Blanden R V, McKenzie I F, Kees U, Melvold R W, Kohn H I
J Exp Med. 1977 Sep 1;146(3):869-80. doi: 10.1084/jem.146.3.869.
The T(c)-cell response to ectromelia virus infection was studied in BALB/c-H-2(db) mice which carry a loss mutation in the H-2D region that results in the absence from cell surfaces of a molecule (D') bearing certain public H-2 specificities. When infected, these mice showed a poor response of T(c) cells that recognize H-2D(d) plus virus-specific determinants on infected macrophage targets, but gave a normal response to H-2K d plus virus-specific antigens. However, their own infected macrophages do display wild-type antigenic patterns involving virus and H-2D(d) since they were killed as efficiently as wild-type (BALB/c,H- 2(d))-infected cells by T(c) cells specific only for H-2D(d) plus viral antigens. When tested in vitro, infected BALB/c-H-2(db) cells stimulated a poor T(c)-cell response to H-2D plus virus-specific antigens, but stimulated a normal response (in comparison with infected BALB/c macrophages) to H-2K(d) plus viral antigens. Uninfected BALB/c-H-2(db) cells stimulated a normal T(c)-cell response to minor H antigens or trinitrophenyl in association with H-2D(d), thus suggesting that the defective response to infection may reside in a failure of the relevant H-2D(d) antigens of mutant cells to physically associate with viral antigens. Close association of viral and H-2D-coded molecules was also suggested by ability of specific anti-H-2K or -H-2D to partially block T(c)-cell-mediated lysis of infected targets. These results were interpreted to mean that H-2Dd-dependent, virus- immune T(c) cells recognized an antigenic pattern consisting of virus- specific and H-2D(d) determinants with the latter borne on an H-2D molecule carrying serologically-defined H-2D(d) private specificities. A second H-2D(d)-coded molecule (D') was not required for recognition and lysis by activated T(c) cells, but was apparently necessary for efficient stimulation of precursor T(c) cells, perhaps by promoting appropriate physical association of viral and H-2D(d) molecules.
在BALB/c-H-2(db)小鼠中研究了T(c)细胞对埃可病毒感染的反应,这些小鼠在H-2D区域携带一个缺失突变,导致细胞表面缺乏一种带有某些公共H-2特异性的分子(D')。感染后,这些小鼠对识别感染巨噬细胞靶标上H-2D(d)加病毒特异性决定簇的T(c)细胞反应较差,但对H-2K d加病毒特异性抗原的反应正常。然而,它们自身被感染的巨噬细胞确实呈现出涉及病毒和H-2D(d)的野生型抗原模式,因为它们被仅针对H-2D(d)加病毒抗原的T(c)细胞杀死的效率与野生型(BALB/c,H-2(d))感染的细胞一样高。在体外测试时,感染的BALB/c-H-2(db)细胞对H-2D加病毒特异性抗原刺激的T(c)细胞反应较差,但对H-2K(d)加病毒抗原刺激的反应正常(与感染的BALB/c巨噬细胞相比)。未感染的BALB/c-H-2(db)细胞对与H-2D(d)相关的次要H抗原或三硝基苯刺激的T(c)细胞反应正常,因此表明对感染的缺陷反应可能在于突变细胞的相关H-2D(d)抗原未能与病毒抗原进行物理结合。特异性抗H-2K或-H-2D能够部分阻断T(c)细胞介导的对感染靶标的裂解,这也提示了病毒和H-2D编码分子的紧密结合。这些结果被解释为意味着依赖H-2Dd的病毒免疫T(c)细胞识别一种由病毒特异性和H-2D(d)决定簇组成的抗原模式,后者存在于携带血清学定义的H-2D(d)私有特异性的H-2D分子上。活化的T(c)细胞进行识别和裂解不需要第二个H-2D(d)编码分子(D'),但它显然是有效刺激T(c)前体细胞所必需的,可能是通过促进病毒和H-2D(d)分子的适当物理结合来实现的。