T cell Dissimilarities in B Cell Activating Factor-Deficient Versus B Cell Activating Factor Receptor 3-Deficient Systemic Lupus Erythematosus-Prone NZM 2328 Mice as Contributors to Their Divergent Clinical Outcomes.


Journal

ACR open rheumatology
ISSN: 2578-5745
Titre abrégé: ACR Open Rheumatol
Pays: United States
ID NLM: 101740025

Informations de publication

Date de publication:
14 Aug 2024
Historique:
revised: 29 05 2024
received: 12 03 2024
accepted: 08 06 2024
medline: 15 8 2024
pubmed: 15 8 2024
entrez: 14 8 2024
Statut: aheadofprint

Résumé

We assessed the contributions of B cell and T cell subsets to the disparate clinical outcomes in NZM.Baff We assessed in NZM wild-type, NZM.Baff In each age and sex cohort, percentages and numbers of CD19 Differences between NZM.Baff

Identifiants

pubmed: 39143363
doi: 10.1002/acr2.11712
doi:

Types de publication

Journal Article

Langues

eng

Informations de copyright

© 2024 The Author(s). ACR Open Rheumatology published by Wiley Periodicals LLC on behalf of American College of Rheumatology.

Références

Chan O, Shlomchik MJ. A new role for B cells in systemic autoimmunity: B cells promote spontaneous T cell activation in MRL‐lpr/lpr mice. J Immunol 1998;160(1):51–59.
Jacob N, Guo S, Mathian A, et al. B Cell and BAFF dependence of IFN‐α‐exaggerated disease in systemic lupus erythematosus‐prone NZM 2328 mice. J Immunol 2011;186(8):4984–4993.
Ramanujam M, Wang X, Huang W, et al. Mechanism of action of transmembrane activator and calcium modulator ligand interactor‐Ig in murine systemic lupus erythematosus. J Immunol 2004;173(5):3524–3534.
Marinov AD, Wang H, Bastacky SI, et al. The type II anti‐CD20 antibody obinutuzumab (GA101) is more effective than rituximab at depleting B cells and treating disease in a murine lupus model. Arthritis Rheumatol 2021;73(5):826–836.
Navarra SV, Guzmán RM, Gallacher AE, et al. Efficacy and safety of belimumab in patients with active systemic lupus erythematosus: a randomised, placebo‐controlled, phase 3 trial. Lancet 2011;377(9767):721–731.
Furie R, Petri M, Zamani O, et al. A phase III, randomized, placebo‐controlled study of belimumab, a monoclonal antibody that inhibits B lymphocyte stimulator, in patients with systemic lupus erythematosus. Arthritis Rheum 2011;63(12):3918–3930.
Stohl W, Schwarting A, Okada M, et al. Efficacy and safety of subcutaneous belimumab in systemic lupus erythematosus: a fifty‐two‐week randomized, double‐blind, placebo‐controlled study. Arthritis Rheumatol 2017;69(5):1016–1027.
Zhang F, Bae SC, Bass D, et al. A pivotal phase III, randomised, placebo‐controlled study of belimumab in patients with systemic lupus erythematosus located in China, Japan and South Korea. Ann Rheum Dis 2018;77(3):355–363.
Kansal R, Richardson N, Neeli I, 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.
Mackensen A, Müller F, Mougiakakos D, et al. Anti‐CD19 CAR T cell therapy for refractory systemic lupus erythematosus. Nat Med 2022;28(10):2124–2132.
Moore PA, Belvedere O, Orr A, et al. BLyS: member of the tumor necrosis factor family and B lymphocyte stimulator. Science 1999;285(5425):260–263.
Schneider P, MacKay F, Steiner V, et al. BAFF, a novel ligand of the tumor necrosis factor family, stimulates B cell growth. J Exp Med. 1999;189(11):1747–1756.
Thompson JS, Schneider P, Kalled SL, et al. BAFF binds to the tumor necrosis factor receptor‐like molecule B cell maturation antigen and is important for maintaining the peripheral B cell population. J Exp Med 2000;192(1):129–135.
