Enriched HLA-E and CD94/NKG2A interaction limits antitumor CD8+ tumor-infiltrating T lymphocyte responses
Immunotherapy treatments with anti-PD-1 boost recovery in less than 30% of treated cancer patients, indicating the complexity of the tumor microenvironment. Expression of HLA-E is linked to poor clinical outcomes in mice and human patients. However, the contributions to immune evasion of HLA-E, a li...
Үндсэн зохиолчид: | Abd Hamid, M, Wang, R, Yao, X, Fan, P, Li, X, Chang, X, Feng, Y, Jones, S, Maldonado-Perez, D, Waugh, C, Verrill, C, Simmons, A, Cerundolo, V, McMichael, A, Conlon, C, Wang, X, Peng, Y, Dong, T |
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Формат: | Journal article |
Хэл сонгох: | English |
Хэвлэсэн: |
American Association for Cancer Research
2019
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Ижил төстэй зүйлс
Ижил төстэй зүйлс
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Enriched HLA-E and CD94/NKG2a interaction limits anti-tumor CD8+ tumor-infiltrating T lymphocyte responses
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HLA-E is expressed on trophoblast and interacts with CD94/NKG2 receptors on decidual NK cells.
-н: King, A, зэрэг
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HLA-E binds to natural killer cell receptors CD94/NKG2A, B and C.
-н: Braud, V, зэрэг
Хэвлэсэн: (1998) -
Regulation of NK cell functions through interaction of the CD94/NKG2 receptors with the nonclassical class I molecule HLA-E.
-н: Braud, V, зэрэг
Хэвлэсэн: (1999) -
HLA class I signal peptide polymorphism determines the level of CD94/NKG2–HLA-E-mediated regulation of effector cell responses
-н: Lin, Z, зэрэг
Хэвлэсэн: (2023)