For this narrative review, a systematic literature search was performed in PubMed and Web of Science database in August 2023, using the following search strategy: “(((((((platelet rich plasma) OR (PRP)) OR (platelet lysate)) OR (PL)) OR (platelet rich fibrin))) OR (PRF)) AND (macrophage polarization)”. Papers were excluded if: 1) the article was written in any language other than English or Spanish 2) duplicates 3) reviews, perspectives, editorials, commentaries, thesis, book chapters 4) no full-text available 5) out of scope 6) did not include macrophages 7) did not include PRP, PRF, PL or similar.

Studies that passed the initial title and abstract evaluation were retrieved for full-text review. For data extraction, an evidence table was created with Microsoft Excel. The following data were included: author and year of publication, study type, field of application, macrophages’ origin, platelet derivatives’ issues (type, origin, sample size, type of anticoagulant, conditions of centrifugation, presence or absence of leukocytes, type of activator), comparison groups, macrophage polarization and summary results.

The reporting quality and the risk of bias were assessed according to the criteria reported by Golbach et al. (53). The reporting quality was determined by the presence (“yes/partly”) or absence (“no”) of critical information. According to the answers (yes”, “partly”, or “no”), the risk of bias was divided into 3 categories: low, moderate and high, respectively.

The reporting quality showed large differences ( Figure 2 ). The lack of information regarding sample size, PRP obtaining process and PRP composition had the greatest impact on the reporting quality as 70%, 66% and 63% of the studies, respectively, did provide partial or no information on these issues. Concerning the risk of bias, the risk associated with the selection bias was the highest detected risk, as only 36% of the articles did specify that animals were randomly assigned.

The great variability of PRP composition and preparation protocols leads to a myriad of biologically distinct products. This issue along with the lack of information in the literature, makes challenging the comparison of results (81, 82). In fact, details such as the sample size, the type of anticoagulant and activator, centrifugation conditions or the composition were often missing in this review. Fifty-nine percent of the articles used PRP in their assays compared to 19% and 15% that used PRF or PL, respectively ( Figure 3A ). Table 2 describes the conditions for obtaining the different platelet derivatives. In only 8 out 27 articles (55, 56, 64, 65, 72, 77–79) were these conditions fully defined. Of those, Cenni et al. (55), Escobar et al. (56), Nishio et al. (65) and Yu et al. (78) completely detailed the cellular composition which was also fully described in other articles (60, 66, 67, 74, 75, 80) where the obtaining protocol was not totally detailed. The origin was human or murine except in two of the articles that PRP from rabbit and mouse (60) or ovine (76) was used. Most used double centrifugation (n = 14) versus single (n = 6). Qian et al. (69) even used both centrifugation methods depending on the type of platelet derivative to be obtained. However, in this regard, conditions such as centrifugal force, speed and time were extremely varied, with as many different protocols as studies. Concerning the cellular composition, 33% of the articles did not provide information about the presence of leukocytes in their studies. Among those that did detail this issue (presence of leukocytes), the majority did not include leukocytes (n = 10), compared to the others (n=6) in which the leukocytes were included. Moreover, the study proposed by Uchiyama et al. (74) was the only one that had two types of platelet derivatives tested, with and without leukocytes, while Kargarpour et al. (61) evaluated several fractions from liquid PRF containing different composition.

As reflected in the data shown in Table 1 , most of the studies used murine macrophages (n = 15), compared to 41% that used human macrophages (n = 11). Only one article used macrophages of ovine origin (76). Regarding the type of macrophages in in vitro studies, tissue resident macrophages were used in only two articles (59, 61) compared to the rest of the studies that used monocyte derived macrophages. Macrophage isolation, culture, differentiation and polarization protocols greatly differed among studies ( Table 3 ). The immunoregulatory effect of platelet derivatives was assessed in several fields of application such as tissue, bone and tendon regeneration, osteoarthritis, cardiovascular diseases, intervertebral disc degeneration, nerve and osteochondral regeneration and skin repair ( Figure 3B ). Although the reported results being diverse, the treatment with platelet derivatives stimulated macrophages to exhibit a reparative phenotype in most of the studies (n = 21) ( Figure 3C ).

