Abstract
Tick saliva has pleiotropic properties that facilitate persistence of the arthropod upon the host. We now describe a feeding-inducible protein in Ixodes scapularis saliva, Salp15, that inhibits CD4(+) T cell activation. The mechanism involves the repression of calcium fluxes triggered by TCR ligation and results in lower production of interleukin-2. Salp15 also inhibits the development of CD4(+) T cell-mediated immune responses in vivo, demonstrating the functional importance of this protein. Salp15 provides a molecular basis for understanding the immunosuppressive activity of I. scapularis saliva and vector-host interactions.
Publication types
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Research Support, Non-U.S. Gov't
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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Amino Acid Sequence
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Animals
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Base Sequence
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CD4-Positive T-Lymphocytes / drug effects*
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Calcium Signaling / drug effects*
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Cell Division / drug effects
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Drosophila
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Female
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Interleukin-2 / biosynthesis
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Ixodes*
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Lymphocyte Activation / drug effects*
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Mice
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Mice, Inbred BALB C
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Molecular Sequence Data
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Rabbits
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Rats
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Receptors, Antigen, T-Cell / drug effects
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Receptors, Interleukin-2 / biosynthesis
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Salivary Proteins and Peptides / isolation & purification
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Salivary Proteins and Peptides / physiology*
Substances
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Interleukin-2
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Receptors, Antigen, T-Cell
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Receptors, Interleukin-2
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Salivary Proteins and Peptides
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Salp15 protein, Ixodes scapularis