4.6 Article

Expression of CD161 (NKR-P1A) defines subsets of human CD4 and CD8 T cells with different functional activities

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JOURNAL OF IMMUNOLOGY
卷 176, 期 1, 页码 211-216

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AMER ASSOC IMMUNOLOGISTS
DOI: 10.4049/jimmunol.176.1.211

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资金

  1. NATIONAL CANCER INSTITUTE [P01CA049605] Funding Source: NIH RePORTER
  2. NATIONAL HEART, LUNG, AND BLOOD INSTITUTE [P01HL075462, P01HL057443, R01HL058250] Funding Source: NIH RePORTER
  3. NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES [R01AI040093, R21AI040093] Funding Source: NIH RePORTER
  4. NCI NIH HHS [CA49605] Funding Source: Medline
  5. NHLBI NIH HHS [HL58250, HL57443, HL75462] Funding Source: Medline
  6. NIAID NIH HHS [AI40093] Funding Source: Medline

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A subset of T cells in human peripheral blood expresses CD161 (NKR-P1A) receptors that are primarily associated with NK cells. In the current study we isolated blood T cell subsets according to the expression of CD161 and examined their contents of naive, central memory, and effector memory cells and their capacities for proliferation, cytokine secretion, and natural cytolysis. We found that CD4(+)D161(-) and CD8(+)D161(-) subsets contained predominantly naive T cells that secreted high levels of IL-2 after in vitro stimulation, and CD4(+)CD161(int) and CD8(+)CD161(int) subsets contained predominantly effector and central memory T cells that secreted high levels of IFN-gamma and TNF-alpha. All of these subsets showed vigorous proliferation after stimulation in vitro, but none had NK lytic activity. Unexpectedly, the CD8(+)D161(+) cells contained an anergic CD8 alpha(+) CD8 beta(low/-) CD161(high) T cell subset that failed to proliferate, secrete cytokines, or mediate NK lytic activity.

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