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Pharmacotherapy of autoimmune rheumatic diseases – from monoclonal antibodies to CAR T cells: 20 years later

https://doi.org/10.47360/1995-4484-2024-262-279

Abstract

Autoimmunity is a pathological process associated with a violation of immunological tolerance to normal structural components of the body (autoantigens), associated with the predominance of active (adaptive) immunity and manifested by hyperproduction of autoantibodies. Systemic autoimmune rheumatic diseases (SARDs) are among the most common and severe nosological forms of this pathology associated with autoimmunity. Problems of pharmacotherapy of SARDs are the subject of intensive research. At the beginning of the 21st century, more than 20 biologic agents were developed for the treatment of rheumatoid arthritis – monoclonal antibodies (mAbs) and recombinant proteins that control inflammation associated with the overproduction of “pro-inflammatory” cytokines, the use of which has dramatically improved the results of pharmacotherapy. However, much less research has been devoted to studying the possibilities of pharmacotherapy aimed at selective suppression of the “autoimmune” component of the pathogenesis of SADRs associated with uncontrolled activation of B cells and restoration of immunological tolerance to autoantigens. In the spectrum of drugs whose mechanism of action is associated with the suppression of pathological activation of B cells, the leading place is occupied by rituximab (RTM). It is noteworthy that 20 years ago (2004), a group of researchers led by prof. J.C. Edwards first demonstrated the effectiveness of RTM in patients with RA, which was soon successfully repositioned to treat a wide range of SARDs. A major achievement in the pharmacotherapy of SARDs is associated with the use of CAR (сhimeric antigen receptor) T cell therapy, developed for the treatment of refractory hematological tumors. The main component of CART-cells is a genetically engineered T-cell receptor that recognizes the target antigen without the participation of the major histocompatibility complex. Although limited, extremely impressive data regarding high remission rates have been obtained by adapting CD19 CART-cell therapy to treat patients with severe systemic lupus erythematosus (SLE) and other SARDs refractory to standard immunosuppressive medications. The article discusses the results of the use of CART-cell therapy in SLE and other SARDs and prospects for further research.

About the Authors

E. L. Nasonov
V.A. Nasonova Research Institute of Rheumatology; I.M. Sechenov First Moscow State Medical University of the Ministry of Health Care of the Russian Federation (Sechenov University)
Russian Federation

Evgeny L. Nasonov

115522, Moscow, Kashirskoye Highway, 34A,

119991, Moscow, Trubetskaya str., 8, building 2



A. G. Rumyantsev
Dmitry Rogachev National Research Center of Pediatric Hematology, Oncology and Immunology
Russian Federation

Alexander G. Rumyantsev

117197, Moscow, Samory Mashela str., 1

 



M. Yu. Samsonov
I.M. Sechenov First Moscow State Medical University of the Ministry of Health Care of the Russian Federation (Sechenov University); R-Pharm, JSC
Russian Federation

Mikhail Yu. Samsonov

119991, Moscow, Trubetskaya str., 8, building 2,

119421, Moscow, Leninsky avenue, 111 



References

1. Theofilopoulos AN, Kono DH, Baccala R. The multiple pathways to autoimmunity. Nat Immunol. 2017;18(7):716-724. doi: 10.1038/ni.3731

2. Nasonov EL. Modern concept of autoimmunity in rheumatology. Nauchno-Prakticheskaya Revmatologia = Rheumatology Science and Practice. 2023;61(4):397-420 (In Russ.). doi: 10.47360/1995-4484-2023-397-420

3. Wang L, Wang FS, Gershwin ME. Human autoimmune diseases: A comprehensive update. J Intern Med. 2015;278(4):369-395. doi: 10.1111/joim.12395

4. Miller FW. The increasing prevalence of autoimmunity and autoimmune diseases: An urgent call to action for improved understanding, diagnosis, treatment, and prevention. Curr Opin Immunol. 2023;80:102266. doi: 10.1016/j.coi.2022.102266

5. Conrad N, Misra S, Verbakel JY, Verbeke G, Molenberghs G, Taylor PN, et al. Incidence, prevalence, and co-occurrence of autoimmune disorders over time and by age, sex, and socioeconomic status: A population-based cohort study of 22 million individuals in the UK. Lancet. 2023;401(10391):1878-1890. doi: 10.1016/S0140-6736(23)00457-9

6. Thomas SL, Griffiths C, Smeeth L, Rooney C, Hall AJ. Burden of mortality associated with autoimmune diseases among females in the United Kingdom. Am J Public Health. 2010;100(11):2279- 2287. doi: 10.2105/AJPH.2009.180273

7. Mitratza M, Klijs B, Hak AE, Kardaun JWPF, Kunst AE. Systemic autoimmune disease as a cause of death: Mortality burden and comorbidities. Rheumatology (Oxford). 2021;60(3):1321-1330. doi: 10.1093/rheumatology/keaa537

8. Szekanecz Z, McInnes IB, Schett G, Szamosi S, Benkő S, Szűcs G. Autoinflammation and autoimmunity across rheumatic and musculoskeletal diseases. Nat Rev Rheumatol. 2021;17(10):585-595. doi: 10.1038/s41584-021-00652-9

9. Pisetsky DS. Pathogenesis of autoimmune disease. Nat Rev Nephrol. 2023;19(8):509-524. doi: 10.1038/s41581-023-00720-1

10. Rubin SJS, Bloom MS, Robinson WH. B cell checkpoints in autoimmune rheumatic diseases. Nat Rev Rheumatol. 2019;15(5):303- 315. doi: 10.1038/s41584-019-0211-0

11. Pouw JN, Leijten EFA, van Laar JM, Boes M. Revisiting B cell tolerance and autoantibodies in seropositive and seronegative autoimmune rheumatic disease (AIRD). Clin Exp Immunol. 2021;203(2):160-173. doi: 10.1111/cei.13542

12. de Gruijter NM, Jebson B, Rosser EC. Cytokine production by human B cells: Role in health and autoimmune disease. Clin Exp Immunol. 2022;210(3):253-262. doi: 10.1093/cei/uxac090

13. Hendriks RW, Corneth OBJ. B cell signaling and activation in autoimmunity. Cells. 2023;12(3):499. doi: 10.3390/cells12030499

14. Zhu Q, Rui K, Wang S, Tian J. Advances of regulatory B cells in autoimmune diseases. Front Immunol. 2021;12:592914. doi: 10.3389/fimmu.2021.592914

15. Walker LSK. The link between circulating follicular helper T cells and autoimmunity. Nat Rev Immunol. 2022;22(9):567-575. doi: 10.1038/s41577-022-00693-5

