Long-term maintenance of lung resident memory T cells is mediated by persistent antigen.
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ABSTRACT: Tissue-resident memory T cells (TRM) in the lungs are pivotal for protection against repeated infection with respiratory viruses. However, the gradual loss of these cells over time and the associated decline in clinical protection represent a serious limit in the development of efficient T cell based vaccines against respiratory pathogens. Here, using an adenovirus expressing influenza nucleoprotein (AdNP), we show that CD8 TRM in the lungs can be maintained for at least 1 year post vaccination. Our results reveal that lung TRM continued to proliferate in situ 8 months after AdNP vaccination. Importantly, this required airway vaccination and antigen persistence in the lung, as non-respiratory routes of vaccination failed to support long-term lung TRM</
SUBMITTER: Uddback I
PROVIDER: S-EPMC7726002 | biostudies-literature | 2021 Jan
REPOSITORIES: biostudies-literature
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