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mirrors a subset of that in humans, suggesting that these preclinical models accurately recapitulate a subset of human disease. Elevated expression in mice and humans Given the

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observed population profiles in most tumors, suggesting the presence of recently activated proliferating and non-senescent intratumoral cells with potential for therapeutic rejuvenation.

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Figure Thumbnail Figure Figure Human Contains Exhausted Show Full Caption View Larger Image Figure Browser Download High Resolution Image Download Next, we studied
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dysfunction in the context of this disease. Humans contain a similarly depleted intratumoral cell population To investigate whether these observations could be extended to humans, we

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tumors. Progenitor cell-like has been shown Evidence is the basis for the proliferative burst in the blocking response Miller et al., Siddiqui et al. What we observed in most tumors, but

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maps and, consistent with our clinical consistent with the previous analysis. with our mouse model Consistently, we observed that eventually exhausted graphs are present in most

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isolated intratumoral cells from freshly resected surgical samples for flow cytometry analysis. Of the samples evaluated, 4 had sufficient range for further immunophenotyping. Consistent

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with previous reports by Stromness et al., most – is maps, reflecting prior antigenic experience, a large fraction of intratumoral cells co-express multiple co-inhibitory receptor

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