Therapeutic CD154 antibody for lupus: promise for the future?

被引:18
作者
Kelsoe, G [1 ]
机构
[1] Duke Univ, Med Ctr 3010, Dept Immunol, Durham, NC 27710 USA
关键词
D O I
10.1172/JCI200320371
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Systemic lupus erythematosus (SLE) is a prototypical systemic autoimmune disease characterized by the production of pathogenic autoantibodies. A new study (see the related article beginning on page 1506) demonstrates that passive antibody specific for the TNF family member, CD 154, ameliorates disease by reducing levels of self-reactive antibody in the serum. This study demonstrates a substantial potential for anti-CD 154 antibody in the treatment of humoral autoimmunity.
引用
收藏
页码:1480 / 1482
页数:3
相关论文
共 22 条
[1]   Increased frequency of pre-germinal center B cells and plasma cell precursors in the blood of children with systemic lupus erythematosus [J].
Arce, E ;
Jackson, DG ;
Gill, MA ;
Bennett, LB ;
Banchereau, J ;
Pascual, V .
JOURNAL OF IMMUNOLOGY, 2001, 167 (04) :2361-2369
[2]   A short course of BG9588 (anti-CD40 ligand antibody) improves serologic activity and decreases hematuria in patients with proliferative lupus glomerulonephritis [J].
Boumpas, DT ;
Furie, R ;
Manzi, S ;
Illei, GG ;
Wallace, DJ ;
Balow, JE ;
Vaishnaw, A .
ARTHRITIS AND RHEUMATISM, 2003, 48 (03) :719-727
[3]   Germinal centers without T cells [J].
de Vinuesa, CG ;
Cook, MC ;
Ball, J ;
Drew, M ;
Sunners, Y ;
Cascalho, M ;
Wabl, M ;
Klaus, GGB ;
MacLennan, ICM .
JOURNAL OF EXPERIMENTAL MEDICINE, 2000, 191 (03) :485-493
[4]   Hyperexpression of CD40 ligand by B and T cells in human lupus and its role in pathogenic autoantibody production [J].
DesaiMehta, A ;
Lu, LJ ;
RamseyGoldman, R ;
Datta, SK .
JOURNAL OF CLINICAL INVESTIGATION, 1996, 97 (09) :2063-2073
[5]   Immune regulation by CD40 and its ligand GP39 [J].
Foy, TM ;
Aruffo, A ;
Bajorath, J ;
Buhlmann, JE ;
Noelle, RJ .
ANNUAL REVIEW OF IMMUNOLOGY, 1996, 14 :591-617
[6]   Visualization of specific B and T lymphocyte interactions in the lymph node [J].
Garside, P ;
Ingulli, E ;
Merica, RR ;
Johnson, JG ;
Noelle, RJ ;
Jenkins, MK .
SCIENCE, 1998, 281 (5373) :96-99
[7]   ALTERED IMMUNOGLOBULIN EXPRESSION AND FUNCTIONAL SILENCING OF SELF-REACTIVE LYMPHOCYTES-B IN TRANSGENIC MICE [J].
GOODNOW, CC ;
CROSBIE, J ;
ADELSTEIN, S ;
LAVOIE, TB ;
SMITHGILL, SJ ;
BRINK, RA ;
PRITCHARDBRISCOE, H ;
WOTHERSPOON, JS ;
LOBLAY, RH ;
RAPHAEL, K ;
TRENT, RJ ;
BASTEN, A .
NATURE, 1988, 334 (6184) :676-682
[8]  
Grammer AC, 1999, J IMMUNOL, V163, P4150
[9]   Abnormal germinal center reactions in systemic lupus erythematosus demonstrated by blockade of CD154-CD40 interactions [J].
Grammer, AC ;
Slota, R ;
Fischer, R ;
Gur, H ;
Girschick, H ;
Yarboro, C ;
Illei, GG ;
Lipsky, PE .
JOURNAL OF CLINICAL INVESTIGATION, 2003, 112 (10) :1506-1520
[10]   IN-SITU STUDIES OF THE PRIMARY IMMUNE-RESPONSE TO (4-HYDROXY-3-NITROPHENYL)ACETYL .4. AFFINITY-DEPENDENT, ANTIGEN-DRIVEN B-CELL APOPTOSIS IN GERMINAL-CENTERS AS A MECHANISM FOR MAINTAINING SELF-TOLERANCE [J].
HAN, SH ;
ZHENG, B ;
PORTO, JD ;
KELSOE, G .
JOURNAL OF EXPERIMENTAL MEDICINE, 1995, 182 (06) :1635-1644