th1 T cell responses in the clearing of infection and provision of protective immunity against chlamydia reinfection (Su and Caldwell, 1995; Gondek et al., 2012; Bakshi et al., 2018; Labuda and McSorley, 2018). The chlamydial major outer membrane protein (MOMP) has been shown to induce an immune response comparable to that seen with live bacteria in mice (Pal et al., 2005), while polymorphic membrane proteins (PMPs), have been explored for their ability to induce cross-species immunogenicity (Pal et al., 2017). MOMP and PMPs have been investigated as vaccine antigens in mice and nonhuman primates. Both antigens have shown suboptimal protection in many studies (Kari et al., 2009; Vasilevsky et al., 2016), hence the search for effective antigen-adjuvant combinations that can induce broad and long-lived protective immune responses continues (de la Maza et al., 2017).

The use of nanotechnology in the development of C. trachomatis vaccines is a promising strategy to enhance the production of long-lived immune protection. Preclinical studies exploring nanoparticle-based vaccines have shown effective delivery of immunogens and the induction of chlamydia-specific immune responses that will be beneficial in translational medicine. Chitosan nanoparticles possess the required size necessary to facilitate uptake by APCs for the induction of immune responses. They are shown to have high encapsulation capacity for stability and antigen protection from enzymatic digestion, making them favorable delivery platforms for chlamydial nucleic acids such as MOMP DNA constructs (Cambridge et al., 2013). Recombinant C. trachomatis fusion antigen CTH522 adjuvanted with glycol-chitosan-coated lipid-polymeric hybrid nanoparticle was shown to induce antigen-specific mucosal immune responses in the lungs and genital tract of mice, characterized by CTH522-specific IgG/IgA antibodies and IFN-γ-producing Th1 cells after nasal immunization (Rose et al., 2018).

PLGA nanoparticles have been extensively explored as vaccine delivery platforms due to their self-adjuvanting properties whereby they possess both antigenic and an adjuvanting moieties, their ability to prolong the release of antigens to stimulate dendritic cells as well as enhance intracellular antigen delivery to activated T-cells via the CD40 co-stimulation mechanism (Makadia and Siegel, 2011; Sneh-Edri et al., 2011; Rosalia et al., 2015). The lactide/glycolide ratio of PLGA nanoparticles is critical for efficient encapsulation and prolonged delivery of both antigens or drugs (Sahu et al., 2020), and PLGA nanoparticles at an 85:15 ratio used for the encapsulation of recombinant MOMP (PLGA-rMOMP) enhanced the activation of dendritic cells, induced chlamydia-specific rMOMP CD4⁺ memory and effector T-cells and activated an antibody adaptive immune response in immunized mice. Mice immunized intranasally with PLGA-rMOMP generated enhanced numbers of CD4⁺ T-cells but not memory and effector T-cells, whereas subcutaneously immunized mice produced both CD4⁺ memory and effector T-cells (Sahu et al., 2020), demonstrating the importance of vaccination route to the resulting immune response. The extended release of rMOMP in this PLGA-rMOMP formulation provided protective immunity against C. muridarum genital challenge and rechallenge (Sahu et al., 2021). PLGA (85:15) nanoparticle encapsulating rMOMP-187 (a peptide derivative of MOMP) induced a significant production of interleukin (IL)-6, IL-12p40, Th1/Th17 cytokines and nitric oxide (NO) by mouse J774 macrophages in a dose dependent manner and with minimal toxicity (Taha et al., 2012). In another preclinical vaccine study, spleen cells from BALB/c mice immunized with PLGA-rMOMP exhibited higher numbers of CD4⁺ and CD8⁺ T-cells and an increased secretion of IFN-γ (Th1) and IL-12p40 versus IL-4 and IL-10 (Th2) cytokines in response to restimulation with purified rMOMP, as well as immunized mice producing higher serum IgG and IgG2a (Th1) than IgG1 (Th2) rMOMP-specific antibodies (Fairley et al., 2013). The ability of PLGA-rMOMP to induce Th1 immune responses in mice makes it an extremely suitable nanoparticle-based vaccine candidate against C. trachomatis to be explored for translational studies.

