HERPESVIRUSES - IMMUNE ESCAPE ARTISTS

被引:99
作者
BANKS, TA [1 ]
ROUSE, BT [1 ]
机构
[1] UNIV TENNESSEE, COLL VET MED, DEPT MICROBIOL, M409 WALTERS LIFE SCI BLDG, KNOXVILLE, TN 37996 USA
关键词
D O I
10.1093/clinids/14.4.933
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Viral persistence depends on the successful avoidance of the host's immunologic surveillance system. This review, which focuses specifically on the herpesviruses, delineates several possible strategies for evading or delaying the immune response. One strategy common to all herpesviruses is the establishment of latency, a state in which the virus may be partially or even completely hidden from the immune system. Other proposed mechanisms of immune evasion include interaction of the virus with components of the humoral immune system, virus-induced modulation of cell-surface recognition structures, and virally mediated interference in antigen processing. Additional strategies include molecular mimicry and the ability of one particular herpesvirus to encode an immunosuppressive cytokine. Although a detailed understanding of the molecular mechanisms of herpesvirus-mediated immune evasion is currently lacking, future studies should identify those critical interactions between host and virus that may prove amenable to therapeutic intervention.
引用
收藏
页码:933 / 941
页数:9
相关论文
共 85 条
[1]  
ABRAMSON JS, 1988, REV INFECT DIS, V10, P326
[2]   HUMAN CYTOMEGALOVIRUS STIMULATES ARACHIDONIC-ACID METABOLISM THROUGH PATHWAYS THAT ARE AFFECTED BY INHIBITORS OF PHOSPHOLIPASE-A2 AND PROTEIN KINASE-C [J].
ABUBAKAR, S ;
BOLDOGH, I ;
ALBRECHT, T .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1990, 166 (02) :953-959
[3]   POSSIBLE ROLE OF FC-RECEPTORS ON CELLS INFECTED AND TRANSFORMED BY HERPESVIRUS - ESCAPE FROM IMMUNE CYTOLYSIS [J].
ADLER, R ;
GLORIOSO, JC ;
COSSMAN, J ;
LEVINE, M .
INFECTION AND IMMUNITY, 1978, 21 (02) :442-447
[4]  
Ahmed R., 1990, VIROLOGY, P241
[5]  
Albrecht T, 1989, Subcell Biochem, V15, P157
[6]   HERPES-SIMPLEX VIRUS TYPE-1-SPECIFIC CYTOTOXIC LYMPHOCYTES-T RECOGNIZE IMMEDIATE-EARLY PROTEIN ICP27 [J].
BANKS, TA ;
ALLEN, EM ;
DASGUPTA, S ;
SANDRIGOLDIN, R ;
ROUSE, BT .
JOURNAL OF VIROLOGY, 1991, 65 (06) :3185-3191
[7]   MEMBRANE-PROTEINS SPECIFIED BY HERPES-SIMPLEX VIRUSES .5. IDENTIFICATION OF AN FC-BINDING GLYCOPROTEIN [J].
BAUCKE, RB ;
SPEAR, PG .
JOURNAL OF VIROLOGY, 1979, 32 (03) :779-789
[8]   HUMAN CYTOMEGALO-VIRUS ENCODES A GLYCOPROTEIN HOMOLOGOUS TO MHC CLASS-I ANTIGENS [J].
BECK, S ;
BARRELL, BG .
NATURE, 1988, 331 (6153) :269-272
[9]  
BIN X, 1989, J GEN VIROL, V70, P893
[10]   HUMAN CYTOMEGALOVIRUS-SPECIFIC CYTO-TOXIC T-CELLS - RELATIVE FREQUENCY OF STAGE-SPECIFIC CTL RECOGNIZING THE 72-KD IMMEDIATE EARLY PROTEIN AND GLYCOPROTEIN-B EXPRESSED BY RECOMBINANT VACCINIA VIRUSES [J].
BORYSIEWICZ, LK ;
HICKLING, JK ;
GRAHAM, S ;
SINCLAIR, J ;
CRANAGE, MP ;
SMITH, GL ;
SISSONS, JGP .
JOURNAL OF EXPERIMENTAL MEDICINE, 1988, 168 (03) :919-931