16. Mouat IC, Goldberg E, Horwitz MS. Age-associated B cells in autoimmune diseases. Cell Mol Life Sci. 2022;79(8):402. doi: 10.1007/s00018-022-04433-9

17. Jenks SA, Cashman KS, Woodruff MC, Lee FE, Sanz I. Extrafollicular responses in humans and SLE. Immunol Rev. 2019;288(1):136-148. doi: 10.1111/imr.12741

18. Avrameas S, Alexopoulos H, Moutsopoulos HM. Natural autoantibodies: An undersugn hero of the immune system and autoimmune disorders – A point of view. Front Immunol. 2018;9:1320. doi: 10.3389/fimmu.2018.01320

19. Skevaki C, Wesemann DR. Antibody repertoire and autoimmunity. J Allergy Clin Immunol. 2023;151(4):898-900. doi: 10.1016/j.jaci.2023.02.008

20. Burbelo PD, Iadarola MJ, Keller JM, Warner BM. Autoantibodies targeting intracellular and extracellular proteins in autoimmunity. Front Immunol. 2021;12:548469. doi: 10.3389/fimmu.2021.548469

21. Ludwig RJ, Vanhoorelbeke K, Leypoldt F, Kaya Z, Bieber K, McLachlan SM, et al. Mechanisms of autoantibody-induced pathology. Front Immunol. 2017;8:603. doi: 10.3389/fimmu.2017.00603

22. Suurmond J, Diamond B. Autoantibodies in systemic autoimmune diseases: Specificity and pathogenicity. J Clin Invest. 2015;125(6):2194-2202. doi: 10.1172/JCI78084

23. Frazzei G, van Vollenhoven RF, de Jong BA, Siegelaar SE, van Schaardenburg D. Preclinical autoimmune disease: A comparison of rheumatoid arthritis, systemic lupus erythematosus, multiple sclerosis and type 1 diabetes. Front Immunol. 2022;13:899372. doi: 10.3389/fimmu.2022.899372

24. Ma WT, Chang C, Gershwin ME, Lian ZX. Development of autoantibodies precedes clinical manifestations of autoimmune diseases: A comprehensive review. J Autoimmun. 2017;83:95-112. doi: 10.1016/j.jaut.2017.07.003

25. Bieber K, Hundt JE, Yu X, Ehlers M, Petersen F, Karsten CM, et al. Autoimmune pre-disease. Autoimmun Rev. 2023;22(2):103236. doi: 10.1016/j.autrev.2022.103236

26. He Y, Aoun M, Holmdahl R. Shoft in perspective: Autoimmunity protecting against rheumatoid arthritis. Ann Rheum Dis. 2024;83(5):550-555. doi: 101136/ard-2023-225237

27. Fugger L, Jensen LT, Rossjohn J. Challenges, progress, and prospects of developing therapies to treat autoimmune diseases. Cell. 2020;181(1):63-80. doi: 10.1016/j.cell.2020.03.007

28. Baker KF, Isaacs JD. Novel therapies for immune-mediated inflammatory diseases: What can we learn from their use in rheumatoid arthritis, spondyloarthritis, systemic lupus erythematosus, psoriasis, Crohn’s disease and ulcerative colitis? Ann Rheum Dis. 2018;77(2):175-187. doi: 10.1136/annrheumdis-2017-211555

29. Nasonov EL. Pharmacotherapy for rheumatoid arthritis: New strategy, new targets. Nauchno-Prakticheskaya Revmatologia = Rheumatology Science and Practice. 2017;55(4):409- 419 (In Russ.). doi: 10.14412/1995-4484-2017-409-419

30. Nasonov EL, Soloviev SK, Arshinov AV. Systemic lupus erythematosus: History and modernity. Nauchno-Prakticheskaya Revmatologia = Rheumatology Science and Practice. 2022;60(4):397-412 (In Russ.). doi: 10.47360/1995-4484-2022-397-412

31. Nasonov EL, Popkova TV, Lila AM. Belimumab in the treatment of systemic lupus erythematosus: 20 years of basic research, 10 years of clinical practice. Nauchno-Prakticheskaya Revmatologia = Rheumatology Science and Practice. 2021;59(4):367-383 (In Russ.). doi: 10.47360/1995-4484-2021-367-383

32. Marinho A, Delgado Alves J, Fortuna J, Faria R, Almeida I, Alves G, et al. Biological therapy in systemic lupus erythematosus, antiphospholipid syndrome, and Sjögren’s syndrome: evidenceand practice-based guidance. Front Immunol. 2023;14:1117699. doi: 10.3389/fimmu.2023.1117699

33. Felten R, Mertz P, Sebbag E, Scherlinger M, Arnaud L. Novel therapeutic strategies for autoimmune and inflammatory rheumatic diseases. Drug Discov Today. 2023;28(7):103612. doi: 10.1016/j.drudis.2023.103612

34. Nasonov EL, Lila AM. Janus kinase inhibitors in immuno-inflammatory rheumatic diseases: New opportunities and prospects. Nauchno-Prakticheskaya Revmatologia = Rheumatology Science and Practice. 2019;57(1):8-16 (In Russ.). doi: 10.14412/1995-4484-2019-8-16

35. McInnes IB, Gravallese EM. Immune-mediated inflammatory disease therapeutics: Past, present and future. Nat Rev Immunol. 2021;21(10):680-686. doi: 10.1038/s41577-021-00603-1

36. Stanway JA, Isaacs JD. Tolerance-inducing medicines in autoimmunity: Rheumatology and beyond. Lancet Rheumatol. 2020;2(9):e565-e575. doi: 10.1016/S2665-9913(20)30100-4

37. Nasonov EL (ed.). Anti-B cell therapy in rheumatology: Focus on rituximab. Moscow:IMA-PRESS;2012 (In Russ.).

38. Lee DSW, Rojas OL, Gommerman JL. B cell depletion therapies in autoimmune disease: Advances and mechanistic insights. Nat Rev Drug Discov. 2021;20(3):179-199. doi: 10.1038/s41573-020-00092-2

39. Nasonov EL, Beketova TV, Ananyeva LP, Vasilyev VI, Solovyev SK, Avdeeva AS Prospects for anti-B-cell therapy in immuno-inflammatory rheumatic diseases. Nauchno-Prakticheskaya Revmatologia = Rheumatology Science and Practice. 2019;57:1-40 (In Russ.). doi: 10.14412/1995-4484-2019-3-40

40. Barnas JL, Looney RJ, Anolik JH. B cell targeted therapies in autoimmune disease. Curr Opin Immunol. 2019;61:92-99. doi: 10.1016/j.coi.2019.09.004

41. Edwards JC, Szczepanski L, Szechinski J, Filipowicz-Sosnowska A, Emery P, Close DR, et al. Efficacy of B-cell-targeted therapy with rituximab in patients with rheumatoid arthritis. N Engl J Med. 2004;350(25):2572-2581. doi: 10.1056/NEJMoa032534

