Yachie A, Miyawaki T, Uwadana N, Ohzeki S, Taniguchi N
J Immunol. 1983 Aug;131(2):731-5.
Recent studies have indicated that a monoclonal antibody, termed anti-Tac, may recognize the receptor sites or closely associated structures for interleukin 2 on activated human T cells. The Tac antigen, definable by anti-Tac antibody and usually found on mitogen- or alloantigen-stimulated T cells, was not expressed to any appreciable extent on normal circulating T cells. In the present study, we showed that an increase in circulating T cells expressing Tac antigen as well as Ia determinants occurred in normal individuals after immunization with tetanus toxoid. The expression of Tac antigen and Ia determinants on T cells was evaluated by the rosette method with Staphylococcal protein A-(SPA) coated bovine red blood cells (BRBC) or the indirect immunofluorescence method with monoclonal anti-Tac and anti-Ia antibodies. An increase in Tac-positive or Ia-positive T cells was more evident with the use of the rosette method with SPA-coated BRBC than with conventional immunofluorescence. The percentage of Ia-positive T cells showed a peak between 24 and 48 hr after toxoid injection, and remained at high levels until 2 wk after immunization. In contrast to Ia-positive T cells, the appearance of Tac-positive T cells was transient and at a rather early period of toxoid immunization. The maximum increase of Tac-positive T cells was apparent around 12 hr after toxoid injection, and Tac-positive T cells disappeared abruptly from circulation by 24 hr after inoculation. Ia-positive T cells were induced in both Leu-2 suppressor/cytotoxic and Leu-3 helper/inducer subsets, whereas Tac-positive T cells were generated only within the Leu-3 subset. The fact that induction of Tac-positive and Ia-positive T cells might occur at different stages of T cell activation and in different subsets of T cells seemed to be important for elucidating their roles in the in vivo T cell proliferation and differentiation.
最近的研究表明,一种名为抗Tac的单克隆抗体可能识别活化的人T细胞上白细胞介素2的受体位点或紧密相关结构。Tac抗原可由抗Tac抗体界定,通常见于有丝分裂原或同种异体抗原刺激的T细胞上,在正常循环T细胞上无明显表达。在本研究中,我们发现,正常个体接种破伤风类毒素后,表达Tac抗原以及Ia决定簇的循环T细胞数量增加。用葡萄球菌蛋白A(SPA)包被的牛红细胞(BRBC)通过花环试验或用单克隆抗Tac和抗Ia抗体通过间接免疫荧光法评估T细胞上Tac抗原和Ia决定簇的表达。与传统免疫荧光法相比,使用SPA包被的BRBC通过花环试验检测到的Tac阳性或Ia阳性T细胞增加更为明显。Ia阳性T细胞的百分比在类毒素注射后24至48小时达到峰值,并在免疫后2周内一直保持在高水平。与Ia阳性T细胞不同,Tac阳性T细胞的出现是短暂的,且在类毒素免疫的相当早期阶段。Tac阳性T细胞的最大增加在类毒素注射后约12小时明显,接种后24小时Tac阳性T细胞从循环中突然消失。Ia阳性T细胞在Leu-2抑制/细胞毒性和Leu-3辅助/诱导亚群中均有诱导,而Tac阳性T细胞仅在Leu-3亚群中产生。Tac阳性和Ia阳性T细胞的诱导可能发生在T细胞活化的不同阶段以及T细胞的不同亚群中,这一事实似乎对于阐明它们在体内T细胞增殖和分化中的作用很重要。