Review of a novel disease entity, immunoglobulin G4-related disease

Abstract

Immunoglobulin G4 (IgG4)-related dacryoadenitis and sialoadenitis (IgG4-DS) are part of a multiorgan fibroinflammatory condition of unknown etiology termed IgG4-related disease (IgG4-RD), which has been recognized as a single diagnostic entity for less than 15 years. Histopathologic examination is critical for diagnosis of IgG4-RD. CD4+ T and B cells, including IgG4-expressing plasma cells, constitute the major inflammatory cell populations in IgG4-RD and are thought to cause organ damage and tissue fibrosis. Patients with IgG4-RD who have active, untreated disease exhibit significant increase of IgG4-secreting plasmablasts in the blood. Considerable insight into the immunologic mechanisms of IgG4-RD has been achieved in the last decade using novel molecular biology approaches, including next-generation and single-cell RNA sequencing. Exploring the interactions between CD4+ T cells and B lineage cells is critical for understanding the pathophysiology of IgG4-RD. Establishment of pathogenic T cell clones and identification of antigens specific to these clones constitutes the first steps in determining the pathogenesis of the disease. Herein, the clinical features and mechanistic insights regarding pathogenesis of IgG4-RD were reviewed.

I. Introduction

Immunoglobulin G4-related disease (IgG4-RD) is a novel clinical disease entity characterized by a chronic fibroinflammatory condition with lymphoplasmacytic infiltration in affected lesions1. The disease mimics many malignant, infectious, and inflammatory disorders with histologic features that are consistently observed across the organs involved. Human IgG can be classified into four subtypes, IgG1, IgG2, IgG3, and IgG4, of which IgG4 is the rarest. However, IgG4-RD is characterized by elevated serum IgG4 concentration and tissue infiltrated by IgG4+ B cells and is termed IgG4 class-switching disease1,2. IgG4-RD may be present in a certain proportion of patients across a wide variety of diseases including Mikuliçz's disease (MD), Küttner's tumor (KT)3, Riedel's thyroiditis, kidney disease, autoimmune pancreatitis, hypophysitis, interstitial pneumonitis, interstitial nephritis, prostatitis, lymphadenopathy, retroperitoneal fibrosis, inflammatory aortic aneurysm, and inflammatory pseudotumor. Thus, this disease can occur in a variety of organs including the pancreas, kidney, lung, lymph nodes, bile duct, liver, aorta, prostate, retroperitoneum, thyroid, and major salivary glands1. The diagnosis of IgG4-RD relies heavily on histopathological analysis and correlation of histology findings with clinical, serological, and radiological data. International consensus statements have been published regarding the nomenclature, pathologic findings, and clinical management of IgG4-RD4,5. Recently, Wallace et al.6 identified four distinctive IgG4-RD phenotypes based on organ involvement and reported that being Asian or female may predispose individuals to disease limited to the head and neck, especially in the salivary and lacrimal glands. The American College of Rheumatology/European League Against Rheumatism Classification Criteria are currently being developed5. Herein, the clinical characteristics of IgG4-RD are described, and up-todate information on mechanistic insights using novel molecular biology approaches is provided.

II. Immunological Insights into the Pathogenesis

1. Imaging of IgG4-RD

Computed tomography (CT), magnetic resonance imaging, and ultrasonography (US) are useful tools to assess organ involvement, monitor therapeutic responses, and guide interventional treatments for IgG4-RD. Furthermore, F-fluorodeoxyglucose (FDG) positron emission tomography/computed tomography (PET/CT) was used to characterize IgG4-RD and showed multi-organ involvement.(Fig. 1. A) FDG-PET/CT enables acquisition of whole-body images and provides functional information regarding disease activity. For example, when focusing on an affected salivary mandibular gland of an IgG4-RD patient, a US image of a lesion showed a hypoechoic area with a reticular pattern in the superficial part and a hypoechoic area with a nodal pattern and high vascularity7,8.(Fig. 1. B)

Fig. 1. Immunoglobulin G4-related disease (IgG4-RD) tends to form tumefactive lesions. A. A 60-year-old male with IgG4-RD showed multi-organ involvement. F-fluorodeoxyglucose (FDG)-positron emission tomography/computed tomography (PET/CT) showed multiple intense uptakes in the bilateral lacrimal glands, submandibular glands, lymph nodes, kidney, pancreas, and retroperitoneum (arrows). B. Ultrasonography shows hypoechoic areas with a nodal pattern and hyperechoic lines (upper). In Doppler mode, the nodal area shows relatively high vascularization (lower). C. Bilateral enlargement of the submandibular glands in an IgG4-RD patient.