Research in human macrophages were performed in 11 articles. In 8 of which a polarization towards the reparative phenotype (M2) was reported after treatment with the platelet derivatives (55, 56, 58, 63, 67, 71, 74, 77). Cenni et al. (55) specified that their PRP impaired osteoclast formation, which is typical of the M2 phenotype. On the contrary, a pro-inflammatory effect was described in only 2 articles (66, 73); however, certain peculiarities must be taken into account, as O´Donnell et al. (66) evaluated a PRP obtained from OA patients and the results reported by Tylek et al. (73) refer to the co-culture of macrophages with mesenchymal stem cells. Both, a hybrid M1/M2 phenotype and a non-polarized state was described by GraÇa et al. (57) according to the type of extracellular vesicle. All the research conducted in this section evaluated the effect of PRP in vitro. Only Yadav et al. (77) did it also in vivo.

Cenni et al. (55) evaluated the effect of bovine thrombin and calcium gluconate-activated PRP on human osteoclasts. Osteoclastogenesis is a multi-step process that requires the delicate coordination of osteoclast progenitors. In this sense, M-CSF (macrophage colony stimulating factor) promotes proliferation of the osteoclast precursor cells and RANKL (receptor activator of NFκB ligand) controls their differentiation (84, 85). Therefore, the authors analyzed the ability of PRP supernatant to influence on osteoclast precursors, both with and without RANKL and M-CSF. They concluded that PRP showed different effects depending on its concentration. Whereas 10% induced a similar number of tartrate-resistant acid phosphatase (TRACP)-positive multinucleated cells to the positive control, higher concentrations of PRP did not induce the generation of multinucleated cells positive for this enzyme considered as a marker of bone resorption. Nevertheless, even when the multinucleated cells were treated with 10%PRP, the bone resorptive activity was also significantly lower. According to the authors, these results could be explained by the fact that PRP at high concentration could recruit osteoclast precursors but inhibit their differentiation. They also suggested that the transforming growth factor-β (TGF-β), present in platelets, could be one of the factors responsible for this inhibition. Also regarding bone regeneration, He et al. (58) studied the effect of different medium suplementations (10% FBS, 10% human platelet lysate (hPL) and 5% hPL) on THP-1-derived macrophage polarization. They concluded that human platelet lysate was a better choice for M1 and M2 polarization as cells treated with 5% hPL exhibited a more consistent morphology with the expected phenotype. In fact, culturing with 10%FBS or with 5% hPL induced opposite patterns for M1 and M2 macrophages. The authors also analyzed the effect of jaw periosteal cells (JPCs) on macrophage polarization in direct coculture. They concluded that low concentration of hPL enhanced the ability of JPCs to inhibit M1 polarization compared to other supplementations. The authors also detected the recently discovered CD169⁺ macrophages. They concluded that the JPCs’ ability to regulate this macrophage population could be enhanced by a low concentration of hPL.

