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Systematic Review

A Scoping Review of the Role of Metalloproteinases in the Pathogenesis of Autoimmune Pemphigus and Pemphigoid

by
Nicola Cirillo
1,* and
Stephen S. Prime
2
1
Melbourne Dental School, University of Melbourne, 720 Swanson Street, Carlton, Melbourne, VIC 3053, Australia
2
Centre for Immunology and Regenerative Medicine, Institute of Dentistry, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, London E1 4NS, UK
*
Author to whom correspondence should be addressed.
Biomolecules 2021, 11(10), 1506; https://doi.org/10.3390/biom11101506
Submission received: 31 August 2021 / Revised: 6 October 2021 / Accepted: 8 October 2021 / Published: 13 October 2021
(This article belongs to the Special Issue Matrix Metalloproteinases in Health and Disease 2.0)
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Abstract

Pemphigus and pemphigoid diseases are potentially life-threatening autoimmune blistering disorders that are characterized by intraepithelial and subepithelial blister formation, respectively. In both disease groups, skin and/or mucosal blistering develop as a result of a disruption of intercellular adhesion (pemphigus) and cell-extracellular matrix (ECM) adhesion (pemphigoid). Given that metalloproteinases can target cell adhesion molecules, the purpose of the present study was to investigate the role of these enzymes in the pathogenesis of these bullous dermatoses. Studies examining MMPs (matrix metalloproteinases) and the ADAM (a disintegrin and metalloproteinase) family of proteases in pemphigus and pemphigoid were selected from articles published in the repository of the National Library of Medicine (MEDLINE/PubMed) and bioRxiv. Multiple phases of screening were conducted, and relevant data were extracted and tabulated, with 29 articles included in the final qualitative analysis. The majority of the literature investigated the role of specific components of the MMP family primarily in bullous pemphigoid (BP) whereas studies that focused on pemphigus were rarer. The most commonly studied metalloproteinase was MMP-9 followed by MMP-2; other MMPs included MMP-1, MMP-3, MMP-8, MMP-12 and MMP-13. Molecules related to MMPs were also included, namely, ADAM5, 8, 10, 15, 17, together with TIMP-1 and TIMP-3. The results demonstrated that ADAM10 and MMP-9 activity is necessary for blister formation in experimental models of pemphigus vulgaris (PV) and BP, respectively. The data linking MMPs to the pathogenesis of experimental BP were relatively strong but the evidence for involvement of metalloproteinases in PV was more tentative. These molecules represent potential candidates for the development of mechanism-based treatments of these blistering diseases.

1. Introduction

Pemphigus and pemphigoid are members of a heterogeneous group of chronic, potentially fatal autoimmune diseases associated with blistering of the skin and mucosae. Once considered part of the same disease spectrum, these bullous dermatoses were first classified as distinct entities by Lever in 1953 [1]. Histologically, pemphigus presents as an intraepithelial split (acantholysis) whereas in pemphigoid, the blisters develop at the dermo-epidermal junction resulting in a subepithelial split.
The two major pemphigus variants, pemphigus vulgaris and pemphigus foliaceus, account for 90–95% of diagnoses [2,3]. Pemphigus diseases are characterized by flaccid blisters and erosions and are treated with high dose corticosteroids and immunosuppressants. By contrast, pemphigoid presents with tense blisters and erosions, a negative Nikolsky sign and, commonly, is controlled using topical steroids although in more severe cases, systemic steroids are an option [2].
The development of molecular techniques has facilitated the further classification of these blistering diseases. The pemphigoid group is now known to include at least eight disorders for which the molecular target antigens have been identified [4], although controversy exists regarding the pathogenic mechanisms of blistering [5]. In pemphigus, distinct autoantibody profiles and, in particular, the presence/absence and type of antibodies to cadherins determines the acantholytic signaling pathways [6,7] and possibly the clinical phenotype [8,9]. Despite advances in understanding the pathophysiology of these disorders, however, the mainstay of treatment is the use of corticosteroids and immune suppressants and, significantly, no mechanism-based treatments have been successfully translated to patient care.
Pemphigus and pemphigoid result from a deficit in cellular adhesion. In pemphigus, cadherin-mediated cell-to-cell adhesion is disrupted due to antibody-mediated signaling pathways and this, in turn, leads to cell-cell detachment (acantholysis) and blister formation [10]. In pemphigoid, both autoantibody and cell-mediated responses induce a disruption of integrin-mediated adhesion between basal keratinocytes and the extracellular matrix (ECM) of the basement membrane [5]. One of the possible mechanisms for the weakening of cell adhesion in these circumstances is that cadherins and/or integrins are digested by proteolytic cleavage [11,12].
Metalloproteinases are proteolytic enzymes with a relatively large spectrum of activity that includes adhesion molecules [13]. Of these, matrix metalloproteinases (MMPs, also known as matrixins) and a disintegrin and metalloproteinase (ADAM) family of endopeptidases, are capable of degrading all kinds of extracellular matrix proteins and extracellular portions of transmembrane proteins, respectively [14]. Metalloproteinases are secreted by both keratinocytes and infiltrating immune cells and modulate a number of physiological and pathological processes in the skin and mucous membranes [15,16]. It is possible, therefore, that these enzymes play a fundamental role in mediating the disruption of intercellular and/or cell-ECM adhesion.
The purpose of the present scoping review was to gather evidence for the involvement of MMPs and ADAMs in the pathophysiology of pemphigus and pemphigoid.

