Abstract
Humans are infected with paramyxoviruses of different genera early
in life, which induce cytotoxic T cells that may recognize conserved epitopes.
This raises the question of whether cross-reactive T cells induced by antecedent
paramyxovirus infections provide partial protection against highly lethal zoonotic
Nipah virus infections. By characterizing a measles virus-specific but paramyxovirus
cross-reactive human T cell clone, we discovered a highly conserved HLA-B*1501-
restricted T cell epitope in the fusion protein. Using peptides, tetramers, and single
cell sorting, we isolated a parainfluenza virus-specific T cell clone from a healthy
adult and showed that both clones cleared Nipah virus-infected cells. We identified
multiple conserved hot spots in paramyxovirus proteomes that contain other potentially
cross-reactive epitopes. Our data suggest that, depending on HLA haplotype
and history of paramyxovirus exposures, humans may have cross-reactive T cells that
provide protection against Nipah virus. The effect of preferential boosting of these
cross-reactive epitopes needs to be further studied in light of paramyxovirus vaccination
studies.
| Original language | English |
|---|---|
| Article number | e00972-20 |
| Pages (from-to) | 1-16 |
| Number of pages | 16 |
| Journal | mBio |
| Volume | 11 |
| Issue number | 4 |
| DOIs | |
| Publication status | Published - 2020 |
Research programs
- EMC OR-01