Immunoregulatory circuits and potential treatment of connective tissue diseases

被引:7
作者
AlcocerVarela, J [1 ]
Llorente, L [1 ]
AlarconSegovia, D [1 ]
机构
[1] INST NACL NUTR SALVADOR ZUBIRAN,DEPT IMMUNOL & RHEUMATOL,MEXICO CITY 14000,DF,MEXICO
关键词
systemic lupus erythematosus; rheumatoid arthritis; interleukin-1; interleukin-2; interleukin-10; monoclonal antibodies;
D O I
10.1159/000237391
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Connective tissue diseases are generated by different immunoregulatory alterations. Their better knowledge may lead to new treatment modalities. In systemic lupus erythematosus (SLE), increased IL-10 production by non-T cells might exert an inhibitory effect on Th1 CD4+ T cells which would explain the decreased T cell functions observed in these patients. In rheumatoid arthritis (RA) patients, there may be a balance within the synovium, where the local production of IFN-gamma may limit the anti-inflammatory properties of IL-10, thus leading to chronic damage. This article shows that rational approaches to therapy need to be individualized. In SLE, the potential therapeutic use of monoclonal antibodies to IL-10 seems to be gathering strength, whereas in RA exactly the opposite is contemplated: IL-10 is tried for its potential therapeutic use.
引用
收藏
页码:348 / 354
页数:7
相关论文
共 50 条
[1]  
ALARCONSEGOVIA D, 1985, CLIN RHEUM DIS, V11, P451
[2]  
ALCOCERVARELA J, 1984, CLIN EXP IMMUNOL, V55, P125
[3]   DECREASED PRODUCTION OF AND RESPONSE TO INTERLEUKIN-2 BY CULTURED LYMPHOCYTES FROM PATIENTS WITH SYSTEMIC LUPUS-ERYTHEMATOSUS [J].
ALCOCERVARELA, J ;
ALARCONSEGOVIA, D .
JOURNAL OF CLINICAL INVESTIGATION, 1982, 69 (06) :1388-1392
[4]   LONGITUDINAL-STUDY ON THE PRODUCTION OF AND CELLULAR-RESPONSE TO INTERLEUKIN A IN PATIENTS WITH SYSTEMIC LUPUS-ERYTHEMATOSUS [J].
ALCOCERVARELA, J ;
ALARCONSEGOVIA, D .
RHEUMATOLOGY INTERNATIONAL, 1995, 15 (02) :57-63
[5]   CYTOKINES AND CYTOKINE INHIBITORS OR ANTAGONISTS IN RHEUMATOID-ARTHRITIS [J].
AREND, WP ;
DAYER, JM .
ARTHRITIS AND RHEUMATISM, 1990, 33 (03) :305-315
[6]  
BENJAMIN D, 1992, BLOOD, V80, P1289
[7]  
Bucht A, 1996, CLIN EXP IMMUNOL, V103, P357
[8]   EPSTEIN-BARR-VIRUS TRANSFORMATION INDUCES LYMPHOCYTES-B TO PRODUCE HUMAN INTERLEUKIN-10 [J].
BURDIN, N ;
PERONNE, C ;
BANCHEREAU, J ;
ROUSSET, F .
JOURNAL OF EXPERIMENTAL MEDICINE, 1993, 177 (02) :295-304
[9]  
CANNON GW, 1993, J RHEUMATOL, V20, P1867
[10]  
DEVELDE AA, 1990, BLOOD, V76, P1392