IMMUNE-RESPONSES AGAINST MULTIPLE EPITOPES

被引:49
作者
NOWAK, MA
MAY, RM
SIGMUND, K
机构
[1] UNIV OXFORD, DEPT ZOOL, S PARKS RD, OXFORD OX1 3PS, ENGLAND
[2] UNIV VIENNA, INST MATH, A-1090 VIENNA, AUSTRIA
基金
英国惠康基金;
关键词
D O I
10.1006/jtbi.1995.0146
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The current understanding of antigenic escape dynamics is based on models with single epitopes. The usual idea is that a mutation which enables a pathogen (virus, bacteria, etc) to escape from a given immune response confers a selective advantage. The ''escape mutant'' may then increase in abundance until it induces a new specific response against itself. In this paper a new picture is developed, based on mathematical models of immune responses against several epitopes; the simplest such models can have very complicated dynamics, with some surprising features. The emergence of an escape mutant can shift the immunodominant response to another epitope. Even in the absence of mutations, antigenic oscillation is found, with distinct peaks of different virus variants and fluctuations in the size and specificity of the immune responses. The model also provides a general theory for immunodominance in the presence of antigenic variation. Immunodominance is determined by the immunogenicity and by the antigenic diversity of the competing epitopes. Antigenic oscillations and fluctuations in the cytotoxic T-lymphocyte response have been observed in infections with the human immunodeficiency virus (HIV). Shifting the immune responses to weaker epitopes can represent a mechanism for disease progression based on evolutionary dynamics and antigenic diversity of the virus. (C) 1995 Academic Press Limited
引用
收藏
页码:325 / 353
页数:29
相关论文
共 26 条
[1]   INVITRO SELECTION OF LYMPHOCYTIC CHORIOMENINGITIS VIRUS ESCAPE MUTANTS BY CYTOTOXIC LYMPHOCYTES-T [J].
AEBISCHER, T ;
MOSKOPHIDIS, D ;
ROHRER, UH ;
ZINKERNAGEL, RM ;
HENGARTNER, H .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (24) :11047-11051
[2]   MATHEMATICAL STUDIES OF PARASITIC INFECTION AND IMMUNITY [J].
ANDERSON, RM .
SCIENCE, 1994, 264 (5167) :1884-1886
[3]   NATURAL VARIANTS OF CYTOTOXIC EPITOPES ARE T-CELL RECEPTOR ANTAGONISTS FOR ANTIVIRAL CYTOTOXIC T-CELLS [J].
BERTOLETTI, A ;
SETTE, A ;
CHISARI, FV ;
PENNA, A ;
LEVRERO, M ;
DECARLI, M ;
FIACCADORI, F ;
FERRARI, C .
NATURE, 1994, 369 (6479) :407-410
[4]  
CAMPOSLIMA P, 1993, SCIENCE, V260, P98
[5]  
Carpenter S., 1990, Applied Virology Research, V2, P99
[6]   NEW OBSERVATIONS ON ANTIGENIC DIVERSIFICATION OF RNA VIRUSES - ANTIGENIC VARIATION IS NOT DEPENDENT ON IMMUNE SELECTION [J].
DOMINGO, E ;
DIEZ, J ;
MARTINEZ, MA ;
HERNANDEZ, J ;
HOLGUIN, A ;
BORREGO, B ;
MATEU, MG .
JOURNAL OF GENERAL VIROLOGY, 1993, 74 :2039-2045
[7]   MOLECULAR ANALYSIS OF THE ASSOCIATION OF HLA-B53 AND RESISTANCE TO SEVERE MALARIA [J].
HILL, AVS ;
ELVIN, J ;
WILLIS, AC ;
AIDOO, M ;
ALLSOPP, CEM ;
GOTCH, FM ;
GAO, XM ;
TAKIGUCHI, M ;
GREENWOOD, BM ;
TOWNSEND, ARM ;
MCMICHAEL, AJ ;
WHITTLE, HC .
NATURE, 1992, 360 (6403) :434-439
[8]  
Hofbauer J., 1988, THEORY EVOLUTION DYN
[9]   CONVERGENT AND DIVERGENT SEQUENCE EVOLUTION IN THE SURFACE ENVELOPE GLYCOPROTEIN OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 WITHIN A SINGLE INFECTED PATIENT [J].
HOLMES, EC ;
ZHANG, LQ ;
SIMMONDS, P ;
LUDLAM, CA ;
BROWN, AJL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (11) :4835-4839
[10]   RETROVIRAL RECOMBINATION AND REVERSE TRANSCRIPTION [J].
HU, WS ;
TEMIN, HM .
SCIENCE, 1990, 250 (4985) :1227-1233