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Современная ревматология

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Роль нейтрофилов при васкулите, ассоциированном с антинейтрофильными цитоплазматическими антителами

https://doi.org/10.14412/1996-7012-2024-6-90-97

Аннотация

Ассоциированный с антинейтрофильными цитоплазматическими антителами васкулит (ААВ) является потенциально опасным аутоиммунным заболеванием и характеризуется некротизирующим воспалением мелких кровеносных сосудов. В патогенезе AAВ как врожденный, так и адаптивный иммунитет тесно связан с функцией нейтрофилов. Изучение патогенетических механизмов активации нейтрофилов при ААВ может послужить предпосылкой для разработки более точных и современных методов лабораторной диагностики, а также новых подходов к лечению, направленных на нейтрофилы. В обзоре представлен анализ исследований, в которых рассматриваются вопросы активации нейтрофилов при ААВ.

Об авторах

Е. Н. Воркель
ФГБНУ «Научно-исследовательский институт ревматологии им. В.А. Насоновой»
Россия

Евгения Николаевна Воркель

115522, Москва, Каширское шоссе, 34А



Т. М. Решетняк
ФГБНУ «Научно-исследовательский институт ревматологии им. В.А. Насоновой»; кафедра ревматологии ФГБОУ ДПО «Российская медицинская академия непрерывного профессионального образования» Минздрава России
Россия

115522, Москва, Каширское шоссе, 34А; 125993, Москва, ул. Баррикадная, 2/1, стр. 1



А. М. Лила
ФГБНУ «Научно-исследовательский институт ревматологии им. В.А. Насоновой»; кафедра ревматологии ФГБОУ ДПО «Российская медицинская академия непрерывного профессионального образования» Минздрава России
Россия

115522, Москва, Каширское шоссе, 34А; 125993, Москва, ул. Баррикадная, 2/1, стр. 1



Литература

1. Jennette JC, Falk RJ, Bacon PA, et al. 2012 revised International Chapel Hill Consensus Conference Nomenclature of Vasculitides. Arthritis Rheum. 2013 Jan;65(1):1-11. doi: 10.1002/art.37715.

2. Бекетова ТВ. Алгоритм диагностики системных васкулитов, ассоциированных с антинейтрофильными цитоплазматическими антителами. Терапевтический архив. 2018;90(5):13-21

3. Новиков ПИ, Семенкова ЕН, Моисеев СВ. Современная номенклатура системных васкулитов. Клиническая фармакология и терапия. 2013;22(1):70-74.

4. Kitching AR, Anders HJ, Basu N, et al. ANCA-associated vasculitis. Nat Rev Dis Primers. 2020 Aug;6(1):71. doi: 10.1038/s41572-020-0204-y.

5. Oristrell J, Loureiro-Amigo J, Solans R, et al. Relapse rate and renal prognosis in ANCA-associated vasculitis according to long-term ANCA patterns. Clin Exp Immunol. 2021 Feb;203(2):209-218. doi: 10.1111/cei.13530.

6. Kolaczkowska E, Kubes P. Neutrophil recruitment and function in health and inflammation. Nat Rev Immunol. 2013 Mar;13(3): 159-75. doi: 10.1038/nri3399.

7. Авдеева АС, Алексанкин АП. Нетоз нейтрофилов: методы лабораторной оценки и роль в патогенезе иммуновоспалительных ревматических заболеваний (обзор литературы). Клиническая лабораторная диагностика. 2024;69(5):206-214.

8. Wigerblad G, Cao Q, Brooks S, et al. Single-Cell Analysis Reveals the Range of Transcriptional States of Circulating Human Neutrophils. J Immunol. 2022 Aug 15;209(4):772- 782. doi: 10.4049/jimmunol.2200154.

9. Shafqat A, Khan JA, Alkachem AY, et al. How Neutrophils Shape the Immune Response: Reassessing Their Multifaceted Role in Health and Disease. Int J Mol Sci. 2023 Dec 18;24(24):17583. doi: 10.3390/ijms242417583.

10. Sheshachalam A, Srivastava N, Mitchell T, et al. Granule protein processing and regulated secretion in neutrophils. Front Immunol. 2014 Sep 19;5:448. doi: 10.3389/fimmu.2014.00448.

