MULTIPLE DEFECTS OF IMMUNE CELL-FUNCTION IN MICE WITH DISRUPTED INTERFERON-GAMMA GENES

被引:1541
作者
DALTON, DK
PITTSMEEK, S
KESHAV, S
FIGARI, IS
BRADLEY, A
STEWART, TA
机构
[1] BAYLOR COLL MED,INST MOLEC GENET,HOUSTON,TX 77030
[2] UNIV OXFORD,SIR WILLIAM DUNN SCH PATHOL,OXFORD OX1 3RE,ENGLAND
[3] GENENTECH INC,S SAN FRANCISCO,CA 94080
关键词
D O I
10.1126/science.8456300
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Interferon-gamma (IFN-gamma) is a pleiotrophic cytokine with immunomodulatory effects on a variety of immune cells. Mice with a targeted disruption of the IFN-gamma gene were generated. These mice developed normally and were healthy in the absence of pathogens. However, mice deficient in IFN-gamma had impaired production of macrophage antimicrobial products and reduced expression of macrophage major histocompatibility complex class II antigens. IFN-gamma-deficient mice were killed by a sublethal dose of the intracellular pathogen Mycobacterium bovis. Splenocytes exhibited uncontrolled proliferation in response to mitogen and alloantigen. After a mixed lymphocyte reaction, T cell cytolytic activity was enhanced against allogeneic target cells. Resting splenic natural killer cell activity was reduced in IFN-gamma-deficient mice. Thus, IFN-gamma is essential for the function of several cell types of the murine immune system.
引用
收藏
页码:1739 / 1742
页数:4
相关论文
共 40 条
[21]   NONSPECIFIC DEFENSE-MECHANISM - THE ROLE OF NITRIC-OXIDE [J].
LIEW, FY ;
COX, FEG .
IMMUNOPARASITOLOGY TODAY-A COMBINED ISSUE OF IMMUNOLOGY TODAY AND PARASITOLOGY TODAY, 1991, (03) :A17-A21
[22]  
LIU Y, 1990, Journal of Experimental Medicine, V172, P1735, DOI 10.1084/jem.172.6.1735
[23]   CELLULAR RESISTANCE TO INFECTION [J].
MACKANESS, GB .
JOURNAL OF EXPERIMENTAL MEDICINE, 1962, 116 (03) :381-&
[24]   THE WNT-1 (INT-1) PROTOONCOGENE IS REQUIRED FOR DEVELOPMENT OF A LARGE REGION OF THE MOUSE-BRAIN [J].
MCMAHON, AP ;
BRADLEY, A .
CELL, 1990, 62 (06) :1073-1085
[25]  
MORRISSEY PJ, 1987, J IMMUNOL, V139, P1113
[26]   MACROPHAGE OXYGEN-DEPENDENT ANTI-MICROBIAL ACTIVITY .3. ENHANCED OXIDATIVE-METABOLISM AS AN EXPRESSION OF MACROPHAGE ACTIVATION [J].
MURRAY, HW ;
COHN, ZA .
JOURNAL OF EXPERIMENTAL MEDICINE, 1980, 152 (06) :1596-1609
[27]   ACTIVATION OF HUMAN MACROPHAGES - COMPARISON OF OTHER CYTOKINES WITH INTERFERON-GAMMA [J].
NATHAN, CF ;
PRENDERGAST, TJ ;
WIEBE, ME ;
STANLEY, ER ;
PLATZER, E ;
REMOLD, HG ;
WELTE, K ;
RUBIN, BY ;
MURRAY, HW .
JOURNAL OF EXPERIMENTAL MEDICINE, 1984, 160 (02) :600-605
[28]   ROLE OF NITRIC-OXIDE SYNTHESIS IN MACROPHAGE ANTIMICROBIAL ACTIVITY [J].
NATHAN, CF ;
HIBBS, JB .
CURRENT OPINION IN IMMUNOLOGY, 1991, 3 (01) :65-70
[29]  
PERUSSIA B, 1980, J IMMUNOL, V125, P1589
[30]   INHIBITION OF CYTOTOXIC T-CELL DEVELOPMENT BY TRANSFORMING GROWTH-FACTOR-BETA AND REVERSAL BY RECOMBINANT TUMOR-NECROSIS-FACTOR-ALPHA [J].
RANGES, GE ;
FIGARI, IS ;
ESPEVIK, T ;
PALLADINO, MA .
JOURNAL OF EXPERIMENTAL MEDICINE, 1987, 166 (04) :991-998