The therapeutic potential of anti-CD20 - What do B-cells do?

被引:105
|
作者
Eisenberg, R [1 ]
Looney, RJ
机构
[1] Univ Penn, Dept Rheumatol, Philadelphia, PA 19104 USA
[2] Univ Rochester, Dept Med, Allergy Immunol & Rheumatol Div, Rochester, NY 14642 USA
关键词
CD20; B-cells; rituximab;
D O I
10.1016/j.clim.2005.08.006
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
B-cells play a major role in the immunopathogenesis of autoimmune diseases. Not only do they produce autoantibodies, but they regulate other cell types, secrete cytokines, and present antigens. They are thus potential targets for therapeutic intervention. CD20 is a B-cell specific cell surface molecule of uncertain function. An anti-CD20 chimeric mAb (rituximab) has been FDA approved for treatment of B-cell lymphomas since 1997. Rituximab also depletes normal B-cells by several mechanisms, including ADCC. Over the past seven years, it has shown promise in a number of autoimmune diseases in phase I trials and anecdotal reports. Efficacy in rheumatoid arthritis has already been demonstrated in randomized control trials (RCTs), and RCTs in SLE, inflammatory myositis, and ANCA associated vasculitis are under way. Safety does not appear to be a major problem, but continued vigilance is warranted. The increased use of rituximab, other anti-CD20 agents, and other B-cell targeting therapies holds great promise for substantial clinical benefits, as well as providing special opportunities to understand better disease pathogenesis. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:207 / 213
页数:7
相关论文
共 50 条
  • [21] Functional characterization of reappearing B cells after anti-CD20 treatment of CNS autoimmune disease
    Haeusler, Darius
    Haeusser-Kinzel, Silke
    Feldmann, Linda
    Torke, Sebastian
    Lepennetier, Gildas
    Bernard, Claude C. A.
    Zamvil, Scott S.
    Brueck, Wolfgang
    Lehmann-Horn, Klaus
    Weber, Martin S.
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2018, 115 (39) : 9773 - 9778
  • [22] Evolution of anti-CD20 monoclonal antibody therapeutics in oncology
    Oflazoglu, Ezogelin
    Audoly, Laurent P.
    MABS, 2010, 2 (01) : 14 - 19
  • [23] Anti-CD20: tales of identical twins?
    Schuh, Anna
    BLOOD, 2011, 118 (19) : 5066 - 5067
  • [24] Anti-CD20 (rituximab) treatment improves atopic eczema
    Simon, Dagmar
    Hosli, Susanne
    Kostylina, Ganna
    Yawalkar, Nikhil
    Simon, Hans-Uwe
    JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2008, 121 (01) : 122 - 128
  • [25] Anti-CD20 Antibody Therapy and Susceptibility to Pneumocystis Pneumonia
    Elsegeiny, Waleed
    Eddens, Taylor
    Chen, Kong
    Kolls, Jay K.
    INFECTION AND IMMUNITY, 2015, 83 (05) : 2043 - 2052
  • [26] IRF8 regulates efficacy of therapeutic anti-CD20 monoclonal antibodies
    Grzelak, Ludivine
    Roesch, Ferdinand
    Vaysse, Amaury
    Biton, Anne
    Legendre, Rachel
    Porrot, Francoise
    Commere, Pierre-Henri
    Planchais, Cyril
    Mouquet, Hugo
    Vignuzzi, Marco
    Bruel, Timothee
    Schwartz, Olivier
    EUROPEAN JOURNAL OF IMMUNOLOGY, 2022, 52 (10) : 1648 - 1661
  • [27] Is there a role for anti-CD20 antibodies in CLL?
    Shah, Harsh R.
    Stephens, Deborah M.
    HEMATOLOGY-AMERICAN SOCIETY OF HEMATOLOGY EDUCATION PROGRAM, 2021, (01) : 68 - 75
  • [28] Rituximab (anti-CD20)-modified AZD-2014-encapsulated nanoparticles killing of B lymphoma cells
    Tang, Xiaolong
    Xie, Chunmei
    Jiang, Zhenyou
    Li, Amin
    Cai, Shiyu
    Hou, Changhao
    Wang, Jian
    Liang, Yong
    Ma, Dong
    ARTIFICIAL CELLS NANOMEDICINE AND BIOTECHNOLOGY, 2018, 46 : 1063 - 1073
  • [29] Rituximab (anti-CD20) zur Behandlung von bullösen AutoimmundermatosenRituximab (anti-CD20) for the treatment of autoimmune bullous diseases
    M. Kasperkiewicz
    D. Zillikens
    Der Hautarzt, 2007, 58 (2): : 115 - 121
  • [30] Improving therapeutic activity of anti-CD20 antibody therapy through immunomodulation in lymphoid malignancies
    Lipowska-Bhalla, Grazyna
    Fagnano, Ester
    Illidge, Timothy M.
    Cheadle, Eleanor J.
    LEUKEMIA & LYMPHOMA, 2016, 57 (06) : 1269 - 1280