The soluble CD40 ligand sCD154 in systemic lupus erythematosus

被引:172
作者
Kato, K
Santana-Sahagún, E
Rassenti, LZ
Weisman, MH
Tamura, N
Kobayashi, S
Hashimoto, H
Kipps, TJ
机构
[1] Univ Calif San Diego, Sch Med, Div Hematol Oncol, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, Sch Med, Div Rheumatol, La Jolla, CA 92093 USA
[3] Juntendo Univ, Sch Med, Dept Rheumatol, Tokyo 113, Japan
关键词
D O I
10.1172/JCI7014
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
We found that the plasma of patients with active systemic lupus erythematosus (SLE) could induce a human B-cell line (Ramos) to express high levels of immune accessory molecules that are commonly found on blood B cells of patients with active SLE. The ability of SLE plasma to induce such phenotypic changes could be abrogated by neutralizing antibodies specific for the CD40 ligand (CD154) but not by antibodies to TNF-a. Immunoprecipitation studies with anti-CD154 identified a 20-kDa protein in the plasma of SLE patients with active disease, but not in plasma of normal donors, indicating that such plasma contained soluble CD154 (sCD154). Using a quantitative ELISA method, we found that the plasma of patients with active disease had levels of sCD154 that were significantly higher than those found in plasma of normal donors. Levels of CD 154 transcripts in SLE blood lymphocytes correlated with the relative concentrations of sCD154 found in SLE plasma. Furthermore, plasma levels of sCD154 correlated with the titers of anti-double-stranded DNA autoantibody and with clinical disease activity. These studies indicate that sCD154 of patients with SLE may act as a functional ligand for CD40 that is associated with SLE disease activity.
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收藏
页码:947 / 955
页数:9
相关论文
共 45 条
[1]   MOLECULAR AND BIOLOGICAL CHARACTERIZATION OF A MURINE LIGAND FOR CD40 [J].
ARMITAGE, RJ ;
FANSLOW, WC ;
STROCKBINE, L ;
SATO, TA ;
CLIFFORD, KN ;
MACDUFF, BM ;
ANDERSON, DM ;
GIMPEL, SD ;
DAVISSMITH, T ;
MALISZEWSKI, CR ;
CLARK, EA ;
SMITH, CA ;
GRABSTEIN, KH ;
COSMAN, D ;
SPRIGGS, MK .
NATURE, 1992, 357 (6373) :80-82
[2]   THE CD40 ANTIGEN AND ITS LIGAND [J].
BANCHEREAU, J ;
BAZAN, F ;
BLANCHARD, D ;
BRIERE, F ;
GALIZZI, JP ;
VANKOOTEN, C ;
LIU, YJ ;
ROUSSET, F ;
SAELAND, S .
ANNUAL REVIEW OF IMMUNOLOGY, 1994, 12 :881-922
[3]   Acquired CD40-ligand deficiency in chronic lymphocytic leukemia [J].
Cantwell, M ;
Hua, T ;
Pappas, J ;
Kipps, TJ .
NATURE MEDICINE, 1997, 3 (09) :984-989
[4]  
CASTLE BE, 1993, J IMMUNOL, V151, P1777
[5]   HOW B-CELLS AND T-CELLS TALK TO EACH OTHER [J].
CLARK, EA ;
LEDBETTER, JA .
NATURE, 1994, 367 (6462) :425-428
[6]   A METALLOPROTEASE INHIBITOR BLOCKS SHEDDING OF THE 80-KD TNF RECEPTOR AND TNF PROCESSING IN T-LYMPHOCYTES [J].
CROWE, PD ;
WALTER, BN ;
MOHLER, KM ;
OTTENEVANS, C ;
BLACK, RA ;
WARE, CF .
JOURNAL OF EXPERIMENTAL MEDICINE, 1995, 181 (03) :1205-1210
[7]   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
[8]   THE ROLE OF CD40 IN THE REGULATION OF HUMORAL AND CELL-MEDIATED-IMMUNITY [J].
DURIE, FH ;
FOY, TM ;
MASTERS, SR ;
LAMAN, JD ;
NOELLE, RJ .
IMMUNOLOGY TODAY, 1994, 15 (09) :406-411
[9]  
Early GS, 1996, J IMMUNOL, V157, P3159
[10]   TREATMENT OF MURINE LUPUS WITH CTLA4IG [J].
FINCK, BK ;
LINSLEY, PS ;
WOFSY, D .
SCIENCE, 1994, 265 (5176) :1225-1227