Profiling the CD8low phenotype, an alternative career choice for CD8 T cells during primary differentiation

N Kienzle, A Baz, A Kelso - Immunology and cell biology, 2004 - Wiley Online Library
N Kienzle, A Baz, A Kelso
Immunology and cell biology, 2004Wiley Online Library
A CD8+ T cell of naive phenotype has multiple career choices during its primary
differentiation into an effector cell population. One of these career options is becoming a
CD8low T cell. We have previously shown by in vitro studies that CD8low T cells have lost
expression of CD8 surface protein and mRNA and are poorly cytolytic. In line with poor
cytolytic function, CD8low T cells express low levels of perforin and granzyme B and C,
mediators of the granule‐exocytosis machinery. However, CD8low T cells express IFN‐γ …
A CD8+ T cell of naive phenotype has multiple career choices during its primary differentiation into an effector cell population. One of these career options is becoming a CD8low T cell. We have previously shown by in vitro studies that CD8low T cells have lost expression of CD8 surface protein and mRNA and are poorly cytolytic. In line with poor cytolytic function, CD8low T cells express low levels of perforin and granzyme B and C, mediators of the granule‐exocytosis machinery. However, CD8low T cells express IFN‐γ and substantial amounts of IL‐4, the signature cytokines of type 1 and type 2 T‐cell polarization, respectively. Here, we argue that the CD8low phenotype is an alternative career choice for any naive CD8+ T cell during primary activation but that the probability of choosing this option is greatly enhanced by both IL‐4 and strong activation conditions. CD8low T cells have downregulated CD8α/β heterodimers and no preferential CD8α/α homodimer expression. As shown by anti‐CD8 Ab blocking experiments, surface CD8 substantially contributes to the CD8 T cell's effector function (i.e. cytokine expression and cytolytic activity). The distinct effector profile of CD8low T cells gives an example of the complexity of different CD8 T cell careers during primary effector differentiation.
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