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相似文献

1
Gamma/delta T cell clones and natural killer cell clones mediate distinct patterns of non-major histocompatibility complex-restricted cytolysis.γ/δ T细胞克隆和自然杀伤细胞克隆介导非主要组织相容性复合体限制的细胞溶解的不同模式。
J Exp Med. 1990 May 1;171(5):1567-79. doi: 10.1084/jem.171.5.1567.
2
Natural killer (NK)-like cytotoxic activity of allospecific T cell receptor-gamma,delta+ T cell clones. Distinct receptor-ligand interactions mediate NK-like and allospecific cytotoxicity.同种异体特异性T细胞受体γ、δ+T细胞克隆的自然杀伤(NK)样细胞毒性活性。不同的受体-配体相互作用介导NK样和同种异体特异性细胞毒性。
J Immunol. 1989 Jun 15;142(12):4161-8.
3
MHC-unrestricted cytotoxic and proliferative responses of two distinct human gamma/delta T cell subsets to Daudi cells.两种不同的人类γ/δ T细胞亚群对Daudi细胞的MHC非限制性细胞毒性和增殖反应。
J Immunol. 1992 Apr 15;148(8):2315-23.
4
[NK-like cytotoxicity of allospecific gamma delta TCR+ T cell clones].[同种特异性γδTCR + T细胞克隆的自然杀伤样细胞毒性]
Hum Cell. 1990 Oct;3(3):220-5.
5
The role of T cell receptors in non-MHC-restricted cytotoxicity.T细胞受体在非主要组织相容性复合体限制的细胞毒性中的作用。
Cell Immunol. 1989 Feb;118(2):265-84. doi: 10.1016/0008-8749(89)90377-8.
6
Human V gamma 9-V delta 2 T cell receptor-gamma delta lymphocytes show specificity to Daudi Burkitt's lymphoma cells.人类Vγ9-Vδ2 T细胞受体γδ淋巴细胞对伯基特氏淋巴瘤细胞Daudi表现出特异性。
J Immunol. 1990 Nov 15;145(10):3202-8.
7
Non-MHC-restricted target-cell lysis by a CD4-CD8- TCR alpha beta T-cell line, as well as by TCR gamma delta T-cell lines, results from lymphokine-activated killing.一条CD4-CD8-TCRαβT细胞系以及TCRγδT细胞系对靶细胞的非MHC限制杀伤作用是由淋巴因子激活的杀伤作用导致的。
Int J Cancer. 1991 Apr 22;48(1):142-7.
8
Functional and phenotypic differences between CD4+ and CD4- T cell receptor-gamma delta clones from peripheral blood.外周血中CD4 +和CD4 - T细胞受体γδ克隆之间的功能和表型差异。
J Immunol. 1991 Aug 15;147(4):1180-8.
9
Cloned CD3+ TcR alpha/beta- Ti gamma A- peripheral blood lymphocytes compared to the Ti gamma A+ counterparts: structural differences of the gamma/delta receptor and functional heterogeneity.与TiγA+外周血淋巴细胞相比,克隆的CD3+T细胞受体α/β-TiγA-外周血淋巴细胞:γ/δ受体的结构差异和功能异质性。
Eur J Immunol. 1988 Nov;18(11):1671-9. doi: 10.1002/eji.1830181104.
10
Patterns of T cell receptor gamma gene rearrangements in human CD3+ clones derived from WT31- or Leu7+ cells in relation to non-MHC-restricted cytotoxic activity.源自WT31或Leu7 +细胞的人CD3 +克隆中T细胞受体γ基因重排模式与非MHC限制性细胞毒性活性的关系。
Nat Immun Cell Growth Regul. 1989;8(6):301-12.