42. Mostkowska A, Rousseau G, Raynal Noël J-M. Repurposing of rituximab biosimilars to treat B cell mediated autoimmune diseases. medRxiv. 2023.09.22.23295633. doi: 10.1101/2023.09.22.23295633

43. Nasonov EL (ed.). Russian clinical guidelines. Moscow:GEOTAR-Media;2017:113-141 (In Russ.).

44. Smolen JS, Landewé R, Breedveld FC, Dougados M, Emery P, Gaujoux-Viala C, et al. EULAR recommendations for the management of rheumatoid arthritis with synthetic and biological disease-modifying antirheumatic drugs. Ann Rheum Dis. 2010;69(6):964-975. doi: 10.1136/ard.2009.126532

45. Fraenkel L, Bathon JM, England BR, St Clair EW, Arayssi T, Carandang K, et al. 2021 American College of Rheumatology guideline for the treatment of rheumatoid arthritis. Arthritis Care Res (Hoboken). 2021;73(7):924-939. doi: 10.1002/acr.24596

46. Fanouriakis A, Kostopoulou M, Andersen J, Aringer M, Arnaud L, Bae SC, et al. EULAR recommendations for the management of systemic lupus erythematosus: 2023 update. Ann Rheum Dis. 2024;83(1):15-29. doi: 10.1136/ard-2023-224762

47. Tektonidou MG, Andreoli L, Limper M, Amoura Z, Cervera R, Costedoat-Chalumeau N, et al. EULAR recommendations for the management of antiphospholipid syndrome in adults. Ann Rheum Dis. 2019;78(10):1296-1304. doi: 10.1136/annrheumdis-2019-215213

48. Jacobs L, Wauters N, Lablad Y, Morelle J, Taghavi M. Diagnosis and management of catastrophic antiphospholipid syndrome and the potential impact of the 2023 ACR/EULAR antiphospholipid syndrome classification criteria. Antibodies (Basel). 2024;13(1):21. doi: 10.3390/antib13010021

49. Bitsadze V, Yakubova F, Khizroeva J, Lazarchuk A, Salnikova P, Vorobev A, et al. Catastrophic antiphospholipid syndrome. Int J Mol Sci. 2024;25(1):668. doi: 10.3390/ijms25010668

50. Chen YH, Wang XY, Jin X, Yang Z, Xu J. Rituximab therapy for primary Sjögren’s syndrome. Front Pharmacol. 2021;12:731122. doi: 10.3389/fphar.2021.731122

51. Ramos-Casals M, Brito-Zerón P, Bombardieri S, Bootsma H, De Vita S, Dörner T, et al.; EULAR-Sjögren Syndrome Task Force Group. EULAR recommendations for the management of Sjögren’s syndrome with topical and systemic therapies. Ann Rheum Dis. 2020;79(1):3-18. doi: 10.1136/annrheumdis-2019-216114

52. Hellmich B, Sanchez-Alamo B, Schirmer JH, Berti A, Blockmans D, Cid MC, et al. EULAR recommendations for the management of ANCA-associated vasculitis: 2022 update. Ann Rheum Dis. 2024;83(1):30-47. doi: 10.1136/ard-2022-223764

53. Beketova TV, Popov IYu, Babak VV. Review of guideline for the management of ANCA-associated vasculitis, presented in 2021 by the American College of Rheumatology/Vasculitis Foundation. Nauchno-Prakticheskaya Revmatologia = Rheumatology Science and Practice. 2021;59(6):684-692 (In Russ.). doi: 10.47360/1995-4484-2021-684-692

54. Xiong A, Yang G, Song Z, Xiong C, Liu D, Shuai Y, et al. Rituximab in the treatment of immune-mediated necrotizing myopathy: A review of case reports and case series. Ther Adv Neurol Disord. 2021;14:1756286421998918. doi: 10.1177/1756286421998918

55. Romero-Bueno F, Diaz Del Campo P, Trallero-Araguás E, RuizRodríguez JC, Castellvi I, Rodriguez-Nieto MJ, Martínez-Becerra MJ, et al.; MEDRA5 (Spanish MDA5 Register) group (listed contributors at the end of the article). Recommendations for the treatment of anti-melanoma differentiation-associated gene 5-positive dermatomyositis-associated rapidly progressive interstitial lung disease. Semin Arthritis Rheum. 2020;50(4):776-790. doi: 10.1016/j.semarthrit.2020.03.007

56. Cambridge G, Leandro MJ, Teodorescu M, Manson J, Rahman A, Isenberg DA, et al. B cell depletion therapy in systemic lupus erythematosus: Effect on autoantibody and antimicrobial antibody profiles. Arthritis Rheum. 2006;54(11):3612-3622. doi: 10.1002/art.22211

57. Lazarus MN, Turner-Stokes T, Chavele KM, Isenberg DA, Ehrenstein MR. B-cell numbers and phenotype at clinical relapse following rituximab therapy differ in SLE patients according to anti-dsDNA antibody levels. Rheumatology (Oxford). 2012;51(7):1208-1215. doi: 10.1093/rheumatology/ker526

58. Tew GW, Rabbee N, Wolslegel K, Hsieh HJ, Monroe JG, Behrens TW, et al. Baseline autoantibody profiles predict normalization of complement and anti-dsDNA autoantibody levels following rituximab treatment in systemic lupus erythematosus. Lupus. 2010;19(2):146-157. doi: 10.1177/0961203309350752

59. Tsanian MÉ, Torgashina AV, Aleksandrova EN, Solovev SK, Nasonov EL. Anti-C1q antibodies in patients with systemic lupus erythematosus treated by rituximab. Terapevticheskii arkhiv. 2013;85(5):53-59 (In Russ.).

