Toll-Like Receptors (TLRs) Expression in Contracted Capsules Compared to Uncontracted Capsules

Silicone breast implants have been widely used for breast augmentation or breast reconstruction after breast cancer [45]. Capsule formation is a normal foreign body reaction occurring around all implants [17, 34]. However, in selected cases this capsule formation around breast implants tends to progress, leading to capsular contracture. This complication presents with signs of hardening and disfiguring of the breast and is often painful [16]. Capsular contracture remains the most common complication after surgical implantation of breast implants with a prevalence ranging from 5 to 17% [18, 26] for breast augmentation and 19–25% [19, 31, 35] for breast reconstruction. The Baker score is used to clinically score the severity of capsular contracture, where Baker scores 1 and 2 represent normal capsules and Baker scores 3 and 4 represent contracted capsules [4].

The etiology of capsular contracture remains unknown [3]. An important observation is the role of the immune system in capsular contracture. All studies investigating the role of the immune system found a chronic inflammation in capsular contracture [13, 15, 22, 27, 37, 38, 49, 50]. A prominent role is seen for elements of innate immunity, such as activated macrophages, which, similar to polymorphonuclear neutrophils (PMNs), have nonspecific immune function. B1a and marginal zone B cells (MZB) are the first antibodies that initiate the process with participation of various interleukins as well as tumor necrosis factor alpha (TNF-α) [15, 27, 30, 38, 49]. This suggests that ongoing activity of the immune system is one of the causative factors in this multifactorial condition. Another important theory is that bacteria peri-prosthetically play a role in the etiology of capsular contracture. Some studies found associations between the presence of bacteria peri-prosthetically and capsular contracture [9, 12, 41, 51]. The bacteria cultured most often were Staphylococcus spp. To date, it is unknown whether bacteria trigger this inflammatory response.

Receptors on immune cells that recognize pathogens such as bacteria are Toll-like receptors (TLRs), previously known as modulins [10, 36]. These receptors recognize pathogenic surface ligands such as peptidoglycan (TLR2) and lipopolysaccharide (TLR4), or, for example, cytosine–guanine pairs intracellularly (TLR9), referred to as pathogen-associated molecular patterns (PAMPs). TLRs also recognize endogenous derived ligands such as oligosaccharides of hyaluronic acid and fibrinogen (TLR4) [10], and ligands that are generated during tissue damage (damage-associated molecular patterns (DAMPs) such as different heat shock proteins [6]. So far, 10 TLR members have been identified in humans. TLR1, TLR2, TLR4, TLR5, TLR6 and TLR10 are transmembrane proteins, while TLR3, TLR7, TLR8 and TLR9 are expressed intracellularly [7]. TLR3, TLR4, TLR5 and TLR9 are activated solely, while TLR 2 can form a heterodimer with TLR1 and TLR6. TLR7 and TLR8 are solely activated as a heterodimer [52]. See Fig. 1 for a simplified schematic representation. Because of their central role in the immune response, TLRs have become an important therapeutic target for the treatment of several diseases. For example, activators of TLRs (TLR agonists) are powerful immunostimulants due to their ability to drive innate and acquired immunity and are therefore used as adjuvants in vaccines [20].

Recognition of ligands by TLRs leads to intracellular signal transduction through the NF-κB pathway that in turn induces an immune cascade resulting in a host response, which is necessary to clear the pathogens [10]. If bacteria indeed play a significant role in the induction of capsular formation and contraction, it seems likely that TLRs are expressed in capsular contraction.

The aim of this study was therefore to investigate the expression of TLRs 1–10 in Baker 1–4 breast capsules.

This was a cross-sectional study. Patient characteristics were retrospectively collected. Consecutive samples were obtained between 2014 and 2016 at the VU University Medical Center, Jan van Goyen Clinic and OLVG location West, in Amsterdam, the Netherlands. The local medical ethical committee approved this study (Study No. 2014.146). Written informed consent was provided by all participants.

The aim of this study was to investigate the expression of TLRs in breast capsules to further elucidate the immune cascade leading to capsular contracture. The current study found a significantly higher expression of TLR2 and TLR6 in contracted capsules (Baker 3 or 4) in comparison with normal capsules (Baker 1 or 2). None of the TLRs displayed a significantly higher expressed in contracted capsules compared to uncontracted capsules.