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CTLs heterogeneity and plasticity: implications for cancer immunotherapy.CTLs 异质性和可塑性:对癌症免疫治疗的影响。
Mol Cancer. 2024 Mar 21;23(1):58. doi: 10.1186/s12943-024-01972-6.
2
Identification and Validation of a DNA Damage Repair-Related Signature for Diffuse Large B-Cell Lymphoma.鉴定和验证弥漫性大 B 细胞淋巴瘤的 DNA 损伤修复相关特征。
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γδ T Cells in the Tumor Microenvironment-Interactions With Other Immune Cells.γδ T 细胞在肿瘤微环境中的作用-与其他免疫细胞的相互作用。
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Comparable Vδ2 Cell Functional Characteristics in Virally Suppressed People Living with HIV and Uninfected Individuals.病毒抑制的HIV感染者与未感染个体中可比的Vδ2细胞功能特征。
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γδ T cells in cancer: a small population of lymphocytes with big implications.癌症中的γδ T细胞:数量少但影响重大的淋巴细胞群体。
Clin Transl Immunology. 2019 Oct 10;8(10):e01080. doi: 10.1002/cti2.1080. eCollection 2019.
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The T-cell Response to Epstein-Barr Virus-New Tricks From an Old Dog.T 细胞对 Epstein-Barr 病毒的反应——老狗新把戏。
Front Immunol. 2019 Sep 18;10:2193. doi: 10.3389/fimmu.2019.02193. eCollection 2019.
7
Expansion and Adoptive Transfer of Human Vδ2 T Cells to Assess Antitumor Effects In Vivo.人Vδ2 T细胞的扩增与过继转移以评估体内抗肿瘤作用
Methods Mol Biol. 2019;1884:57-72. doi: 10.1007/978-1-4939-8885-3_4.
8
BTN3A1 Discriminates γδ T Cell Phosphoantigens from Nonantigenic Small Molecules via a Conformational Sensor in Its B30.2 Domain.BTN3A1通过其B30.2结构域中的构象传感器区分γδT细胞磷酸抗原与非抗原性小分子。
ACS Chem Biol. 2017 Oct 20;12(10):2631-2643. doi: 10.1021/acschembio.7b00694. Epub 2017 Sep 14.
9
Apoptosis Induced Gamma Delta T Cell Antigen Receptor "Blocking" Antibodies: A Cautionary Tale.γδT细胞抗原受体“阻断”抗体诱导的细胞凋亡:一则警示故事
Front Immunol. 2017 Jun 30;8:776. doi: 10.3389/fimmu.2017.00776. eCollection 2017.
10
Adoptively transferred Vγ9Vδ2 T cells show potent antitumor effects in a preclinical B cell lymphomagenesis model.在临床前B细胞淋巴瘤发生模型中,过继转移的Vγ9Vδ2 T细胞显示出强大的抗肿瘤作用。
JCI Insight. 2017 Jul 6;2(13). doi: 10.1172/jci.insight.93179.

本文引用的文献

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Phenotypic and functional heterogeneity of human cloned natural killer cell lines.人克隆自然杀伤细胞系的表型和功能异质性。
Nature. 1983 Jan 13;301(5896):158-60. doi: 10.1038/301158a0.
2
Rapidly expanded activated human killer cell clones have strong antitumor cell activity and have the surface phenotype of either T gamma, T-non-gamma, or null cells.快速扩增的活化人杀伤细胞克隆具有强大的抗肿瘤细胞活性,并且具有Tγ、T非γ或裸细胞的表面表型。
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3
Selective rejection of H-2-deficient lymphoma variants suggests alternative immune defence strategy.对H-2缺陷型淋巴瘤变体的选择性排斥表明存在替代免疫防御策略。
Nature. 1986;319(6055):675-8. doi: 10.1038/319675a0.
4
Evidence that the T cell antigen receptor may not be involved in cytotoxicity mediated by gamma/delta and alpha/beta thymic cell lines.有证据表明,T细胞抗原受体可能不参与由γ/δ和α/β胸腺细胞系介导的细胞毒性作用。
J Exp Med. 1987 Nov 1;166(5):1579-84. doi: 10.1084/jem.166.5.1579.
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The T cell receptor.T细胞受体。
Science. 1987 Nov 20;238(4830):1073-9. doi: 10.1126/science.3317824.
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Two forms of the T-cell receptor gamma protein found on peripheral blood cytotoxic T lymphocytes.在外周血细胞毒性T淋巴细胞上发现的两种形式的T细胞受体γ蛋白。
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A T-cell receptor gamma/CD3 complex found on cloned functional lymphocytes.在克隆的功能性淋巴细胞上发现的一种T细胞受体γ/CD3复合物。
Nature. 1987;325(6106):683-8. doi: 10.1038/325683a0.
8
Two antigen-independent adhesion pathways used by human cytotoxic T-cell clones.人类细胞毒性T细胞克隆所使用的两种抗原非依赖性黏附途径。
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9
T-cell antigen receptor genes and T-cell recognition.T细胞抗原受体基因与T细胞识别
Nature. 1988 Aug 4;334(6181):395-402. doi: 10.1038/334395a0.
10
Distinct molecular forms of human T cell receptor gamma/delta detected on viable T cells by a monoclonal antibody.通过单克隆抗体在活T细胞上检测到的人T细胞受体γ/δ的不同分子形式。
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γ/δ T细胞克隆和自然杀伤细胞克隆介导非主要组织相容性复合体限制的细胞溶解的不同模式。