Do RKG, Hatada E, Lee H, et al. Attenuation of apoptosis underlies B lymphocyte stimulator enhancement of humoral immune response. J Exp Med 2000;192(7):953–964.
Batten M, Groom J, Cachero TG, et al. BAFF mediates survival of peripheral immature B lymphocytes. J Exp Med 2000;192(10):1453–1466.
Gross JA, Dillon SR, Mudri S, et al. TACI‐Ig neutralizes molecules critical for B cell development and autoimmune disease. impaired B cell maturation in mice lacking BLyS. Immunity 2001;15(2):289–302.
Schiemann B, Gommerman JL, Vora K, et al. An essential role for BAFF in the normal development of B cells through a BCMA‐independent pathway. Science 2001;293(5537):2111–2114.
Mackay F, Woodcock SA, Lawton P, et al. Mice transgenic for BAFF develop lymphocytic disorders along with autoimmune manifestations. J Exp Med 1999;190(11):1697–1710.
Gross JA, Johnston J, Mudri S, et al. TACI and BCMA are receptors for a TNF homologue implicated in B‐cell autoimmune disease. Nature 2000;404(6781):995–999.
Laabi Y, Gras MP, Brouet JC, et al. The BCMA gene, preferentially expressed during B lymphoid maturation, is bidirectionally transcribed. Nucleic Acids Res 1994;22(7):1147–1154.
vonBülow GU, Bram RJ. NF‐AT activation induced by a CAML‐interacting member of the tumor necrosis factor receptor superfamily. Science 1997;278(5335):138–141.
Thompson JS, Bixler SA, Qian F, et al. BAFF‐R, a newly identified TNF receptor that specifically interacts with BAFF. Science 2001;293(5537):2108–2111.
Yan M, Brady JR, Chan B, et al. Identification of a novel receptor for B lymphocyte stimulator that is mutated in a mouse strain with severe B cell deficiency. Curr Biol 2001;11(19):1547–1552.
Harless SM, Lentz VM, Sah AP, et al. Competition for BLyS‐mediated signaling through Bcmd/BR3 regulates peripheral B lymphocyte numbers. Curr Biol. 2001;11(24):1986–1989.
Sasaki Y, Casola S, Kutok JL, et al. TNF family member B cell‐activating factor (BAFF) receptor‐dependent and ‐independent roles for BAFF in B cell physiology. J Immunol. 2004;173(4):2245–2252.
Shulga‐Morskaya S, Dobles M, Walsh ME, et al. B cell‐activating factor belonging to the TNF family acts through separate receptors to support B cell survival and T cell‐independent antibody formation. J Immunol 2004;173(4):2331–2341.
Xu S, Lam KP. B‐cell maturation protein, which binds the tumor necrosis factor family members BAFF and APRIL, is dispensable for humoral immune responses. Mol Cell Biol 2001;21(12):4067–4074.
vonBülow GU, vanDeursen JM, Bram RJ. Regulation of the T‐independent humoral response by TACI. Immunity 2001;14(5):573–582.
Yan M, Wang H, Chan B, et al. Activation and accumulation of B cells in TACI‐deficient mice. Nat Immunol. 2001;2(7):638–643.
Jacob CO, Pricop L, Putterman C, et al. Paucity of clinical disease despite serological autoimmunity and kidney pathology in lupus‐prone New Zealand mixed 2328 mice deficient in BAFF. J Immunol. 2006;177(4):2671–2680.
Jacob CO, Yu N, Guo S, et al. Development of systemic lupus erythematosus in NZM 2328 mice in the absence of any single BAFF receptor. Arthritis Rheum 2013;65(4):1043–1054.
Stohl W, Yu N, Wu Y. B cell and T cell dissimilarities in BAFF‐deficient versus BR3‐deficient C57BL/6 mice. J Immunol 2022;209(11):2133–2140.
Jacob CO, Guo S, Jacob N, et al. Dispensability of APRIL to the development of systemic lupus erythematosus in NZM 2328 mice. Arthritis Rheum 2012;64(5):1610–1619.