2. Methods

2.1. Search Strategy

The review was designed to analyze the role of metalloproteinases in the autoimmune blistering diseases pemphigus and pemphigoid. Evidence was gathered for a variety of experimental settings (in vitro, in vivo, and human studies) from peer-reviewed articles published in MEDLINE/PubMed, as well as from pre-prints available in bioRxiv. The results were reported according to the methodology outlined by the most recent Preferred Reporting Items for Systematic Reviews and Meta-analyses extension for Scoping Reviews (PRISMA-ScR) guidelines [17].
The search was conducted in August 2021 and the following search string was applied to the databases:
(metalloproteinase OR metalloprotease OR gelatinase OR disintegrin OR ADAM) and (Pemphigus OR Pemphigoid).

2.2. Eligibility Criteria

As this review aimed to determine the role of metalloproteinases in autoimmune blistering diseases, articles were included if they involved either disease specimens or disease models and were related to metalloproteinases. Studies were excluded if they were not in English, were review articles, reported on non-autoimmune blistering diseases or did not assess MMPs or ADAMs. There was no time restriction. Only autoimmune forms of pemphigus (i.e., vulgaris, vegetans, foliaceus, erythematosus) were included, whereas non-immune-mediated forms such as Hailey–Hailey disease (benign chronic familial pemphigus) were excluded.

2.3. Data Selection, Collection and Synthesis

After applying the exclusion criteria, a title and abstract screening was conducted to determine if an article was relevant. Articles were excluded if they did not mention pemphigus, pemphigoid, or metalloproteinases. Adhering to the Cochrane guidelines, a lenient policy was adopted during the selection process where there was any uncertainty. In the final phase, full-text screening of each article was performed by two independent reviewers. Data were extracted from the selected articles and tabulated. The main outcomes were evaluated on the basis of (1) the expression of metalloproteinases in pemphigus and pemphigoid, and (2) whether these metalloproteinases were essential for disease development. The pathogenicity criterion was satisfied if the study met the following: (i) serum, IgG, or disease-specific monoclonal antibodies induced pemphigus or pemphigoid-like phenotype in vivo or cell-cell or cell-ECM detachment in vitro; or study in humans; and (ii) a specific pharmacological block, knock-out, knock-down, silencing or inactivation, knock-in or activation, of metalloproteinases prevented or significantly reduced disease phenotype in vivo, cell detachment in vitro, or ameliorated blistering/clinical manifestations in pemphigus or pemphigoid patients.

