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
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