2. Affected salivary glands

Both major and minor salivary glands can be affected by IgG4-related dacryoadenitis and sialoadenitis (IgG4-DS).(Fig. 1. C) IgG4-DS is commonly encountered by oral surgeons in the context of MD or KT, especially in Asians, which comprises simultaneous bilateral and symmetrical enlargement of the lacrimal and salivary glands. Some patients, however, only exhibit lacrimal gland disease or may present with unilateral submandibular gland involvement. For many decades, MD was thought to represent a subtype of Sjögren's syndrome (SS); however, now these two diseases are known to be different9.

Comprehensive diagnostic criteria have been proposed for IgG4-RD. Furthermore, organ-specific criteria have been proposed for IgG4-DS9. Using these criteria, biopsies of affected lesions can be used to exclude diseases that often mimic IgG4-DS, including lymphoma, SS, sarcoidosis, sialodocholithiasis, granulomatosis with polyangiitis, and multicentric Castleman's disease10,11. An incisional or excisional biopsy of affected submandibular glands is often the best method for establishing a definitive diagnosis of IgG4-DS9,12.

3. Genetic background of IgG4-RD patients

In numerous previous studies, have investigated risk factors for IgG4-RD, especially type I autoimmune pancreatitis (IgG4-related pancreatitis), were investigated. The HLA-DRB1*0405 and HLA-DQB1*0401 haplotypes were frequently found in Japanese patients with IgG4-related pancreatitis13. In addition to HLA risk loci described in previous reports, several non-human leukocyte antigen (HLA) genes have been identified as risk genes of IgG4-RD. Terao et al.14 reported that, because HLA loci usually showed stronger associations with autoimmune diseases compared with non-HLA loci, detailed analyses of the HLA regions with finemapping genome-wide association study (GWAS) signals using next-generation sequencing and prioritizing amino acid variants or positions critical for IgG4-RD should be conducted as sub-analyses of GWAS.

4. Histopathology of IgG4-RD

Histopathology is critical for diagnosis of IgG4-RD. Major central pathology features include lymphocytic infiltration, obliterate phlebitis, and storiform fibrosis in the affected lesions.(Fig. 2. A) IgG4+ B cells and CD4+ and CD8+ T cells are commonly present (Fig. 2. B–D), and most IgG in the affected organs is IgG4.(Fig. 2. F, 2. G) The finding of abundant IgG4+ plasma cells is helpful to differentiate IgG4-RD from other mimic disorders with a similar presentation. However, IgG4-RD cannot be diagnosed based only on IgG4+ cell infiltration because these plasma cells are present in many other inflammatory disorders15.

Fig. 2. Histopathological features of a submandibular gland affected by fibro-inflammation in an immunoglobulin G4-related dacryoadenitis and sialoadeniti (IgG4-DS) patient. The inflammatory cell infiltrate mainly consists of lymphocytes and plasma cells, and fibrosis is evident throughout the tissue. A. Staining with H&E (×200) shows dense fibrosis with lymphocytes, plasma cells, and occasional eosinophils embedded within. B–D. Immunostaining for CD3 (×200), CD4 (×200), and CD8 (×200) shows that T cells are diffusely distributed. E, F. Immunostaining for IgG (×200) and IgG4 (×200) shows that most IgG-positive cells in affected tissues are also IgG4-positive.

IgG4 is generally considered a non-inflammatory immunoglobulin due to its limited ability to fix complement and bind activating Fc receptors16. Notably, there is no evidence that IgG4 has a primary role in the pathophysiology of IgG4-RD. Furthermore, the activity of IgG4-RD does not always correlate well with serum IgG4 concentration17.

