Culling of Activated CD4 T Cells during Typhoid Is Driven by Salmonella Virulence Genes
Author(s) -
Aparna Srinivasan,
Minelva R. Nanton,
Amanda Griffin,
Stephen J. McSorley
Publication year - 2009
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.0900382
Subject(s) - salmonella , pathogen , microbiology and biotechnology , biology , immune system , culling , virulence , salmonella enterica , immunity , t cell , immunology , bacteria , gene , biochemistry , zoology , genetics , herd
Pathogen-specific CD4 T cells are activated within a few hours of oral Salmonella infection and are essential for protective immunity. However, CD4 T cells do not participate in bacterial clearance until several weeks after infection, suggesting that Salmonella can inhibit or evade CD4 T cells that are activated at early time points. Here, we describe the progressive culling of initially activated CD4 T cells in Salmonella-infected mice. Loss of activated CD4 T cells was independent of early instructional programming, T cell precursor frequency, and Ag availability. In contrast, apoptosis of Ag-specific CD4 T cells was actively induced by live bacteria in a process that required Salmonella pathogenicity island-2 and correlated with increased expression of PD-L1. These data demonstrate efficient culling of initially activated Ag-specific CD4 cells by a microbial pathogen and document a novel strategy for bacterial immune evasion.
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