Forman J, Ciavarra R, Vitetta E S
J Exp Med. 1981 Nov 1;154(5):1357-68. doi: 10.1084/jem.154.5.1357.
C.B-20 mice were immunized with splenocytes or B leukemia cells (BCL1) from Ig H chain allotype congenic strains. Spleen cells from these immunized mice were rechallenged in vitro to generate H-2-restricted cytotoxic T cells that were specific for target antigens controlled by genes linked to the Ig H chain locus. The anti-Ig H cytotoxic T cells detected an antigen(s) expressed only on surface Ig+ cells. Thus, T cell lymphoblasts, eight BALB/c myeloma cell lines, and a T cell lymphoma were not lysed by the effector cells. In contrast, B cell lymphoblasts and the surface Ig+ BCL1 cells were sensitive to lysis. A surface Ig- hybridoma (which secretes the IgM from the BCL1 cells) generated by fusing BCL1 cells to X63 myeloma cells was not killed by the effector cells. These data indicate that cytotoxic T cells specific for antigenic determinants on either surface IgM+ or IgD+ or on a molecule that is coordinately expressed on IgM+ or IgD+ cells can be generated and that such cells might play a role in regulating the growth of normal B cells or surface Ig+ tumor cells in vivo.
用来自Ig H链同种异型基因纯合子品系的脾细胞或B白血病细胞(BCL1)对C.B - 20小鼠进行免疫。将这些免疫小鼠的脾细胞在体外再次刺激,以产生对与Ig H链基因座连锁的基因所控制的靶抗原具有特异性的H - 2限制性细胞毒性T细胞。抗Ig H细胞毒性T细胞检测到仅在表面Ig⁺细胞上表达的一种抗原。因此,效应细胞不能裂解T细胞淋巴母细胞、8种BALB/c骨髓瘤细胞系和1种T细胞淋巴瘤。相反,B细胞淋巴母细胞和表面Ig⁺的BCL1细胞对裂解敏感。通过将BCL1细胞与X63骨髓瘤细胞融合产生的表面Ig⁻杂交瘤(分泌来自BCL1细胞的IgM)不被效应细胞杀死。这些数据表明,可以产生对表面IgM⁺或IgD⁺上的抗原决定簇或对在IgM⁺或IgD⁺细胞上协同表达的分子具有特异性的细胞毒性T细胞,并且这些细胞可能在体内调节正常B细胞或表面Ig⁺肿瘤细胞的生长中发挥作用。