Schmidt H, Forsthuber T, Bühring H J, Müller C A
Immunobiology. 1987 Jan;174(1):51-66. doi: 10.1016/S0171-2985(87)80084-0.
Mouse L(tk-) cells were transfected with recombinant genomic clones encoding the human major histocompatibility antigens HLA-A2 or HLA-B7. The exposure of 15 different transfected cell clones to mouse interferon resulted in an up to 2.9-fold enhancement of the HLA-A2 antigen at the cell surface but in an up to 5.5-fold enhancement of the HLA-B7 antigen as shown by quantitative radioimmunoassay with monoclonal antibodies directed against different HLA epitopes. Using the HLA-Bw6 specific monoclonal antibody 2BC4, an even higher increase of the HLA-B7 antigen (up to 12-fold) could be observed. This higher inducibility of an HLA-B versus HLA-A locus gene may reflect distinct regulatory mechanism controlling the expression of HLA class I subregion antigens.
用编码人类主要组织相容性抗原HLA - A2或HLA - B7的重组基因组克隆转染小鼠L(tk-)细胞。15个不同的转染细胞克隆暴露于小鼠干扰素后,通过针对不同HLA表位的单克隆抗体进行定量放射免疫测定表明,细胞表面的HLA - A2抗原最多增强了2.9倍,而HLA - B7抗原最多增强了5.5倍。使用HLA - Bw6特异性单克隆抗体2BC4,可观察到HLA - B7抗原更高的增加(高达12倍)。HLA - B基因座基因相对于HLA - A基因座基因的这种更高诱导性可能反映了控制HLA I类亚区抗原表达的不同调节机制。