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Explaining the Paucity of Intratumoral T Cells: A Construction Out of Known Entities
Author(s) -
Douglas T. Fearon
Publication year - 2016
Publication title -
cold spring harbor symposia on quantitative biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.615
H-Index - 77
eISSN - 1943-4456
pISSN - 0091-7451
DOI - 10.1101/sqb.2016.81.030783
Subject(s) - cxcr3 , chemokine , chemokine receptor , context (archaeology) , cxcr4 , immune system , biology , function (biology) , immunology , receptor , microbiology and biotechnology , cxc chemokine receptors , cancer research , genetics , paleontology
This essay addresses the question of how tumors escape control by the immune system. The literature strongly points to inadequate accumulation of T cells among cancer cells as being the proximate cause, but this observation has no acceptable explanation as yet. An approach to this problem is adopted wherein the chemokines and chemokine receptors that normally mediate the trafficking of T cells to inflamed tissues are reviewed and considered in the context of their relative levels of expression in a transplanted colorectal tumor model. This method of reasoning-consistent with Bertrand Russell's (1985) advice, "Whenever possible, substitute constructions out of known entities for inferences to unknown entities"-leads to the proposal that signaling via the chemokine receptor, CXCR4, impairs the function of CXCR3 on the immune cells that are responsible for suppressing the growth of cancers.

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