The encapsulation of chlamydial antigens in Poly (lactic acid)-poly (ethylene glycol) or PLA-PEG, another self-adjuvating, biodegradable co-polymeric nanoparticle, has been shown to induce potent anti-C. trachomatis immune responses. M278, a recombinant peptide derived from C. trachomatis MOMP encapsulated in PLA-PEG, showed an enhancement of long-lasting chlamydia-specific CD4⁺ T-cell effector responses facilitated by caveolin-mediated endosomal antigen processing and MHC class II-dependent antigen presentation (Dixit et al., 2018). More specifically, there was an enhanced expression of pathogen-sensing receptors, such as TLR2 and Nod1, surface activation markers, including, Cd1d2 and Fcgr1, effector cytokines and chemokines, MHC class I and II molecules, as well as co-stimulatory molecules including CD40, CD80 and CD86 (Dixit et al., 2018). Subcutaneous immunization of M278 encapsulated in PLA-PEG was shown to induce secretion of IFN-γ, resulting in the differentiation of chlamydia-specific CD4⁺ T-cells to memory and effector phenotypes. Significant protection of immunized mice characterized by reduced vaginal bacterial loads after a genital tract challenge was observed and associated to elevated mucosal IgG1 and MOMP-specific IgA in the mice. Additionally, immune sera with functional neutralizing antibodies collected from mice immunized with PLA-PEG-encapsulated M278 prevented the infection of McCoy cells by C. muridarum (Verma et al., 2018). In another study, mice immunized with PLA-PEG encapsulated M278 generated higher T-cell cytokines [Th1 (IFN-γ, IL-2), Th17 (IL-17)] and antibodies [Th1 (IgG2a), Th2 (IgG1, IgG2b)] when compared to mice immunized with unencapsulated M278 (Dixit et al., 2014).

We recently encapsulated MOMP from C. muridarum (mMOMP) in the membrane-like environment of NLPs and demonstrated that vaccination with MOMP-NLPs provided a balanced T cell response with partial protection in a respiratory challenge model (He et al., 2017; Tifrea et al., 2021). We used an Escherichia coli-based cell-free system to express a MOMP protein from C. muridarum (mMOMP) and supported it within a telodendrimer nanolipoprotein particle (mMOMP–tNLP) co-localized with CpG oligodeoxynucleotide 1826 (CpG), a single-stranded synthetic DNA adjuvant, functionalized with a cholesterol tag to enable conjugation to the lipid nanoparticle. This mMOMP-tNLP complex induced an enhanced antigen-specific IgG response in vaccinated mice (He et al., 2017; Tifrea et al., 2021). We first reported a C. muridarum-exosomes vaccine formulated with CpG plus Montanide as adjuvants that elicited robust Th1 humoral and cell-mediated immune responses against a respiratory challenge with C. muridarum EB in vaccinated mice as well as producing high levels of C. muridarum-specific neutralizing antibodies in their serum (Pal et al., 2020).

