Clinical and immunological variants of ANCA-associated systemic vasculitis: a look at the phenomenon of IgG4 overproduction. Literature review and own observations
https://doi.org/10.47360/1995-4484-2020-550-559
Abstract
About the Authors
T. V. BeketovaRussian Federation
Tatiana V. Beketova
115522, Moscow, Kashirskoe highway, 34a
N. V. Kokosadze
Russian Federation
N.V. Kokosadze
115478, Moscow, Kashirskoe highway, 23
References
1. Jennette J.C., Falk R.J., Bacon P.A., et al. 2012 revised International Chapel Hill Consensus Conference Nomenclature of Vasculitides. Arthritis Rheum. 2013;65(1):1–11. DOI: 10.1002/art.37715
2. Beketova T.V. Diagnostic algorithm for antineutrophil cytoplasmic antibody-associated systemic vasculitis. Terapevticheskii arkhiv = Therapeutic archive. 2018;90(5):13–21 (In Russ.). DOI: 10.26442/terarkh201890513-21
3. Watts R., Lane S., Hanslik T., et al. Development and validation of a consensus methodology for the classification of the ANCAassociated vasculitides and polyarteritis nodosa for epidemiological studies. Ann Rheum Dis. 2007;66(2):222–227. DOI: 10.1136/ard.2006.054593
4. Comarmond C., Crestani B., Tazi A., et al. Pulmonary fibrosis in antineutrophil cytoplasmic antibodies (ANCA)-associated vasculitis: a series of 49 patients and review of the literature. Medicine (Baltimore). 2014;93(24):340–349. DOI: 10.1097/MD.0000000000000217
5. Beketova T.V., Frolova N.F., Stolyarevich E.S., et al. Problems in the diagnosis and treatment of ANCA-associated systemic vasculitis: in the focus of ANCA-negative pauci-immune glomerulonephritis. Nauchno-prakticheskaya revmatologiya = Rheumatology Science and Practice. 2016;54(5):543–552 (In Russ.). DOI: 10.14412/1995-4484-2016-543-552
6. Lindic J., Vizjak A., Ferluga D., et al. Clinical outcome of patients with coexistent antineutrophil cytoplasmic antibodies and antibodies against glomerular basement membrane. Ther Apher Dial. 2009;13(4):278–281. DOI: 10.1111/j.1744-9987.2009.00724.x
7. Chen L.Y.C., Mattman A., Seidman M.A., Carruthers M.N. IgG4-related disease: what a hematologist needs to know. Haematologica. 2019;104(3)444–455. DOI: 10.3324/haematol.2018.205526
8. Vasilyev V.I., Safonova T.N., Socol E.V., et al. Diagnosis of IgG4 – related ophthalmic disease in a group of patients with various lesions of the eye and orbits. Terapevticheskii arkhiv = Therapeutic archive. 2018;90(5):61–71 (In Russ.). DOI: 10.26442/terarkh201890561-71
9. Sokol E.V. IgG4-related disease: what do we know after 20 years. Terapevticheskii arkhiv = Therapeutic archive. 2020; 92 (5): 104–109. DOI: 10.26442/00403660.2020.05.00063
10. Kamisawa T., Anjiki H., Egawa N., Kubota N. Allergic manifestations in autoimmune pancreatitis. Eur J Gastroenterol Hepatol. 2009;21(10):1136–1139. DOI: 10.1097/meg.0b013e3283297417
11. Deshpande V., Zen Y., Chan J.K., et al. Consensus statement on the pathology of IgG4-related disease. Mod Pathol. 2012;25(9):1181–1192. DOI: 10.1038/modpathol.2012.72
12. Dhall D., Suriawinata A.A., Tang L.H., et al. Use of immunohistochemistry for IgG4 in the distinction of autoimmune pancreatitis from peritumoral pancreatitis. Hum Pathol. 2010 May;41(5):643–652. DOI: 10.1016/j.humpath.2009.10.019
13. Deshpande V. The pathology of IgG4-related disease: critical issues and challenger. Seminars in Diagnostic Pathology. 2012;29(4):191–196. DOI: 10.1053/j.semdp.2012.08.001
