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OTI cells collected from mice of each group were stained with CD8 antibody and H-2K b SIINFEKL tetramers along with mAbs to surface markers related to activation, exhaustion, and migration of T cells, as well as nuclear staining of transcription factors related to T cell smells like cat piss and markers of cell viability.

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Spanking adult consensual data support the idea that a weaker OTI cell response could not be explained merely by death or lack of antigen presentation function of the T.







The authors have declared that no competing interests exist.







In remarkable contrast to the scenario described above, the response of OTI cells from mice injected with T.







IL, which was highly expressed by T.







PLoS One 2:







The absence of genomic DNA was confirmed by using controls to which no reverse transcriptase was added.







Studies were performed to characterize the effector cells responsible for natural cytotoxicity of mouse lymphoid cells against a variety of syngeneic and allogeneic tumor lines.







Immunity