Spencer J S, Freed J H, Kubo R T
Department of Medicine, National Jewish Center for Immunology and Respiratory Medicine, Denver, CO 80206.
J Immunol. 1993 Dec 15;151(12):6822-32.
Mixed isotype MHC class II molecules (E alpha dA beta d) occur at extremely low levels on the surface of normal mouse B cells and macrophages, as determined by surface staining with an E alpha dA beta d-specific hamster mAb, H71-258.41. The surface levels of mixed isotype on the B cell lymphoma line A20 are approximately 1 to 2% that of surface I-A, whereas the levels of these molecules on normal mouse B cells were estimated to be at least two to four times less than those on A20. Nevertheless, other investigators have recently reported that immunization of normal H-2d mice with the sperm whale myoglobin peptide 110-121 (SWM(110-121)) elicits T cells, predominantly, V beta 8.2+, that recognize the peptide only in context of E alpha A beta. We have characterized a large number of SWM(110-121)-specific T cell hybridomas from several strains of H-2d haplotype mice. All of the V beta 8.2+ 110-121-specific hybridomas were found to be restricted by E alpha dA beta d, whereas, of the V beta 8.2- 110-121-specific group, approximately half recognized the peptide through E alpha dA beta d whereas the remainder were restricted by either I-Ad or I-Ed. mAb inhibition experiments revealed that 14-4-4S (E alpha-specific) could block presentation by mixed isotype completely, while MK-D6 (A beta d-specific) and H71-258.41 (E alpha dA beta d-specific) only inhibited presentation when the concentration of peptide was limiting. Although A20 expresses very low levels of mixed isotype, 10 to 100 nmol of the peptide produced a detectable response, illustrating the remarkable efficiency in presenting this peptide through E alpha dA beta d. The ability of normal mouse APC to use this restriction element despite its extremely low expression has important implications for the activation of T cells by low levels of peptide-MHC complexes.
混合同种型MHC II类分子(EαdAβd)在正常小鼠B细胞和巨噬细胞表面的表达水平极低,这是通过用EαdAβd特异性仓鼠单克隆抗体H71 - 258.41进行表面染色确定的。B细胞淋巴瘤系A20上混合同种型的表面水平约为表面I - A的1%至2%,而正常小鼠B细胞上这些分子的水平估计比A20上的水平至少低两到四倍。然而,其他研究人员最近报道,用抹香鲸肌红蛋白肽110 - 121(SWM(110 - 121))免疫正常H - 2d小鼠会引发T细胞,主要是Vβ8.2 +,这些T细胞仅在EαAβ的背景下识别该肽。我们从几株H - 2d单倍型小鼠中鉴定了大量SWM(110 - 121)特异性T细胞杂交瘤。所有Vβ8.2 + 110 - 121特异性杂交瘤都被发现受EαdAβd限制,而在Vβ8.2 - 110 - 121特异性组中,约一半通过EαdAβd识别该肽,其余则受I - Ad或I - Ed限制。单克隆抗体抑制实验表明,14 - 4 - 4S(Eα特异性)可完全阻断混合同种型的呈递,而MK - D6(Aβd特异性)和H71 - 258.41(EαdAβd特异性)仅在肽浓度有限时抑制呈递。尽管A20表达的混合同种型水平非常低,但10至100 nmol的肽产生了可检测的反应,说明通过EαdAβd呈递该肽的效率非常高。尽管正常小鼠抗原呈递细胞中这种限制元件的表达极低,但它仍能利用该元件,这对于低水平肽 - MHC复合物激活T细胞具有重要意义。