14. Umehara H., Okazaki K., Masaki Y., et al. Comprehensive diagnostic criteria for IgG4-related disease (IgG4-RD), 2011. Mod Rheumatol. 2012 Feb;22(1):21–30. DOI: 10.1007/s10165011-0571-z
15. Brouwer E., Tervaert J.W., Horst G., et al. Predominance of IgG1 and IgG4 subclasses of anti-neutrophil cytoplasmic autoantibodies (ANCA) in patients with Wegener’s granulomatosis and clinically related disorders. Clin Exp Immunol. 1991;83(3):379–386. DOI: 10.1111/j.1365-2249.1991.tb05647.x
16. Holland M., Hewins P., Goodall M., et al. Anti-neutrophil cytoplasm antibody IgG subclasses in Wegener’s granulomatosis: a possible pathogenic role for the IgG4 subclass. Clin Exp Immunol. 2004;138(1):183–192. DOI: 10.1111/j.1365-2249.2004.02566.x
17. Yamamoto M., Takahashi H., Suzuki C., et al. Analysis of serum IgG subclasses in Churg-Strauss syndrome-the meaning of elevated serum levels of IgG4. Intern Med. 2010;49(14):1365–1370. DOI: 10.2169/internalmedicine.49.3532
18. Stone J.H., Zen Y., Deshpande V. IgG4-related disease. N Engl J Med. 2012;366(6):539–551. DOI: 10.1056/NEJMra1104650
19. Aalberse R.C., Platts-Mills T.A., Rispens T. The developmental history of IgE and IgG4 antibodies in relation to atopy, eosinophilic esophagitis, and the modified TH2 response. Curr Allergy Asthma Rep. 2016;16(6):45. DOI: 10.1007/s11882-016-0621-x
20. Lo A.S., Mao X., Mukherjee E.M., et al. Pathogenicity and epitope characteristics do not differ in IgG subclass-switched anti-desmoglein 3 IgG1 and IgG4 autoantibodies in pemphigus vulgaris. PLoS One. 2016;11(6):e0156800. DOI: 10.1371/journal.pone.0156800
21. Huijbers M.G., Zhang W., Klooster R., et al. MuSK IgG4 autoantibodies cause myasthenia gravis by inhibiting binding between MuSK and Lrp4. Proc Natl Acad Sci U S A. 2013;110(51):2078320788. DOI: 10.1073/pnas.1313944110
22. Zen Y., Fujii T., Harada K., et al. Th2 and regulatory immune reactions are increased in immunoglobin G4-related sclerosing pancreatitis and cholangitis. Hepatology. 2007;45(6):1538–1546. DOI: 10.1002/hep.21697
23. Kanari H., Kagami S., Kashiwakuma D., et al. Role of Th2 cells in IgG4-related lacrimal gland enlargement. Int Arch Allergy Immunol. 2010;152(Suppl 1):47–53. DOI: 10.1159/000312125
24. Detlefsen S., Sipos B., Zhao J., et al. Autoimmune pancreatitis: expression and cellular source of profibrotic cytokines and their receptors. Am J Surg Pathol. 2008;32(7):986–995. DOI: 10.1097/PAS.0b013e31815d2583
25. Okazaki K., Umehara H. Current Concept of IgG4-Related Disease. Curr Top Microbiol Immunol. 2017;401:1–17. DOI: 10.1007/82_2016_47
26. Valenzuela L.M., Draibe J.B., Oliveras X.F., et al. T-lymphocyte in ANCA-associated vasculitis: what do we know? A pathophysiological and therapeutic approach. Clinical Kidney Journal. 2019;12(4):503–511. DOI: 10.1093/ckj/sfz029
27. Sokol E.V., Vasilyev V.I. Treatment of IgG-related disease. Nauchno-prakticheskaya revmatologiya = Rheumatology Science and Practice. 2016;54(3):352–360 (In Russ.). DOI: 10.14412/1995-4484-2016-352-360
28. Sedyshev S.K., Vasil’ev V.I., Kovrigina A.M., et al. IgG4-related disease: patient group characterization and rituximab therapy. Terapevticheskii arkhiv =Therapeutic archive. 2013;85(2):48–53 (In Russ.).
