Carr William H, Little Ann-Margaret, Mocarski Edward, Parham Peter
Department of Structural Biology, Stanford University, California 94305-5126, USA.
Clin Immunol. 2002 Nov;105(2):126-40. doi: 10.1006/clim.2002.5273.
Lysis of human cytomegalovirus (HCMV)-infected fibroblasts by autologous natural killer (NK) cells was examined in vitro. For NK cell clones, receptor expression was determined at the level of mRNA and cell-surface protein and compared to the lysis of HCMV AD169 strain-infected fibroblasts in which HLA class I was >70% downregulated. The clones ranged broadly in their ability to lyse AD169-infected fibroblasts, correlating neither with the expression of inhibitory KIR, leukocyte inhibitory receptor-1, or CD94:NKG2A receptors nor with the number of different inhibitory KIR expressed per clone. Some lines of polyclonal NK cells preferentially lysed AD169-infected cells and similarly lysed fibroblasts infected with mutant virus RV798, which lacks the genes for downregulating HLA class I. These results demonstrate that NK cell lysis of HCMV-infected autologous fibroblasts is more complex than a simple missing-self mechanism involving downregulation of HLA class I and failure to engage inhibitory self-specific KIR.
在体外检测了自体自然杀伤(NK)细胞对人巨细胞病毒(HCMV)感染的成纤维细胞的裂解作用。对于NK细胞克隆,在mRNA和细胞表面蛋白水平测定受体表达,并与HLA I类下调>70%的HCMV AD169株感染的成纤维细胞的裂解情况进行比较。这些克隆在裂解AD169感染的成纤维细胞的能力上差异很大,既不与抑制性杀伤细胞免疫球蛋白样受体(KIR)、白细胞抑制受体-1或CD94:NKG2A受体的表达相关,也不与每个克隆表达的不同抑制性KIR的数量相关。一些多克隆NK细胞系优先裂解AD169感染的细胞,并且同样裂解被缺乏下调HLA I类基因的突变病毒RV798感染的成纤维细胞。这些结果表明,NK细胞对HCMV感染的自体成纤维细胞的裂解比涉及HLA I类下调和未能结合抑制性自身特异性KIR的简单的缺失自我机制更为复杂。