Hercend T, Meuer S, Brennan A, Edson M A, Acuto O, Reinherz E L, Schlossman S F, Ritz J
Cell Immunol. 1984 Jul;86(2):381-92. doi: 10.1016/0008-8749(84)90393-9.
A monoclonal antibody termed anti-NKTb has been generated following immunization of mice with cloned human cells (JT9) displaying natural killer (NK)-like activity. This antibody has the capacity to block cytotoxicity of the immunizing clone against several targets. In the present study, anti-NKTb was compared with a monoclonal antibody termed anti-NKTa that had previously been generated against JT9 cells and that had also been shown to block the NK-like function of these cells. The expression of a NKTb determinant, like that of NKTa, was found to be restricted to two NK active clones derived from the same individual, JT9 and JT10, both of which have the same mature T-cell phenotype (T3+, T8+, T11+). Comodulation, immunoprecipitation, and competitive binding experiments showed that both antibodies are directed to the same 90-kDa heterodimer associated with the T3 structure on the cell surface. However, cytotoxicity blocking studies suggested that NKTa and NKTb may represent functionally distinct epitopes of this 90-kDa molecule. Anti-NKTa uniformly blocked the cytotoxicity of both JT9 and JT10 cells when tested against 11 randomly selected target cell lines. In contrast, anti-NKTb totally blocked the cytotoxicity of these cloned cells against some targets (i.e., HPB-ALL, Nalm-1) but had very little effect when cytotoxicity was measured against other target cells (i.e., K562, U937, KG-1). This selective blocking effect, therefore, supports the notion that the heterodimer defined by the NKT antibodies is involved in the process of target cell recognition rather than in the cytolytic pathway of the cloned effector cells. Moreover, the unique functional effects of anti-NKTb suggest that additional levels of complexity exist in the specific recognition mechanisms of these clonal populations of NK active mature T lymphocytes.
用具有自然杀伤(NK)样活性的克隆人细胞(JT9)免疫小鼠后,产生了一种名为抗NKTb的单克隆抗体。该抗体能够阻断免疫克隆对多个靶标的细胞毒性。在本研究中,将抗NKTb与一种名为抗NKTa的单克隆抗体进行了比较,抗NKTa先前已针对JT9细胞产生,并且也已证明可阻断这些细胞的NK样功能。发现NKTb决定簇的表达与NKTa一样,仅限于来自同一个体的两个具有NK活性的克隆JT9和JT10,二者均具有相同的成熟T细胞表型(T3 +、T8 +、T11 +)。共调节、免疫沉淀和竞争性结合实验表明,两种抗体均针对与细胞表面T3结构相关的相同90 kDa异二聚体。然而,细胞毒性阻断研究表明,NKTa和NKTb可能代表该90 kDa分子在功能上不同的表位。当针对11个随机选择的靶细胞系进行测试时,抗NKTa均能阻断JT9和JT10细胞的细胞毒性。相比之下,抗NKTb完全阻断了这些克隆细胞对某些靶标(即HPB - ALL、Nalm - 1)的细胞毒性,但在针对其他靶细胞(即K562、U937、KG - 1)测量细胞毒性时作用很小。因此,这种选择性阻断作用支持了以下观点,即由NKT抗体定义的异二聚体参与靶细胞识别过程,而不是克隆效应细胞的溶细胞途径。此外,抗NKTb的独特功能效应表明,这些具有NK活性的成熟T淋巴细胞克隆群体的特异性识别机制存在额外的复杂层面。