• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

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。

相似文献

1
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.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。
J Immunol. 1985 May;134(5):2953-9.
2
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。
J Immunol. 1986 Oct 1;137(7):2080-8.
3
Modulation of F1 cytotoxic potentials by GvHR: role and mode of action of non-MHC genes that determine the hybrid resistance to GvHR-associated suppression of F1 cytotoxic potential.移植物抗宿主反应对F1细胞毒性潜能的调节:决定杂种对移植物抗宿主反应相关的F1细胞毒性潜能抑制的杂种抗性的非主要组织相容性复合体基因的作用及作用方式
J Immunol. 1984 May;132(5):2218-25.
4
Modulation of F1 cytotoxic potentials by graft-vs-host reaction. Cooperative non-H-2- and H-2D region-gene control of F1 natural resistance to graft-vs-host reaction-associated immunosuppression.移植物抗宿主反应对F1细胞毒性潜能的调节。F1对移植物抗宿主反应相关免疫抑制的天然抗性的非H-2和H-2D区域基因协同控制。
J Immunol. 1989 Mar 1;142(5):1495-9.
5
Modulation of F1 cytotoxic potentials by GvHR. Host- and donor-derived cytotoxic lymphocytes arise in the unirradiated F1 host spleens under the condition of GvHR-associated immunosuppression.移植物抗宿主反应对F1细胞毒性潜能的调节。在移植物抗宿主反应相关免疫抑制条件下,宿主和供体来源的细胞毒性淋巴细胞在未受照射的F1宿主脾脏中产生。
J Immunol. 1983 Sep;131(3):1142-8.
6
Cytotoxic T lymphocyte response to minor H-43a alloantigen in H-43b mice. Privileged H-2Kb restriction to the response is not due to immunodominance or epistatic effect but due to Ir gene function of H-2Kb itself.H-43b小鼠中细胞毒性T淋巴细胞对次要H-43a同种抗原的应答。对该应答的特权性H-2Kb限制并非由于免疫显性或上位效应,而是由于H-2Kb自身的Ir基因功能。
J Immunol. 1988 Jan 1;140(1):44-51.
7
In vivo priming of mouse CTL precursors directed to product of a newly defined minor H-42 locus is under a novel control of class II MHC gene.针对新定义的次要H-42位点产物的小鼠CTL前体的体内启动受II类MHC基因的新型调控。
J Immunol. 1985 Dec;135(6):3681-5.
8
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。
J Immunol. 1988 Feb 1;140(3):723-9.
9
Cell surface expression of cytotoxic T lymphocyte-defined, AKR/Gross leukemia virus-associated tumor antigens by normal AKR.H-2b splenic B cells.正常AKR.H-2b脾B细胞对细胞毒性T淋巴细胞定义的、AKR/格罗斯白血病病毒相关肿瘤抗原的细胞表面表达。
J Immunol. 1983 Dec;131(6):3078-84.
10
H-41, a new minor histocompatibility locus. I. Histogenetic analysis.H-41,一个新的次要组织相容性位点。I. 组织发生学分析。
J Immunol. 1984 Dec;133(6):2950-4.

引用本文的文献

1
Mouse chromosome 17.小鼠17号染色体。
Mamm Genome. 1991;1 Spec No:S280-300. doi: 10.1007/BF00656498.
2
Maps of mouse chromosome 17: first report. Committee for Mouse Chromosome 17.小鼠第17号染色体图谱:首次报告。小鼠第17号染色体委员会。
Mamm Genome. 1991;1(1):5-29.
3
Mouse chromosome 17.小鼠17号染色体。
Mamm Genome. 1992;3 Spec No:S241-60. doi: 10.1007/BF00648435.