Calnexin induces expansion of antigen-specific CD4(+) T cells that confer immunity to fungal ascomycetes via conserved epitopes.

Abstract

Fungal infections remain a threat due to the lack of broad-spectrum fungal vaccines and protective antigens. Recent studies showed that attenuated Blastomyces dermatitidis confers protection via T cell recognition of an unknown but conserved antigen. Using transgenic CD4(+) T cells recognizing this antigen, we identify an amino acid determinant within the chaperone calnexin that is conserved across diverse fungal ascomycetes. Calnexin, typically an ER protein, also localizes to the surface of yeast, hyphae, and spores. T cell epitope mapping unveiled a 13-residue sequence conserved across Ascomycota. Infection with divergent ascomycetes, including dimorphic fungi, opportunistic molds, and the agent causing white nose syndrome in bats, induces expansion of calnexin-specific CD4(+) T cells. Vaccine delivery of calnexin in glucan particles induces fungal antigen-specific CD4(+) T cell expansion and resistance to lethal challenge with multiple fungal pathogens. Thus, the immunogenicity and conservation of calnexin make this fungal protein a promising vaccine target.

• Authors: Marcel Wüthrich, Tristan T Brandhorst, Thomas D Sullivan, Hanna Filutowicz, Alana Sterkel, Douglas Stewart, Mengyi Li, Tassanee Lerksuthirat, Vanessa LeBert, Zu Ting Shen, Gary Ostroff, George S Deepe Jr, Chiung Yu Hung, Garry Cole, Jennifer A Walter, Marc K Jenkins, Bruce Klein
• Journal: Cell host & microbe (Cell Host Microbe) Vol. 17 Issue 4 Pg. 452-65 (Apr 08 2015) ISSN: 1934-6069 [Electronic] United States
• PMID: 25800545 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
• Copyright: Copyright © 2015 Elsevier Inc. All rights reserved.

Chemical References

• Antigens, Fungal
• Epitopes
• Calnexin

Topics

• Animals
• Antigens, Fungal (immunology)
• Ascomycota (immunology)
• CD4-Positive T-Lymphocytes (drug effects, immunology)
• Calnexin (immunology)
• Cell Proliferation (drug effects)
• Epitopes (immunology)
• Mice