Memory T lymphocytes

被引:8
作者
Ashton-Rickardt, PG
Opferman, JT
机构
[1] Univ Chicago, Gwen Knapp Ctr Lupus & Immunol Res, Comm Immunol, Chicago, IL 60637 USA
[2] Univ Chicago, Gwen Knapp Ctr Lupus & Immunol Res, Comm Dev Biol, Chicago, IL 60637 USA
[3] Univ Chicago, Gwen Knapp Ctr Lupus & Immunol Res, Dept Pathol, Chicago, IL 60637 USA
关键词
immunological memory; T lymphocyte; antigen; host defense; lymphocyte survival; immunity to infection; vaccine; apoptosis;
D O I
10.1007/s000180050007
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Immunological memory protects organisms from recurrent challenge by pathogens. The persistence of a heightened reactive state initiated by antigenic challenge is mediated by long-lived memory lymphocytes. The survival of memory T cells is thought to require stimulation through the T cell receptor (TCR), sometimes by persistent antigen. However, memory T cells can survive in the absence of antigen, in which case TCR stimulation provided by cell surface self-peptide/ major histocompatibility complex (MHC) molecules and cytokines are required to sustain memory T cells. Recent work using mouse models has provided insights into the origin of memory T cells. Understanding the mechanisms that underlie the differentiation and persistence of memory T cells may improve the effectiveness of vaccines through the induction of T cell memory.
引用
收藏
页码:69 / 77
页数:9
相关论文
共 78 条
[1]   Immunological memory and protective immunity: Understanding their relation [J].
Ahmed, R ;
Gray, D .
SCIENCE, 1996, 272 (5258) :54-60
[2]   RADIATION CHIMAERA, HOST H-2 ANTIGENS DETERMINE IMMUNE RESPONSIVENESS OF DONOR CYTOTOXIC CELLS [J].
BEVAN, MJ .
NATURE, 1977, 269 (5627) :417-418
[3]   IS T-CELL MEMORY MAINTAINED BY CROSS-REACTIVE STIMULATION [J].
BEVERLEY, PCL .
IMMUNOLOGY TODAY, 1990, 11 (06) :203-205
[4]   GROWTH-FACTORS CAN ENHANCE LYMPHOCYTE SURVIVAL WITHOUT COMMITTING THE CELL TO UNDERGO CELL-DIVISION [J].
BOISE, LH ;
MINN, AJ ;
JUNE, CH ;
LINDSTEN, T ;
THOMPSON, CB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (12) :5491-5495
[5]   CD28 COSTIMULATION CAN PROMOTE T-CELL SURVIVAL BY ENHANCING THE EXPRESSION OF BCL-X(L) [J].
BOISE, LH ;
MINN, AJ ;
NOEL, PJ ;
JUNE, CH ;
ACCAVITTI, MA ;
LINDSTEN, T ;
THOMPSON, CB .
IMMUNITY, 1995, 3 (01) :87-98
[6]   Survival of mature CD4 T lymphocytes is dependent on major histocompatibility complex class II-expressing dendritic cells [J].
Brocker, T .
JOURNAL OF EXPERIMENTAL MEDICINE, 1997, 186 (08) :1223-1232
[7]   ON THE CELLULAR BASIS OF IMMUNOLOGICAL T-CELL MEMORY [J].
BRUNO, L ;
KIRBERG, J ;
VONBOEHMER, H .
IMMUNITY, 1995, 2 (01) :37-43
[8]   Interleukin-15 protects from lethal apoptosis in vivo [J].
BulfonePaus, S ;
Ungureanu, D ;
Pohl, T ;
Lindner, G ;
Paus, R ;
Ruckert, R ;
Krause, H ;
Kunzendorf, U .
NATURE MEDICINE, 1997, 3 (10) :1124-1128
[9]   Lymphocyte homing and homeostasis [J].
Butcher, EC ;
Picker, LJ .
SCIENCE, 1996, 272 (5258) :60-66
[10]  
Cerwenka A, 1998, J IMMUNOL, V161, P97