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.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5701006PMC
http://dx.doi.org/10.1038/s41467-017-01886-6DOI Listing

Publication Analysis

Top Keywords

tgf-β mimic
8
treg cells
8
mammalian tgf-β
8
tgf-β
7
structurally distinct
4
distinct tgf-β
4
mimic intestinal
4
intestinal helminth
4
helminth parasite
4
parasite potently
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!