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细胞毒性T淋巴细胞(CTL)的发育与功能。I. 在无明显增殖的情况下,CTL前体在体内成熟是同种异体免疫的正常结果。

Development and function of cytotoxic T lymphocytes (CTL). I. In vivo maturation of CTL precursors in the absence of detectable proliferation results as a normal consequence of alloimmunization.

作者信息

Kimura A K, Wigzell H

出版信息

J Immunol. 1983 May;130(5):2056-61.

PMID:6220076
Abstract

In the experiments reported here, we examine the need for cell division as a critical component in the clonal expansion of alloreactive CTL precursors. Unlike previous attempts to inhibit DNA synthesis and cell division non-specifically, we have chosen to follow the normal unimpeded development of CTL in two of the most commonly used in vivo and in vitro allograft systems. The development and relative contribution of CTL lymphoblast-associated cytotoxicity has been followed by density gradient separation and functional analysis of the various fractions of lymphocytes obtained throughout the entire course of sensitization. In addition to the physical parameters (size and density), even more convincing data have been obtained from in vivo administration of 3H-TdR during the entire allograft reaction. The results presented here clearly confirm CTL precursor proliferation in vitro but provide strong evidence that in vivo CTL normally arise via a mechanism independent of blast formation and cellular proliferation. Interpretations of these findings in relationship to the concept of "clonal expansion" for the generation of mature CTL are discussed.

摘要

在本文报道的实验中,我们研究了细胞分裂作为同种异体反应性CTL前体细胞克隆扩增关键组成部分的必要性。与以往非特异性抑制DNA合成和细胞分裂的尝试不同,我们选择在两种最常用的体内和体外同种异体移植系统中追踪CTL的正常无阻碍发育。通过密度梯度分离和对整个致敏过程中获得的淋巴细胞不同组分的功能分析,追踪了CTL淋巴母细胞相关细胞毒性的发育及其相对贡献。除了物理参数(大小和密度)外,在整个同种异体移植反应期间体内给予³H-TdR还获得了更有说服力的数据。此处呈现的结果清楚地证实了CTL前体在体外的增殖,但提供了强有力的证据表明,体内CTL通常通过一种独立于母细胞形成和细胞增殖的机制产生。讨论了这些发现与成熟CTL产生的“克隆扩增”概念相关的解释。

相似文献

1
Development and function of cytotoxic T lymphocytes (CTL). I. In vivo maturation of CTL precursors in the absence of detectable proliferation results as a normal consequence of alloimmunization.细胞毒性T淋巴细胞(CTL)的发育与功能。I. 在无明显增殖的情况下,CTL前体在体内成熟是同种异体免疫的正常结果。
J Immunol. 1983 May;130(5):2056-61.
2
The origin of cytotoxic T lymphocyte precursors (CTL-P): MHC-restricted and alloreactive CTL-P in the spleen during regeneration after a sublethal dose of cyclophosphamide (Cy).细胞毒性T淋巴细胞前体(CTL-P)的起源:在亚致死剂量环磷酰胺(Cy)后再生过程中脾脏中的MHC限制性和同种反应性CTL-P。
J Immunol. 1983 Mar;130(3):1077-83.
3
Regulatory mechanisms in cytotoxic T lymphocyte development. I. A suppressor T cell subset that regulates the proliferative stage of CTL development.细胞毒性T淋巴细胞发育中的调节机制。I. 调节CTL发育增殖阶段的抑制性T细胞亚群。
J Immunol. 1983 Feb;130(2):527-32.
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Monoclonal anti-Lyt-2 antibodies block the activation of cytolytic T lymphocyte precursors.单克隆抗Lyt-2抗体可阻断细胞毒性T淋巴细胞前体的激活。
J Immunol. 1983 Apr;130(4):1552-5.
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In vivo mechanisms of alloreactivity. I. Frequency of donor-reactive cytotoxic T lymphocytes in sponge matrix allografts.同种异体反应的体内机制。I. 海绵基质同种异体移植物中供体反应性细胞毒性T淋巴细胞的频率。
Transplantation. 1986 Jan;41(1):75-83.
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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.
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The frequency of mutant-specific killer precursors in related and unrelated mouse strains.相关和不相关小鼠品系中突变特异性杀伤前体的频率。
Eur J Immunol. 1982 Oct;12(10):892-5. doi: 10.1002/eji.1830121017.
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Limiting dilution analysis of alloreactive cytotoxic precursor cells in aging mice.
J Immunol. 1983 Nov;131(5):2215-8.
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Early loss of precursors of CTL and IL 2-producing cells in the development of neonatal tolerance to alloantigens.新生儿对同种异体抗原产生耐受过程中,CTL和产生IL-2细胞前体的早期丢失。
J Immunol. 1984 Jul;133(1):45-51.
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The cytolytic T lymphocyte response to the murine cytomegalovirus. I. Distinct maturation stages of cytolytic T lymphocytes constitute the cellular immune response during acute infection of mice with the murine cytomegalovirus.针对小鼠巨细胞病毒的细胞毒性T淋巴细胞反应。I. 细胞毒性T淋巴细胞的不同成熟阶段构成了小鼠感染小鼠巨细胞病毒急性感染期间的细胞免疫反应。
J Immunol. 1984 Jan;132(1):482-9.

引用本文的文献

1
In vivo proliferation of naïve and memory influenza-specific CD8(+) T cells.初始和记忆性流感特异性CD8(+) T细胞的体内增殖
Proc Natl Acad Sci U S A. 1999 Jul 20;96(15):8597-602. doi: 10.1073/pnas.96.15.8597.
2
Oligoclonal expansion of major histocompatibility complex class I-restricted cytolytic T lymphocytes during a primary immune response in vivo: direct monitoring by flow cytometry and polymerase chain reaction.体内初次免疫应答期间主要组织相容性复合体I类限制性细胞毒性T淋巴细胞的寡克隆扩增:通过流式细胞术和聚合酶链反应进行直接监测
J Exp Med. 1993 May 1;177(5):1487-92. doi: 10.1084/jem.177.5.1487.
3
Characteristics of lymphoblasts appearing in efferent lymph in response to immunization with vaccinia virus.
接种牛痘病毒后出现在输出淋巴液中的成淋巴细胞的特征。
Immunology. 1985 Sep;56(1):23-31.
4
Identification and characterization of a tumor-derived immunosuppressive glycoprotein from murine melanoma K-1735.从小鼠黑色素瘤K-1735中鉴定和表征一种肿瘤衍生的免疫抑制糖蛋白。
Cancer Immunol Immunother. 1985;19(2):90-100. doi: 10.1007/BF00199715.
5
Clonal expansion of T cells: a cytotoxic T-cell response in vivo that involves precursor cell proliferation.T细胞的克隆性扩增:一种体内细胞毒性T细胞反应,涉及前体细胞增殖。
Proc Natl Acad Sci U S A. 1986 Aug;83(16):6089-92. doi: 10.1073/pnas.83.16.6089.