Immunological memory to viral infections

被引:159
作者
Welsh, RM [1 ]
Selin, LK [1 ]
Szomolanyi-Tsuda, E [1 ]
机构
[1] Univ Massachusetts, Sch Med, Dept Pathol, Worcester, MA 01655 USA
关键词
T cells; B cells; antibody; cytotoxicity; vaccine;
D O I
10.1146/annurev.immunol.22.012703.104527
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The purpose of immunological memory is to protect the host from reinfection, to control persistent infections, and, through maternal antibody, to protect the host's immunologically immature offspring from primary infections. Immunological memory is an exclusive property of the acquired immune system, where in the presence of CD4 T cell help, T cells and B cells clonally expand and differentiate to provide effector systems that protect the host from pathogens. Here we describe how T and B cell memory is generated in response to virus infections and how these cells respond when the host is infected again by similar or different viruses.
引用
收藏
页码:711 / 743
页数:35
相关论文
共 238 条
[1]   Heterologous immunity provides a potent barrier to transplantation tolerance [J].
Adams, AB ;
Williams, MA ;
Jones, TR ;
Shirasugi, N ;
Durham, MM ;
Kaech, SM ;
Wherry, EJ ;
Onami, T ;
Lanier, JG ;
Kokko, KE ;
Pearson, TC ;
Ahmed, R ;
Larsen, CP .
JOURNAL OF CLINICAL INVESTIGATION, 2003, 111 (12) :1887-1895
[2]   A multivalent minigene vaccine, containing B-cell, cytotoxic T-lymphocyte, and T-h epitopes from several microbes, induces appropriate responses in vivo and confers protection against more than one pathogen [J].
An, LL ;
Whitton, JL .
JOURNAL OF VIROLOGY, 1997, 71 (03) :2292-2302
[3]   INFLUENZA BASIC POLYMERASE-2 PEPTIDES ARE RECOGNIZED BY INFLUENZA NUCLEOPROTEIN-SPECIFIC CYTOTOXIC LYMPHOCYTES-T [J].
ANDERSON, RW ;
BENNINK, JR ;
YEWDELL, JW ;
MALOY, WL ;
COLIGAN, JE .
MOLECULAR IMMUNOLOGY, 1992, 29 (09) :1089-1096
[4]   Memory CD8+ T cells vary in differentiation phenotype in different persistent virus infections [J].
Appay, V ;
Dunbar, PR ;
Callan, M ;
Klenerman, P ;
Gillespie, GMA ;
Papagno, L ;
Ogg, GS ;
King, A ;
Lechner, F ;
Spina, CA ;
Little, S ;
Havlir, DV ;
Richman, DD ;
Gruener, N ;
Pape, G ;
Waters, A ;
Easterbrook, P ;
Salio, M ;
Cerundolo, V ;
McMichael, AJ ;
Rowland-Jones, SL .
NATURE MEDICINE, 2002, 8 (04) :379-385
[5]   HIV-specific CD8+ T cells produce antiviral cytokines but are impaired in cytolytic function [J].
Appay, V ;
Nixon, DF ;
Donahoe, SM ;
Gillespie, GMA ;
Dong, T ;
King, A ;
Ogg, GS ;
Spiegel, HML ;
Conlon, C ;
Spina, CA ;
Havlir, DV ;
Richman, DD ;
Waters, A ;
Easterbrook, P ;
McMichael, AJ ;
Rowland-Jones, SL .
JOURNAL OF EXPERIMENTAL MEDICINE, 2000, 192 (01) :63-75
[6]   THE INFLUENCE OF ANTIGEN ORGANIZATION ON B-CELL RESPONSIVENESS [J].
BACHMANN, MF ;
ROHRER, UH ;
KUNDIG, TM ;
BURKI, K ;
HENGARTNER, H ;
ZINKERNAGEL, RM .
SCIENCE, 1993, 262 (5138) :1448-1451
[7]   Induction of long-lived germinal centers associated with persisting antigen after viral infection [J].
Bachmann, MF ;
Odermatt, B ;
Hengartner, H ;
Zinkernagel, RM .
JOURNAL OF EXPERIMENTAL MEDICINE, 1996, 183 (05) :2259-2269
[8]   Regulation of CD8+ T cells undergoing primary and secondary responses to infection in the same host [J].
Badovinac, VP ;
Messingham, KAN ;
Hamilton, SE ;
Harty, JT .
JOURNAL OF IMMUNOLOGY, 2003, 170 (10) :4933-4942
[9]   Regulation of antigen-specific CD8+ T cell homeostasis by perforin and interferon-γ [J].
Badovinac, VP ;
Tvinnereim, AR ;
Harty, JT .
SCIENCE, 2000, 290 (5495) :1354-1357
[10]   Cutting edge: Rapid in vivo killing by memory CD8 T cells [J].
Barber, DL ;
Wherry, EJ ;
Ahmed, R .
JOURNAL OF IMMUNOLOGY, 2003, 171 (01) :27-31