Wofsy D, Seaman WE. Successful treatment of autoimmunity in NZB/NZW F1 mice with monoclonal antibody to L3T4. J Exp Med 1985;161(2):378–391.
Wofsy D, Seaman WE. Reversal of advanced murine lupus in NZB/NZW F1 mice by treatment with monoclonal antibody to L3T4. J Immunol 1987;138(10):3247–3253.
Hori S, Nomura T, Sakaguchi S. Control of regulatory T cell development by the transcription factor Foxp3. Science 2003;299(5609):1057–1061.
Fontenot JD, Gavin MA, Rudensky AY. Foxp3 programs the development and function of CD4+CD25+ regulatory T cells. Nat Immunol. 2003;4(4):330–336.
Khattri R, Cox T, Yasayko SA, et al. An essential role for Scurfin in CD4+CD25+ T regulatory cells. Nat Immunol 2003;4(4):337–342.
Komatsu N, Okamoto K, Sawa S, et al. Pathogenic conversion of Foxp3+ T cells into TH17 cells in autoimmune arthritis. Nat Med 2014;20(1):62–68.
Collins CE, Dall'Era M, Kan H, et al. Response to belimumab among patients with systemic lupus erythematosus in clinical practice settings: 24‐month results from the OBSErve study in the USA. Lupus Sci Med 2016;3(1):e000118.
Schwarting A, Schroeder JO, Alexander T, et al. First real‐world insights into belimumab use and outcomes in routine clinical care of systemic lupus erythematosus in Germany: results from the OBSErve Germany Study. Rheumatol Ther 2016;3(2):271–290.
Touma Z, Sayani A, Pineau CA, et al. Belimumab use, clinical outcomes and glucocorticoid reduction in patients with systemic lupus erythematosus receiving belimumab in clinical practice settings: results from the OBSErve Canada Study. Rheumatol Int 2017;37(6):865–873.
Isenberg D, Gordon C, Licu D, et al. Efficacy and safety of atacicept for prevention of flares in patients with moderate‐to‐severe systemic lupus erythematosus (SLE): 52‐week data (APRIL‐SLE randomised trial). Ann Rheum Dis 2015;74(11):2006–2015.
Isenberg DA, Petri M, Kalunian K, et al. Efficacy and safety of subcutaneous tabalumab in patients with systemic lupus erythematosus: results from ILLUMINATE‐1, a 52‐week, phase III, multicentre, randomised, double‐blind, placebo‐controlled study. Ann Rheum Dis 2016;75(2):323–331.
Merrill JT, Shanahan WR, Scheinberg M, et al. 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.
Wu D, Li J, Xu D, 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.
Dhillon S. Telitacicept: first approval. Drugs. 2021;81(14):1671–1675.
Sun L, Shen Q, Gong Y, et al. Safety and efficacy of telitacicept in refractory childhood‐onset systemic lupus erythematosus: a self‐controlled before‐after trial. Lupus 2022;31(8):998–1006.
Stohl W, Hiepe F, Latinis KM, et al. Belimumab reduces autoantibodies, normalizes low complement levels, and reduces select B cell populations in patients with systemic lupus erythematosus. Arthritis Rheum 2012;64(7):2328–2337.
Merrill JT, vanVollenhoven RF, Buyon JP, 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.
Mayne CG, Amanna IJ, Nashold FE, et al. Systemic autoimmunity in BAFF‐R‐mutant A/WySnJ strain mice. Eur J Immunol 2008;38(2):587–598.
Hao Y, O'Neill P, Naradikian MS, et al. A B‐cell subset uniquely responsive to innate stimuli accumulates in aged mice. Blood. 2011;118(5):1294–1304.
Rubtsov AV, Rubtsova K, Fischer A, et al. Toll‐like receptor 7 (TLR7)‐driven accumulation of a novel CD11c+ B‐cell population is important for the development of autoimmunity. Blood 2011;118(5):1305–1315.
Sutherland APR, Ng LG, Fletcher CA, et al. BAFF augments certain Th1‐associated inflammatory responses. J Immunol 2005;174(9):5537–5544.
