Key result
Listeria infection disproportionately expands splenic CD8+ T cells specific to four MHC class I epitopes.
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Infection of mice with Listeria monocytogenes results in a robust T lymphocyte response that clears the pathogen and provides long term immunity from reinfection. The number of splenic CD4+ and CD8+ T cells and natural killer cells increases during primary and recall infection with L. monocytogenes, however the proportional increase is greatest for CD8+ T cells. The proportion of CD8 T cells expressing low levels of CD62L, a sign of activation, was increased among immune splenocytes, suggesting a substantial expansion of L. monocytogenes specific CTL. Analysis of CTL specific for the immunodominant LLO 91-99 epitope showed that essentially all were CD62Llo during the primary response, but that many upregulated expression of CD62L during the memory phase. Interestingly, the antigen specificity of nearly all additional CD62Llo CTL detected in spleens during recall L. monocytogenes infection can be accounted for with MHC class I tetramers complexed with four different epitopes. These studies demonstrate the complex T lymphocyte dynamics during infection with intracellular pathogens.
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Busch et al. (1999) studied Listeria monocytogenes infection. Listeria monocytogenes infection was evaluated on Splenic CD4+ and CD8+ T cell and natural killer cell dynamics and CD62L expression. Listeria monocytogenes infection in mice disproportionately increased splenic CD8+ T cells, with recall CD62Llo CTL specificity accounted for by MHC class I tetramers complexed with 4 epitopes.
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