O´Donnell et al. (66) and Uchiyama et al. (74) conducted their research on osteoarthritis (OA), although with very different approaches. O´Donnell et al. (66) compared leukocyte-poor PRP from healthy young male donors with the PRP from older male patients with severe knee OA. They also grouped the samples according to the concentration of inflammatory mediators and growth factors into high and low. They reported that according to age and disease state the composition of PRP was different, as PRP from older OA patients showed increased levels of inflammatory cytokines and less growth factors and platelets. These differences were reflected in the response of macrophages to treatment with PRP from these two groups. OA-PRP upregulated mRNA for inflammatory proteins in human monocyte-derived macrophages, thus promoting the inflammatory macrophage phenotype. The authors therefore suggested that these two factors (age and disease condition) may influence the bioactivity of PRP and hence their clinical effect. On the other hand, Uchiyama et al. (74), compared two types of PRP purification kits that resulted in two PRP of different composition (leukocyte-poor PRP (LP-PRP) and leukocyte-rich PRP (APS LR-PRP)) on macrophage phenotypes. They found higher concentrations of both M1 and M2 macrophages related factors in APS. The addition of PRP supernatants decreased the expression of M1 macrophage markers, such as IL-1β, TNF-α, CD80 and CD86, when compared to the monocyte derived macrophages alone, while there were no detected differences in the purification kits. Regarding M2 markers, they showed higher expression of MRC1 when macrophages were cultured with both PRP supernatants with regard to negative control, while the gene expression of IL-10 and TGF-β was increased in cells treated with APS or LP-PRP, respectively. In contrast, cell surface markers of the M2 phenotype (CD163 and CD206) were not altered after PRP culture. They also reported that both types of PRP promoted the repolarization of monocyte-derived M1 macrophages to the M2 phenotype; however, according to the authors, they gave rise to different M2 subpopulations. While LP-PRP promoted polarization toward the M2c subset, mainly related to tissue repair, APS promoted towards M2a, related to anti-inflammatory activity. Nevertheless, this information should be interpreted with caution. M2 macrophages further divide into subsets based on their distinct gene expression profiles. However, many of these subpopulations share markers. Thus, M2a, M2c and M2d subsets are characterized by the secretion of IL-10 and TGF-β, making accurate classification difficult (28). The authors stated that an increase in the ratio M1/M2 macrophages leads to a progression in OA disease. Therefore, they concluded that PRP treatment could improve symptoms in these patients by reducing the imbalance of M1/M2 macrophages.

When it comes to tissue regeneration or wound healing, several articles were also included. Both the study groups and the experimental design were also different in all studies. Escobar et al. (56) evaluated the biological effects of two platelet preparations on the phenotype of human monocyte-derived macrophages. They compared a leukocyte-depleted pure platelet-rich plasma without activation (P-PRP) and the supernatant released from that P-PRP after CaCl₂ activation (S-PRP). Their findings showed that P-PRP and S-PRP generated different profiles of tissue-repair macrophages. Both preparations stimulated the expression of the M2 marker, CD206. In addition, only P-PRP enhanced the production of the potent anti-inflammatory cytokine IL-10. On the other hand, S-PRP also induced higher levels of expression of another M2 marker (CD163) compared with P-PRP; however, the expression of the pro-inflammatory marker CD86 was also enhanced after S-PRP treatment. Those results suggested different clinical regenerative potentials for both platelet preparations. Recent developments in platelet biology have led to new insights. In this regard, the platelet derived extracellular vesicles (EVs) and their role in intercellular communication are of interest (86). In this sense, the work of GraÇa et al. (57) evaluated the effect of two different EV populations (small EVs and medium EVs) derived from platelet lysates. Macrophage responses varied depending on the EV population they were treated with. sEVs induced polarization towards a hybrid M1/M2 phenotype, while mEVs induced a more non-polarized state. The authors stated that hybrid macrophages, which also exist in vivo, promote a more native-like extracellular matrix compared to a predominantly M2 macrophage phenotype. They also suggested that this difference in macrophage response to treatment could be useful as an effective strategy in modulating the process of tissue repair by sequentially using sEVs and mEVs in early and later healing stages, respectively. The immunoregulatory role of another platelet concentrate product in macrophage functional activities was also included (63). In this case, the authors tested different concentrations of conditioned medium (CCM) from concentrated growth factor (CGF). They reported reduced secretion of inflammatory cytokines (such as IL-1β) and enhanced chemokine production (such as RANTES) by CGF-stimulated macrophages, thus promoting M2 polarization. The Akt pathway was also determined to be involved in the immunoregulatory role of this concentrated growth factor. Papait el al (67). analyzed the effect of allogenic PRP mismatched for AB0 and Rh antigens on macrophages differentiation and function. Two types of preparations were used, standard (ST) and leucodepleted (LD). Macrophage cultures with GM-CSF, IL-4 and 10% FCS were referred as immature dendritic cells (iDC), while the addition of 5% ST-PRP or LD-PRP to that treatment were referred to as DC-ST or DC-LD, respectively. Combination of GM-CSF and IL-4 is generally used for the differentiation of human monocytes into dendritic cells (DC) (87, 88). The mononuclear phagocyte system (MPS) has been defined as a family of cells comprising monocytes, dendritic cells and macrophages. Their functional and phenotypical characteristics are often overlapping, making the distinction and classification of these cell types truly challenging. In fact, many of the proposed unique markers and functions are shared between cell types. This has added much confusion about their identity and function, opening the debate regarding which subsets represents distinct cell types and which are versions of the same cell type, thus leading to a possible misinterpretation of the results (89, 90). In fact, authors reported difficulty in clearly defining the type of DC induced by PRP. Their findings showed that PRP could inhibit macrophage differentiation to CD1a⁺ iDC; on the contrary, PRP induced type 2 macrophages, as they expressed high levels of CD163 and CD206. Moreover, release of IL-10 and PGE2 was also induced by PRP, even in the presence of LPS. Although both ST-PRP and LD-PRP induced DC with similar features, the authors stated that the inclusion of leukocytes did influence the secretion of those immunoregulatory factors, as more IL-10 and PGE-2 were reported with DC-LD, however, the white cell content was practically nil in both preparations. Taken together, data suggested that PRP promoted a regulatory anti-inflammatory phenotype thus supporting wound healing. The effects of platelet lysate (PL) on macrophages phenotype and functions were also examined in two other studies with different scopes (71, 73). Scopelliti et al. (71) used a commercial PL to conduct their assays in order to limit individual variation; however, as they stated, this also involved a drawback, as information about its composition was also missing. The authors exposed M1-polarized macrophages to 10% PL. They demonstrated that PL treatment reduced the expression of M1 markers (such as CD80 and CD86) and enhanced the expression of M2 markers (such as CD206, CD200R, PPAR and arginase). In addition, TNF-α and NFκB expression was significantly reduced. On the other hand, the release of TGF-β and VEGF, both largely involved in the wound healing process, was significantly increased along with the expression of STAT3, STAT6, SMAD2 and SMAD4. Therefore, the authors concluded that PL repolarized M1 macrophages towards a M2-like phenotype, thus favoring the regenerative process. Tylek et al. (73) evaluated another commercial platelet lysate as an alternative for in vitro culture of macrophages as well as for co-culture with hMSCs. The authors concluded that hPL, especially without adding heparin, was the best performing supplement both for the in vitro culture of human monocyte-derived macrophages and for the co-culture system, compared to human serum and fetal calf serum.

