Fischer A, Beverley P, Feldmann M, Smith S
Immunology. 1983 Jan;48(1):177-86.
Influenza virus-specific (A/X31) long-term cultured human T-cell lines belonging to the helper/inducer T-cell set, produce high potency antigen specific helper factors which induce in vitro antibody production to A/X31 by autologous B cells, as well as small and variable amounts of non-specific helper factors. When added to unseparated peripheral blood mononuclear cells, both cultured T cells and their supernatants suppress in vitro antibody synthesis as measured by a solid phase enzyme-linked immunoassay, and T-cell proliferation to antigens and allogeneic cells, but not to mitogens. This phenomenon was further analysed and could be separated into several steps: (i) the production of suppressor inducer factor(s) by the T-cell lines which are distinct from the helper molecules; (ii) activation of T cells belonging to the suppressor/cytotoxic subset as defined by monoclonal antibodies, a process which is antigen-independent and non-genetically restricted, and is optimal with 18 hr incubation; (iii) the activated T cells non-specific suppress antibody production and antigen-induced or allogeneic cell-induced T-cell proliferation. Thus, antigen-specifically activated T-inducer cells exert multiple activities, including specific and non-specific help and non-specific induction of T suppressor cells.
属于辅助/诱导性T细胞组的流感病毒特异性(A/X31)长期培养的人T细胞系,产生高效力的抗原特异性辅助因子,该因子可在体外诱导自体B细胞产生针对A/X31的抗体,以及少量且可变的非特异性辅助因子。当添加到未分离的外周血单个核细胞中时,培养的T细胞及其上清液均可抑制体外抗体合成(通过固相酶联免疫测定法测定),以及T细胞对抗原和同种异体细胞的增殖,但不抑制对有丝分裂原的增殖。对这一现象进行了进一步分析,并可分为几个步骤:(i)T细胞系产生与辅助分子不同的抑制诱导因子;(ii)由单克隆抗体定义的属于抑制/细胞毒性亚群的T细胞的激活,这一过程不依赖抗原且不受基因限制,在孵育18小时时最为理想;(iii)活化的T细胞非特异性抑制抗体产生以及抗原诱导或同种异体细胞诱导的T细胞增殖。因此,抗原特异性活化的T诱导细胞发挥多种活性,包括特异性和非特异性辅助以及T抑制细胞的非特异性诱导。