Although not completely understood, an ongoing immune response is observed in capsular contracture [13, 15, 22, 27, 37, 38, 49, 50]. Activated macrophages and monocytes secrete cytokines and chemokines such as IL-8 and TNF-α which induce a pro-inflammatory immune response [15, 27, 38, 49]. Hereafter, activation of NK cells and fibroblast is seen [14, 39]. It is unknown which pathogen or signaling factor induces this immune response. However, there is evidence that bacteria in situ might be involved in the etiopathogenesis of capsular contracture. The presence of bacteria has been described in several studies [9, 12, 41, 51]. Multiple studies have found a higher number of bacteria in contracted capsules compared to normal breast capsules [9, 12, 41, 51]. In these studies, the most common cultured bacteria were coagulase-negative staphylococci such as Staphylococcus epidermidis. Other frequently cultured bacteria were Staphylococcus aureus and Propionibacterium acnes. Although several studies found associations between the presence of bacteria, conflicting data exist [1]. Nonetheless, it has never been investigated whether these bacteria induce an immune response via, for example, TLR activation in relation to capsular contracture.

Staphylococcus epidermidis is a commensal gram-positive bacterium which contains phenol-soluble modulin ligands [10] on its surface which is recognized by TLR2 receptors. In the current study, TLR2 was significantly more often expressed in Baker 3 (40% positive) capsules compared to Baker 2 (6.3% positive) capsules. There was, however, no difference in the mean concentration of cDNA between contracted and uncontracted capsules. Staphylococcus aureus and Propionibacterium acnes are also commensal skin bacteria, but with peptidoglycan (PGN) ligands on their surface which is also recognized by TLR2 [48]. If bacterial infection with S. epidermidis, S. aureus or P. acnes would have activated an immune reaction, much higher TLR2 expression would have been expected in the capsules. In our study, there was also a significant higher expression of TLR6 (Baker 2 vs. Baker 3, 31.3% vs. 90%) observed in contracted capsules compared to non-contracted capsules inversely with a significant higher mean concentration for uncontracted (Baker 2) versus contracted capsules (Baker 3). TLR6 can form a heterodimer with TLR2 [47]. Together, they function as a receptor for (gram-positive) recognition of diacyl lipopeptides ligands on, for example, Mycoplasma spp [10]. It is, however, unlikely that a Mycoplasma infection occurs around breast implants. This would result in a fulminant clinical infection which has not been reported by our patients. Moreover, all capsules have been tested for microbial presence in our former study finding no Mycoplasma spp. on the capsules [1]. In that study, we investigated the presence of bacteria on the same set of capsules using a highly sensitive PCR method. Here, we observed that breast capsules are generally sterile. Moreover, no association was found between the presence of bacteria and the Baker score.

TLR8 was significantly more often expressed in Baker 1 capsules compared to Baker 2 and Baker 4 capsules. TLR8, which is expressed intracellularly, is known to interact with single-stranded RNA from viruses, and small synthetic compounds [10]. Our former study on the same capsules, however, did not find any viruses in the capsules [1].

None of the TLRs displayed a significantly higher expressed in contracted capsules compared to uncontracted capsules. This is thought to be less important since TLRs expression does not correlate well with the TLRs on the membrane (or intracellularly), and it therefore just a measurement for expression.

Only one study investigated the role of TLR expression in breast capsules. Segreto et al. [42], investigated the expression of TLR4 and its relationship with estrogen receptor expression. They found TLR4 expression in fibroblasts and myofibroblasts with a positive correlation with estrogen receptor-β expression in capsular contracture. They postulate that estrogen receptor-β increases the TGF-β production which is a stimulus involved in myofibroblast differentiation and contraction. This study suggests a role for hormonal signaling in the etiology of capsular contracture. TLR4 is, however, mostly known to be one of the major receptors for the recognition of lipopolysaccharide (LPS), a ligand on Gram-negative bacteria [10, 29]. Upregulation in contracted capsules as observed by Segreto et al. [42] could suggest that TLR4 is activated by the presence of bacteria. It would have been valuable if they would also have investigated bacterial presence on their capsules to strengthen this theory. In our study, we also observed upregulation of TLR4 in all four groups. However, no differences in expression of concentrations of cDNA were observed between the four investigated groups. Our follow-up time was much longer (a mean of 11 years in comparison with a mean of 1 year by Segreto et al.), with the possibility of a decline of TLR expression over time.