3. Results

3.1. Overview of the Search Process

Following the implementation of the search strategy, 108 titles were identified on databases. Of these, 29 articles [18,19,20,21,22,23,24,25,26,27,28,29,30,31,32,33,34,35,36,37,38,39,40,41,42,43,44,45,46] met the inclusion criteria and were included in the qualitative synthesis (Figure 1).
The majority of the selected studies focused on pemphigoid (n = 27) whereas only 5 studies were related to pemphigus (Table 1). The most common pemphigoid subtype was bullous pemphigoid (BP, n = 24), followed by ocular mucous membrane (cicatricial) pemphigoid (OCP, n = 4). Pemphigus vulgaris (PV) was exclusively examined in the pemphigus category. In seven studies, two or more blistering diseases were assessed for the expression of metalloproteinases, and diseases also included the autoimmune skin disorders dermatitis herpetiformis (DH, n = 4) and epidermolysis bullosa acquisita (EBA, n = 2).
The expression of MMPs and ADAMs was examined by immunohistochemistry, western blotting, protein arrays, ELISA, DNA microarrays, PCR, and in situ hybridization; MMP2/9 activity was investigated using gelatin zymography and colorimetric MMP assays (Supplementary Table S1). The most commonly studied metalloproteinase was MMP-9 (n = 23) and in six articles, MMP-2 was also investigated. The expression of other MMPs (MMP-1, MMP-3, MMP-8, MMP-12, and MMP-13), ADAM family members (ADAM10 and ADAM17) and TIMPs (TIMP-1) were also reported.

3.2. Summary of Findings

The majority of studies (n = 18) used human samples and assessed metalloproteinase expression in patients’ skin and blister fluid. In vitro and in vivo models were used in 15 and six studies, respectively. In vitro experiments were often carried out in association with either human or animal studies (n = 8). In general, the expression of MMPs was dysregulated in lesional skin of patients with autoimmune blistering diseases. MMP-9 activity was found to be pathogenic in animal models of BP [38,42]. Specifically, mice deficient in functional MMP-9 failed to develop skin blisters in response to anti-mBP180 IgG [42]. In PV, inhibition of ADAM10 prevented blister formation in mice injected with PV IgG that did not contain anti-Dsc antibodies [21].
For a detailed description of individual studies, see Table 1 and Supplementary Table S1.
Table 1. Summary of studies assessing metalloproteinases in pemphigus and pemphigoid.
Table 1. Summary of studies assessing metalloproteinases in pemphigus and pemphigoid.
Ref.First Author, Year TypeDiseaseTarget
[18]Woodward et al., 2020HumanOCPMMP9
[19]Le Jan et al., 2019In vitroBPMMP9
[20]Riani et al., 2019In vitro, humanBPMMP9
[21]Ivars et al., 2020In vivoPVADAM10
[22]de Graauw et al., 2018In vitroBPMMP2/9
[23]Shen et al., 2018HumanBPADAM10
[24]Riani et al., 2017In vitroBPMMP9
[25]Fujimura et al., 2017HumanPV, BPMMP12
[26]Zebrowska et al., 2014HumanBP, DHMMP9
[27]Massie et al., 2015In vitroOCPMMP2/9
[28]Le Jan et al., 2014In vitro, humanBPMMP9
[29]Arafat et al., 2014HumanBPMMP8, MMP9, TIMP1
[30]Zebrowska et al., 2012HumanBP, DHADAM17
[31]Oswald et al., 2012In vitroBPMMP9
[32]Lin et al., 2011In vitro, in vivoBPMMP9
[33]Chan et al., 2011HumanOCPMMP9
[34]Saw et al., 2011In vitroOCPMMP3/8/13
[35]Zebrowska et al., 2009HumanBP, DHADAM8/15/17
[36]Cirillo et al., 2007In vitro, in vivoPVTIMP3, ADAM5, MMP9
[37]Niimi et al., 2006HumanBPMMP2/9/13
[38]Liu et al., 2005In vitro, in vivoBPMMP3/9
[39]Shimanovich et al., 2004In vitroBP, EBAMMP9
[40]Verraes et al., 2001In vitro, humanBPMMP2/9, TIMP1
[41]Liu et al., 2000In vitro, in vivoBPMMP9
[42]Liu et al., 1998In vivoBPMMP9
[43]Saarialho-Kere et al., 1995HumanEB, PV, BPMMP1
[44]Ståhle-Bäckdahl et al., 1994In vitro, humanBPMMP9
[45]Oikarinen et al., 1993HumanBPMMP2/9
[46]Oikarinen et al., 1983HumanBP, DH, PV
BP, bullous pemphigoid; OCP, ocular cicatricial pemphigoid; PV, pemphigus vulgaris; DH, dermatitis herpetiformis; EBA, epidermolysis bullosa acquisita.

4. Discussion

The purpose of this scoping review was to assess the role of metalloproteinases in the pathogenesis of pemphigus and pemphigoid. Despite the relatively limited evidence that is available, a pathogenic role for MMPs and ADAMs in mouse models could successfully be established for both autoimmune blistering diseases.

