Quillet A, Presse F, Marchiol-Fournigault C, Harel-Bellan A, Benbunan M, Ploegh H, Fradelizi D
Laboratoire d'Immunologie, Institut Gustave Roussy, Villejuif, France.
J Immunol. 1988 Jul 1;141(1):17-20.
Experiments in several laboratories have shown that target susceptibility to NK and lymphokine-activated killer (LAK) cytotoxicity is inversely correlated with the target expression of HLA Class I molecules. We present the first direct evidence, obtained by gene transfection, that target cell HLA, A, B expression increases the resistance to the "so-called" non-MHC-restricted cytotoxicity. We have co-transfected, by electroporation, the human beta 2-microglobulin gene and the gene carrying the resistance to geneticin into Daudi cell line. Geneticin selection in culture followed by FACS sorting on the basis of strong positivity with the mAb W6/32 (which is specific for the HLA class I H chain associated to beta 2-microglobulin) have led to the establishment of a HLA+ Daudi cell line permanently expressing HLA A10, A11, and B17 molecules. Studies were performed in vitro to evaluate the susceptibility of these cells to either NK and LAK cytotoxicity. The HLA class I+ Daudi cells exhibit an increased resistance to killing by non-MHC-restricted killer cells (both NK and LAK) as compared with their HLA-Daudi counterpart.
多个实验室的实验表明,靶细胞对自然杀伤细胞(NK)和淋巴因子激活的杀伤细胞(LAK)细胞毒性的敏感性与HLA I类分子的靶细胞表达呈负相关。我们通过基因转染获得了首个直接证据,即靶细胞HLA-A、B表达增加了对“所谓的”非主要组织相容性复合体(MHC)限制性细胞毒性的抗性。我们通过电穿孔将人β2-微球蛋白基因和携带对遗传霉素抗性的基因共转染到Daudi细胞系中。在培养物中进行遗传霉素筛选,然后基于与mAb W6/32(对与β2-微球蛋白相关的HLA I类重链具有特异性)的强阳性通过荧光激活细胞分选(FACS),从而建立了永久表达HLA A10、A11和B17分子的HLA+ Daudi细胞系。进行体外研究以评估这些细胞对NK和LAK细胞毒性的敏感性。与HLA- Daudi对应细胞相比,HLA I类+ Daudi细胞对非MHC限制性杀伤细胞(NK和LAK)的杀伤表现出更高的抗性。