• 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

混合淋巴细胞培养中的T细胞增殖不一定会导致细胞毒性T效应细胞的产生。

T cell proliferation in the mixed lymphocyte culture does not necessarily result in the generation of cytotoxic T effector cells.

作者信息

Röllinghoff M, Pfizenmeier K, Trostmann H, Wagner H

出版信息

Eur J Immunol. 1975 Aug;5(8):560-4. doi: 10.1002/eji.1830050811.

DOI:10.1002/eji.1830050811
PMID:135689
Abstract

It was tested whether T lymphocytes, when stimulated in vitro by M locus-coded lymphocyte activating determinants (LAD), are able to mediate cytotoxic effector functions. The assay for cytotoxicity included both the use of purified appropriate target cells (i.e. purified lipopolysaccharide blasts) as well as the use of phytohemagglutinin dependent cytolysis as a model for detecting cytotoxic T lymphocytes (CTL). Although strong proliferative responses were obtained in the mixed lymphocyte culture, the T cell blast generated did not display any detectable cytotoxic effector function. Thus, it is concluded that LAD, at least in the M locus-dependent system, do have the capacity to induce T cell proliferation but do not induce CTL.

摘要

测试了T淋巴细胞在体外受到M位点编码的淋巴细胞激活决定簇(LAD)刺激时,是否能够介导细胞毒性效应功能。细胞毒性测定方法既包括使用纯化的合适靶细胞(即纯化的脂多糖母细胞),也包括使用植物血凝素依赖性细胞溶解作为检测细胞毒性T淋巴细胞(CTL)的模型。尽管在混合淋巴细胞培养中获得了强烈的增殖反应,但产生的T细胞母细胞未显示出任何可检测到的细胞毒性效应功能。因此,得出结论,至少在M位点依赖性系统中,LAD确实有能力诱导T细胞增殖,但不能诱导CTL。

相似文献

1
T cell proliferation in the mixed lymphocyte culture does not necessarily result in the generation of cytotoxic T effector cells.混合淋巴细胞培养中的T细胞增殖不一定会导致细胞毒性T效应细胞的产生。
Eur J Immunol. 1975 Aug;5(8):560-4. doi: 10.1002/eji.1830050811.
2
Cytotoxic effects of antigen- and mitogen-induced T cells on various targets.抗原和丝裂原诱导的T细胞对各种靶标的细胞毒性作用。
J Immunol. 1975 Feb;114(2 Pt 1):559-65.
3
Effector functions and specificities of normal murine T cells stimulated by syngeneic blasts.同基因胚细胞刺激的正常小鼠T细胞的效应功能和特异性
Eur J Immunol. 1986 May;16(5):471-7. doi: 10.1002/eji.1830160502.
4
Cellular responses to murine alloantigens of the major histocompatibility complex: the role of cell subpopulations that express different quantities of H-2 associated antigenic markers.细胞对主要组织相容性复合体小鼠同种异体抗原的反应:表达不同数量H-2相关抗原标记的细胞亚群的作用。
Eur J Immunol. 1976 Mar;6(3):180-7. doi: 10.1002/eji.1830060308.
5
Cell-free media of mixed lymphocyte cultures augmenting sensitization in vitro of mouse T lymphocytes against allogeneic fibroblasts.混合淋巴细胞培养的无细胞培养基增强小鼠T淋巴细胞体外对同种异体成纤维细胞的致敏作用。
Eur J Immunol. 1976 Jul;5(7):437-44. doi: 10.1002/eji.1830050702.
6
Stimulation of mixed lymphocyte cultures and cytotoxic responses: evidence that T cells express SD but not LD antigens, whereas B cells express both.混合淋巴细胞培养的刺激及细胞毒性反应:证据表明T细胞表达SD抗原但不表达LD抗原,而B细胞则同时表达这两种抗原。
Eur J Immunol. 1976 Jul;5(7):456-61. doi: 10.1002/eji.1830050706.
7
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.
8
Lymphoid cell subpopulations. I. Synergy between lymph node cells and thymocytes in response to alloantigens and mitogens.淋巴细胞亚群。I. 淋巴结细胞与胸腺细胞在对同种异体抗原和有丝分裂原反应中的协同作用。
J Immunol. 1975 Nov;115(5):1227-32.
9
Effects of sodium periodate modification of lymphocytes on the sensitization and lytic phases of T cell-mediated lympholysis.高碘酸钠对淋巴细胞的修饰作用对T细胞介导的淋巴细胞溶解的致敏阶段和溶解阶段的影响。
J Immunol. 1976 Apr;116(4):947-58.
10
Lymphocyte-mediated cytotoxicity against tumor cells. III Differentiation of concanavalin A-activated cytotoxic effector cells.淋巴细胞介导的对肿瘤细胞的细胞毒性。III. 伴刀豆球蛋白A激活的细胞毒性效应细胞的分化
Eur J Immunol. 1976 May;6(5):317-20. doi: 10.1002/eji.1830060503.

