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.
机构:
Univ Washington, Dept Immunol, Howard Hughes Med Inst, Seattle, WA 98195 USAUniv Washington, Dept Immunol, Howard Hughes Med Inst, Seattle, WA 98195 USA
Butz, EA
;
Bevan, MJ
论文数: 0引用数: 0
h-index: 0
机构:
Univ Washington, Dept Immunol, Howard Hughes Med Inst, Seattle, WA 98195 USAUniv Washington, Dept Immunol, Howard Hughes Med Inst, Seattle, WA 98195 USA
机构:
Univ Washington, Dept Immunol, Howard Hughes Med Inst, Seattle, WA 98195 USAUniv Washington, Dept Immunol, Howard Hughes Med Inst, Seattle, WA 98195 USA
Butz, EA
;
Bevan, MJ
论文数: 0引用数: 0
h-index: 0
机构:
Univ Washington, Dept Immunol, Howard Hughes Med Inst, Seattle, WA 98195 USAUniv Washington, Dept Immunol, Howard Hughes Med Inst, Seattle, WA 98195 USA