Suppr超能文献

由同基因亲本脾脏细胞诱导的F1细胞毒性T淋巴细胞的靶次要组织相容性抗原由与H-2相关的基因编码。

The target minor H antigen for F1 cytotoxic T lymphocytes induced by Igh-congenic parental spleen cells is coded for by gene linked to H-2.

作者信息

Ishikawa H, Kubota E, Suzuki H, Saito K

出版信息

J Immunol. 1985 May;134(5):2953-9.

PMID:2580009
Abstract

Graft-vs-host reaction (GvHR) induced in (B10.BR X CWB)F1 (BWF1; H-2k/b, Ighb/b) by i.v. injection with CWB (H-2b, Ighb) spleen cells resulted in complete suppression of cytotoxic T lymphocyte (CTL) responsiveness of the F1 host spleen cells (GvHR-associated immunosuppression). In contrast, GvHR induced in BWF1 mice with CSW (H-2b, Ighj; Igh-congenic to CWB) spleen cells did not affect CTL responsiveness of the F1 host spleen cells at all. The BWF1 hosts undergoing the CSW-induced GvHR generated anti-CSW CTL in their spleens, and the subsequent culture of such BWF1 spleen cells with CSW stimulator cells, augmented the CTL activity. The BWF1 anti-CSW CTL lysed both Con A- and LPS-induced splenic blasts from mouse strains carrying the Ighj allele in the context of self H-2Kb. However, determination of the Igh haplotype in the serum IgG and of the susceptibility of the splenic lymphocytes to the BWF1 anti-CSW CTL on backcross mice, which carry either Ighb/j or Ighb/b in the context of H-2b/b or H-2b/k, showed clearly that Ighj and the gene coding for the target antigen for the BWF1 anti-CSW CTL segregated at ratios close to 1:1. The study in which linkage between the gene(s) coding for the target antigen for the BWF1 anti-CSW CTL and H-2 was examined on CWB X (C3H X CWB)F1 backcross mice and (B10.BR X CSW)F1 X B10 mice demonstrated that the gene, most likely a single gene, coding for the target antigen for the BWF1 anti-CSW CTL is located at 8.5 +/- 4.3 cross-over units to the right or left of the H-2 complex. We designated the minor H antigen to be recognized by the BWF1 anti-CSW CTL as H-X+, and we discuss the distinction between the H-X+ locus and the other minor H loci on chromosome 17.

摘要

通过静脉注射CWB(H-2b,Ighb)脾细胞在(B10.BR×CWB)F1(BWF1;H-2k/b,Ighb/b)小鼠中诱导的移植物抗宿主反应(GvHR)导致F1宿主脾细胞的细胞毒性T淋巴细胞(CTL)反应性完全受到抑制(GvHR相关的免疫抑制)。相比之下,用CSW(H-2b,Ighj;与CWB Igh基因同源)脾细胞在BWF1小鼠中诱导的GvHR对F1宿主脾细胞的CTL反应性完全没有影响。经历CSW诱导的GvHR的BWF1宿主在其脾脏中产生了抗CSW CTL,并且随后将这种BWF1脾细胞与CSW刺激细胞一起培养增强了CTL活性。BWF1抗CSW CTL在自身H-2Kb背景下裂解了来自携带Ighj等位基因的小鼠品系的Con A和LPS诱导的脾母细胞。然而,对回交小鼠血清IgG中的Igh单倍型以及脾淋巴细胞对BWF1抗CSW CTL的敏感性进行测定,这些回交小鼠在H-2b/b或H-2b/k背景下携带Ighb/j或Ighb/b,结果清楚地表明Ighj和编码BWF1抗CSW CTL靶抗原的基因以接近1:1的比例分离。在CWB×(C3H×CWB)F1回交小鼠和(B10.BR×CSW)F1×B10小鼠上进行的研究,检测了编码BWF1抗CSW CTL靶抗原的基因与H-2之间的连锁关系,结果表明,编码BWF1抗CSW CTL靶抗原的基因很可能是单个基因,位于H-2复合体右侧或左侧8.5±4.3个交换单位处。我们将BWF1抗CSW CTL识别的次要H抗原命名为H-X+,并讨论了H-X+基因座与17号染色体上其他次要H基因座之间的区别。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验