Brondz B D, Karaulov A V, Chervonsky A V, Blandova Z K
Immunogenetics. 1982;15(2):167-76. doi: 10.1007/BF00621949.
Specific suppressor T cells (SSTC), primed in vivo with H-2 antigens, have been shown previously to inhibit DNA synthesis in the one-way, three-cell mixed lymphocyte reaction (MLR) provided that (a) the stimulator cells bear the priming H-2 antigens, and (b) the responder cells possess IC + S regions homologous to those of the SSTC. Anti-B10.A B10.A(2R) SSTC (anti-Dd) and anti-A.AL A.TL SSTC (anti-Kk) are shown here to be able to inhibit the DNA synthesis triggered in MLR, not only by the corresponding antigens, Dd and Kk, respectively, but also by irrelevant, third-party H-2 and Mls products provided that the corresponding and third-party antigens are presented on the same stimulator cell. If stimulator H-2 regions, whose products interact with SSTC and responders, are located on different stimulator cells within the particular MLR, SSTC activity is not elicited. Participation of cytotoxic T lymphocytes in DNA-synthesis suppression is ruled out. Direct contact or location of the inhibited responder cell very close to SSTC is considered to be required for the development of SSTC activity.
以前的研究表明,用H-2抗原在体内致敏的特异性抑制性T细胞(SSTC),在单向三细胞混合淋巴细胞反应(MLR)中能抑制DNA合成,条件是:(a)刺激细胞带有致敏的H-2抗原,以及(b)应答细胞拥有与SSTC同源的IC + S区域。本文显示,抗B10.A B10.A(2R) SSTC(抗Dd)和抗A.AL A.TL SSTC(抗Kk)不仅能够分别抑制由相应抗原Dd和Kk引发的MLR中的DNA合成,而且还能抑制由不相关的第三方H-2和Mls产物引发的DNA合成,前提是相应抗原和第三方抗原呈递在同一个刺激细胞上。如果在特定的MLR中,其产物与SSTC和应答细胞相互作用的刺激细胞H-2区域位于不同的刺激细胞上,则不会引发SSTC活性。细胞毒性T淋巴细胞参与DNA合成抑制作用被排除。抑制性应答细胞与SSTC的直接接触或非常接近的位置被认为是SSTC活性发挥所必需的。