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跨越I-Ab突变差异产生的细胞毒性T淋巴细胞针对携带Ia抗原的分子。

Cytotoxic T lymphocytes generated across and I-Ab mutant difference are directed against a molecule bearing Ia antigens.

作者信息

de Waal L P, Melief C J, Melvold R W

出版信息

Eur J Immunol. 1981 Mar;11(3):258-65. doi: 10.1002/eji.1830110317.

DOI:10.1002/eji.1830110317
PMID:6165590
Abstract

The recently discovered B6.C-H-2bm12 (bm12) histocompatibility mutant bears a mutation of the I-A subregion of the H-2b haplotype. We have studied cytotoxic T lymphocytes (CTL) generated in secondary mixed lymphocyte culture (MLC) between the bm12 mutant and the strain of origin C57BL/6 (B6). In both directions, strong CTL responses were generated against lipopolysaccharide-stimulated, but not against concanavalin A-stimulated target cells. Studies of the specificity of the bm12 anti-B6 CTL response, using target cells from a panel of H-2 recombinants, showed that the CTL were directed against specificities of the I-Ab subregion. This conclusion was confirmed by the observation that the bm12 anti-B6 CTL could be specifically blocked by anti-Iab, but not by anti-Kb antisera. EL4 tumor cells, which express Kb and Db but not Iab antigens, were not lysed by the CTL. The combined data confirm that bm12 is an I-A subregion mutant and indicate that the I-A subregion antigens, recognized by antibody and those recognized by CTL, are probably present on the same molecules. The CTL effector cells generated in secondary MLC across the I-Ab mutant difference had the surface phenotype Lyt 1- 2+.

摘要

最近发现的B6.C-H-2bm12(bm12)组织相容性突变体带有H-2b单倍型I-A亚区的突变。我们研究了在bm12突变体与亲本菌株C57BL/6(B6)之间的二次混合淋巴细胞培养(MLC)中产生的细胞毒性T淋巴细胞(CTL)。在两个方向上,针对脂多糖刺激的靶细胞产生了强烈的CTL反应,但对刀豆蛋白A刺激的靶细胞没有产生反应。使用一组H-2重组体的靶细胞对bm12抗B6 CTL反应的特异性进行研究,结果表明CTL针对的是I-Ab亚区的特异性。抗Iab抗体可特异性阻断bm12抗B6 CTL,而抗Kb抗血清则不能,这一观察结果证实了该结论。表达Kb和Db但不表达Iab抗原的EL4肿瘤细胞未被CTL裂解。综合数据证实bm12是I-A亚区突变体,并表明抗体识别的I-A亚区抗原和CTL识别的抗原可能存在于同一分子上。在跨越I-Ab突变差异的二次MLC中产生的CTL效应细胞具有Lyt 1- 2+的表面表型。

相似文献

1
Cytotoxic T lymphocytes generated across and I-Ab mutant difference are directed against a molecule bearing Ia antigens.跨越I-Ab突变差异产生的细胞毒性T淋巴细胞针对携带Ia抗原的分子。
Eur J Immunol. 1981 Mar;11(3):258-65. doi: 10.1002/eji.1830110317.
2
Nonresponsiveness to the male antigen H-Y in H-2 I-A-mutant B6.C-H-2bm12 is not caused by defective antigen presentation.在H-2 I-A突变体B6.C-H-2bm12中对雄性抗原H-Y无反应性并非由抗原呈递缺陷所致。
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Induction and characterization of minor histocompatibility antigens. Specific primary cytotoxic T lymphocyte responses in vitro.次要组织相容性抗原的诱导与特性。体外特异性原发性细胞毒性T淋巴细胞反应。
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T cell responses to select Ia determinants using the I-A mutant mouse strain B6.C-H-2bm12.使用I-A突变小鼠品系B6.C-H-2bm12对选定Ia决定簇的T细胞应答。
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Recognition of H-2Kb mutant target cells by Moloney virus-specific cytotoxic T lymphocytes from bm13 (H-2Db mutant) mice. I. Full recognition of Kbm11 by Kb-restricted CTL.来自bm13(H-2Db突变体)小鼠的莫洛尼病毒特异性细胞毒性T淋巴细胞对H-2Kb突变靶细胞的识别。I. Kb限制性细胞毒性T淋巴细胞对Kbm11的完全识别。
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Cytotoxic T lymphocyte response to minor H-42a alloantigen in H-42b mice: clonal inactivation of the precursor cytotoxic T lymphocytes by veto-like spleen cells that express the H-42a antigen.H-42b小鼠对次要H-42a同种抗原的细胞毒性T淋巴细胞反应:表达H-42a抗原的类否决脾细胞对细胞毒性T淋巴细胞前体的克隆失活。
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引用本文的文献

1
Gain/loss of poly(Glu50Tyr50)/poly(Glu60Ala30Tyr10) responsiveness in the bm12 mutant strain.bm12突变株中聚(Glu50Tyr50)/聚(Glu60Ala30Tyr10)反应性的获得/丧失
J Exp Med. 1982 Aug 1;156(2):596-609. doi: 10.1084/jem.156.2.596.
2
I-A subregion control of the transfer of delayed type hypersensitivity (DTH).迟发型超敏反应(DTH)转移的I-A亚区控制
Immunogenetics. 1982;15(6):615-9. doi: 10.1007/BF00347057.
3
Graft-vs.-host-associated immune suppression is activated by recognition of allogeneic murine I-A antigens.移植物抗宿主相关的免疫抑制是通过识别同种异体小鼠I-A抗原而激活的。
J Exp Med. 1983 Mar 1;157(3):936-46. doi: 10.1084/jem.157.3.936.
4
Allosuppressor and allohelper T cells in acute and chronic graft-vs.-host disease. II. F1 recipients carrying mutations at H-2K and/or I-A.急性和慢性移植物抗宿主病中的同种抑制性和同种辅助性T细胞。II. 在H-2K和/或I-A携带突变的F1受体。
J Exp Med. 1983 Feb 1;157(2):755-71. doi: 10.1084/jem.157.2.755.
5
The murine bm12 gene conversion provides evidence that T cells recognize predominantly Ia conformation.小鼠bm12基因转换提供了T细胞主要识别Ia构象的证据。
Proc Natl Acad Sci U S A. 1985 Oct;82(20):7058-62. doi: 10.1073/pnas.82.20.7058.
6
Cytotoxic T-cell response to H-Y antigen by B6.C-H-2bm12 and B10.BR mice.B6.C-H-2bm12和B10.BR小鼠对H-Y抗原的细胞毒性T细胞反应。
Immunology. 1985 Aug;55(4):671-5.