11. Насонов ЕЛ, Авдеева АС, Решетняк ТМ и др. Роль нетоза в патогенезе иммуновоспалительных ревматических заболеваний. Научно-практическая ревматология. 2023;61(5):513-530

12. Brinkmann V, Reichard U, Goosmann C, et al. Neutrophil extracellular traps kill bacteria. Science. 2004 Mar 5;303(5663):1532-5. doi: 10.1126/science.1092385.

13. Sorensen OE, Borregaard N. Neutrophil extracellular traps – the dark side of neutrophils. J Clin Invest. 2016 May 2;126(5): 1612-20. doi: 10.1172/JCI84538.

14. Воробьева НВ, Черняк БВ. Нетоз: молекулярные механизмы, роль в физиологии и патологии. Биохимия. 2020;85:1383-97.

15. Hakkim A, Fürnrohr BG, Amann K, et al. Impairment of neutrophil extracellular trap degradation is associated with lupus nephritis. Proc Natl Acad Sci U S A. 2010 May 25;107(21): 9813-8. doi: 10.1073/pnas.0909927107.

16. Silvestre-Roig C, Fridlender ZG, Glogauer M, Scapini P. Neutrophil Diversity in Health and Disease. Trends Immunol. 2019 Jul;40(7):565-583. doi: 10.1016/j.it.2019.04.012.

17. Rosales C. Neutrophils at the crossroads of innate and adaptive immunity. J Leukoc Biol. 2020 Jul;108(1):377-396. doi: 10.1002/JLB.4MIR0220-574RR.

18. Bert S, Nadkarni S, Perretti M. Neutrophil-T cell crosstalk and the control of the host inflammatory response. Immunol Rev. 2023 Mar;314(1):36-49. doi: 10.1111/imr.13162.

19. Супоницкая ЕВ, Александрова ЕН, Насонов ЕЛ. Клиническое значение BAFF/BLyS и APRIL при системной красной волчанке и ревматоидном артрите. Научно-практическая ревматология. 2014;52(5):545-52. [

20. Wigerblad G, Kaplan MJ. Neutrophil extracellular traps in systemic autoimmune and autoinflammatory diseases. Nat Rev Immunol. 2023 May;23(5):274-288. doi: 10.1038/s41577-022-00787-0.

21. Ge S, Zhu X, Xu Q, et al. Neutrophils in ANCA-associated vasculitis: Mechanisms and implications for management. Front Pharmacol. 2022 Sep 23;13:957660. doi: 10.3389/fphar.2022.957660.

22. Kronbichler A, Lee KH, Denicolт S, et al. Immunopathogenesis of ANCA-Associated Vasculitis. Int J Mol Sci. 2020 Oct 3;21(19): 7319. doi: 10.3390/ijms21197319.

23. Walulik A, Lysak K, Blaszkiewicz M, et al. The Role of Neutrophils in ANCA-Associated Vasculitis: The Pathogenic Role and Diagnostic Utility of Autoantibodies. Int J Mol Sci. 2023 Dec 7;24(24):17217. doi: 10.3390/ijms242417217.

24. d'Alessandro M, Conticini E, Bergantini L, et al. Neutrophil Extracellular Traps in ANCA-Associated Vasculitis and Interstitial Lung Disease: A Scoping Review. Life (Basel). 2022 Feb 20;12(2):317. doi: 10.3390/life12020317.

25. Michailidou D, Kuley R, Wang T, et al. Neutrophil extracellular trap formation in anti-neutrophil cytoplasmic antibody-associated and large-vessel vasculitis. Clin Immunol. 2023 Apr;249:109274. doi: 10.1016/j.clim.2023.109274.

26. Shiratori-Aso S, Nakazawa D. The involvement of NETs in ANCA-associated vasculitis. Front Immunol. 2023 Sep 14;14:1261151. doi: 10.3389/fimmu.2023.1261151.

27. Aymonnier K, Amsler J, Lamprecht P, et al. The neutrophil: A key resourceful agent in immune-mediated vasculitis. Immunol Rev. 2023 Mar;314(1):326-356. doi: 10.1111/imr.13170.

28. Bader L, Koldingsnes W, Nossent J. B-lymphocyte activating factor levels are increased in patients with Wegener's granulomatosis and inversely correlated with ANCA titer. Clin Rheumatol. 2010 Sep;29(9):1031-5. doi: 10.1007/s10067-010-1526-z.

29. Brilland B, Garnier AS, Chevailler A, et al. Complement alternative pathway in ANCAassociated vasculitis: Two decades from bench to bedside. Autoimmun Rev. 2020 Jan;19(1): 102424. doi: 10.1016/j.autrev.2019.102424.

