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Treg-Cell-Derived IL-35-Coated Extracellular Vesicles Promote Infectious Tolerance.

ABSTRACT: Interleukin-35 (IL-35) is an immunosuppressive cytokine composed of Epstein-Barr-virus-induced protein 3 (Ebi3) and IL-12α chain (p35) subunits, yet the forms that IL-35 assume and its role in peripheral tolerance remain elusive. We induce CBA-specific, IL-35-producing T regulatory (Treg) cells in Treg^Ebi3WT C57BL/6 reporter mice and identify IL-35 producers by expression of Ebi3^TdTom gene reporter plus Ebi3 and p35 proteins. Curiously, both subunits of IL-35 are displayed on the surface of tolerogen-specific Foxp3⁺ and Foxp3^neg (iTr35) T cells. Furthermore, IL-35 producers, although rare, secrete Ebi3 and p35 on extracellular vesicles (EVs) targeting a 25- to 100-fold higher number of T and B lymphocytes, causing them to acquire surface IL-35. This surface IL-35 is absent when EV production is inhibited or if Ebi3 is genetically deleted in Treg cells. The unique ability of EVs to coat bystander lymphocytes with IL-35, promoting exhaustion in, and secondary suppression by, non-Treg cells identifies a novel mechanism of infectious tolerance.

SUBMITTER: Sullivan JA

PROVIDER: S-EPMC7042971 | biostudies-literature |

REPOSITORIES: biostudies-literature

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Cutting edge: Human regulatory T cells require IL-35 to mediate suppression and infectious tolerance.

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| S-EPMC6311537 | biostudies-literature

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