Effect of rituximab on human in vivo antibody immune responses

被引:80
|
作者
Pescovitz, Mark D. [2 ,3 ]
Torgerson, Troy R. [4 ,5 ]
Ochs, Hans D. [4 ,5 ]
Ocheltree, Elizabeth [4 ,5 ]
McGee, Paula [6 ]
Krause-Steinrauf, Heidi [6 ]
Lachin, John M. [6 ]
Canniff, Jennifer [7 ]
Greenbaum, Carla [10 ]
Herold, Kevan C. [11 ,12 ]
Skyler, Jay S. [1 ]
Weinberg, Adriana [8 ,9 ]
机构
[1] Univ Miami, Miller Sch Med, Diabet Res Inst, Miami, FL 33136 USA
[2] Indiana Univ, Dept Surg, Indianapolis, IN 46204 USA
[3] Indiana Univ, Dept Microbiol & Immunol, Indianapolis, IN 46204 USA
[4] Univ Washington, Dept Pediat, Seattle, WA 98195 USA
[5] Seattle Childrens Res Inst, Seattle, WA USA
[6] George Washington Univ, Ctr Biostat, Rockville, MD USA
[7] Univ Colorado Denver, Dept Pediat, Aurora, CO USA
[8] Univ Colorado Denver, Dept Med, Aurora, CO USA
[9] Univ Colorado Denver, Dept Pathol, Aurora, CO USA
[10] Benaroya Res Inst, Seattle, WA USA
[11] Yale Univ, Dept Immunobiol, New Haven, CT USA
[12] Yale Univ, Dept Internal Med, New Haven, CT USA
基金
美国国家卫生研究院;
关键词
B lymphocytes; human; diabetes; antibodies; immunization; CD20; ANTI-CD20; MONOCLONAL-ANTIBODY; BETA-CELL FUNCTION; SEROLOGICAL MEMORY; HUMORAL IMMUNITY; CLINICAL-TRIAL; LYMPHOMA; THERAPY; TRANSPLANTATION; IDEC-C2B8; DEPLETION;
D O I
10.1016/j.jaci.2011.08.008
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Background: B-lymphocyte depletion with rituximab has been shown to benefit patients with various autoimmune diseases. We have previously demonstrated that this benefit is also apparent in patients with newly diagnosed type 1 diabetes. Objectives: The effect of rituximab on in vivo antibody responses, particularly during the period of B-lymphocyte depletion, is incompletely determined. This study was designed to assess this knowledge void. Methods: In patients with recent-onset type 1 diabetes treated with rituximab (n = 46) or placebo (n = 29), antibody responses to neoantigen phiX174 during B-lymphocyte depletion and with hepatitis A (as a second neoantigen) and tetanus/diphtheria (as recall antigens) after B-lymphocyte recovery were studied. Anti-tetanus, diphtheria, mumps, measles, and rubella titers were measured before and after treatment by means of ELISA. Antibody titers and percentage IgM versus percentage IgG to phiX174 were measured by means of phage neutralization. B-lymphocyte subsets were determined by means of flow cytometry. Results: No change occurred in preexisting antibody titers. Tetanus/diphtheria and hepatitis A immunization responses were protective in the rituximab-treated subjects, although significantly blunted compared with those seen in the controls subjects, when immunized at the time of B-lymphocyte recovery. Anti-phiX174 responses were severely reduced during the period of B-lymphocyte depletion, but with B-lymphocyte recovery, anti-phiX174 responses were within the normal range. Conclusions: During the time of B-lymphocyte depletion, rituximab recipients had a decreased antibody response to neoantigens and significantly lower titers after recall immunization with diphtheria and tetanus toxoid. With recovery, immune responses return toward normal. Immunization during the time of B-lymphocyte depletion, although ineffective, does not preclude a subsequent response to the antigen. (J Allergy Clin Immunol 2011;128:1295-302.)
引用
收藏
页码:1295 / U655
页数:13
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