60. Cambridge G, Leandro MJ, Lahey LJ, Fairhead T, Robinson WH, Sokolove J. B cell depletion with rituximab in patients with rheumatoid arthritis: Multiplex bead array reveals the kinetics of IgG and IgA antibodies to citrullinated antigens. J Autoimmun. 2016;70:22-30. doi: 10.1016/j.jaut.2016.03.010

61. Modi S, Soejima M, Levesque MC. The effect of targeted rheumatoid arthritis therapies on anti-citrullinated protein autoantibody levels and B cell responses. Clin Exp Immunol. 2013;173(1):8-17. doi: 10.1111/cei.12114

62. Lindenberg L, Spengler L, Bang H, Dorner T, Maslyanskiy AL, Lapin SV, et al. Restrictive IgG antibody response against mutated citrullinated vimentin predicts response to rituximab in patients with rheumatoid arthritis. Arthritis Res Ther. 2015;17(1):206. doi: 10.1186/s13075-015-0717-z

63. Cortazar FB, Pendergraft WF 3rd, Wenger J, Owens CT, Laliberte K, Niles JL. Effect of continuous B cell depletion with rituximab on pathogenic autoantibodies and total IgG levels in antineutrophil cytoplasmic antibody-associated vasculitis. Arthritis Rheumatol. 2017;69(5):1045-1053. doi: 10.1002/art.40032

64. Ananyeva LP, Garzanova LA, Koneva OA, Starovoytova MN, Desinova OV, Ovsyannikova OB, et al. Antitopoisomerase 1 antibody level changes after B сell depletion therapy in systemic sclerosis. Nauchno-Prakticheskaya Revmatologia = Rheumatology Science and Practice. 2022;60(1):57-63 (In Russ.) doi: 10.47360/1995-4484-2022-57-63

65. Moazedi-Fuerst FC, Kielhauser SM, Hermann J, Meilinger M, Demel U, Stradner MH, et al. Decrease in autoantibody titres during long-term treatment of scleroderma with rituximab: A promising surveillance marker of therapy? Scand J Rheumatol. 2015;44(6):519-520. doi: 10.3109/03009742.2015.1069888

66. Crickx E, Weill JC, Reynaud CA, Mahévas M. Anti-CD20-mediated B-cell depletion in autoimmune diseases: Successes, failures and future perspectives. Kidney Int. 2020;97(5):885-893. doi: 10.1016/j.kint.2019.12.025

67. Chatzidionysiou K, Lie E, Nasonov E, Lukina G, Hetland ML, Tarp U, et al. Highest clinical effectiveness of rituximab in autoantibody-positive patients with rheumatoid arthritis and in those for whom no more than one previous TNF antagonist has failed: Pooled data from 10 European registries. Ann Rheum Dis. 2011;70(9):1575-1580. doi: 10.1136/ard.2010.148759

68. Cooles FAH, Isaacs JD. The interferon gene signature as a clinically relevant biomarker in autoimmune rheumatic disease. Lancet Rheumatol. 2022;4(1):e61-e72. doi: 10.1016/S2665-9913(21)00254-X

69. Rivellese F, Nerviani A, Giorli G, Warren L, Jaworska E, Bombardieri M, et al.; STRAP collaborative group. Stratification of biological therapies by pathobiology in biologic-naive patients with rheumatoid arthritis (STRAP and STRAP-EU): Two parallel, open-label, biopsy-driven, randomised trials. Lancet Rheumatol. 2023;5(11):e648-e659. doi: 10.1016/S2665-9913(23)00241-2

70. Rodziewicz M, Mendoza-Pinto C, Dyball S, Munguía-Realpozo P, Parker B, Bruce IN. Predictors and prognostic factors influencing outcomes of anti-CD20 monoclonal antibodies in systemic lupus erythematosus: A systematic review update. Semin Arthritis Rheum. 2024;65:152346. doi: 10.1016/j.semarthrit.2023.152346

71. Gerlag DM, Safy M, Maijer KI, Tang MW, Tas SW, StarmansKool MJF, et al. Effects of B-cell directed therapy on the preclinical stage of rheumatoid arthritis: The PRAIRI study. Ann Rheum Dis. 2019;78(2):179-185. doi: 10.1136/annrheumdis-2017-212763

72. Werner A, Schäfer S, Zaytseva O, Albert H, Lux A, Krištić J, et al. Targeting B cells in the pre-phase of systemic autoimmunity globally interferes with autoimmune pathology. iScience. 2021;24(9):103076. doi: 10.1016/j.isci.2021.103076

73. Kaegi C, Wuest B, Crowley C, Boyman O. Systematic review of safety and efficacy of second- and third-generation CD20-targeting biologics in treating immune-mediated disorders. Front Immunol. 2022;12:788830. doi: 10.3389/fimmu.2021.788830

74. Furie RA, Aroca G, Cascino MD, Garg JP, Rovin BH, Alvarez A, et al. B-cell depletion with obinutuzumab for the treatment of proliferative lupus nephritis: A randomised, double-blind, placebocontrolled trial. Ann Rheum Dis. 2022;81(1):100-107. doi: 10.1136/annrheumdis-2021-220920

75. Rovin BH, Furie RA, Ross Terres JA, Giang S, Schindler T, Turchetta A, et al. Kidney outcomes and preservation of kidney function with obinutuzumab in patients with lupus nephritis: A post hoc analysis of the NOBILITY trial. Arthritis Rheumatol. 2024;76(2):247-254. doi: 10.1002/art.42734

76. Thurlings RM, Vos K, Wijbrandts CA, Zwinderman AH, Gerlag DM, Tak PP. Synovial tissue response to rituximab: Mechanism of action and identification of biomarkers of response. Ann Rheum Dis. 2008;67(7):917-925. doi: 10.1136/ard.2007.080960

77. Kamburova EG, Koenen HJ, Borgman KJ, ten Berge IJ, Joosten I, Hilbrands LB. A single dose of rituximab does not deplete B cells in secondary lymphoid organs but alters phenotype and function. Am J Transplant. 2013;13(6):1503-1511. doi: 10.1111/ajt.12220

78. Robinson JI, Md Yusof MY, Davies V, Wild D, Morgan M, Taylor JC, et al.; MATURA Consortia; MASTERPLANS Consortia. Comprehensive genetic and functional analyses of Fc gamma receptors influence on response to rituximab therapy for autoimmunity. EBioMedicine. 2022;86:104343. doi: 10.1016/j.ebiom.2022.104343

79. Frampton JE. Inebilizumab: First approval. Drugs. 2020;80(12):1259-1264. doi: 10.1007/s40265-020-01370-4

80. Nie T, Blair HA. Inebilizumab: A review in neuromyelitis optica spectrum disorder. CNS Drugs. 2022;36(10):1133-1141. doi: 10.1007/s40263-022-00949-7

81. Merrill JT, Guthridge J, Smith M, June J, Koumpouras F, Machua W, et al. Obexelimab in systemic lupus erythematosus with exploration of response based on gene pathway co-expression patterns: A double-blind, randomized, placebo-controlled, phase 2 trial. Arthritis Rheumatol. 2023;75(12):2185-2194. doi: 10.1002/art.42652

82. Boyles JS, Sadowski D, Potter S, Vukojicic A, Parker J, Chang WY, et al. A nondepleting anti-CD19 antibody impairs B cell function and inhibits autoimmune diseases. JCI Insight. 2023;8(13):e166137. doi: 10.1172/jci.insight.166137

