Differences in maintenance of CD8+ and CD4+ bacteria-specific effector-memory T cell populations

被引:38
作者
Schiemann, M [1 ]
Busch, V [1 ]
Linkemann, K [1 ]
Huster, KM [1 ]
Busch, DH [1 ]
机构
[1] Tech Univ Munich, Inst Med Microbiol Immunol & Hyg, D-81675 Munich, Germany
关键词
protective immunity; T cells; bacterial infection; CD4/CD8 memory T cells;
D O I
10.1002/eji.200324224
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Our knowledge about the kinetics and dynamics of complex pathogen-specific CD8(+) T cell responses and the in vivo development of CD8(+) memory T cells has increased substantially over the past years; in comparison, relatively little is known about the CD4(+) T cell compartment. We monitored and directly compared the phenotypical changes of pathogen (Listeria monocytogenes)-specific CD8(+) and CD4(+)T cell responses under conditions leading to effective and long-lasting protective immunity. We found that the general kinetics of bacteria-specific CD8(+) and CD4(+) T cells during the effector and post-effector phases are synchronized. However, later during the memory phase, CD8(+) and CD4(+) T cell populations differ substantially. Whereas CD8(+) memory T cell populations with immediate effector function are readily detectable in lymphoid and non-lymphoid tissues and remain remarkably stable in size, antigen-specific CD4(+) effector-memory T cells decline continuously in frequency over time. These findings have important implications for the better understanding of the in vivo development of protective immunity towards intracellular pathogens.
引用
收藏
页码:2875 / 2885
页数:11
相关论文
共 36 条
[11]   A Listeria monocytogenes pentapeptide is presented to cytolytic T lymphocytes by the H2-M3 MHC class Ib molecule [J].
Gulden, PH ;
Fischer, P ;
Sherman, NE ;
Wang, W ;
Engelhard, VH ;
Shabanowitz, J ;
Hunt, DF ;
Pamer, EG .
IMMUNITY, 1996, 5 (01) :73-79
[12]   Differential regulation of antiviral T-cell immunity results in stable CD8+ but declining CD4+ T-cell memory [J].
Homann, D ;
Teyton, L ;
Oldstone, MBA .
NATURE MEDICINE, 2001, 7 (08) :913-919
[13]   CD4+ T cells are required for secondary expansion and memory in CD8+ T lymphocytes [J].
Janssen, EM ;
Lemmens, EE ;
Wolfe, T ;
Christen, U ;
von Herrath, MG ;
Schoenberger, SP .
NATURE, 2003, 421 (6925) :852-856
[14]   Memory CD8+ T cell differentiation:: initial antigen encounter triggers a developmental program in naive cells [J].
Kaech, SM ;
Ahmed, R .
NATURE IMMUNOLOGY, 2001, 2 (05) :415-422
[15]   VISUALIZATION OF PEPTIDE-SPECIFIC T-CELL IMMUNITY AND PERIPHERAL TOLERANCE INDUCTION IN-VIVO [J].
KEARNEY, ER ;
PAPE, KA ;
LOH, DY ;
JENKINS, MK .
IMMUNITY, 1994, 1 (04) :327-339
[16]   Dynamics of memory T cell proliferation under conditions of heterologous immunity and bystander stimulation [J].
Kim, SK ;
Brehm, MA ;
Welsh, RM ;
Selin, LK .
JOURNAL OF IMMUNOLOGY, 2002, 169 (01) :90-98
[17]   Regulatory CD4+CD25+ T cells restrict memory CD8+ T cell responses [J].
Kursar, M ;
Bonhagen, K ;
Fensterle, J ;
Köhler, A ;
Hurwitz, R ;
Kamradt, T ;
Kaufmann, SHE ;
Mittrücker, HW .
JOURNAL OF EXPERIMENTAL MEDICINE, 2002, 196 (12) :1585-1592
[18]   Progressive differentiation and selection of the fittest in the immune response [J].
Lanzavecchia, A ;
Sallusto, F .
NATURE REVIEWS IMMUNOLOGY, 2002, 2 (12) :982-987
[19]   Identification of an H2-M3-restricted Listeria epitope: Implications for antigen presentation by M3 [J].
Lenz, LL ;
Dere, B ;
Bevan, MJ .
IMMUNITY, 1996, 5 (01) :63-72
[20]   A new look at T cells [J].
McMichael, AJ ;
O'Callaghan, CA .
JOURNAL OF EXPERIMENTAL MEDICINE, 1998, 187 (09) :1367-1371