Finally, Yadav et al. (77) focused their research on nerve regeneration and conducted their assays both in vitro and in vivo. The authors studied, in vitro, the effect of different percentages of PRGF on M0 and M1 macrophage polarization. PRGF treatment inhibited the M1 phenotype. Consistent with Scopelliti et al. (71) they also showed a decrease in TNF-α, in addition to IL-1β and IL-6. However, in contrast to Scopelliti et al., who used a platelet lysate, the PRGF used in this experimental setting did increase IL-10 secretion. The therapeutic effects of PRGF were further investigated on nerve tissue regeneration by using a sciatic nerve transection model in rats. As was the case in the in vitro assays, the pro-inflammatory cytokines TNF-α, IL-1β and IL-6 were reduced in the PRGF group compared to the saline control group. In fact, treatment with the platelet preparation decreased M1-type macrophages, thus suggesting that its administration may modulate the inflammatory microenvironment to promote sciatic nerve regeneration via macrophage polarization among others.

Fifteen investigations were included in this section. In most of them (12 out of 15), the results were that treatment with platelet derivatives modulated the polarization of macrophages towards the M2 phenotype. Only one article (75) reported a stimulation towards the pro-inflammatory phenotype. Nishio et al. (65) described both situations, depending on the type of PRP used. No modulation of macrophage polarization was reported by Hudgens et al. (59). The studies covered different fields of application and responses were evaluated both in vitro and in vivo.

