| Literature DB >> 34715017 |
Emilie V Russler-Germain1, Jisun Jung1, Aidan T Miller1, Shannon Young1, Jaeu Yi1, Alec Wehmeier1, Lindsey E Fox1, Kristen J Monte1, Jiani N Chai1, Devesha H Kulkarni2, Lisa J Funkhouser-Jones3, Georgia Wilke3, Vivek Durai4, Bernd H Zinselmeyer4, Rafael S Czepielewski4, Suellen Greco5, Kenneth M Murphy4, Rodney D Newberry2, L David Sibley6, Chyi-Song Hsieh7.
Abstract
Cryptosporidium can cause severe diarrhea and morbidity, but many infections are asymptomatic. Here, we studied the immune response to a commensal strain of Cryptosporidium tyzzeri (Ct-STL) serendipitously discovered when conventional type 1 dendritic cell (cDC1)-deficient mice developed cryptosporidiosis. Ct-STL was vertically transmitted without negative health effects in wild-type mice. Yet, Ct-STL provoked profound changes in the intestinal immune system, including induction of an IFN-γ-producing Th1 response. TCR sequencing coupled with in vitro and in vivo analysis of common Th1 TCRs revealed that Ct-STL elicited a dominant antigen-specific Th1 response. In contrast, deficiency in cDC1s skewed the Ct-STL CD4 T cell response toward Th17 and regulatory T cells. Although Ct-STL predominantly colonized the small intestine, colon Th1 responses were enhanced and associated with protection against Citrobacter rodentium infection and exacerbation of dextran sodium sulfate and anti-IL10R-triggered colitis. Thus, Ct-STL represents a commensal pathobiont that elicits Th1-mediated intestinal homeostasis that may reflect asymptomatic human Cryptosporidium infection.Entities:
Keywords: IFNγ; IL-12; T cell differentiation; TCR sequencing; Th1; cDC1; commensal protist; cryptosporidiosis; cryptosporidium; dendritic cell; intestine; microbiome
Mesh:
Year: 2021 PMID: 34715017 PMCID: PMC8716016 DOI: 10.1016/j.immuni.2021.10.002
Source DB: PubMed Journal: Immunity ISSN: 1074-7613 Impact factor: 31.745