Su R C, Kung S K, Gariépy J, Barber B H, Miller R G
Department of Medical Biophysics, Ontario Cancer Institute, University of Toronto, Canada.
J Immunol. 1998 Jul 15;161(2):755-66.
NK recognition and lysis of targets are mediated by activation receptor(s) whose effects may be over-ridden by inhibitory receptors recognizing class I MHC on the target. Incubation of normal lymphoblasts with a peptide that can bind to their class I MHC renders them sensitive to lysis by syngeneic NK cells. By binding to class I MHC, the peptide alters or masks the target structure recognized by an inhibitory NK receptor(s). This target structure is most likely an "empty" dimer of class I heavy chain and beta2m as opposed to a "full" class I trimer formed by binding of specific peptide that is recognized by CTL.
NK细胞对靶标的识别和裂解是由激活受体介导的,其作用可能会被识别靶标上I类MHC的抑制性受体所抑制。用能与其I类MHC结合的肽孵育正常淋巴细胞,可使其对同基因NK细胞的裂解敏感。通过与I类MHC结合,该肽改变或掩盖了抑制性NK受体所识别的靶标结构。这种靶标结构很可能是I类重链和β2m的“空”二聚体,而不是由CTL所识别的特异性肽结合形成的“完整”I类三聚体。