Five studies explored the in vitro response of murine macrophages to different platelet derivatives (54, 59, 61, 64, 75). Both Cao et al. (54) and Kargarpour et al. (61) focused on bone regeneration, and although the treatments and the approach were different, their outcomes supported the same conclusion that platelet derivatives possessed anti-inflammatory activity by promoting macrophage M2 polarization. Cao et al. (54) evaluated the immunomodulatory role of PRP in combination with methacrylated gelatin (GelMA) and methacrylated alginate (AlgMA) (GA) hydrogel alone or together with Laponite nanoparticles. The authors concluded that M1 and M2-type genes were decreased and increased, respectively, for both PRP-containing hydrogels. Different fractions of liquid PRF were studied by Kargarpour et al. (61): platelet poor plasma (PPP), the buffy coat (BC or C-PRF), the remaining red clot (RC) and albumin gels (Alb-gel) from heating PPP. The results of their research indicated that lysates of both BC and PPP inhibited the inflammatory response of macrophages exposed to different TLR agonists, as evidenced by the significant decrease of IL-6 and COX-2. This was further confirmed with a reduction in p65 phosphorylation and NFκB nuclear translocation. Both types of lysates repolarized the M1-like macrophages as deduced from the increased expression of M2 phenotype markers, ARG1 and YM1. Not only did these fractions exert a potent anti-inflammatory effect but they also inhibited osteoclastogenesis, finding that has also been reported by other authors (55) as already mentioned above.

The study performed by Hudgens et al. (59) compared the effect of PPP and PRP on macrophage polarization in tendon disorders. In contrast to most studies, they used resident macrophages, specifically rat resident peritoneal macrophages. They concluded that PRP had no obvious effect on modulating macrophage polarization. However, as they suggested, multiple PRP doses should have been evaluated as well as changes in protein expression beyond the gene response.

In the context of tissue regeneration, Nasirzade et al. (64) studied the effect of PRF lysates, produced by freeze-thawing the membranes, and the PRF conditioned medium, that is, its secretome, on macrophages exposed to saliva and LPS. Their findings were in line with those already discussed from Kargarpour et al. (61) (authors from the same working group). Briefly, PRF possessed anti-inflammatory activity and shifted the macrophage polarization from M1 toward M2 phenotype. Further, NF-κB p65 signalling activation was strongly reduced by PRF lysates. The authors reported that the transition between M1 and M2 was partially mediated via activation of TGF-β signalling. They also described that PRF could modulate the expression of lipoxygenases (ALOX5, ALOX12 and ALOX15) thus supporting the production of pro-resolving lipid mediators. Still in the field of wound healing, Ulivi et al. (75) showed that PL supports macrophages in a proinflammatory state, thus enhancing the key initial inflammatory response to the injury. However, it should be noted that the outcome described in this article is not a direct but a paracrine effect of the PL. That is, the collected conditioned media from MSCs exposed to PL were used to treat bone marrow-derived macrophages and to assay its effect on their phenotype.

In the field of bone healing, the M2 polarized macrophages are critical in the osteogenic microenvironment for effective bone regeneration (91). In this sense, Li et al. (62) developed hybrid hydrogels composed of injectable platelet-rich fibrin (i-PRF) and polycaprolactone/hydroxyapatite composite nanofibers by using enriched polydopamine (PDA) as linker (PnP-iPRF). To simulate the biodegradation process in vivo, i-PRF-containing hydrogels were treated with plasmin. RAW 264.7 macrophages were then incubated with those degradation products. The authors reported that the immunomodulatory activity of the PnP-iPRF could be attributed to the PDA component, as this hybrid hydrogel effectively induced M2 macrophage activation in a sustained manner. Cytokines secreted by these PnP-iPRF-treated macrophages also promoted the osteoblastic differentiation of BMSCs. PnP nanofibers were considered to be responsible for enhancing this osteogenic activity of i-PRF hydrogels. However, i-PRF hydrogel produced a moderate and unsustainable induction towards the M2 phenotype. The authors created a critical cranial defect in rats to further investigate the osteogenic effect of this hybrid hydrogel in vivo. The results were in line with those obtained in the in vitro assays. PnP-iPRF hydrogels could effectively induce M2 macrophage phenotype at 4 weeks post-surgery, as deduced from expression of CD206 and iNOS, markers of M2 and M1 respectively. Therefore, in this study, the added value was provided by the PnP rather than by the i-PRF.