In another study, a peptide derived from Pmp-G, a chlamydial polymorphic membrane protein, which functions as an autotransporter adhesin and plays an essential role in the initial phase of chlamydial infection (Vasilevsky et al., 2016) was encapsulated in vault nanoparticles, made from a natural nanocapsule engineered from hollow barrel-shaped eukaryotic ribonucleoprotein complexes. This vaccine formulation was shown to significantly reduce the genital bacterial burden and histopathologic inflammation in immunized mice following a C. muridarum challenge. Protection correlated with the induction of a systemic antigen-specific cellular immune response, characterized by an increase in PmpG-specific splenic CD4⁺ central memory T-cells and IFN-γ+ natural killer (NK) cells, a decrease in the number of inflammatory cells, such as neutrophils and TNF-α+ CD8⁺ T-cells in the genital tract, and the secretion of IFN-γ, TNF-α, IL-17, and IL-2 by splenic CD4⁺ T-cells (Jiang et al., 2017). Lastly, the self-assembly of lipid phytantriol and the immunopotentiator monomycoloyl glycerol-1 into nanocarriers with an internal hexagonal phase encapsulating chlamydial MOMP induced stronger MOMP-specific IgG humoral responses and antigen-specific CD4⁺ T-cell responses than MOMP surface-adsorbed to CAF04 liposome [a cationic liposomal adjuvant formulation containing monomycolyl glycerol [MMG] and N,N-dimethyl-N,N-dioctadecylammonium (DDA)] or unadjuvanted MOMP in immunized mice. However, CAF04 liposomes elicited more robust effector T-cell responses than the MOMP encapsulated nanocarrier, suggesting that the nanostructural composition of the lipid-based delivery system exerts a significant impact on both the type and magnitude of the induced immune responses (Rodrigues et al., 2018). Reports from the phase I clinical trial of the first in-human vaccine against C. trachomatis infections has shown that the use of CTH522 adjuvanted with either CAF01, a cationic liposomal adjuvant or aluminum hydroxide was safe and well tolerated (Abraham et al., 2019) (NCT02787109). While further investigation is needed, positive results from this first clinical trial showed that CTH522 formulated with CAF01 induced better humoral immunogenicity than CTH522 formulated with aluminum hydroxide (Abraham et al., 2019). These results led to another phase I clinical trial for trachoma (NCT03926728) and indicates a bright future for nanoparticle-based vaccines against C. trachomatis.

As with other human STIs, there is an urgent need for the development of efficacious vaccines against the spirochete Treponema pallidum, etiological agent for the multistage STI syphilis. Syphilis is the cause of STI-related deaths, second to only acquired immune deficiency syndrome (AIDS) (Zhao et al., 2011; Zhao et al., 2013). Syphilis exhibits alternating asymptomatic and symptomatic disease stages with different clinical manifestations. It is associated with systemic disease ranging from multiple organ impairment in adults to adverse pregnancy outcomes including abortions, premature births, stillbirths, and congenital diseases (Walker et al., 2019). Although penicillin has been an effective treatment for syphilis, its effectiveness depends on such limitations as accurate diagnosis, patient compliance, drug availability, and disease stage (Cameron and Lukehart, 2014). Hence, the need for efficacious vaccine formulations that will prevent infection and provide robust protection against all T. pallidum strains remains.

Despite the critical need for effective vaccines against T. pallidum, only a limited number of preclinical vaccine studies were conducted for decades, partly due to the fragility of the T. pallidum outer membrane proteins (OMPs) and limited research on T. pallidum biology. Current vaccine studies are investigating the role of OMPs in the induction of opsonization and phagocytosis, as well as their role as potentiators of T. pallidum virulence. Some of these studies utilized conventional vaccine strategies such as whole cell attenuated, aged, and γ-irradiated T. pallidum, while other studies have utilized T. pallidum specific antigens for immunization. However, only rabbits immunized with γ-irradiated T. pallidum, Nichols strain, over a 37-week period were shown to be fully protected against challenge with homologous treponemes but with no protection against challenge with the T. pallidum subspecies pallidum strain (Lithgow and Cameron, 2017). Significantly reduced bacterial organ burden in immunized rabbits after a T. pallidum challenge was seen in a recent study that utilized Tp0751 (a vascular adhesin of T. pallidum subspecies pallidum) as a vaccine candidate against the T. pallidum subspecies pallidum strain. The transfer of popliteal lymph nodes from Tp0751-immunized, T. pallidum-challenged rabbits to naive rabbits also conferred sterile protection against a T. pallidum-challenge (Lithgow et al., 2017). While these studies were conducted in the absence of nanoparticle formulations, these promising findings suggest that nanoparticles vaccine carriers combining these protective T. pallidum antigens with adjuvants could provide efficacious vaccine formulations with robust protection against all T. pallidum strains.