Since upregulation of all TLRs is observed after a mean implant duration of 11 years, it seems likely that an ongoing stimulus activates TLR expression. It is expected that after 11 years bacteria are resolved by the immune system, as has been confirmed in our sterile samples [1], making PAMPs an unlikely factor for the observed TLR expression. DAMPs, however, can be generated over a long period of time. Different types of DAMPs, such as heat shock proteins (HSPs), are released under conditions of stress or tissue injury such as traumatic lesions, burns and oxidative stress [11, 28]. The major HSPs that are generated during tissue damage are HSP 47 and 70 [24, 46]. These HSPs are then recognized by pattern recognition receptors such as TLRs and contribute to an immune response causing tissue damage [5]. HSP 70, for example, is recognized by TLR2 [32, 53]. HSP 47 and 70 have been associated with different fibrotic diseases such as keloids, lung fibrosis and cardiac hypertrophy [21, 23, 33]. Therefore, it seems not unlikely that the same process occurs in capsular contracture. We hypothesize that HSPs are released as a consequence of mechanical friction of the implant in the surrounding tissue causing cell injury. The release of these molecules might cause an expression of TLR2, as has been found to be significantly higher in our contracture group, leading to an immune response causing tissue damage. This hypothesis may explain the high rates of capsular contracture in patients with textured or smooth implants [2, 8, 25] which can move freely in the surrounding tissue and cause mechanical stress in contrast to polyurethane implants [43] that usually grow within the surrounding tissue and cause minimal mechanical stress. Further research, however, should provide more insight in the release of DAMPs in capsular contracture.

To our knowledge, this is the first study investigating expression of the full human TLR set in the context of capsular contracture. There are nonetheless several limitations to the present study. First of all, we included mostly female patients who underwent the primary surgical procedure for cosmetic reasons, but we also included two female patients who underwent breast reconstruction as a primary indication. Secondly, the implant duration in our study was quite long. It is possible that bacteria or any other factor have triggered initial TLR expression, but that this expression has declined over time as bacteria were cleared by the host immune system. There is also a significant difference between the Baker scores in implant duration. This difference alone could be an explanation for the difference between the groups. Also, data on “time to complaint” are not available since it was difficult for patients to mention the start of their complaints. This would have been beneficial since bacterial activity and immune response would be different at different time intervals independent of capsular contracture. Third, TLR expression was measured based on mRNA expression, which is rapidly degradable. Therefore, samples were immediately collected and transported in liquid nitrogen to prevent degradation. Samples were placed in dry ice during laboratory testing as much as possible. Although samples were handled with care during transportation and laboratory testing, it is inevitable that some of the mRNA degraded during sample transportation and laboratory testing. This may have influenced the results and makes it difficult to reproduce this test even though standardized assays were used. Fourth, there are also routes other than TLRs activation by which the immune system can be activated [44]. Staphylococcus aureus and group A streptococci, for example, produce superantigens. These superantigens first bind to MHC class II and then to T cell receptors inducing a signaling pathway resulting in the production of several cytokines. This mechanism bypasses the TLR route. In such a case, the TLR mechanism is less relevant in the pathogenesis of capsular contracture. Fifth, the Baker score was used to grade the degree of contracture. Patients with some palpable firmness and pain were therefore automatically categorized as Baker 4. Because this scale is not completely objective, some error might have been introduced.

More and larger studies are needed to confirm our findings. First, it would be valuable to perform a follow-up study in which samples with a lower implant duration were collected to test the theory that there could be a decline in TLR expression over time. Furthermore, it should be investigated whether DAMPs indeed are released in breast and capsular tissue. Also, intracellular signaling after TLR activation occurs through the MyD88, MAL, TRIF, TRAM or TAK-1 pathway [10]. Further research is needed to investigate which of these intracellular signaling pathways is activated in capsular contracture. This could give more insight into the exact immune cascade leading to capsular contracture. Lastly, other receptors on immune cells have been identified and should be investigated to give more insight into the activation and signaling pathways leading to capsular contracture.

The present study shows that TLR2 and TLR6 are more often expressed in contracted capsules compared to non-contracted capsules. We suggest that bacteria are not per se involved in the activation of an immune cascade leading to capsular contracture, but hypothesize that other ligands, such as DAMPs, might be involved.