Specific T cell responses are central for protection against infection with . Here we show that mycobacteria-specific CD4 and CD8 T cells accumulated in the lung but not in the mediastinal lymph node (MLN) at different time points after infection or BCG immunization. Proliferating specific T cells were found in the lung after infection and immunization. Pulmonary, but not MLN-derived CD4 and CD8 T cells, from -infected mice secreted IFN-γ after stimulation with different mycobacterial peptides. Mycobacteria-specific resident memory CD4 and CD8 T cells (TRM) expressing PD-1 accumulated in the lung after aerosol infection and intratracheal (i.t.) -but not subcutaneous (s.c.)- BCG immunization. Chemical inhibition of recirculation indicated that TRM were generated in the lung after BCG i.t. immunization. In summary, mycobacteria specific-TRM accumulate in the lung during i.t. but not s.c. immunization or infection. Collectively our data suggests that priming, accumulation and/or expansion of specific T cells during BCG immunization and infection occurs in the lung.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7643023 | PMC |
http://dx.doi.org/10.3389/fimmu.2020.566319 | DOI Listing |
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