Control of T cell viability

P Marrack, J Kappler - Annu. Rev. Immunol., 2004 - annualreviews.org
P Marrack, J Kappler
Annu. Rev. Immunol., 2004annualreviews.org
▪ Abstract The factors affecting T cell viability vary depending on the type and status of the T
cell involved. Naļve T cells die via a Bcl-2/Bim dependent route. Their deaths are prevented
in animals by IL-7 and contact with MHC. Activated T cells die in many different ways.
Among these is a pathway involving signals that come from outside the T cell and affect it via
surface receptors such as Fas. Activated T cells also die through a pathway driven by
signals generated within the T cell itself, a cell autonomous route. This pathway involves …
▪ Abstract 
The factors affecting T cell viability vary depending on the type and status of the T cell involved. Naļve T cells die via a Bcl-2/Bim dependent route. Their deaths are prevented in animals by IL-7 and contact with MHC. Activated T cells die in many different ways. Among these is a pathway involving signals that come from outside the T cell and affect it via surface receptors such as Fas. Activated T cells also die through a pathway driven by signals generated within the T cell itself, a cell autonomous route. This pathway involves members of the Bcl-2 family, in particular Bcl-2, Bcl-xl, Bim, and probably Bak. The viability of CD8+ and CD4+ memory T cells is controlled in different ways. CD8+ memory T cells are maintained by IL-15 and IL-7. The control of CD4+ memory T cells is more mysterious, with roles reported for IL-7 and/or contact via the TCR.
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