Forman J, Trial J, Tonkonogy S, Flaherty L
J Exp Med. 1982 Mar 1;155(3):749-67. doi: 10.1084/jem.155.3.749.
B6.KI mice were immunized with spleen cells from B6.K2, a Qa2-subregion congenic strain. Cytotoxic T cells were generated that recognize two target antigens controlled by this region. One of the target antigens is Qa-2. This was demonstrated by the findings that pretreatment of target cells with monoclonal anti-Qa-2 antibody blocked lysis of target cells, and Qa-2 target antigens and serological determinants had a concordant distribution on a panel of B10.W (wild) mice. The gene controlling the Qa-2 target antigen is not polymorphic because B6.K2 and three strains of Qa-2(+) B10.W mice express the same antigens, as determined by a CTL cold target competition assay. Anti-Qa-2 CTL were H-2 unrestricted because effector cells lysed Qa-2(+) targets irrespective of their H-2 haplotype, including five B 10.W strains, and lysis was not inhibited by pretreating target cells with anti-H-2 sera. The Qa2 subregion does not act as a restricting locus for anti-minor-H antigen CTL. A second target antigen was detected that was associated with the expression of the Qa-5 determinant. However, CTL activity could not be blocked by pretreating target cells with monoclonal anti-Qa-5. Therefore, the CTL target antigen may be expressed on a Qa-5(-) molecule. Although the Qa-5 associated CTL specificity is only detected on H-2D(b) strains, it is unlikely that CTL recognition is H-2 restricted because anti-H-2(b) sera has no effect in blocking this reactivity. Qa-2 and H-2 class I antigens share a similar structure and serve as target antigens for unrestricted CTL. However, unlike class I H-2 genes, Qa-2 neither restricts antigen-specific CTL nor is polymorphie. Therefore, it is likely that Qa-2 and H-2 are derived from a common ancestral gene and have evolved to serve different functions.
用来自 Qa2 亚区同源品系 B6.K2 的脾细胞对 B6.KI 小鼠进行免疫。产生了识别该区域控制的两种靶抗原的细胞毒性 T 细胞。其中一种靶抗原是 Qa-2。这一点通过以下发现得以证明:用单克隆抗 Qa-2 抗体预处理靶细胞可阻断靶细胞的裂解,并且 Qa-2 靶抗原和血清学决定簇在一组 B10.W(野生)小鼠上具有一致的分布。控制 Qa-2 靶抗原的基因不是多态性的,因为通过细胞毒性 T 淋巴细胞冷靶竞争试验确定,B6.K2 和三株 Qa-2(+) B10.W 小鼠表达相同的抗原。抗 Qa-2 细胞毒性 T 淋巴细胞不受 H-2 限制,因为效应细胞可裂解 Qa-2(+)靶细胞,而不论其 H-2 单倍型如何,包括五株 B10.W 品系,并且用抗 H-2 血清预处理靶细胞不会抑制裂解。Qa2 亚区不作为抗次要组织相容性抗原细胞毒性 T 淋巴细胞的限制位点。检测到第二种与 Qa-5 决定簇表达相关的靶抗原。然而,用单克隆抗 Qa-5 预处理靶细胞并不能阻断细胞毒性 T 淋巴细胞活性。因此,细胞毒性 T 淋巴细胞靶抗原可能在 Qa-5(-)分子上表达。尽管与 Qa-5 相关的细胞毒性 T 淋巴细胞特异性仅在 H-2D(b)品系上检测到,但细胞毒性 T 淋巴细胞识别不太可能受 H-2 限制,因为抗 H-2(b)血清对阻断这种反应性没有作用。Qa-2 和 H-2 I 类抗原具有相似的结构,并作为不受限制的细胞毒性 T 淋巴细胞的靶抗原。然而,与 I 类 H-2 基因不同,Qa-2 既不限制抗原特异性细胞毒性 T 淋巴细胞,也不是多态性的。因此,Qa-2 和 H-2 很可能源自一个共同的祖先基因,并已进化以发挥不同的功能。