To date, the only nanoparticle-based vaccine studies against T. pallidum have utilized plasmids expressing IL-2 and Tp92, a T. pallidum OMP, encapsulated in chitosan nanoparticles individually or in combination. Both the IL-2 and Tp92 plasmid-encapsulated chitosan nanoparticle-based vaccines increased anti-Tp92 antibody levels while the combination of both plasmids encapsulated in chitosan nanoparticles showed the greatest amplification of anti-Tp92 antibodies and T-cell proliferation, which resulted in significant protection against challenge with T. pallidum in immunized male New Zealand white rabbits (Zhao et al., 2011). Similar effects were seen with T. pallidum Gpd DNA vaccine adjuvanted with IL-2 and chitosan nanoparticles (Zhao et al., 2013). These findings indicate promising vaccine outcomes from DNA complexed with nanoparticles and the need for more research on developing T. pallidum vaccines.

Neisseria gonorrhoeae is the bacterial agent responsible for the STI gonorrhea that poses a critical public health problem worldwide due to its resistance to multiple antimicrobials (Rowley et al., 2019). Infection with N. gonorrhoeae is often asymptomatic but can lead to serious complications in both men and women including urethritis, cervicitis, proctitis, pelvic inflammatory diseases, chronic pelvic pain, infertility, ectopic pregnancy, and increased susceptibility to acquiring HIV (Workowski et al., 2008; Li et al., 2013; Rice et al., 2017). The development of effective vaccine candidates against gonococcal infection is critical for the prevention and eradication of gonorrhea; however, the extraordinary ability of N. gonorrhoeae to change its surface antigen composition, and a lack of knowledge regarding protective correlates of immunity in humans significantly complicates vaccine development (Rotman and Seifert, 2014; Edwards et al., 2016; Gulati et al., 2019; Russell et al., 2019). Some of the gonococcal surface antigens that have been considered as vaccine targets include the porin PorB, lipo-oligosaccharide glycan structures, type IV gonococcal surface pili, and gonococcal colony opacity-associated (Opa) proteins (Russell et al., 2019).

While the nanotechnology-based preclinical studies have focused on therapeutic approaches against N. gonorrheae (Li et al., 2013; Lucío et al., 2020), in this study (Gala et al., 2018), the microparticles were made containing spray dried, inactivated whole-cell gonococci strain CDC-F62 loaded in biodegradable crosslinked albumin-based particulate matrix for prolonged slow antigen release. This novel nanovaccine was administered transdermally to 6–8-week-old Swiss Webster female mice using biodegradable microneedle skin patches. The immune response of vaccinated mice was monitored for 10 weeks starting immediately after the prime vaccination, followed by two booster vaccination regimens, scheduled 1 week apart. When compared to either subcutaneous or microneedle transdermal administration of N. gonorrhoeae antigen in suspension, the novel nanovaccine induced a higher antigen-specific IgG antibody titer from week 2 with significantly higher titers at weeks 6 and 8. At week 10, all three vaccinated groups had significantly higher levels of antigen-specific CD4⁺ and CD8⁺ T lymphocytes when compared to empty microneedles and unvaccinated mice (Gala et al., 2018). Although this whole-cell-based nanovaccine did not address the current challenge of N. gonorrhoeae immune evasion due to surface antigen mutations, this preclinical study opens an avenue for the possibility of N. gonorrhoeae infection prevention with nanoparticle-based vaccines, where multiple N. gonorrhoeae strains with different immunogenic epitopes can be packaged and delivered in a nanocarrier. If successful, such a nanoparticle-based vaccine will limit immune evasion by providing protection against potential N. gonorrhoeae strains, eliminate the strenuous processes involved in the identification of a single immunogenic epitope, and ultimately reduce the rate of acquiring multi-drug resistant infections. Hence, further exploration of the immunopotentiating capacity of nanoparticle-based vaccines for novel strategies will be essential for the development of vaccines capable of overcoming the adaptive capability of N. gonorrhoeae.