SUPPRESSION OF RAT CYTOMEGALOVIRUS REPLICATION BY ANTIBODIES AGAINST GAMMA-INTERFERON

被引:22
作者
HAAGMANS, BL
VANDERMEIDE, PH
STALS, FS
VANDENEERTWEGH, AJM
CLAASSEN, E
BRUGGEMAN, CA
HORZINEK, MC
SCHIJNS, VECJ
机构
[1] UNIV UTRECHT, FAC VET, DEPT INFECT DIS & IMMUNOL, DIV VIROL, 3584 CL UTRECHT, NETHERLANDS
[2] TNO, ITRI, DEPT INFECT & CHRON DIS, RIJSWIJK, NETHERLANDS
[3] UNIV LIMBURG, DEPT MED MICROBIOL, MAASTRICHT, NETHERLANDS
[4] TNO, MED BIOL LAB, DEPT IMMUNOL & MED MICROBIOL, 2280 AA RIJSWIJK, NETHERLANDS
关键词
D O I
10.1128/JVI.68.4.2305-2312.1994
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The role of gamma interferon (IFN-gamma) in the resolution of rat cytomegalovirus (RCMV) infection was investigated. In the spleen, IFN-gamma-producing cells reached maximum numbers on day 7 after infection. Prophylactic treatment with high doses of recombinant rat IFN-gamma exerted antiviral activity in fibroblasts and protected immunosuppressed rats against a lethal RCMV challenge. Remarkably, in immunocompetent rats, neutralization of endogenous IFN-gamma activity significantly reduced the numbers of RCMV antigen-expressing cells in the spleen, the predominant site of viral replication. Moreover, protection of radiation-immunosuppressed infected rats by transferred immune T cells was enhanced by coinjection of IFN-gamma neutralizing antibodies. The observations were paralleled by in vitro findings: low concentrations of IFN-gamma enhanced viral replication in both macrophages and fibroblasts. These data suggest that IFN-gamma can play different and even opposite roles in the regulation of RCMV replication in vivo; T lymphocytes may contribute to the progression of RCMV infection by secreting IFN-gamma.
引用
收藏
页码:2305 / 2312
页数:8
相关论文
共 45 条
[1]   ANTAGONISTIC MODULATION OF HUMAN CYTOMEGALOVIRUS REPLICATION BY TRANSFORMING GROWTH-FACTOR-BETA AND BASIC FIBROBLASTIC GROWTH-FACTOR [J].
ALCAMI, J ;
PAYA, CV ;
VIRELIZIER, JL ;
MICHELSON, S .
JOURNAL OF GENERAL VIROLOGY, 1993, 74 :269-274
[2]  
BELOSEVIC M, 1989, J IMMUNOL, V143, P266
[3]   INTERFERON-GAMMA INDUCES THE EXPRESSION OF HUMAN-IMMUNODEFICIENCY-VIRUS IN PERSISTENTLY INFECTED PROMONOCYTIC CELLS (U1) AND REDIRECTS THE PRODUCTION OF VIRIONS TO INTRACYTOPLASMIC VACUOLES IN PHORBOL-MYRISTATE ACETATE DIFFERENTIATED U1 CELLS [J].
BISWAS, P ;
POLI, G ;
KINTER, AL ;
JUSTEMENT, JS ;
STANLEY, SK ;
MAURY, WJ ;
BRESSLER, P ;
ORENSTEIN, JM ;
FAUCI, AS .
JOURNAL OF EXPERIMENTAL MEDICINE, 1992, 176 (03) :739-750
[4]  
BRUGGEMAN CA, 1985, FEMS MICROBIOL LETT, V27, P263
[5]   ISOLATION OF A CYTOMEGALOVIRUS-LIKE AGENT FROM WILD RATS [J].
BRUGGEMAN, CA ;
MEIJER, H ;
DORMANS, PHJ ;
DEBIE, WMH ;
GRAULS, GELM ;
VANBOVEN, CPA .
ARCHIVES OF VIROLOGY, 1982, 73 (3-4) :231-241
[6]   MULTIPLE DEFECTS OF IMMUNE CELL-FUNCTION IN MICE WITH DISRUPTED INTERFERON-GAMMA GENES [J].
DALTON, DK ;
PITTSMEEK, S ;
KESHAV, S ;
FIGARI, IS ;
BRADLEY, A ;
STEWART, TA .
SCIENCE, 1993, 259 (5102) :1739-1742
[7]   REDUCED MORTALITY IN MURINE CYTOMEGALO-VIRUS INFECTED MICE FOLLOWING PROPHYLACTIC MURINE INTERFERON-GAMMA TREATMENT [J].
FENNIE, EH ;
LIE, YS ;
LOW, MAL ;
GRIBLING, P ;
ANDERSON, KP .
ANTIVIRAL RESEARCH, 1988, 10 (1-3) :27-39
[8]  
FONG TAT, 1990, J IMMUNOL, V144, P1744
[9]   TREATMENT OF AIDS-RELATED KAPOSI-SARCOMA WITH RECOMBINANT GAMMA-INTERFERON [J].
GANSER, A ;
BRUCHER, W ;
BRODT, HR ;
BUSCH, W ;
BRANDHORST, I ;
HELM, EB ;
HOELZER, D .
ONKOLOGIE, 1986, 9 (03) :163-&
[10]  
GESSNER A, 1990, J IMMUNOL, V144, P3160