5. Role of T-B interactions in IgG4-RD

It is important to determine which cells are crucial for pathogenesis of IgG4-RD. The first reliable report on the pathophysiology of this disease was from preliminary studies of rituximab (RTX) therapy (anti-CD20 B cell depletion therapy) showing that B cell depletion induced disease remission and led to clinical improvement18,19,20. Active and untreated IgG4-RD patients have an oligoclonally expanded population of circulating plasmablasts with a restricted oligoclonal B cell receptor repertoire21, strongly indicating that IgG4-RD is an antigen-driven disease22. Clonally expanded plasmablasts from IgG4-RD blood are a hallmark of active IgG4-RD. In flow cytometry studies after RTX therapy, clinical improvement correlated with selective depletion of this B cell subpopulation. Oligoclonal proliferation of antibody-producing cells was correlated with disease activity, and marked clinical responsiveness to B cell depletion indicated the importance of B cells in the pathophysiology of IgG4-RD21,23,24.

T cells are also implicated in the pathogenesis of IgG4-RD for several reasons, the most obvious is the histological observation that many CD4+ T cells are present in affected tissues4.(Fig. 2. C) In addition, IgG4-RD was linked to HLA class II based on a GWAS of a Japanese population. T cell responses have long been considered central to the pathophysiology of IgG4-RD; however, interest regarding the T cell population has recently shifted. IgG4-RD has long been considered a CD4+ type 2 helper T (Th2)/CD4+ regulatory helper T (Treg)-driven condition. The presence of dense fibrotic tissues and abundant IgG4+ plasma cells is consistent with an underlying “modified Th2 immune reaction,” which is associated with production of both Th2 (interleukin [IL]-4 and IL-13) and Treg-related cytokines (transforming growth factor [TGF]-β1 and IL-10)25. A novel population of effector memory CD4+ T cells with a cytotoxic function (CD4+ CTLs) was described in IgG4-RD patients using next-generation sequencing20,26. CD4+ CTLs might be antigen-experienced T cells with features of both CD4+ and CD8+ T lymphocytes, which retain the ability to kill target cells in an major histocompatibility complex (MHC) class II-restricted manner27. This cell population likely arises from chronic antigenic stimulation. Notably, a significant reduction of circulating CD4+ CTLs and circulating plasmablasts was observed following RTX therapy20,28 or glucocorticoid therapy in IgG4-RD29. In contrast, circulating naïve CD4+ T cells remained stable after treatment interventions20,28, indicating that this cell population has an important role in the pathophysiology of IgG4-RD.

Pillai et al.30 showed that B cell depletion therapy was effective in autoimmune diseases with somatically hypermutated B cells or plasmablasts at disease sites, which likely serve as critical antigen-presenting cells for a subset of disease-causing T cells. Taken together, these findings strongly indicate an antigen-driven process that requires a critical interaction between CD4+ CTLs and activated B cells31. Regarding pathophysiology, dominantly expanded B cells possibly maintain or present antigens to a subset of expanded CD4+ CTLs in affected tissue sites of IgG4-RD patients31.

A clonally expanded activated B cell population and multiple subsets of T cells are hallmarks of IgG4-RD. New molecular biological technologies have increased the understanding of the pathogenesis of this disease related to activation-causing B cells and CD4+ CTLs. Currently, the focus of research is shifting to follicular helper T (Tfh) cells. Generally, Tfh cells help B cells during T-dependent immune responses. Tfh cells are essential for germinal center formation and affinity maturation, as well as development of most high-affinity antibodies and memory B cells, indicating that disease-specific Tfh cells promote specific class switching to IgG432. Recently, an increased number of blood memory type 2 Tfh (Tfh2) cells has been noted in patients with IgG4-RD33,34,35. Especially, Akiyama et al.34 reported that circulating Tfh2 (cTfh2) cells, but not cTfh1 or cTfh17 cells, induced differentiation of naïve B cells into CD19+ plasmablasts and enhanced production of IgG4 in patients with IgG4-RD. Tfh cells in germinal centers cooperate with B cells in production of antibodies. However, there is no evidence connecting subsets of Tfh cells in the blood with functional counterparts in secondary or tertiary lymphoid organs.

6. Autoantibodies in IgG4-RD

Four different autoantigens have been described as potential triggers for IgG4-RD: prohibitin, annexin A11, laminin 511, and galectin-336,37,38. Shiokawa et al.38 reported antilaminin 511 in 51% of Japanese IgG4-RD patients. However, Liu et al.39 recently reported anti-laminin 511 in only 7% of Caucasian IgG4-RD patients. They reported that the higher prevalence of HLA class II molecules suggests that East Asians compared with Caucasians might be more efficient at presenting immune-dominant peptides from laminin 511 to activated CD4+ T cells, thereby permitting IgG or IgG4 antibody responses. This highlights the importance of cross-validation studies in patients of both East Asian and Western descent39.

