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A structurally distinct TGF-β mimic from an intestinal helminth parasite potently induces regulatory T cells.

Chris J C JohnstonDanielle J SmythRavindra B KodaliMadeleine P J WhiteYvonne HarcusKara J FilbeyJames P HewitsonCynthia S HinckAlasdair IvensAndrea M KemterAnna O KildemoesThierry Le BihanDinesh C SoaresStephen M AndertonThomas BrennStephen J WigmoreHannah V WoodcockRachel C ChambersAndrew P HinckHenry J McSorleyRick M Maizels
Published in: Nature communications (2017)
Helminth parasites defy immune exclusion through sophisticated evasion mechanisms, including activation of host immunosuppressive regulatory T (Treg) cells. The mouse parasite Heligmosomoides polygyrus can expand the host Treg population by secreting products that activate TGF-β signalling, but the identity of the active molecule is unknown. Here we identify an H. polygyrus TGF-β mimic (Hp-TGM) that replicates the biological and functional properties of TGF-β, including binding to mammalian TGF-β receptors and inducing mouse and human Foxp3+ Treg cells. Hp-TGM has no homology with mammalian TGF-β or other members of the TGF-β family, but is a member of the complement control protein superfamily. Thus, our data indicate that through convergent evolution, the parasite has acquired a protein with cytokine-like function that is able to exploit an endogenous pathway of immunoregulation in the host.
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