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继发性细胞介导的淋巴细胞溶解:H-2 LD和SD因子的重要性。

Secondary cell-mediated lympholysis: importance of H-2 LD and SD factors.

作者信息

Alter B J, Grillot-Courvalin C, Bach M L, Zier K S, Sondel P M, Bach F H

出版信息

J Exp Med. 1976 May 1;143(5):1005-14. doi: 10.1084/jem.143.5.1005.

DOI:10.1084/jem.143.5.1005
PMID:131173
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2190188/
Abstract

Lymphocytes stimulated in mixed leukocyte cultures and left for 13-17 days, i.e. beyond their peak proliferative and cytotoxic reactivities, can be restimulated to give a secondary-type rapid and strong proliferative and cytotoxic response when confronted with cells of the original sensitizing cell donor. We have concerned ourselves primarily with the requirements of restimulation for the presence of LD and/or SD stimuli on the restimulating cells. (a) The low level cell-mediated lympholysis (CML) associated with LD differences in a primary CML can be restimulated to give a secondary-type response by those same LD antigens. (b) If the original sensitizing cells differ from the responding cells by both LD and SD antigens, restimulation with only the LD antigens, or third-party cells presumably carrying cross-reactive LD antigens, can restimulate the secondary CML responses directed against the SD antigens on the original sensitizing cells. (c) The presence of SD antigens on the restimulating cells that are cross-reactive with the primary sensitizing SD antigens (as determined in a primary CML) leads to the preferential activation of cytotoxic T lymphocytes reactive to those antigens although maximum cytotoxicity is still directed at cells carrying the original sensitizing SD antigens. A model to explain these results is presented.

摘要

在混合白细胞培养物中受到刺激并放置13 - 17天(即超过其增殖和细胞毒性反应峰值)的淋巴细胞,当与原始致敏细胞供体的细胞相遇时,可被再次刺激以产生二次型快速且强烈的增殖和细胞毒性反应。我们主要关注再次刺激时对再次刺激细胞上存在LD和/或SD刺激的要求。(a) 与初次细胞介导的淋巴细胞溶解(CML)中LD差异相关的低水平细胞介导的淋巴细胞溶解可被相同的LD抗原再次刺激以产生二次型反应。(b) 如果原始致敏细胞与反应细胞在LD和SD抗原方面均不同,仅用LD抗原或可能携带交叉反应性LD抗原的第三方细胞进行再次刺激,可再次刺激针对原始致敏细胞上SD抗原的二次CML反应。(c) 再次刺激细胞上存在与初次致敏SD抗原交叉反应的SD抗原(如在初次CML中所确定),尽管最大细胞毒性仍针对携带原始致敏SD抗原的细胞,但会导致对那些抗原具有反应性的细胞毒性T淋巴细胞优先活化。本文提出了一个解释这些结果的模型。

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Secondary cell-mediated lympholysis: importance of H-2 LD and SD factors.继发性细胞介导的淋巴细胞溶解:H-2 LD和SD因子的重要性。
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Requirements for activation of CD8+ murine T cells. I. Development of cytolytic activity.CD8 + 小鼠T细胞激活的要求。I. 细胞溶解活性的发展。
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本文引用的文献

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Replacement of T-cell function by a T-cell product.用一种T细胞产物替代T细胞功能。
Nat New Biol. 1972 May 3;237(70):15-7. doi: 10.1038/newbio237015a0.
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Serologically defined and lymphocyte-defined components of the major histocompatibility complex in the mouse.小鼠主要组织相容性复合体的血清学定义成分和淋巴细胞定义成分。
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Generation of cytotoxic T lymphocytes in vitro. II. Effect of repeated exposure to alloantigens on the cytotoxic activity of long-term mixed leukocyte cultures.体外细胞毒性T淋巴细胞的产生。II. 反复接触同种异体抗原对长期混合淋巴细胞培养物细胞毒性活性的影响。
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Generation of cytotoxic T lymphocytes in vitro. I. Response of normal and immune mouse spleen cells in mixed leukocyte cultures.体外细胞毒性T淋巴细胞的产生。I. 混合白细胞培养中正常和免疫小鼠脾细胞的反应。
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The involvement of LD- and SD-region differences in MLC and CML: a three-cell experiment.MLC和CML中LD区与SD区差异的参与:一项三细胞实验。
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Specific priming of mouse thymus-dependent lymphocytes to allogeneic cells in vitro.小鼠胸腺依赖性淋巴细胞在体外对同种异体细胞的特异性致敏
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Cell-mediated lympholysis. Importance of serologically defined H-2 regions.细胞介导的淋巴细胞溶解。血清学定义的H-2区域的重要性。
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Cell mediated immunity: separation of cells involved in recognitive and destructive phases.细胞介导免疫:参与识别阶段和破坏阶段的细胞分离。
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Demonstration by MLR test of a previously unsuspected intra-H-2 crossover in the B10.HTT strain: implications concerning location of MLR determinants in the Ir region.通过混合淋巴细胞反应(MLR)试验证明B10.HTT品系中先前未被怀疑的H-2复合体内交叉:关于MLR决定簇在Ir区域定位的意义。
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10
Functional subclasses of T lymphocytes bearing different Ly antigens. II. Cooperation between subclasses of Ly+ cells in the generation of killer activity.带有不同Ly抗原的T淋巴细胞功能亚类。II. Ly+细胞亚类在杀伤活性产生中的合作。
J Exp Med. 1975 Jun 1;141(6):1390-9. doi: 10.1084/jem.141.6.1390.