83. Clowse ME, Wallace DJ, Furie RA, Petri MA, Pike MC, Leszczyński P, et al.; EMBODY Investigator Group. Efficacy and safety of epratuzumab in moderately to severely active systemic lupus erythematosus: Results from two phase III randomized, double-blind, placebo-controlled trials. Arthritis Rheumatol. 2017;69(2):362-375. doi: 10.1002/art.39856

84. Gottenberg JE, Dörner T, Bootsma H, Devauchelle-Pensec V, Bowman SJ, Mariette X, et al. Efficacy of epratuzumab, an antiCD22 monoclonal IgG antibody, in systemic lupus erythematosus patients with associated Sjögren’s syndrome: Post hoc analyses from the EMBODY trials. Arthritis Rheumatol. 2018;70(5):763- 773. doi: 10.1002/art.40425

85. Hiepe F, Radbruch A. Plasma cells as an innovative target in autoimmune disease with renal manifestations. Nat Rev Nephrol. 2016;12(4):232-240. doi: 10.1038/nrneph.2016.20

86. Holzer MT, Ruffer N, Huber TB, Kötter I, Ostendorf L, Krusche M. Daratumumab for autoimmune diseases: A systematic review. RMD Open. 2023;9(4):e003604. doi: 10.1136/rmdopen-2023-003604

87. Stohl W, Hilbert DM. The discovery and development of belimumab: The anti-BLyS-lupus connection. Nat Biotechnol. 2012;30(1):69-77. doi: 10.1038/nbt.2076

88. Nasonov EL, Popkova TV, Lila AM. Belimumab in the treatment of systemic lupus erythematosus: 20 years of basic research, 10 years of clinical practice. Nauchno-Prakticheskaya Revmatologia = Rheumatology Science and Practice. 2021;59(4):367-383 (In Russ.). doi: 10.47360/1995-4484-2021-367-383

89. Vincent FB, Morand EF, Schneider P, Mackay F. The BAFF/ APRIL system in SLE pathogenesis. Nat Rev Rheumatol. 2014;10(6):365-373. doi: 10.1038/nrrheum.2014.33

90. Wise LM, Stohl W. Belimumab and rituximab in systemic lupus erythematosus: A tale of two B cell-targeting agents. Front Med (Lausanne). 2020;7:303. doi: 10.3389/fmed.2020.00303

91. Shipa M, Santos LR, Nguyen DX, Embleton-Thirsk A, Parvaz M, Heptinstall LL, et al. Identification of biomarkers to stratify response to B-cell-targeted therapies in systemic lupus erythematosus: An exploratory analysis of a randomised controlled trial. Lancet Rheumatol. 2022;5(1):e24-e35. doi: 10.1016/S2665-9913(22)00332-0

92. Kaegi C, Steiner UC, Wuest B, Crowley C, Boyman O. Systematic review of safety and efficacy of atacicept in treating immunemediated disorders. Front Immunol. 2020;11:433. doi: 10.3389/fimmu.2020.00433.

93. Merrill JT, Shanahan WR, Scheinberg M, Kalunian KC, Wofsy D, Martin RS. Phase III trial results with blisibimod, a selective inhibitor of B-cell activating factor, in subjects with systemic lupus erythematosus (SLE): Results from a randomised, double-blind, placebo-controlled trial. Ann Rheum Dis. 2018;77(6):883-889. doi: 10.1136/annrheumdis-2018-213032

94. Merrill JT, van Vollenhoven RF, Buyon JP, Furie RA, Stohl W, Morgan-Cox M, et al. Efficacy and safety of subcutaneous tabalumab, a monoclonal antibody to B-cell activating factor, in patients with systemic lupus erythematosus: Results from ILLUMINATE-2, a 52-week, phase III, multicentre, randomised, double-blind, placebo-controlled study. Ann Rheum Dis. 2016;75(2):332-340. doi: 10.1136/annrheumdis-2015-207654

95. Wu D, Li J, Xu D, Merrill JT, van Vollenhoven RF, Liu Y, et al. Telitacicept in patients with active systemic lupus erythematosus: results of a phase 2b, randomised, double-blind, placebo-controlled trial. Ann Rheum Dis. 2024;83(4):475-487. doi: 10.1136/ard-2023-224854

96. Greco R, Alexander T, Del Papa N, Müller F, Saccardi R, Sanchez-Guijo F, et al. Innovative cellular therapies for autoimmune diseases: Expert-based position statement and clinical practice recommendations from the EBMT practice harmonization and guidelines committee. EClinicalMedicine. 2024;69:102476. doi: 10.1016/j.eclinm.2024.102476

97. Schett G, Mackensen A, Mougiakakos D. CAR T-cell therapy in autoimmune diseases. Lancet. 2023;402(10416):2034-2044. doi: 10.1016/S0140-6736(23)01126-1

98. Chasov V, Zmievskaya E, Ganeeva I, Gilyazova E, Davletshin D, Khaliulin M, et al. Immunotherapy strategy for systemic autoimmune diseases: Betting on CAR-T cells and antibodies. Antibodies (Basel). 2024;13(1):10. doi: 10.3390/antib13010010

99. Merino-Vico A, Frazzei G, van Hamburg JP, Tas SW. Targeting B cells and plasma cells in autoimmune diseases: From established treatments to novel therapeutic approaches. Eur J Immunol. 2023;53(1):e2149675. doi: 10.1002/eji.202149675

100. Mitra A, Barua A, Huang L, Ganguly S, Feng Q, He B. From bench to bedside: The history and progress of CAR T cell therapy. Front Immunol. 2023;14:1188049. doi: 10.3389/fimmu.2023.1188049

101. Cappell KM, Kochenderfer JN. Long-term outcomes following CAR T cell therapy: What we know so far. Nat Rev Clin Oncol. 2023;20(6):359-371. doi: 10.1038/s41571-023-00754-1

102. Mougiakakos D, Krönke G, Völkl S, Kretschmann S, Aigner M, Kharboutli S, et al. CD19-targeted CAR T cells in refractory systemic lupus erythematosus. N Engl J Med. 2021;385(6):567-569. doi: 10.1056/NEJMc2107725

103. Mackensen A, Müller F, Mougiakakos D, Böltz S, Wilhelm A, Aigner M, et al. Anti-CD19 CAR T cell therapy for refractory systemic lupus erythematosus. Nat Med. 2022;28(10):2124-2132. doi: 10.1038/s41591-022-02017-5

104. Taubmann J, Müller F, Aigner M, Minopoulou I, Knitza J, Werner D, et al. Tolerability of CAR T cell therapy in autoimmune disease. Arthritis Rheumatol. 2023;75(Suppl 9). URL: https://acrabstracts.org/abstract/tolerability-of-car-t-cell-therapyin-autoimmune-disease/ (Accessed: 6th May 2024).