30. Gupta AK, Giaglis S, Hasler P, Hahn S. Efficient neutrophil extracellular trap induction requires mobilization of both intracellular and extracellular calcium pools and is modulated by cyclosporine A. PLoS One. 2014 May 12;9(5):e97088. doi: 10.1371/journal.pone. 0097088.

31. Tessarz P, Kouzarides T. Histone core modifications regulating nucleosome structure and dynamics. Nat Rev Mol Cell Biol. 2014 Nov;15(11):703-8. doi: 10.1038/nrm3890.

32. Wang Y, Li M, Stadler S, et al. Histone hypercitrullination mediates chromatin decondensation and neutrophil extracellular trap formation. J Cell Biol. 2009 Jan 26;184(2): 205-13. doi: 10.1083/jcb.200806072.

33. Metzler KD, Goosmann C, Lubojemska A, et al. A myeloperoxidase-containing complex regulates neutrophil elastase release and actin dynamics during NETosis. Cell Rep. 2014 Aug 7;8(3):883-96. doi: 10.1016/j.celrep.2014.06.044.

34. Sun XJ, Li ZY, Chen M. Pathogenesis of anti-neutrophil cytoplasmic antibody-associated vasculitis. Rheumatol Immunol Res. 2023 Apr 18;4(1):11-21. doi: 10.2478/rir2023-0003.

35. Muсoz LE, Lauber K, Schiller M, et al. The role of defective clearance of apoptotic cells in systemic autoimmunity. Nat Rev Rheumatol. 2010 May;6(5):280-9. doi: 10.1038/nrrheum.2010.46.

36. Ma YH, Ma TT, Wang C, et al. High-mobility group box 1 potentiates antineutrophil cytoplasmic antibody-inducing neutrophil extracellular traps formation. Arthritis Res Ther. 2016 Jan 6;18:2. doi: 10.1186/s13075-015-0903-z.

37. Wang C, Wang H, Chang DY, et al. High mobility group box 1 contributes to anti-neutrophil cytoplasmic antibody-induced neutrophils activation through receptor for advanced glycation end products (RAGE) and Toll-like receptor 4. Arthritis Res Ther. 2015 Mar 18;17(1):64. doi: 10.1186/s13075-015-0587-4.

38. Nakazawa D, Masuda S, Tomaru U, Ishizu A. Pathogenesis and therapeutic interventions for ANCA-associated vasculitis. Nat Rev Rheumatol. 2019 Feb;15(2):91-101. doi: 10.1038/s41584-018-0145-y. Erratum in: Nat Rev Rheumatol. 2019 Feb;15(2):123. doi: 10.1038/s41584-019-0168-z.

39. Kuklina E. Semaphorin 4D as a guidance molecule in the immune system. Int Rev Immunol. 2021;40(4):268-273. doi: 10.1080/08830185.2021.1905807.

40. Ito D, Nojima S, Kumanogoh A. The role of semaphorin family in immune systems. Nihon Rinsho Meneki Gakkai Kaishi. 2014;37(1): 1-10. doi: 10.2177/jsci.37.1.

41. Hong L, Li F, Tang C, al. Semaphorin 7A promotes endothelial to mesenchymal transition through ATF3 mediated TGF-β2/Smad signaling. Cell Death Dis. 2020 Aug 10;11(8): 695. doi: 10.1038/s41419-020-02818-x.

42. Nishide M, Nojima S, Ito D, et al. Semaphorin 4D inhibits neutrophil activation and is involved in the pathogenesis of neutrophilmediated autoimmune vasculitis. Ann Rheum Dis. 2017 Aug;76(8):1440-1448. doi: 10.1136/annrheumdis-2016-210706.

43. Ui Mhaonaigh A, Coughlan AM, Dwivedi A, et al. Low Density Granulocytes in ANCA Vasculitis Are Heterogenous and Hypo-Responsive to Anti-Myeloperoxidase Antibodies. Front Immunol. 2019 Nov 7;10:2603. doi: 10.3389/fimmu.2019.02603.

44. Jones BE, Herrera CA, Agosto-Burgos C, et al. ANCA autoantigen gene expression highlights neutrophil heterogeneity where expression in normal-density neutrophils correlates with ANCA-induced activation. Kidney Int. 2020 Sep;98(3):744-757. doi: 10.1016/j.kint.2020.04.037.

