Jones B, Janeway C A
Immunogenetics. 1982;16(3):243-55. doi: 10.1007/BF00343313.
To test whether Mls determinants like other non-MHC or nominal antigens, are recognized by T-cells in association with H-2 determinants, the in vitro proliferative responses of T-cell lines and clones were studied. Lines and clones were prepared by soft agar cloning (B10.BR X BALB/c)F1 (H-2k/H-2d Mlsb/Mlsb) t-cells responding in a primary MLR to AKD2F1 (H-2k/H-2d, Mlsa/Mlsa) stimulator cells. All the T-cell clones obtained could respond equally well in a proliferative assay to the Mlsa determinant in association with the H-2 haplotype of either parent, i.e., DBA/2 (H-2d, Mls), and AKR (H-2K, Mlsa) both stimulated equally well. When the T-cell lines and clones were screened against stimulators from recombinant inbred (RI) strains, it became apparent that strains exhibiting the H-2b, Mlsa genotype stimulated poorly or not at all. This shows that the T-cell response to Mlsa involves MHC recognition, and raises the possibility that the response to Mlsa can involve recognition of H-2 specificities shared between the H-2k and H-2d haplotypes.
为了检测诸如其他非MHC或普通抗原的Mls决定簇是否与H-2决定簇相关联而被T细胞识别,我们研究了T细胞系和克隆的体外增殖反应。细胞系和克隆是通过软琼脂克隆法从(B10.BR×BALB/c)F1(H-2k/H-2d Mlsb/Mlsb)T细胞制备而来,这些T细胞在初次混合淋巴细胞反应中对AKD2F1(H-2k/H-2d,Mlsa/Mlsa)刺激细胞产生反应。获得的所有T细胞克隆在增殖试验中对与任一亲本H-2单倍型相关联的Mlsa决定簇反应同样良好,即DBA/2(H-2d,Mls)和AKR(H-2K,Mlsa)刺激效果相同。当用重组近交(RI)品系的刺激细胞对T细胞系和克隆进行筛选时,很明显,表现出H-2b、Mlsa基因型的品系刺激效果很差或根本没有刺激作用。这表明T细胞对Mlsa的反应涉及MHC识别,并增加了对Mlsa的反应可能涉及识别H-2k和H-2d单倍型之间共有的H-2特异性的可能性。