105. Müller F, Taubmann J, Bucci L, Wilhelm A, Bergmann C, Völkl S, et al. CD19 CAR T-cell therapy in autoimmune disease – A case series with follow-up. N Engl J Med. 2024;390(8):687-700. doi: 10.1056/NEJMoa2308917

106. Bergmann C, Müller F, Distler JHW, Györfi AH, Völkl S, Aigner M, et al. Treatment of a patient with severe systemic sclerosis (SSc) using CD19-targeted CAR T cells. Ann Rheum Dis. 2023;82(8):1117-1120. doi: 10.1136/ard-2023-223952

107. Merkt W, Freitag M, Claus M, Kolb P, Falcone V, Röhrich M, et al. Third-generation CD19 CAR-T cell-containing combination therapy in Scl70+ systemic sclerosis. Ann Rheum Dis. 2024;83(4):543-546. doi: 10.1136/ard-2023-225174

108. Bergmann C, Müller F, Auth J, Taubmann J, Aigner M, Werner D, et al. 6 months-follow up data of systemic sclerosis patients treated with CD19 targeting CAR-T cells. Arthritis Rheumatol. 2023;75(Suppl 9). URL: https://acrabstracts.org/abstract/6-months-follow-up-data-of-systemic-sclerosis-patients-treatedwith-cd-19-targeting-car-t-cells/ (Accessed: 3rd May 2024).

109. Feng J, Hu Y, Chang AH, Huang H. Safety and efficacy of CD19 CAR-T cells for refractory systemic sclerosis: A Phase I clinical trial. Blood. 2022;140 (Suppl 1):10335-10336. doi: 10.1182/blood-2022-169265

110. Müller F, Boeltz S, Knitza J, Aigner M, Völkl S, Kharboutli S, et al. CD19-targeted CAR T cells in refractory antisynthetase syndrome. Lancet. 2023;401(10379):815-818. doi: 10.1016/S0140-6736(23)00023-5

111. Pecher AC, Hensen L, Klein R, Schairer R, Lutz K, Atar D, et al. CD19-targeting CAR T cells for myositis and interstitial lung disease associated with antisynthetase syndrome. JAMA. 2023;329(24):2154-2162. doi: 10.1001/jama.2023.8753

112. Taubmann J, Knitza J, Müller F, Völkl S, Aigner M, Kleyer A, et al. Rescue therapy of antisynthetase syndrome with CD19-targeted CAR-T cells after failure of several B-cell depleting antibodies. Rheumatology (Oxford). 2024;63(1):e12-e14. doi: 10.1093/rheumatology/kead330

113. Kaul A, Gordon C, Crow MK, Touma Z, Urowitz MB, van Vollenhoven R, et al. Systemic lupus erythematosus. Nat Rev Dis Primers. 2016;2:16039. doi: 10.1038/nrdp.2016.39

114. Tsokos GC, Lo MS, Costa Reis P, Sullivan KE. New insights into the immunopathogenesis of systemic lupus erythematosus. Nat Rev Rheumatol. 2016;12(12):716-730. doi: 10.1038/nrrheum

115. Kansal R, Richardson N, Neeli I, Khawaja S, Chamberlain D, Ghani M, et al. Sustained B cell depletion by CD19-targeted CAR T cells is a highly effective treatment for murine lupus. Sci Transl Med. 2019;11(482):eaav1648. doi: 10.1126/scitranslmed.aav1648

116. Jin X, Xu Q, Pu C, Zhu K, Lu C, Jiang Y, et al. Therapeutic efficacy of anti-CD19 CAR-T cells in a mouse model of systemic lupus erythematosus. Cell Mol Immunol. 2021;18(8):1896-1903. doi: 10.1038/s41423-020-0472-1

117. Schett G, Munoz L, Taubmann J, Aigner M, Bergmann C, Knitza J, et al. CAR T cell therapy leads to long-term abrogation of autoimmunity in SLE patients while vaccination responses are maintained. Arthritis Rheumatol. 2023;75(Suppl 9). URL: https://acrabstracts.org/abstract/car-t-cell-therapy-leadsto-long-term-abrogation-of-autoimmunity-in-sle-patients-whilevaccination-responses-are-maintained (Accessed 9th May 2024).

118. Taubmann J, Müller F, Boeltz S, Völkl S, Aigner M, Kleyer A, et al. Long term safety and efficacy of CAR-T cell treatment in refractory systemic lupus erythematosus – Data from the first seven patients. Ann Rheum Dis. 2023;82:93-94. doi: annrheumdis2023-eular.3736

119. Krickau T, Naumann-Bartsch N, Aigner M, Kharboutli S, Kretschmann S, Spoerl S, et al. CAR T-cell therapy rescues adolescent with rapidly progressive lupus nephritis from haemodialysis. Lancet. 2024;403(10437):1627-1630. doi: 10.1016/S0140-6736(24)00424-0

120. Nunez D, Patel D, Volkov J, Wong S, Vorndran Z, Müller F, et al. Cytokine and reactivity profiles in SLE patients following anti-CD19 CART therapy. Mol Ther Methods Clin Dev. 2023;31:101104. doi: 10.1016/j.omtm.2023.08.023

121. Feng J, Hu Y, Chang AH, Huang H. CD19/BCMA CAR-T cell therapy for refractory systemic lupus erythematosus – Safety and preliminary efficacy data from a phase I clinical study. Blood. 2023;142(Suppl 1):4835. doi: 10.1182/blood-2023-186669

122. Wang W, He S, Zhang W, Zhang H, DeStefano VM, Wada M, et al. BCMA-CD19 compound CAR T cells for systemic lupus erythematosus: A phase 1 open-label clinical trial. Ann Rheum Dis. 2024 May 22. doi: 10.1136/ard-2024-225785

123. Bodansky A, Yu DJ, Rallistan A, Kalaycioglu M, Boonyaratanakornkit J, Green DJ, et al. Unveiling the autoreactome: Proteomewide immunological fingerprints reveal the promise of plasma cell depleting therapy. medRxiv. 2023:2023.12.19.23300188. doi: 10.1101/2023.12.19.23300188

124. Mueller F., Schwingen R, Stabel L, Aingner M, Taubman J, Kretschmann S, et al. CAR-T cell therapy in patients with refractory autoimmune diseases exhibits less inflammation, toxicities and different cellular dynamics compared to patients with B cell lymphoma. Blood. 2023;142(Suppl 1):6871. doi: 10.1182/blood2023-188830

125. Lodka D, Zschummel M, Bunse M, Rousselle A, Sonnemann J, Kettritz R, et al. CD19-targeting CAR T cells protect from ANCA-induced acute kidney injury. Ann Rheum Dis. 2024;83(4):499-507. doi: 10.1136/ard-2023-224875