Leukocyte rich PRP was select by Jiang et al. (60) for incorporation into the GelMA hydrogel on macrophages and to study its resulting influence on osteochondral regeneration. The addition of 20% PRP-GelMA significantly reduced the in vitro expression of several M1 markers (IL-1β, IL-6, iNOS, CCR7) in the LPS-treated macrophage culture when compared with pure GelMA or control. In this regard, M2 markers (Arg-1, IL-1ra, IL-10 and CD206) exhibited higher expression in PRP-GelMA than in the other groups. The authors indicated that the PRP-GelMA hydrogel not only inhibited the transition from M0 to M1 but also promoted M2 polarization. This hydrogel combination was further investigated in a rabbit model of osteochondral defect and showed early onset (12 weeks) and the persistence (18 weeks) of the M2c macrophage subset, and the reduction of M1 phenotype, thus suggesting that osteochondral regeneration was mediated by M2 polarization. Although not directly comparable, as the composition of PRP and hydrogel were different, the addition of the platelet derivative in this study did lead to an improvement in the performance of the hydrogel in contrast to that reported by Li et al. (62).

Macrophage infiltration and polarization have been increasingly associated with the degree of intervertebral disc degeneration (IDD) (92). Therefore, Qian et al. (70) addressed the underlying mechanisms involved in IDD pathology. They compared the effect of PRP with that of PRP-derived exosomes. The authors showed that both PRP and PRP-derived exosomes inhibited the polarization of M1-type macrophages through the inhibition of genes associated with this pro-inflammatory phenotype. This occurred via suppressing NF-κB and MAPK signalling by targeting TRAF6. The inhibitory ability was more pronounced in the case of PRP-derived exosomes. On the other hand, PRP-derived exosomes promoted M2 macrophage polarization via the STAT6 signaling pathway. The strongest inhibitory effect was exerted with respect to IL-1β, which led the authors to explore the effect of PRP-derived exosomes on NLRP3 inflammasome in macrophages. The NLRP3 inflammasome is a multiprotein complex critical in the innate immune system that assembles in response to pathogens and other stressors leading to the activation of caspase-1, the secretion of proinflammatory cytokines (Il-1β, IL-18) and the induction of pyroptosis (93–95). The authors reported the inhibition of NLRP3 inflammasome activation by PRP-derived exosomes. They also used rat models of IDD to address the issue in vivo. As it was reported in vitro, the expression of inflammasome-related proteins was also reduced in the PRP-derived exosomes group in vivo. The results of this study differ somewhat from those obtained by Graca et al. (57) where the extracellular vesicles did not clearly polarize towards the M2 phenotype. However, the comparison between these two studies is challenging, since the origin of the vesicles, PRP and macrophages is different, as well as the platelet derivative’s composition.

Several authors (72, 79, 80) have carried out studies in terms of wound healing and despite their different approaches, all results consistently showed that platelet derivatives stimulated polarization towards the M2 phenotype. Tang et al. (72) developed a thermosensitive injectable hydrogel known as the thermosensitive decellularized adipose tissue/platelet-rich plasma interpenetrating polymer network (t-DPI) hydrogel based on decellularized adipose tissue (DAT) and temperature-controlled platelet-rich plasma (t-PRP). All the treatments (t-PRP, DAT hydrogel and t-DPI hydrogel) promoted M2 macrophage polarization in vitro compared to the control. However, the t-DPI hydrogel group was the treatment that induced the highest polarization. Same results were obtained in vivo in a nude mouse model. The authors concluded that the biologically active ingredients present in the t-PRP and DAT contributed to the therapeutic effect of t-DPI hydrogel via M2 macrophage polarization, among others. On the other hand, Zhang et al. (79) concluded that i-PRF had greater anti-inflammatory response than whole blood (WB). In fact, i-PRF reduced the expression of IL-6, TNF-α, and INOS2 in LPS-treated murine-derived macrophage compared with WB. Moreover, p65 phosphorylation and TLR4 expression was also decreased after treatment with this platelet concentrate. The inhibition of NFκB signalling was consistent with that reported by other authors already included in this review (61, 64, 70, 71), that also showed the ability of the different platelet derivatives to stimulate the M2 phenotype. In this study, i-PRF also increased the M2-polarized macrophage phenotype-associated cytokines. Results also showed an anti-inflammatory response in vivo. i-PRF reduced the amount of local innate immune cells in a rat muscle defect model. Finally, Zhao et al. (80) evaluated PRP as an additive to develop an alginate-gelatin (AG) composite hydrogel bioink. Different concentrations of PRP were incorporated. Macrophages were seeded on the 3D bioprinted double-layered skin substitutes under inflammatory conditions (LPS). The addition of 5% PRP (AG-5P) led to greater decrease and increase of iNOS and Arg-1, respectively, than the control and AG groups. The same results were obtained in the in-situ 3D bioprinting repair of a rat dorsal full-thickness wound model. In addition, the AG-5P reduced the inflammatory response and macrophage infiltration after transplantation, as suggested by the lowest level of CD3, CD68 and MPO that were detected compared with control and AG group. Therefore, the authors concluded that the PRP incorporation regulated the immune response and tissue regeneration by promoting the macrophage polarization towards an M2 phenotype.

