Viral escape mechanisms - escapology taught by viruses

被引:78
作者
Lucas, M [1 ]
Karrer, U
Lucas, A
Klenerman, P
机构
[1] Univ Oxford, John Radcliffe Hosp, Buffield Dept Med, Oxford OX3 9DU, England
[2] Univ Oxford, Sir William Dunn Sch Pathol, Oxford OX1 3RE, England
关键词
lymphocytic choriomeningitis virus; murine cytomegalovirus; virus; persistence; T lymphocyte; CD8; CD4; escape; HCV; HIV;
D O I
10.1046/j.1365-2613.2001.00204.x
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Viruses have 'studied' immunology over millions of years of coevolution with their hosts. During this ongoing education they have developed countless mechanisms to escape from the host's immune system. To illustrate the most common strategies of viral immune escape we have focused on two murine models of persistent infection, lymphocytic choriomeningitis virus (LCMV) and murine cytomegalovirus (MCMV). LCMV is a fast replicating small RNA virus with a genome prone to mutations. Therefore, LCMV escapes from the immune system mainly by two strategies: 'speed' and 'shape change'. At the opposite extreme, MCMV is a large, complex DNA virus with a more rigid genome and thus the strategies used by LCMV are no option. However, MCMV has the coding capacity for additional genes which interfere specifically with the immune response of the host, These escape strategies have been described as 'camouflage' and 'sabotage'. Using these simple concepts we describe the spectrum of viral escapology, giving credit not only to the researchers who uncovered this fascinating area of immunology but also to the viruses themselves, who still have a few lessons to teach.
引用
收藏
页码:269 / 286
页数:18
相关论文
共 129 条
[51]   EXPRESSION OF INTERLEUKIN-10 ACTIVITY BY EPSTEIN-BARR-VIRUS PROTEIN BCRF1 [J].
HSU, DH ;
MALEFYT, RD ;
FIORENTINO, DF ;
DANG, MN ;
VIEIRA, P ;
DEVRIES, J ;
SPITS, H ;
MOSMANN, TR ;
MOORE, KW .
SCIENCE, 1990, 250 (4982) :830-832
[52]   IMMUNE-RESPONSE IN MICE THAT LACK THE INTERFERON-GAMMA RECEPTOR [J].
HUANG, S ;
HENDRIKS, W ;
ALTHAGE, A ;
HEMMI, S ;
BLUETHMANN, H ;
KAMIJO, R ;
VILCEK, J ;
ZINKERNAGEL, RM ;
AGUET, M .
SCIENCE, 1993, 259 (5102) :1742-1745
[53]  
JONES S, 2000, ALMOST LIKE WHALE
[54]   Human cytomegalovirus US2 destabilizes major histocompatibility complex class I heavy chains [J].
Jones, TR ;
Sun, L .
JOURNAL OF VIROLOGY, 1997, 71 (04) :2970-2979
[55]   Human cytomegalovirus US3 impairs transport and maturation of major histocompatibility complex class I heavy chains [J].
Jones, TR ;
Wiertz, EJHJ ;
Sun, L ;
Fish, KN ;
Nelson, JA ;
Ploegh, HL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (21) :11327-11333
[56]   ANTIBODIES ARE NOT ESSENTIAL FOR THE RESOLUTION OF PRIMARY CYTOMEGALOVIRUS-INFECTION BUT LIMIT DISSEMINATION OF RECURRENT VIRUS [J].
JONJIC, S ;
PAVIC, I ;
POLIC, B ;
CRNKOVIC, I ;
LUCIN, P ;
KOSZINOWSKI, UH .
JOURNAL OF EXPERIMENTAL MEDICINE, 1994, 179 (05) :1713-1717
[57]   SITE-RESTRICTED PERSISTENT CYTOMEGALO-VIRUS INFECTION AFTER SELECTIVE LONG-TERM DEPLETION OF CD4+ LYMPHOCYTES-T [J].
JONJIC, S ;
MUTTER, W ;
WEILAND, F ;
REDDEHASE, MJ ;
KOSZINOWSKI, UH .
JOURNAL OF EXPERIMENTAL MEDICINE, 1989, 169 (04) :1199-1212
[58]   The roles of perforin- and Fas-dependent cytotoxicity in protection against cytopathic and noncytopathic viruses [J].
Kagi, D ;
Seiler, P ;
Pavlovic, J ;
Ledermann, B ;
Burki, K ;
Zinkernagel, RM ;
Hengartner, H .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1995, 25 (12) :3256-3262
[59]   CYTOTOXICITY MEDIATED BY T-CELLS AND NATURAL-KILLER-CELLS IS GREATLY IMPAIRED IN PERFORIN DEFICIENT MICE [J].
KAGI, D ;
LEDERMANN, B ;
BURKI, K ;
SEILER, P ;
ODERMATT, B ;
OLSEN, KJ ;
PODACK, ER ;
ZINKERNAGEL, RM ;
HENGARTNER, H .
NATURE, 1994, 369 (6475) :31-37
[60]  
Kalams SA, 1995, CURR TOP MICROBIOL, V202, P79