4.6 Article

HLA-F and MHC Class I Open Conformers Are Ligands for NK Cell Ig-like Receptors

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JOURNAL OF IMMUNOLOGY
卷 191, 期 7, 页码 3553-3562

出版社

AMER ASSOC IMMUNOLOGISTS
DOI: 10.4049/jimmunol.1300081

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资金

  1. National Institute of Child Health and Human Development [HD45813]
  2. University of Washington Center for AIDS Research, a National Institutes of Health [P30 AI027757]
  3. National Institutes of Health Institutes and Centers: National Institute of Allergy and Infectious Diseases
  4. National Cancer Institute
  5. National Institute of Mental Health
  6. National Institute on Drug Abuse
  7. National Institute of Child Health and Human Development
  8. National Heart, Lung, and Blood Institute
  9. National Center for Complementary and Alternative Medicine
  10. Clinical Research Division at the Fred Hutchinson Cancer Research Center

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Killer Ig-like receptors (KIRs) are innate immune receptors expressed by NK and T cells classically associated with the detection of missing self through loss of their respective MHC ligand. Some KIR specificities for allelic classical class IMHC (MHC-I) have been described, whereas other KIR receptor-ligand relationships, including those associated with nonclassical MHC-I, have yet to be clearly defined. We report in this article that KIR3DL2 and KIR2DS4 and the nonclassical Ag HLA-F, expressed as a free form devoid of peptide, physically and functionally interact. These interactions extend to include classical MHC-I open conformers as ligands, defining new relationships between KIR receptors and MHC-I. The data collectively suggest a broader, previously unrecognized interaction between MHC-I open conformers-including prototypical HLA-F-and KIR receptors, acting in an immunoregulatory capacity centered on the inflammatory response.

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