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• W1970597521 abstract "A variety of murine tumor cell lines was studied for its binding of exogeneously added human β2-microglobulin (hβ2m). Three T lymphomas and one IL-2-dependent T-cell line (HT-1) bound substantial amounts of hβ2m, whereas P815 mastocytoma cells, an Abelson virus-infected pre-B cell line (ABLS-8), X63 B-lymphoma cells and YAC cells did not bind hβ2m. In two of the T lymphomas, EL4 and BW5147, binding of hβ2m led to an increase in major histocompatibility complex class I (MHC-I) heavy-chain epitope expression as measured by anti-H-2K/D antibody binding and FACS analysis. EL4 cells which had bound hβ2m decreased their rate of constitutive IL-2 secretion and became resistant to activated natural killer (NK) cell killing. The present data suggest that binding of hβ2m to mouse T cells leads to conformational changes of MHC-I heavy chains which influence both effector and target functions of the cell." @default.
• W1970597521 created "2016-06-24" @default.
• W1970597521 creator A5067530823 @default.
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• W1970597521 date "1994-02-01" @default.
• W1970597521 modified "2023-10-12" @default.
• W1970597521 title "Binding of human β2-microglobulin to murine EL4 thymoma cells upregulates MHC class I heavy-chain epitopes, inhibits IL-2 secretion and induces resistance to killing by natural killer cells" @default.
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• W1970597521 doi "https://doi.org/10.1016/0165-2478(94)90107-4" @default.
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