Human Anti-fungal Th17 Immunity and Pathology Rely on Cross-Reactivity against Candida albicans
Author(s) -
Petra Bächer,
Thordis Hohnstein,
Eva Beerbaum,
Marie Röcker,
Matthew G. Blango,
Svenja Kaufmann,
Jobst Röhmel,
Patience Eschenhagen,
Claudia Grehn,
K. Seidel,
Volker Rickerts,
Laura Lozza,
Ulrik Stervbo,
Mikalai Nienen,
Nina Babel,
Julia Milleck,
Mario Assenmacher,
Oliver A. Cornely,
Maren Ziegler,
Hilmar Wisplinghoff,
Guido Heine,
Margitta Worm,
Britta Siegmund,
Jochen Maul,
Petra Creutz,
Christoph Tabeling,
Christoph RuwweGlösenkamp,
Leif Erik Sander,
Christoph Knosalla,
Sascha Brunke,
Bernhard Hube,
Olaf Kniemeyer,
Axel A. Brakhage,
C. Schwarz,
Alexander Scheffold
Publication year - 2019
Publication title -
cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 26.304
H-Index - 776
eISSN - 1097-4172
pISSN - 0092-8674
DOI - 10.1016/j.cell.2019.01.041
Subject(s) - candida albicans , biology , immunology , aspergillus fumigatus , immune system , inflammation , immunity , microbiology and biotechnology , corpus albicans , heterologous , biochemistry , gene
Th17 cells provide protection at barrier tissues but may also contribute to immune pathology. The relevance and induction mechanisms of pathologic Th17 responses in humans are poorly understood. Here, we identify the mucocutaneous pathobiont Candida albicans as the major direct inducer of human anti-fungal Th17 cells. Th17 cells directed against other fungi are induced by cross-reactivity to C. albicans. Intestinal inflammation expands total C. albicans and cross-reactive Th17 cells. Strikingly, Th17 cells cross-reactive to the airborne fungus Aspergillus fumigatus are selectively activated and expanded in patients with airway inflammation, especially during acute allergic bronchopulmonary aspergillosis. This indicates a direct link between protective intestinal Th17 responses against C. albicans and lung inflammation caused by airborne fungi. We identify heterologous immunity to a single, ubiquitous member of the microbiota as a central mechanism for systemic induction of human anti-fungal Th17 responses and as a potential risk factor for pulmonary inflammatory diseases.
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