4.8 Article

Human Anti-fungal Th17 Immunity and Pathology Rely on Cross-Reactivity against Candida albicans

Journal

CELL
Volume 176, Issue 6, Pages 1340-+

Publisher

CELL PRESS
DOI: 10.1016/j.cell.2019.01.041

Keywords

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Funding

  1. Christiane Herzog Stiftung, Stuttgart, Germany
  2. Mukoviszidose e.V., Bonn
  3. German Cystic Fibrosis Association
  4. Deutsche Forschungsgemeinschaft (DFG, German Research Foundation) under Germany's Excellence Strategy [EXC 2167-390884018, CRC/TR 241, CRC/TR 124, CRC/TR 84 C8]
  5. Infect ERA-NET Program FunComPath [BMBF 031L0001A]
  6. Center for Sepsis Control and Care (CSCC) [BMBF 01EO1002]
  7. Cystic Fibrosis Foundation (USA) [SCHEFF15G0]
  8. German Federal Ministry of Education and Science (BMBF) InfectControl 2020 Project ART4Fun [BMBF 03ZZ0813A+C]
  9. German Federal Ministry of Education and Science (BMBF) InfectControl 2020 Project DIAT [BMBF 03ZZ0827A+C]
  10. German Federal Ministry of Education and Science (BMBF) InfectControl 2020 Project Transsektorale Forschungsplattform-TV1 [BMBF 03ZZ0802A]
  11. German Federal Ministry of Education and Science (BMBF) InfectControl 2020 Project EXASENS [BMBF13N13861]

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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 antifungal Th17 responses and as a potential risk factor for pulmonary inflammatory diseases.

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