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Publication : Human gut mycobiota tune immunity via CARD9-dependent induction of anti-fungal IgG antibodies.

First Author  Doron I Year  2021
Journal  Cell Volume  184
Issue  4 Pages  1017-1031.e14
PubMed ID  33548172 Mgi Jnum  J:306002
Mgi Id  MGI:6508474 Doi  10.1016/j.cell.2021.01.016
Citation  Doron I, et al. (2021) Human gut mycobiota tune immunity via CARD9-dependent induction of anti-fungal IgG antibodies. Cell 184(4):1017-1031.e14
abstractText  Antibodies mediate natural and vaccine-induced immunity against viral and bacterial pathogens, whereas fungi represent a widespread kingdom of pathogenic species for which neither vaccine nor neutralizing antibody therapies are clinically available. Here, using a multi-kingdom antibody profiling (multiKAP) approach, we explore the human antibody repertoires against gut commensal fungi (mycobiota). We identify species preferentially targeted by systemic antibodies in humans, with Candida albicans being the major inducer of antifungal immunoglobulin G (IgG). Fungal colonization of the gut induces germinal center (GC)-dependent B cell expansion in extraintestinal lymphoid tissues and generates systemic antibodies that confer protection against disseminated C. albicans or C. auris infection. Antifungal IgG production depends on the innate immunity regulator CARD9 and CARD9(+)CX3CR1(+) macrophages. In individuals with invasive candidiasis, loss-of-function mutations in CARD9 are associated with impaired antifungal IgG responses. These results reveal an important role of gut commensal fungi in shaping the human antibody repertoire through CARD9-dependent induction of host-protective antifungal IgG.
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