45. Lipka S, Ostendorf L, Schneider U, et al. Increased levels of immature and activated low density granulocytes and altered degradation of neutrophil extracellular traps in granulomatosis with polyangiitis. PLoS One. 2023 Mar 15;18(3):e0282919. doi: 10.1371/journal.pone.0282919.

46. Montaldo E, Lusito E, Bianchessi V, et al. Cellular and transcriptional dynamics of human neutrophils at steady state and upon stress. Nat Immunol. 2022 Oct;23(10):1470- 1483. doi: 10.1038/s41590-022-01311-1.

47. Arnold S, Kitching AR, Witko-Sarsat V, et al. Myeloperoxidase-specific antineutrophil cytoplasmic antibody-associated vasculitis. Lancet Rheumatol. 2024 May;6(5):e300-e313. doi: 10.1016/S2665-9913(24)00025-0.

48. Kronbichler A, Leierer J, Shin JI, et al. Association of Pulmonary Hemorrhage, Positive Proteinase 3, and Urinary Red Blood Cell Casts With Venous Thromboembolism in Antineutrophil Cytoplasmic Antibody-Associated Vasculitis. Arthritis Rheumatol. 2019 Nov;71(11): 1888-1893. doi: 10.1002/art.41017.

49. Michailidou D, Duvvuri B, Kuley R, et al. Neutrophil activation in patients with antineutrophil cytoplasmic autoantibody-associated vasculitis and large-vessel vasculitis. Arthritis Res Ther. 2022 Jun 29;24(1):160. doi: 10.1186/s13075-022-02849-z.

50. Soderberg D, Kurz T, Motamedi A, et al. Increased levels of neutrophil extracellular trap remnants in the circulation of patients with small vessel vasculitis, but an inverse correlation to anti-neutrophil cytoplasmic antibodies during remission. Rheumatology (Oxford). 2015 Nov;54(11):2085-94. doi: 10.1093/rheumatology/kev217.

51. Wang H, Sha LL, Ma TT, et al. Circulating Level of Neutrophil Extracellular Traps Is Not a Useful Biomarker for Assessing Disease Activity in Antineutrophil Cytoplasmic Antibody-Associated Vasculitis. PLoS One. 2016 Feb 3;11(2):e0148197. doi: 10.1371/journal.pone.0148197.

52. Moore S, Juo HH, Nielsen CT, et al. Role of Neutrophil Extracellular Traps Regarding Patients at Risk of Increased Disease Activity and Cardiovascular Comorbidity in Systemic Lupus Erythematosus. J Rheumatol. 2020 Nov 1; 47(11):1652-1660. doi: 10.3899/jrheum.190875.

53. Нурбаева КС, Решетняк ТМ, Лила АМ. Нетоз в патогенезе антифосфолипидного синдрома и системной красной волчанки. Современная ревматология. 2021;15(5): 96-102. doi: 10.14412/1996-7012-2021-5-96-102.

54. Manfredi M, Van Hoovels L, Benucci M, et al. Circulating Calprotectin (cCLP) in autoimmune diseases. Autoimmun Rev. 2023 May;22(5):103295. doi: 10.1016/j.autrev.2023.103295.

55. Ometto F, Friso L, Astorri D, et al. Calprotectin in rheumatic diseases. Exp Biol Med (Maywood). 2017 Apr;242(8):859-873. doi: 10.1177/1535370216681551.

56. Pepper RJ, Hamour S, Chavele KM, et al. Leukocyte and serum S100A8/S100A9 expression reflects disease activity in ANCA-associated vasculitis and glomerulonephritis. Kidney Int. 2013 Jun;83(6):1150-8. doi: 10.1038/ki.2013.2.

57. Anton-Pampols P, Martinez Valenzuela L, Fernandez Lorente L, et al. Combining neutrophil and macrophage biomarkers to detect active disease in ANCA vasculitis: a combinatory model of calprotectin and urine CD163. Clin Kidney J. 2022 Dec 7;16(4):693-700. doi: 10.1093/ckj/sfac257.

58. Romand X, Paclet MH, Chuong MV, et al. Serum calprotectin and renal function decline in ANCA-associated vasculitides: a post hoc analysis of MAINRITSAN trial. RMD Open. 2023 Oct;9(4):e003477. doi: 10.1136/rmdopen-2023-003477.

59. Martinez Valenzuela L, Draibe J, Quero Ramos M, et al. Calprotectin as a smoldering activity detection tool and renal prognosis biomarker in ANCA associated vasculitis. PLoS One. 2018 Oct 22;13(10):e0205982. doi: 10.1371/journal.pone.0205982.