Four articles were included in this section. Despite the fact that the experimental design and the type and composition of PRP were different, 3 out of 4 studies concluded that platelet derivatives stimulated the anti-inflammatory phenotype. In the case of the study of Nishio et al. (65) polarization depended on the type of PRP, as LP-PRP induced the M2 phenotype, while LR-PRP induced the pro-inflammatory M1 phenotype.

In line with the studies of hybrid hydrogels, Qian et al. (69) reported the combination of PRP and lyophilized platelet-rich fibrin (Ly-PRF) with alginate-hyaluronic acid hydrogel as a novel approach for the treatment of myocardial infarction. They concluded that in this cardiovascular condition, Ly-PRF improved the immunological response by reducing the M1 macrophages and by stimulating their polarization towards the M2 phenotype.

Park et al. (68) evaluated the effect of PRP on an acute UVB-induced skin photodamage model in rats. They reported that the addition of PRP modulated the immune response depending on the stage of wound healing. That is, PRP enhanced the inflammatory or the repair response 7 days or 28 days after treatment, respectively, thus, finally reducing skin tissue inflammation. This regulation of macrophage polarization was performed via the activin receptor-follistatin system.

Two studies (65, 78) addressed tendon healing. As already mentioned, Nishio et al. (65) evaluated the influence of the leukocyte inclusion in the PRP on macrophage recruitment and polarization. They created full-thickness defects in the central third of patellar tendons in mice. As already described in the findings of Park et al. (68), macrophage modulation was dependent on the stage of tendon healing. They demonstrated that both types of PRP enhanced the tendon healing and promoted the recruitment of macrophages to injured tissue. However, leukocytes did influence the effect that PRP has on the balance between M1 and M2. In fact, LR-PRP preferentially stimulated the activity of the M1 phenotype, whereas LP-PRP did so with M2 macrophages. Nevertheless, the authors also noted that the effect of the PRP groups could be due to a foreign body reaction as the control group was not well-designed. On the other hand, Yu et al. (78) evaluated the effect of PRP releasate (released from platelets after PRP was activated) on the early stages of tendon healing. A rat model of Achilles tendon injury was used. In contrast to Nishio et al. (65), saline solution was used as a control. They reported lower levels of CD68⁺ (ED1⁺) macrophages, which have been suggested to stimulate tendon catabolism, in the samples treated with PRP as compared with the control group in the early healing stage (day 5 post injury), thus promoting tissue recovery.

Wessely-Szponder et al. (76) used ovine monocyte-derived macrophage cultures to assess the influence of autologous ovine PRP and rabbit antimicrobial peptide extracts. Macrophages were previously stimulated with LPS or dexamethasone. The proinflammatory cytokines superoxide and nitric oxide (NO) were increased in macrophage cultures after PRP treatment both alone and in combination with LPS, although the addition of the latter exacerbated this response. The use of dexamethasone reduced the proinflammatory response to PRP. Therefore, the authors concluded that PRP treatment induced a pro-inflammatory rather than repair phenotype rather than a repair one. Although this response might enhance antimicrobial activity, they suggested that the application of this platelet derivative should be restricted in cases of severe inflammation.