29. Danlos F.X., Rossi G.M., Blockmans D., et al. Antineutrophil cytoplasmic antibody-associated vasculitides and IgG4-related disease: A new overlap syndrome. Autoimmun Rev. 2017;16(10):1036–1043. DOI: 10.1016/j.autrev.2017.07.020
30. Kawashima H., Utsugi A., Shibamiya A., et al. Consideration concerning similarities and differences between ANCA-associated vasculitis and IgG-4-related diseases: case series and review of literature. Immunol Res. 2019;67(1):99–107. DOI: 10.1007/s12026019-9070-7
31. Akiyama K., Yonezaki M., Dobashi H., et al. Case of EGPA and Eosinophilic Chronic Rhinosinusitis Concomitant with IgG4 Related Disease. Nihon Jibiinkoka Gakkai Kaiho. 2017 Feb;120(2):123–130. DOI: 10.3950/jibiinkoka.120.123. PMID: http://www.ncbi.nlm.nih.gov/pubmed/30033930
32. Chang S.Y., Keogh K.A., Lewis J.E., et al. IgG4-positive plasma cells in granulomatosis with polyangiitis (Wegener’s): a clinicopathologic and immunohistochemical study on 43 granulomatosis with polyangiitis and 20 control cases. Hum Pathol. 2013;44(11):2432–2437. DOI: 10.1016/j.humpath.2013.05.023
33. Piao Y., Zhang Y., Yue C., et al. Immunoglobulin G4-related chronic rhinosinusitis: a pitfall in the differential diagnosis of granulomatosis with polyangiitis, Rosai-Dorfman disease, and fungal rhinosinusitis. Hum Pathol. 2018;73:82–88. DOI: 10.1016/j.humpath.2017.12.011
34. Yoo J., Ahn S.S., Jung S.M., et al. No overlap between IgG4related disease and microscopic polyangiitis and granulomatosis with polyangiitis despite elevated serum IgG4 at diagnosis: a retrospective monocentric study. Clin Rheumatol. 2019;38(4):11471154. DOI: 10.1007/s10067-018-4402-x
35. Vaglio A., Strehl J.D., Manger B., et al. IgG4 immune response in Churg-Strauss syndrome. Ann Rheum Dis. 2012;71(3):390–393. DOI: 10.1136/ard.2011.155382
36. Alba M.A., Milisenda J., Fernandez S., et al. Small-vessel vasculitis with prominent IgG4 positive plasma cell infiltrates as potential part of the spectrum of IgG4-related disease: a case report. Clin Exp Rheumatol. 2015;33(2 Suppl 89):138–141.