60. Yoshida M, Sasaki M, Sugisaki K, et al. Neutrophil extracellular trap components in fibrinoid necrosis of the kidney with myeloperoxidase-ANCA-associated vasculitis. Clin Kidney J. 2013 Jun;6(3):308-12. doi: 10.1093/ckj/sft048.

61. O'Sullivan KM, Lo CY, Summers SA, et al. Renal participation of myeloperoxidase in antineutrophil cytoplasmic antibody (ANCA)-associated glomerulonephritis. Kidney Int. 2015 Nov;88(5):1030-46. doi: 10.1038/ki.2015.202.

62. Takeuchi H, Kawasaki T, Shigematsu K, et al. Neutrophil extracellular traps in neuropathy with anti-neutrophil cytoplasmic autoantibody-associated microscopic polyangiitis. Clin Rheumatol. 2017 Apr;36(4):913-917. doi: 10.1007/s10067-017-3546-4.

63. Matsuda Y, Hamayasu H, Seki A, et al. Presence of Citrullinated Histone H3-Positive Neutrophils in Microscopic Polyangiitis from the Early Phase: An Autopsy Proven Case. Pathol Int. 2016 Aug;66(8):466-71. doi: 10.1111/pin.12434.

64. Nakazawa D, Tomaru U, Yamamoto C, et al. Abundant neutrophil extracellular traps in thrombus of patient with microscopic polyangiitis. Front Immunol. 2012 Nov 12; 3:333. doi: 10.3389/fimmu.2012.00333.

65. Leffler J, Martin M, Gullstrand B, et al. Neutrophil extracellular traps that are not degraded in systemic lupus erythematosus activate complement exacerbating the disease. J Immunol. 2012 Apr 1;188(7):3522-31. doi: 10.4049/jimmunol.1102404.

66. Bach M, Moon J, Moore R, et al. A Neutrophil Activation Biomarker Panel in Prognosis and Monitoring of Patients With Rheumatoid Arthritis. Arthritis Rheumatol. 2020 Jan;72(1):47-56. doi: 10.1002/art.41062.

67. Frangou E, Vassilopoulos D, Boletis J, Boumpas DT. An emerging role of neutrophils and NETosis in chronic inflammation and fibrosis in systemic lupus erythematosus (SLE) and ANCA-associated vasculitides (AAV): Implications for the pathogenesis and treatment. Autoimmun Rev. 2019 Aug;18(8):751- 760. doi: 10.1016/j.autrev.2019.06.011.

68. Negreros M, Flores-Suarez LF. A proposed role of neutrophil extracellular traps and their interplay with fibroblasts in ANCAassociated vasculitis lung fibrosis. Autoimmun Rev. 2021 Apr;20(4):102781. doi: 10.1016/j.autrev.2021.102781.

69. Moiseev S, Lee JM, Zykova A, et al. The alternative complement pathway in ANCAassociated vasculitis: further evidence and a meta-analysis. Clin Exp Immunol. 2020 Dec;202(3):394-402. doi: 10.1111/cei.13498.

70. Massberg S, Grahl L, von Bruehl ML, et al. Reciprocal coupling of coagulation and innate immunity via neutrophil serine proteases. Nat Med. 2010 Aug;16(8):887-96. doi: 10.1038/nm.2184.

71. Харламова ЕН, Решетняк ТМ, Тарасова ГМ. Факторы риска тромбозов при АНЦА-ассоциированных васкулитах. Современная ревматология. 2023;17(2):93-99. doi: 10.14412/1996-7012-2023-2-93-99.


Рецензия

Для цитирования:


Воркель ЕН, Решетняк ТМ, Лила АМ. Роль нейтрофилов при васкулите, ассоциированном с антинейтрофильными цитоплазматическими антителами. Современная ревматология. 2024;18(6):90-97. https://doi.org/10.14412/1996-7012-2024-6-90-97

For citation:


Vorkel EN, Reshetnyak TM, Lila AM. The role of neutrophils in vasculitis associated with antineutrophil cytoplasmic antibodies. Sovremennaya Revmatologiya=Modern Rheumatology Journal. 2024;18(6):90-97. (In Russ.) https://doi.org/10.14412/1996-7012-2024-6-90-97

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ISSN 1996-7012 (Print)
ISSN 2310-158X (Online)