4.1. MMP-9 and Pemphigoid

An array of descriptive research linking metalloproteinases, particularly MMP-9, to pemphigoid has already been published but there remains a paucity of mechanistic studies. Early work reported 72 and 92 kd collagenases, now known as MMP-2 and MMP-9, in skin blisters of pemphigoid patients [46]. MMP-2 was thought to be produced predominantly by fibroblasts whereas MMP-9 was localized to the epidermis and endothelial cells [45]; later, MMP-9 was also found to be secreted by eosinophils at the site of blister formation [40]. More recently, other sources of MMP-9 in BP blisters have been identified including T cells and monocyte-derived macrophages [20]. It is now well documented that MMP-2 is constitutively expressed in several tissues whereas MMP-9 expression appears to be regulated by a number of cell type-specific signaling pathways, for example during inflammation and in response to a changing redox state [47]. This is consistent with the fact that MMP-9 is highly expressed in inflammatory cells, including macrophages, lymphocytes, neutrophils, and eosinophils [48], which are found in the inflammatory infiltrate of BP blisters.
In a landmark study in 1998, a genetically engineered mouse featuring targeted disruption of the gelatinase B (GB; MMP-9; 92 kD gelatinase) gene was used to explore the immunopathogenesis of pemphigoid [42]. GB-deficient mice were resistant to the blistering effect of intracutaneous anti-mBP180 antibodies but when the mice were reconstituted with normal neutrophils, blister formation occurred, thus implicating neutrophil-derived GB/MMP-9 in the pathogenesis of experimental pemphigoid. A subsequent study from the same group used GB −/− and neutrophil elastase (NE) −/− mice to show that GB acts upstream to regulate NE activity by inactivating alpha1-proteinase inhibitor and that only NE, but not GB/MMP-9, degrades BP180 to produce a dermal-epidermal separation in vivo [41]. This pathogenic pathway was further categorized by the demonstration that the plasminogen (Plg) cascade was also involved in Pemphigoid blister formation. In particular, Plg-deficient mice reconstituted locally with the active form of MMP-9, but not the proenzyme form of MMP-9, develop pemphigoid, thus showing that the Plg/plasmin system is epistatic to MMP-9 activation and subsequent dermal-epidermal separation [38].
Mechanistically, MMP-9 has been shown to cleave the extracellular domain of the 180 kd bullous pemphigoid autoantigen in vitro [44], but not in vivo [41], thus questioning its direct role in causing the dermo-epidermal split. It is worth noting that MMP-9 can cleave BP180 into small tripeptides, which significantly enhance neutrophil chemotaxis and NE release in vivo [28]. Therefore, it is likely that the effects of MMP-9 overexpression in BP are more prominent upstream of the degradation of BP180 and that MMP-9 acts by amplifying the inflammatory cascade and activating proteolytic enzymes, whereas NE is the final executioner of BP180 cleavage [49].
While considerable progress has been made regarding the role of MMPs in the pathogenesis of experimental pemphigoid, no mechanism-based treatments for the disease have been developed to date. This may partially be due to the difference between experimental models and human disease. MMP-9, for example, is essential for blister formation induced by anti-BP180 antibodies in mice, but pemphigoid patients develop autoantibodies against other junctional molecules including BP230, laminin 311, type VII collagen and α6β4 integrin [4,5]. While MMP-9 can target ECM proteins such as type VII collagen and β4 integrin in vitro [50], the capacity of MM9 to induce a dermo-epidermal split in vivo remains to be established.
Interestingly, only the proenzymes of MMP-2/9 could be found in lesional skin and in blister fluid of pemphigoid patients [40] which contrasts to the situation in experimental mice where both the pro- and active forms of MMP-9 were detected in lesional and non-lesional skin samples [32]. This raises the question as to whether the pathophysiological events underlying MMP-9 activation in mouse models also takes place in BP in humans.
Taken together with the lack of clinical translation of MMP inhibitors for the treatment of BP patients, these data suggest that the pathogenic role of MMP-9 in human BP may be more complex than previously anticipated in animal models.