引用本文的文献

1
Generation of primary cytotoxic lymphocytes against non-major histocompatibility complex antigens by anti-Ia serum plus complement-treated lymphocytes.通过抗Ia血清加补体处理的淋巴细胞产生针对非主要组织相容性复合体抗原的原发性细胞毒性淋巴细胞。
J Exp Med. 1980 May 1;151(5):1305-10. doi: 10.1084/jem.151.5.1305.
2
T cell recognition of antigen in vivo: role of the H-2 complex.体内T细胞对抗原的识别:H-2复合体的作用。
Springer Semin Immunopathol. 1980 Aug;3(2):213-45. doi: 10.1007/BF02053976.
3
Proliferative patterns of lymphocytes in lymph nodes during tumour development: involvement of T and B cell areas.
肿瘤发展过程中淋巴结内淋巴细胞的增殖模式:T细胞区和B细胞区的累及情况
Br J Cancer. 1984 Apr;49(4):477-84. doi: 10.1038/bjc.1984.75.
4
Suppressor T cells activated in a primary in vitro response to non-major histocompatibility alloantigens.在对非主要组织相容性同种异体抗原的初次体外应答中被激活的抑制性T细胞。
J Exp Med. 1982 Nov 1;156(5):1398-414. doi: 10.1084/jem.156.5.1398.
5
T cell clones with dual specificity for M1s and various major histocompatibility complex determinants.对M1s和各种主要组织相容性复合体决定簇具有双重特异性的T细胞克隆。
J Exp Med. 1981 Dec 1;154(6):1970-4. doi: 10.1084/jem.154.6.1970.
6
Absence of H-2 restriction in primary and secondary mixed-lymphocyte reactions to strong M1s determinants.对强M1s决定簇的初次和再次混合淋巴细胞反应中H-2限制的缺失。
J Exp Med. 1980 Feb 1;151(2):407-17. doi: 10.1084/jem.151.2.407.
7
Participation of the H-2 antigens of tumor cells in their lysis by syngeneic T cells.肿瘤细胞的H-2抗原在同基因T细胞介导的细胞裂解中的作用。
J Exp Med. 1976 Mar 1;143(3):601-14. doi: 10.1084/jem.143.3.601.
8
Effect of niridazole in cellular immunity in vivo and in vitro.硝唑咪对体内和体外细胞免疫的影响。
Clin Exp Immunol. 1978 Jun;32(3):411-8.
9
Secondary in vitro responses of T lymphocytes to non-H-2 alloantigens self-H-2-restricted responses induced in heterologous serum are not dependent on primary-stimulating non-H-2 alloantigens.T淋巴细胞对非H-2同种抗原的继发性体外反应——在异种血清中诱导的自身H-2限制性反应——不依赖于初次刺激的非H-2同种抗原。
J Exp Med. 1977 Apr 1;145(4):802-18. doi: 10.1084/jem.145.4.802.
10
Cyclophosphamide-sensitive T lymphocytes suppress the in vivo generation of antigen-specific cytotoxic T lymphocytes.环磷酰胺敏感的T淋巴细胞抑制抗原特异性细胞毒性T淋巴细胞的体内生成。
J Exp Med. 1977 Feb 1;145(2):455-9. doi: 10.1084/jem.145.2.455.