Impaired T cell activation and increased Th2 lineage commitment in Annexin‐1‐deficient T cells

F D'Acquisto, N Paschalidis… - European journal of …, 2007 - Wiley Online Library
European journal of immunology, 2007Wiley Online Library
Annexin‐1 is a well‐known endogenous anti‐inflammatory protein that modulates the
activation of cells of the innate immune system such as neutrophils and macrophages. We
have recently reported a positive role for the exogenous protein on T cell differentiation,
however, whether such a role holds true for the endogenous protein has yet to be
determined. This aspect has been investigated here finding that Annexin‐1‐deficient T cells
display an impaired activation and proliferation in response to anti‐CD3 plus anti‐CD28 …
Abstract
Annexin‐1 is a well‐known endogenous anti‐inflammatory protein that modulates the activation of cells of the innate immune system such as neutrophils and macrophages. We have recently reported a positive role for the exogenous protein on T cell differentiation, however, whether such a role holds true for the endogenous protein has yet to be determined. This aspect has been investigated here finding that Annexin‐1‐deficient T cells display an impaired activation and proliferation in response to anti‐CD3 plus anti‐CD28 stimulation. Furthermore, differentiation of T cells from Annexin‐1‐deficient mice in Th0/Th1/Th2 or Th17 skewing conditions demonstrated an increased Th2 phenotype compared to cells from control littermates. Similar results were obtained when we analyzed the Th1/Th2 profile of lymph node cells obtained from mice immunized with keyhole limpet hemocyanin or the inflammatory infiltrate in mouse model of allergic inflammation. These results demonstrate a novel modulatory role of endogenous Annexin‐1 in TCR signaling and T cell differentiation and suggest this protein might play a dual and complementary role in the innate and adaptive immune response.
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