Lupus nephritis and B-cell targeting therapy

被引:33
作者
Cassia, Matthias [1 ,2 ]
Alberici, Federico [1 ]
Gallieni, Maurizio [1 ,2 ]
Jayne, David [3 ]
机构
[1] San Carlo Borromeo Hosp, Nephrol & Immunol Unit, ASST Santi Paolo & Carlo, Milan, Italy
[2] Univ Milan, Dept Biomed & Clin Sci L Sacco, Milan, Italy
[3] Univ Cambridge, Dept Med, Cambridge, England
关键词
Auto-antibodies; belimumab; B cell; lupus; lymphocytes; nephritis; rituximab; BRUTONS TYROSINE KINASE; ANCA-ASSOCIATED VASCULITIS; DEPLETES PLASMA-CELLS; GAMMA RECEPTOR IIB; OFF-LABEL USE; MURINE LUPUS; RHEUMATOID-ARTHRITIS; MONOCLONAL-ANTIBODY; AUTOIMMUNE-DISEASE; DOUBLE-BLIND;
D O I
10.1080/1744666X.2017.1366855
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Introduction: Lupus Nephritis (LN) is a severe manifestation of Systemic Lupus Erythematosus (SLE) with a significant prognostic impact. Over a prolonged course, an exhaustion of treatment alternatives may occur and further therapeutic options are needed. B cells play a pivotal role in disease pathogenesis and represent an attractive therapeutic target. Areas covered: This review provides an update regarding targeting B cells in LN. The rational for this approach, as well as currently available and future targets are discussed. Expert commentary: Despite its wide clinical use and the encouraging results from retrospective studies, a role of rituximab in LN has not been prospectively confirmed. Trial design methodologies as well as intrinsic limitations of this approach may be responsible and rituximab use is currently limited as a rescue treatment or in settings where a strong steroid sparing effect is warranted. Despite belimumab now being licensed for use in SLE, the evidence in LN is weak although prospective trials are on-going. The combination of different targeted approaches as well as a focus on new clinical end-points may be strategies to identify new therapeutic options.
引用
收藏
页码:951 / 962
页数:12
相关论文
共 132 条
[21]  
2-S
[22]   The Pathogenesis and Therapeutic Implications of Tubulointerstitial Inflammation in Human Lupus Nephritis [J].
Clark, Marcus R. ;
Trotter, Kimberly ;
Chang, Anthony .
SEMINARS IN NEPHROLOGY, 2015, 35 (05) :455-464
[23]   Efficacy and Safety of Epratuzumab in Moderately to Severely Active Systemic Lupus Erythematosus Results From Two Phase III Randomized, Double-Blind, Placebo-Controlled Trials [J].
Clowse, Megan E. B. ;
Wallace, Daniel J. ;
Furie, Richard A. ;
Petri, Michelle A. ;
Pike, Marilyn C. ;
Leszczynski, Piotr ;
Neuwelt, C. Michael ;
Hobbs, Kathryn ;
Keiserman, Mauro ;
Duca, Liliana ;
Kalunian, Kenneth C. ;
Galateanu, Catrinel ;
Bongardt, Sabine ;
Stach, Christian ;
Beaudot, Carolyn ;
Kilgallen, Brian ;
Gordon, Caroline .
ARTHRITIS & RHEUMATOLOGY, 2017, 69 (02) :362-375
[24]   Prospective observational single-centre cohort study to evaluate the effectiveness of treating lupus nephritis with rituximab and mycophenolate mofetil but no oral steroids [J].
Condon, Marie B. ;
Ashby, Damien ;
Pepper, Ruth J. ;
Cook, H. Terence ;
Levy, Jeremy B. ;
Griffith, Megan ;
Cairns, Tom D. ;
Lightstone, Liz .
ANNALS OF THE RHEUMATIC DISEASES, 2013, 72 (08) :1280-1286
[25]  
Cottone S, 2008, J NEPHROL, V21, P175
[26]   Complement-mediated lysis by anti-CD20 mAb correlates with segregation into lipid rafts [J].
Cragg, MS ;
Morgan, SM ;
Chan, HTC ;
Morgan, BP ;
Filatov, AV ;
Johnson, PWM ;
French, RR ;
Glennie, MJ .
BLOOD, 2003, 101 (03) :1045-1052
[27]   Regulation of CD40 ligand expression in systemic lupus erythematosus [J].
Crow, MK ;
Kirou, KA .
CURRENT OPINION IN RHEUMATOLOGY, 2001, 13 (05) :361-369
[28]   Cutting edge: Reversal of murine lupus nephritis with CTLA4Ig and cyclophosphamide [J].
Daikh, DI ;
Wofsy, D .
JOURNAL OF IMMUNOLOGY, 2001, 166 (05) :2913-2916
[29]   Reduced B lymphocyte and immunoglobulin levels after atacicept treatment in patients with systemic lupus erythematosus [J].
Dall'Era, Maria ;
Chakravarty, Eliza ;
Wallace, Daniel ;
Genovese, Mark ;
Weisman, Michael ;
Kavanaugh, Arthur ;
Kalunian, Kenneth ;
Dhar, Patricia ;
Vincent, Emmanuelle ;
Pena-Rossi, Claudia ;
Wofsy, David ;
Serono, Merck .
ARTHRITIS AND RHEUMATISM, 2007, 56 (12) :4142-4150
[30]   Selectivity of BAFF/BLyS and APRIL for binding to the TNF family receptors BAFFR/BR3 and BCMA [J].
Day, ES ;
Cachero, TG ;
Qian, F ;
Sun, Y ;
Wen, D ;
Pelletier, M ;
Hsu, YM ;
Whitty, A .
BIOCHEMISTRY, 2005, 44 (06) :1919-1931