7. Innate immunity in IgG4-RD

Innate immunity was also recently shown to have a role in initiation of IgG4-RD. Macrophages, especially CD68+ CD163+ alternatively activated (M2) macrophages, were abundant in affected IgG4-RD tissues and expressed profibrotic factors (CCL18 and TGF-β)40,41,42. Furthermore, in several studies, B cell activating factor (BAFF) secreted by macrophages and basophils reportedly induced IgG4 production by B cells via activation of Toll-like receptors (TLR)43,44. Thus, activated TLR signaling might promote IgG4 production in this disease. Although IgG4-RD model mice have not been established, we recently reported that human TLR7 transgenic (huTlr7) Tg mice developed fibrosis and lymphocytic infiltration in the salivary mandibular glands (SMGs), pancreas, and lung45. A more thorough understanding of how macrophages contribute to IgG4-RD might help elucidate the mechanism of fibrosis in this disease. However, additional research is required to establish a mouse model of IgG4-RD.

8. Targeted treatment results

Most clinical manifestations of IgG4-RD respond to glucocorticoids, which are the first-line, standard care approach for most patients1,46. Masaki et al.47 reported a multicenter phase II prospective clinical trial of glucocorticoid therapy in Japanese patients with IgG4-RD. Hong et al.48 reported that glucocorticoid therapy was beneficial for induction and maintenance therapy in Chinese patients with IgG4-DS. In a randomized, controlled trial of long-term maintenance corticosteroid therapy, Masamune et al.49 reported that maintenance glucocorticoid therapy was effective in reducing relapse in Japanese patients with IgG4-related pancreatitis. One conventional treatment included an initial prednisolone dose of 0.6 to 1.0 mg/kg daily; after 2 to 4 weeks, the dose was tapered by 5 mg every 1 to 2 weeks based on clinical response50. Clinical improvement after initiation of glucocorticoid therapy is rapid, and a follow-up serological evaluation should be performed approximately 2 weeks after therapy. PET/CT may be useful for assessment of treatment responses. A poor response to glucocorticoid therapy might be indicative of other diagnoses, particularly cancer. Furthermore, response to glucocorticoids varies with respect to affected organs and degree of fibrosis. After therapy, salivary secretion in patients with IgG4-DS is more likely to be improved, contrary to glandular function in SS51. These clinical conditions consistent with histologically ductal epithelial cell apoptosis are characteristic of SS but not IgG4-DS.

RTX therapy is typically used for patients who do not respond to glucocorticoids or who experience disease flares during or after glucocorticoid tapers. Important mechanistic insights correlating with pathogenesis of IgG4-RD have been reported after B cell depletion18,19,20,21,31.

III. Conclusion

Fig. 3 shows immunological responses in IgG4-RD subjects who harbor plasmablasts or other activated B cells specific for a subset of autoantigens, including galectin-3, which exhibit oligoclonal restriction resulting in clonal expansion of CD4+ CTLs in tissues. The B lineage cells might also present antigens to relevant Tfh cells52. Furthermore, in IgG4-RD, IL-4-secreting Tfh cells are increased in blood and tissues, which might enable a subset of B cells to undergo differentiation and somatic mutation. In recent studies, interactions among clonally expanded CD4+ CTLs, Tfh cells and B cells were critical for pathogenesis of IgG4-RD. M2 macrophages are the dominant population in affected tissues and might contribute to fibrosis through production of pro-fibrotic cytokines. The important of several findings for the pathogenesis of IgG4-RD has been reported in Table 119,20,21,22,24,25,28,29,33,34,36,37,38,39,42,45,51,52,53,54,55,56,57,58,59,60,61,62,63,64,65,66,67,68,69,70,71,72,73,74,75.