Walters S, Webster KE, Sutherland A, et al. Increased CD4+Foxp3+ T cells in BAFF‐transgenic mice suppress T cell effector responses. J Immunol 2009;182(2):793–801.
Stohl W, Yu N. Promotion of T regulatory cells in mice by B cells and BAFF. J Immunol 2020;204(9):2416–2428.
Marsters SA, Yan M, Pitti RM, et al. Interaction of the TNF homologues BLyS and APRIL with the TNF receptor homologues BCMA and TACI. Curr Biol 2000;10(13):785–788.
Yu G, Boone T, Delaney J, et al. APRIL and TALL‐I and receptors BCMA and TACI: system for regulating humoral immunity. Nat Immunol 2000;1(3):252–256.
Wu Y, Bressette D, Carrell JA, et al. Tumor necrosis factor (TNF) receptor superfamily member TACI is a high affinity receptor for TNF family members APRIL and BLyS. J Biol Chem 2000;275(45):35478–35485.
Rennert P, Schneider P, Cachero TG, et al. A soluble form of B cell maturation antigen, a receptor for the tumor necrosis factor family member APRIL, inhibits tumor cell growth. J Exp Med 2000;192(11):1677–1684.
Tivol EA, Borriello F, Schweitzer AN, et al. Loss of CTLA‐4 leads to massive lymphoproliferation and fatal multiorgan tissue destruction, revealing a critical negative regulatory role of CTLA‐4. Immunity. 1995;3(5):541–547.
Waterhouse P, Penninger JM, Timms E, et al. Lymphoproliferative disorders with early lethality in mice deficient in Ctla‐4. Science 1995;270(5238):985–988.
Stohl W, Yu N, Wu Y. Preferential expansion of Foxp3+ T regulatory cells in CTLA‐4‐deficient and CTLA‐4‐haploinsufficient C57BL/6 mice. Immunohorizons 2022;6(7):507–514.
McCormick N, Yokose C, Challener GJ, et al. Serum urate and recurrent gout. JAMA 2024;331(5):417–424.
Jacob CO, Yu N, Sindhava V, et al. Differential development of systemic lupus erythematosus in NZM 2328 mice deficient in discrete pairs of BAFF receptors. Arthritis Rheumatol 2015;67(9):2523–2535.
Cambridge G, Isenberg DA, Edwards JCW, et al. B cell depletion therapy in systemic lupus erythematosus: relationships among serum B lymphocyte stimulator levels, autoantibody profile and clinical response. Ann Rheum Dis 2008;67(7):1011–1016.
Carter LM, Isenberg DA, Ehrenstein MR. Elevated serum BAFF levels are associated with rising anti‐double‐stranded DNA antibody levels and disease flare following B cell depletion therapy in systemic lupus erythematosus. Arthritis Rheum 2013;65(10):2672–2679.
Merrill JT, Neuwelt CM, Wallace DJ, et al. Efficacy and safety of rituximab in moderately‐to‐severely active systemic lupus erythematosus: the randomized, double‐blind, phase II/III systemic lupus erythematosus evaluation of rituximab trial. Arthritis Rheum 2010;62(1):222–233.
Rovin BH, Furie R, Latinis K, et al. Efficacy and safety of rituximab in patients with active proliferative lupus nephritis: the Lupus Nephritis Assessment with Rituximab study. Arthritis Rheum 2012;64(4):1215–1226.
Bowman SJ, Fox R, Dörner T, et al. Safety and efficacy of subcutaneous ianalumab (VAY736) in patients with primary Sjögren's syndrome: a randomised, double‐blind, placebo‐controlled, phase 2b dose‐finding trial. Lancet 2022;399(10320):161–171.
Huard B, Schneider P, Mauri D, et al. T cell costimulation by the TNF ligand BAFF. J Immunol. 2001;167(11):6225–6231.

Auteurs

William Stohl (W)

University of Southern California Keck School of Medicine, Los Angeles.

Ying Wu (Y)

University of Southern California Keck School of Medicine, Los Angeles.

Malka Stohl (M)

New York State Psychiatric Institute, New York City.

Classifications MeSH