126. Wang J, Alkrekshi A, Dasari S, Lin HC, Elantably D, Armashi ARA. CD19-targeted chimeric antigen receptor T-cell therapy in patients with concurrent B-cell non-Hodgkin lymphoma and rheumatic autoimmune diseases: A propensity score matching study. Bone Marrow Transplant. 2023;58(11):1223-1228. doi: 10.1038/s41409-023-02086-1

127. Bachanova V, Nachman PH. Two for one? CAR-T therapy for lymphoma benefits concurrent autoimmune disorders. Bone Marrow Transplant. 2023;58(11):1175-1176. doi: 10.1038/s41409-023-02084-3

128. Schmelz JL, Navsaria L, Goswamy R, Chuang HH, Miranda RN, Lee HJ. Chimeric antigen receptor T-cell therapy’s role in antiphospholipid syndrome: A case report. Br J Haematol. 2020;188(3):e5-e8. doi: 10.1111/bjh.16266

129. Sheng L, Zhang Y, Song Q, Jiang X, Cao W, Li L, et al. Concurrent remission of lymphoma and Sjögren̓s disease following antiCD19 chimeric antigen receptor-T cell therapy for diffuse large B-cell lymphoma: A case report. Front Immunol. 2023;14:1298815. doi: 10.3389/fimmu.2023.1298815

130. Konig MF. The rise of precision cellular therapies. Nat Rev Rheumatol. 2024;20(2):69-70. doi: 10.1038/s41584-023-01073-6

131. Aghajanian H, Rurik JG, Epstein JA. CAR-based therapies: Opportunities for immuno-medicine beyond cancer. Nat Metab. 2022;4(2):163-169. doi: 10.1038/s42255-022-00537-5

132. Mog B, Shaw E, Hwang M, Pearlman A, DiNapoli S, Paul S, et al. Chimeric autoantigen-T cell receptor (CATCR)-T cell therapies to selectively target autoreactive B cells. Arthritis Rheumatol. 2022;74(Suppl 9). URL: https://acrabstracts.org/abstract/chimeric-autoantigen-t-cell-receptor-catcr-t-cell-therapies-to-selectively-target-autoreactive-b-cells

133. Solé C, Royo M, Sandoval S, Moliné T, Gabaldón A, CortésHernández J. Precise targeting of autoantigen-specific B cells in lupus nephritis with chimeric autoantibody receptor T cells. Int J Mol Sci. 2024;25(8):4226. doi: 10.3390/ijms25084226

134. Meng H, Sun X, Song Y, Zou J, An G, Jin Z, et al. La/SSB chimeric autoantibody receptor modified NK92MI cells for targeted therapy of autoimmune disease. Clin Immunol. 2018;192:40-49. doi: 10.1016/j.clim.2018.04.006

135. Whittington KB, Prislovsky A, Beaty J, Albritton L, Radic M, Rosloniec EF. CD8+ T cells expressing an HLA-DR1 chimeric antigen receptor target autoimmune CD4+ T cells in an antigen-specific manner and inhibit the development of autoimmune arthritis. J Immunol. 2022;208(1):16-26. doi: 10.4049/jimmunol.2100643

136. Zhang R, Miao J, Zhu P. Regulatory T cell heterogeneity and therapy in autoimmune diseases. Autoimmun Rev. 2021;20(5):102715. doi: 10.1016/j.autrev.2020.102715

137. Doglio M, Ugolini A, Bercher-Brayer C, Camisa B, Toma C, Norata R, et al. Regulatory T cells expressing CD19-targeted chimeric antigen receptor restore homeostasis in systemic lupus erythematosus. Nat Commun. 2024;15(1):2542. doi: 10.1038/s41467-024-46448-9

138. Pushpakom S, Iorio F, Eyers PA, Escott KJ, Hopper S, Wells A, et al. Drug repurposing: Progress, challenges and recommendations. Nat Rev Drug Discov. 2019;18(1):41-58. doi: 10.1038/nrd.2018.168

139. Kingsmore KM, Grammer AC, Lipsky PE. Drug repurposing to improve treatment of rheumatic autoimmune inflammatory diseases. Nat Rev Rheumatol. 2020;16(1):32-52. doi: 10.1038/s41584-019-0337-0

140. Orvain C, Boulch M, Bousso P, Allanore Y, Avouac J. Is there a place for chimeric antigen receptor-T cells in the treatment of chronic autoimmune rheumatic diseases? Arthritis Rheumatol. 2021;73(11):1954-1965. doi: 10.1002/art.41812

141. Daamen AR, Lipsky PE. Potential and pitfalls of repurposing the CAR-T cell regimen for the treatment of autoimmune disease. Ann Rheum Dis. 2024;83(6):696-699. doi: 10.1136/ard-2024-225638

142. Mullard A. CAR T cell therapies raise hopes – and questions – for lupus and autoimmune disease. Nat Rev Drug Discov. 2023;22(11):859-861. doi: 10.1038/d41573-023-00166-x

143. Blache U, Tretbar S, Koehl U, Mougiakakos D, Fricke S. CAR T cells for treating autoimmune diseases. RMD Open. 2023;9(4):e002907. doi: 10.1136/rmdopen-2022-002907

144. Schett G, Mielenz D, Nagy G, Kronke G. B-cell depletion in autoimmune diseases. Ann Rheum Dis. 2024 May 22. doi: 10.1136/ard-2024-225727

145. Lyu X, Gupta L, Tholouli E, Chinoy H. Chimeric antigen receptor T cell therapy: A new emerging landscape in autoimmune rheumatic diseases. Rheumatology (Oxford). 2024;63(5):1206- 1216. doi: 10.1093/rheumatology/kead616

146. Salazar-Camarena DC, Palafox-Sánchez CA, Cruz A, MarínRosales M, Muñoz-Valle JF. Analysis of the receptor BCMA as a biomarker in systemic lupus erythematosus patients. Sci Rep. 2020;10(1):6236. doi: 10.1038/s41598-020-63390-0

147. Leung WK, Ayanambakkam A, Heslop HE, Hill LC. Beyond CD19 CAR-T cells in lymphoma. Curr Opin Immunol. 2022;74:46-52. doi: 10.1016/j.coi.2021.09.009

148. Davila ML, Riviere I, Wang X, Bartido S, Park J, Curran K, et al. Efficacy and toxicity management of 19-28z CART cell therapy in B cell acute lymphoblastic leukemia. Sci Transl Med. 2014;6(224):224ra25. doi: 10.1126/scitranslmed.3008226

149. Enocsson H, Karlsson J, Li HY, Wu Y, Kushner I, Wetterö J, et al. The complex role of C-reactive protein in systemic lupus erythematosus. J Clin Med. 2021;10(24):5837. doi: 10.3390/jcm10245837