Fig. 3. Immunological responses in immunoglobulin G4-related disease (IgG4-RD). Chronic stimulation via activated antigen-presenting cells induces differentiation of naïve T cells into CD4+ CTLs and follicular helper T (Tfh) cells. In secondary lymphoid organs, Tfh cells collaborate with B cells to drive IgG4 class switching, somatic hypermutation, and plasmablast differentiation of antigen-detecting B cells. Clonally expanded CD4+ CTLs and activated B cells, including IgG4 secreting plasmablasts, might cause IgG4-RD. Reactivation of CD4+ CTLs may require presentation of antigens, including galectin-3, by plasmablasts or other activated B cells at affected tissue sites. Activated CD4+ CTLs and CD8+ cytotoxic T cells may mediate fibrosis and inflammation associated with cytokine secretion or induction of cell death. Activated macrophages may contribute to fibrosis associated with pro-fibrotic cytokine expression.

Table 1. Principal findings regarding the pathogenesis of IgG4-RD.

Involvement in the pathogenesis of IgG4-RD	Reference No.
Organs and conditions associated with IgG4-RD
Orbit	53
Salivary glands (Mikuliçz's disease, Küttner's tumor)	9,51,54,55
Ears, nose, throat, and maxillary mass	56
Thyroid gland (Riedel's thyroiditis)	57
Lymph nodes (lymphadenopathy)	58
Aorta	59
Retroperitoneum (idiopathic retroperitoneal fibrosis, Ormond's disease)	60
Lungs	61
Kidneys	62
Pancreas (type II autoimmune pancreatitis)	63
IgG4-related sclerosing cholangitis	64
B cell phenotype in IgG4-RD
Oligoclonally expanded IgG4-secreting plasmablasts	21
Plasmablasts as a biomarker for IgG4-RD	28
Clinical improvement correlated with B cell depletion therapy	20,24,28
T cell phenotype in IgG4-RD
Th2 responses may result from concomitant atopic manifestations	65
IL-33 might contribute to pathogenesis via aberrant activation of Th2 immune responses	42
Th2 and Treg cells are important for IgG4 production in IgG4-DS	25
Overexpression of IL-21 promotes tertiary lymphoid organ formation and IgG4 production in salivary glands of IgG4-DS patients	66
Clonally expanded CD4+ CTL in IgG4-RD is decreased following rituximab treatment	20
CD4+ CTLs are increased in IgG4-RD and decreased following glucocorticoid treatment	29
Clonally expanded CD4+ CTL and pathogenesis of IgG4-RD; review	19
Circulating IgG4+ plasmablasts are oligoclonally expanded in active and relapsing IgG4-RD	21
Plasmablasts as a biomarker for IgG4-RD independent of serum IgG4 level	28
Increased IL-4-secreting Tfh cells are associated with IgG4 class switching in vivo	52
Increased circulating Tfh2 cells and their capacity to help naïve B cells differentiate into plasmablasts and IgG4 production in vitro	33,34
Tfh cells in the pathogenesis of IgG4-RD; review	67
Lesional Tfh cells in the pathogenesis of IgG4-RD	68
Peripheral helper T cells in IgG4-RD	69
Principal findings regarding autoantigens in IgG4-RD
Identification of galectin-3 as an autoantigen in IgG4-RD	70
Pathogenicity of IgG1 and IgG4 in IgG4-related pancreatitis	71
Laminin 511 is a target antigen in IgG4-related pancreatitis	38
Specific antigen in IgG4-RD; review	22
Annexin A11 is targeted by IgG4 and IgG1 autoantibodies in IgG4-RD	37
Prohibitin is involved in IgG4-RD	36
Disease severity is associated with increased autoantibody diversity in IgG4-RD	39
Macrophages in IgG4-RD
CD68+CD163+ type 2 macrophages contribute to fibrosis in IgG4-RD	72
MARCO expressing type 2 macrophages in IgG4-RD	73
TLR7 expressing type 2 macrophages may promote activation of Th2 immune responses via IL-33 secretion	45
Useful IgG4-RD reviews
IgG4-related disease	1
Treatment of IgG4-RD: current and future approaches	74
Immunological mechanism in IgG4-RD	19
Emerging treatment models in rheumatology	75
Clinical features and mechanistic insights regarding IgG4-DS	9

(IgG4-RD: immunoglobulin G4-related disease, Th2: type 2 helper T, IL: interleukin, IgG4-DS: immunoglobulin G4-related dacryoadenitis and sialoadenitis, Tfh: follicular helper T, MARCO: macrophage receptor with collagenous structure, TLR: Toll-like receptor)