| Literature DB >> 32122997 |
Véronique Corbière1, Jérôme Segers2, Rémi Desmet2, Sophie Lecher2, Marc Loyens2, Emmanuelle Petit2, Oleg Melnyk2, Camille Locht2, Françoise Mascart3,4.
Abstract
T cell epitopes are mostly nonmodified peptides, although posttranslationally modified peptide epitopes have been described, but they originated from viral or self-proteins. In this study, we provide evidence of a bacterial methylated T cell peptide epitope. The mycobacterial heparin-binding hemagglutinin (HBHA) is a protein Ag with a complex C-terminal methylation pattern and is recognized by T cells from humans latently infected with Mycobacterium tuberculosis By comparing native HBHA with recombinant HBHA produced in Mycobacterium smegmatis (rHBHA-Ms), we could link antigenic differences to differences in the methylation profile. Peptide scan analyses led to the discovery of a peptide containing methyl lysines recognized by a mAb that binds to native HBHA ∼100-fold better than to rHBHA-Ms This peptide was also recognized by T cells from latently infected humans, as evidenced by IFN-γ release upon peptide stimulation. The nonmethylated peptide did not induce IFN-γ, arguing that the methyl lysines are part of the T cell epitope.Entities:
Year: 2020 PMID: 32122997 DOI: 10.4049/jimmunol.1901214
Source DB: PubMed Journal: J Immunol ISSN: 0022-1767 Impact factor: 5.422