37. Su T., Yang L., Cui Z., et al. Concurrent IgG4-related tubulointerstitial nephritis and IgG4 myeloperoxidase-anti-neutrophil cytoplasmic antibody positive crescentic glomerulonephritis: A case report. Medicine (Baltimore). 2017;96(20):e6707. DOI: 10.1097/MD.0000000000006707
38. Al-Soudi A., Doorenspleet M.E., Esveldt R.E., et al. IgG4:IgG RNA ratio differentiates active disease from remission in granulomatosis with polyangiitis: a new disease activity marker? A cross-sectional and longitudinal study. Arthritis Res Ther. 2019;21(1):43. DOI: 10.1186/s13075-018-1806-6
39. Tosovský M., Bradna P., Laco J., et al. Case 1-2012: ANCA associated glomerulonephritis in combination with IgG4-positive mediastinal mass in a patient with ankylosing spondylitis treated with TNF alpha inhibitors. Acta Medica (Hradec Kralove). 2012;55(1):42–46. DOI: 10.14712/18059694.2015.74
40. Hanioka Y., Yamagami K., Yoshioka K., et al. Churg-Strauss syndrome concomitant with chronic symmetrical dacryoadenitis suggesting Mikulicz’s disease. Intern Med. 2012;51(17):2457–2461. DOI: 10.2169/internalmedicine.51.7725
41. Paulus Y.M., Cockerham K.P., Cockerham G.C., et al. IgG4positive sclerosing orbital inflammation involving the conjunctiva: a case report. Ocul Immunol Inflamm. 2012;20(5):375–377. DOI: 10.3109/09273948.2012.709574
42. Kotani S., Wakamatsu R., Itoh A., et al. Proteinase 3 anti-neutrophil cytoplasmic antibody (PR3-ANCA) positive IgG4-related retroperitoneal fibrosis: utility of PET-CT with 18F-fluorodeoxy glucose (FDG). Intern Med. 2012;51(7):755–758. DOI: 10.2169/internalmedicine.51.6599
43. Iguchi A., Wada Y., Kobayashi D., et al. A case of MPO- and PR3-ANCA-positive hypertrophic cranial pachymeningitis with elevated serum IgG4. Mod Rheumatol. 2013;23(1):151–155. DOI: 10.1007/s10165-012-0613-1
44. Aragonès J.M., Arias-Rivero M., García-Barrionuevo J.M., et al. IgG4- and MPO-ANCA-associated hypertrophic pachymeningitis. Rev Neurol. 2015;61(10):454–457. DOI: 10.33588/rn.6110.2015121
45. Popkirov S., Kowalski T., Schlegel U., et al. ImmunoglobulinG4-related hypertrophic pachymeningitis with antineutrophil cytoplasmatic antibodies effectively treated with rituximab. J Clin Neurosci 2015;22(6):1038–1040. DOI: 10.1016/j.jocn.2014.12.020
46. Ohno K., Matsuda Y., Arai T., et al. Myeloperoxidaseantineutrophil cytoplasmic antibody-positive otitis media and rhinosinusitis with pathological features of immunoglobulin G4-related disease: a case report. Ann Otol Rhinol Laryngol. 2016;125(6):516–521. DOI: 10.1177/0003489415625072
47. Alexandraki K.I., Kaltsatou M., Chatzellis E., et al. Hypophysitis in IgG4-related disease associated with p-ANCA vasculitis. Am J Med. 2016;129(6):25–27. DOI: 10.1016/j.amjmed.2015.11.021
48. Della-Torre E., Lanzillotta M., Campochiaro C., et al. Antineutrophil cytoplasmic antibody positivity in IgG4-related disease: A case report and review of the literature. Medicine (Baltimore). 2016;95(34):e4633. DOI: 10.1097/MD.0000000000004633
49. Bravais J., Pogliaghi M., Polivka M., et al. IgG4-related disease and ANCA positivity: an overlap syndrome? QJM. 2017;110(11):749–750. DOI: 10.1093/qjmed/hcx134
50. Touge H., Tomita K., Yamasaki A., Shimizu E. A case of proteinase 3 anti-neutrophil cytoplasmic antibody (PR3-ANCA) positive/IgG4-related lung disease. Respir Med Case Rep. 2017;20:92–94. DOI: 10.1016/j.rmcr.2017.01.001
51. Sato S., Morimoto J., Oguchi Y., et al. A Case of Eosinophilic Granulomatosis with Polyangiitis Complicated with A IgG4 Related Disease Like Symptoms. Case Reports Immunol. 2018;2018:3763084. DOI: 10.1155/2018/3763084
Review
For citations:
Beketova T.V., Kokosadze N.V. Clinical and immunological variants of ANCA-associated systemic vasculitis: a look at the phenomenon of IgG4 overproduction. Literature review and own observations. Rheumatology Science and Practice. 2020;58(5):550-559. (In Russ.) https://doi.org/10.47360/1995-4484-2020-550-559