4.2. Metalloproteinases in Pemphigus

Despite the well-known ability of metalloproteinases to cleave the extracellular domain of desmogleins (Dsgs) and other cell adhesion molecules [51,52,53], data relating to their involvement in the pathogenesis of PV are scanty. An increase in the expression of ADAM5 and MMP-9, together with the downregulation of TIMP3, occurs in the skin of mice injected with PV sera [36]. Further, MMP-12 has been detected in the upper layer of epidermis and superficial dermis in PV lesions [25]. Interestingly, PV IgG triggers a significant increase in ADAM10 activity in a Src-dependent manner; inhibition of ADAM10 prevents histological acantholysis and skin blistering in mice injected with IgG from PV patients with a typical autoantibody profile, but not with PV IgG containing antibodies to desmocollins [21]. The authors propose that anti-Dsg IgG-dependent ADAM10 activity leads to EGFR activation and acantholysis but it is also known that ADAM10 targets epithelial cell adhesion molecules by direct cleavage [54]. Overall, these findings indicate that anti-Dsg1/3 antibodies trigger a signaling pathway culminating in pathogenic ADAM10 activation, whereas non-Dsg antibodies in PV induce blistering in an ADAM10-independent manner.

4.3. Limitations and Future Directions

This study has limitations in terms of internal and external validity. The use of only one search engine (PubMed) for peer-reviewed articles together with one pre-print server (bioRxiv) may have failed to identify relevant studies from other databases. Furthermore, our search string focused on a relatively new nomenclature. MMP-1 and MMP-8, for example, were once known as interstitial collagenase and neutrophil collagenase, respectively, and this may have resulted in the exclusion of older studies. Finally, some articles may have been overlooked due to the strict exclusion criteria adopted and the search string used.
The differences between passive transfer mouse models and human disease may hinder the potential translational applications of our results. For example, despite the important role of MMPs in many human diseases, none of the broad-range synthetic MMP inhibitors that have been designed have successfully passed clinical trials [55], partly due to broad-spectrum inhibition of MMPs resulting in severe side effects. Novel classes of selective inhibitors against gelatinases, collagenases, membrane-type and elastase subgroups are being developed [56] and will likely pave the path to new therapeutic strategies.

5. Conclusions

Despite the relatively limited number of studies investigating the role of MMPs in autoimmune blistering diseases, inactivation of ADAM10 and MMP-9 were shown to prevent blister formation in experimental models of pemphigus and pemphigoid, respectively. These molecules and their related pathways represent potential candidates for clinical translation and for developing mechanism-based treatments of these conditions.

Supplementary Materials

The following are available online at https://www.mdpi.com/article/10.3390/biom11101506/s1, Table S1: Detailed list of included studies.

Author Contributions

N.C., conceptualization, methodology, formal analysis, writing—original draft preparation; S.S.P., formal analysis, writing—review and editing. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

Not applicable.

Data Availability Statement

Supplementary results are available with the article. All data items not included in the manuscript are available upon reasonable request to the corresponding author.

Acknowledgments

N.C. gratefully acknowledges the support of the Melbourne Dental School, The University of Melbourne.

Conflicts of Interest

The authors declare no conflict of interest.

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Biomolecules 11 01506 g001
Figure 1. Flowchart of data selection process in accordance with PRISMA-ScR guidelines.
Figure 1. Flowchart of data selection process in accordance with PRISMA-ScR guidelines.
Biomolecules 11 01506 g001
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Cirillo, N.; Prime, S.S. A Scoping Review of the Role of Metalloproteinases in the Pathogenesis of Autoimmune Pemphigus and Pemphigoid. Biomolecules 2021, 11, 1506. https://doi.org/10.3390/biom11101506

AMA Style

Cirillo N, Prime SS. A Scoping Review of the Role of Metalloproteinases in the Pathogenesis of Autoimmune Pemphigus and Pemphigoid. Biomolecules. 2021; 11(10):1506. https://doi.org/10.3390/biom11101506

Chicago/Turabian Style

Cirillo, Nicola, and Stephen S. Prime. 2021. "A Scoping Review of the Role of Metalloproteinases in the Pathogenesis of Autoimmune Pemphigus and Pemphigoid" Biomolecules 11, no. 10: 1506. https://doi.org/10.3390/biom11101506

APA Style

Cirillo, N., & Prime, S. S. (2021). A Scoping Review of the Role of Metalloproteinases in the Pathogenesis of Autoimmune Pemphigus and Pemphigoid. Biomolecules, 11(10), 1506. https://doi.org/10.3390/biom11101506

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