150. Kretschmann S, Völkl S, Reimann H, Krönke G, Schett G, Achenbach S, et al. Successful generation of CD19 chimeric antigen receptor T cells from patients with advanced systemic lupus erythematosus. Transplant Cell Ther. 2023;29(1):27-33. doi: 10.1016/j.jtct.2022.10.004

151. Viallard JF, Mercié P, Faure I, Pellegrin JL, Leng B. Successful treatment of lupus with fludarabine. Lupus. 1999;8(9):767-769. doi: 10.1191/096120399678840954

152. Illei GG, Yarboro CH, Kuroiwa T, Schlimgen R, Austin HA, Tisdale JF, et al. Long-term effects of combination treatment with fludarabine and low-dose pulse cyclophosphamide in patients with lupus nephritis. 2007;46(6):952-926. doi: 10.1093/rheumatology/kem001

153. Li Y, Cui Q, Liu S, Liu L, Li M, Gao J, et al. Rituximab potentially improves clinical outcomes of CAR-T therapy for r/r B-ALL via sensitizing leukemia cells to CAR-T-mediated cytotoxicity and reducing CAR-T exhaustion. Cell Oncol (Dordr). 2024 Apr 25. doi: 10.1007/s13402-024-00945-7

154. Cambier JC. Therapeutic tactics for targeting B lymphocytes in autoimmunity and cancer. Eur J Immunol. 2024;54(1):e2249947. doi: 10.1002/eji.202249947

155. Shah K, Leandro M, Cragg M, Kollert F, Schuler F, Klein C, et al. Disrupting B and T cell collaboration in autoimmune disease: T cell engagers versus CAR T cell therapy? Clin Exp Immunol. 2024 Apr 20: uxae031. doi: 10.1093/cei/uxae031

156. Yuan AQ, Yang I, Yuan RQ, Zhao L, Bai L, Meng Q. Targeting CD19 for the treatment of B-cell related autoimmune diseases with a novel T cell engager. bioRxiv 2024.02.17.580750; doi: 10.1101/2024.02.17.580750

157. Perico L, Casiraghi F, Sônego F, Todeschini M, Corna D, Cerullo D, et al. Bi-specific autoantigen-T cell engagers as targeted immunotherapy for autoreactive B cell depletion in autoimmune diseases. Front Immunol. 2024;15:1335998. doi: 10.3389/fimmu.2024.1335998

158. Nelson R. FDA investigating safety risks in CAR T-cell recipients. Lancet. 2023;402(10418):2181. doi: 10.1016/S0140-6736(23)02747-2

159. Wiedmeier-Nutor JE, Iqbal M, Rosenthal AC, Bezerra ED, Garcia-Robledo JE, Bansal R, et al. Response to COVID-19 vaccination post-CAR T therapy in patients with non-Hodgkin lymphoma and multiple myeloma. Clin Lymphoma Myeloma Leuk. 2023;23(6):456-462. doi: 10.1016/j.clml.2023.03.002

160. Turesson C, Matteson EL. Malignancy as a comorbidity in rheumatic diseases. Rheumatology (Oxford). 2013;52(1):5-14. doi: 10.1093/rheumatology/kes189

161. Nasonov EL. Coronavirus disease 2019 (COVID-19) pandemic and autoimmune rheumatic diseases: Outcomes and prospects. Nauchno-Prakticheskaya Revmatologia = Rheumatology Science and Practice. 2024;62(1):32-54 (In Russ.). doi: 10.47360/1995-4484-2024-32-54

162. Parayath NN, Stephan SB, Koehne AL, Nelson PS, Stephan MT. In vitro-transcribed antigen receptor mRNA nanocarriers for transient expression in circulating T cells in vivo. Nat Commun. 2020;11(1):6080. doi: 10.1038/s41467-020-19486-2

163. Granit V, Benatar M, Kurtoglu M, Miljković MD, Chahin N, Sahagian G, et al.; MG-001 Study Team. Safety and clinical activity of autologous RNA chimeric antigen receptor T-cell therapy in myasthenia gravis (MG-001): A prospective, multicentre, open-label, non-randomised phase 1b/2a study. Lancet Neurol. 2023;22(7):578-590. doi: 10.1016/S1474-4422(23)00194-1

164. Blache U, Popp G, Dünkel A, Koehl U, Fricke S. Potential solutions for manufacture of CAR T cells in cancer immunotherapy. Nat Commun. 2022;13(1):5225. doi: 10.1038/s41467-022-32866-0

165. Samsonov NYu, Lomonosov AM. Towards personal gene and cell therapy: Accelerating factors and roadblocks on point-of-care production approach. Cell Ther Transp. 2024;13(1):6-15. doi: 10.18620/ctt-1866-8836-13-1-6-15

166. Li Y, Hu Z, Li Y, Wu X. Charting new paradigms for CAR-T cell therapy beyond current Achilles heels. Front Immunol. 2024;15:1409021. doi: 10.3389/fimmu.2024.1409021

167. Zhao J, Lin Q, Song Y, Liu D. Universal CARs, universal T cells, and universal CAR T cells. J Hematol Oncol. 2018;11(1):132. doi: 10.1186/s13045-018-0677-2

168. Wilhelm A, Chambers D, Müller F, Bozec A, Grieshaber-Bouyer R, Winkler T, et al. Selective CAR-T cell mediated B cell depletion suppresses interferon signature in SLE. JCI Insight. 2024 May 9:e179433. doi: 10.1172/jci.insight.179433

169. Leandro MJ, Cambridge G, Ehrenstein MR, Edwards JC. Reconstitution of peripheral blood B cells after depletion with rituximab in patients with rheumatoid arthritis. Arthritis Rheum. 2006;54(2):613-620. doi: 10.1002/art.21617

170. Londe AC, Fernandez-Ruiz R, Julio PR, Appenzeller S, Niewold TB. Type I interferons in autoimmunity: Implications in clinical phenotypes and treatment response. J Rheumatol. 2023;50(9):1103-1113. doi: 10.3899/jrheum.2022-0827

171. Jiang J, Zhao M, Chang C, Wu H, Lu Q. Type I interferons in the pathogenesis and treatment of autoimmune diseases. Clin Rev Allergy Immunol. 2020;59(2):248-272. doi: 10.1007/s12016-020-08798-2


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Nasonov E.L., Rumyantsev A.G., Samsonov M.Yu. Pharmacotherapy of autoimmune rheumatic diseases – from monoclonal antibodies to CAR T cells: 20 years later. Rheumatology Science and Practice. 2024;62(3):262-279. (In Russ.) https://doi.org/10.47360/1995-4484-2024-262-279

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