The interplay between host and viral factors in shaping the outcome of cytomegalovirus infection

被引:76
作者
Scalzo, Anthony A.
Corbett, Alexandra J.
Rawlinson, William D.
Scott, Gillian M.
Degli-Esposti, Mariapia A.
机构
[1] Lions Eye Inst, Ctr Expt Immunol, Nedlands, WA 6009, Australia
[2] Univ Western Australia, Ctr Optometry & Visual Sci, Immunol & Virol Program, Nedlands, WA 6009, Australia
[3] Prince Wales Hosp, SEALS, Dept Microbiol, Div Virol, Randwick, NSW 2031, Australia
[4] Prince Wales Hosp, POWH & UNSW Res Labs, Randwick, NSW 2031, Australia
基金
英国惠康基金;
关键词
viral infection; genetic variability; immune evasion; cytomegalovirus; NK cells; CTL;
D O I
10.1038/sj.icb.7100013
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Cytomegalovirus (CMV) remains a major human pathogen causing significant morbidity and mortality in immumosuppressed or immunoimmature individuals. Although significant advances have been made in dissecting out certain features of the host response to human CMV (HCMV) infection, the strict species specificity of CMVs means that most aspects of antiviral immunity are best assessed in animal models. The mouse model of murine CMV (MCMV) infection is an important tool for analysis of in vivo features of host-virus interactions and responses to antiviral drugs that are difficult to assess in humans. Important studies of the contribution of host resistance genes to infection outcome, interplays between innate and adaptive host immune responses, the contribution of virus immune evasion genes and genetic variation in these genes to the establishment of persistence and in vivo studies of resistance to antiviral drugs have benefited from the well-developed MCMV model. In this review, we discuss recent advances in the immunobiology of host-CMV interactions that provide intriguing insights into the complex interplay between host and virus that ultimately facilitates viral persistence. We also discuss recent studies of genetic responses to antiviral therapy, particularly changes in DNA polymerase and protein kinase genes of MCMV and HCMV.
引用
收藏
页码:46 / 54
页数:9
相关论文
共 122 条
[11]   Cutting edge:: Conventional CD8α+ dendritic cells are generally involved in priming CTL immunity to viruses [J].
Belz, GT ;
Smith, CM ;
Eichner, D ;
Shortman, K ;
Karupiah, G ;
Carbone, FR ;
Heath, WK .
JOURNAL OF IMMUNOLOGY, 2004, 172 (04) :1996-2000
[12]   Genetic dissection of innate immunity to infection: the mouse cytomegalovirus model [J].
Beutler, B ;
Crozat, K ;
Koziol, JA ;
Georgel, P .
CURRENT OPINION IN IMMUNOLOGY, 2005, 17 (01) :36-43
[13]  
Biron CA, 1999, CURR OPIN MICROBIOL, V2, P374
[14]   Outcome of reduction mammaplasty - a patient's perspective [J].
Brown, AP ;
Hill, C ;
Khan, K .
BRITISH JOURNAL OF PLASTIC SURGERY, 2000, 53 (07) :584-587
[15]   Vital involvement of a natural killer cell activation receptor in resistance to viral infection [J].
Brown, MG ;
Dokun, AO ;
Heusel, JW ;
Smith, HRC ;
Beckman, DL ;
Blattenberger, EA ;
Dubbelde, CE ;
Stone, LR ;
Scalzo, AA ;
Yokoyama, WM .
SCIENCE, 2001, 292 (5518) :934-937
[16]   A COMPLEX BETWEEN THE MHC CLASS-I HOMOLOG ENCODED BY HUMAN CYTOMEGALOVIRUS AND BETA-2 MICROGLOBULIN [J].
BROWNE, H ;
SMITH, G ;
BECK, S ;
MINSON, T .
NATURE, 1990, 347 (6295) :770-772
[17]   Gain of virulence caused by loss of a gene in murine cytomegalovirus [J].
Bubic, I ;
Wagner, M ;
Krmpotic, A ;
Saulig, T ;
Kim, S ;
Yokoyama, WM ;
Jonjic, S ;
Koszinowski, UH .
JOURNAL OF VIROLOGY, 2004, 78 (14) :7536-7544
[18]   PATHOGENESIS OF MURINE CYTOMEGALOVIRUS-INFECTION IN NATURAL-KILLER CELL-DEPLETED MICE [J].
BUKOWSKI, JF ;
WODA, BA ;
WELSH, RM .
JOURNAL OF VIROLOGY, 1984, 52 (01) :119-128
[19]   ADOPTIVE TRANSFER STUDIES DEMONSTRATING THE ANTIVIRAL EFFECT OF NATURAL-KILLER CELLS INVIVO [J].
BUKOWSKI, JF ;
WARNER, JF ;
DENNERT, G ;
WELSH, RM .
JOURNAL OF EXPERIMENTAL MEDICINE, 1985, 161 (01) :40-52
[20]  
CEBONI C, 2006, EUR J IMMUNOL, V36, P732