CD8+T cell immunosurveillance dynamics influence the outcome of intracellular infections and cancer. Here we used two-photon intravital microscopy to visualize the responses of CD8+resident memory T cells (TRMcells) within the reproductive tracts of live female mice. We found that mucosal TRMcells were highly motile, but paused and underwent in situ division after local antigen challenge. TRMcell reactivation triggered the recruitment of recirculating memory T cells that underwent antigen-independent TRMcell differentiation in situ. However, the proliferation of pre-existing TRMcells dominated the local mucosal recall response and contributed most substantially to the boosted secondary TRMcell population. We observed similar results in skin. Thus, TRMcells can autonomously regulate the expansion of local immunosurveillance independently of central memory or proliferation in lymphoid tissue.
Nature Immunology(2018)
doi:10.1038/s41590-017-0029-3