Gamma/delta T cell clones and natural killer cell clones mediate distinct patterns of non-major histocompatibility complex-restricted cytolysis.

作者信息

Fisch P, Malkovsky M, Braakman E, Sturm E, Bolhuis R L, Prieve A, Sosman J A, Lam V A, Sondel P M

机构信息

Department of Human Oncology, University of Wisconsin, Madison 53792.

出版信息

J Exp Med. 1990 May 1;171(5):1567-79. doi: 10.1084/jem.171.5.1567.

DOI:10.1084/jem.171.5.1567
PMID:2185329
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2187884/
Abstract

Non-MHC-restricted killer cells are cytotoxic lymphocytes that can mediate cytolysis of most tumor targets without apparent selectivity and restriction by the MHC, particularly when activated with IL-2. These effector cells include predominantly NK cells and T cells expressing the TCR-gamma/delta. We found that TCR-gamma/delta-1+, delta TSC1-, BB3+, Ti gamma A+ T cell clones mediate a characteristic cytolytic pattern of non-MHC-restricted cytolysis that is markedly different from NK clones and alpha/beta T cell clones derived from the peripheral blood of the same normal individuals. The characteristic finding is that all BB3/Ti gamma A+ gamma/delta clones mediate strong cytolysis of Daudi cells but they do not lyse Raji cells. In contrast, NK clones from the same donors mediate strong cytolysis of both Daudi and Raji targets. Cytotoxicity by the gamma/delta clones on certain target cells such as Daudi and Molt 4 can be specifically inhibited by mAbs reactive against the TCR-gamma/delta. Therefore, the TCR-gamma/delta on these clones either directly recognizes target epitopes on some tumor targets or it is involved in the regulation of their cytotoxic function. The expression of TCR-gamma/delta products reacting with the BB3 and Ti gamma A mAbs reflects the usage of identical TCR-gamma/delta V region genes that appear to be associated with the characteristic pattern of non-MHC-restricted cytotoxicity displayed by this major subset of human peripheral blood gamma/delta cells.

摘要

非MHC限制杀伤细胞是细胞毒性淋巴细胞,能够介导对大多数肿瘤靶标的细胞溶解,且不受MHC明显的选择性和限制,尤其是在用白细胞介素-2激活时。这些效应细胞主要包括自然杀伤细胞(NK细胞)和表达TCR-γ/δ的T细胞。我们发现,TCR-γ/δ-1+、δTSC1-、BB3+、TiγA+ T细胞克隆介导一种非MHC限制细胞溶解的特征性细胞溶解模式,这与来自相同正常个体外周血的NK细胞克隆和α/β T细胞克隆明显不同。特征性发现是,所有BB3/TiγA+γ/δ克隆均介导对Daudi细胞的强烈细胞溶解,但它们不裂解Raji细胞。相反,来自相同供体的NK细胞克隆介导对Daudi和Raji靶标的强烈细胞溶解。γ/δ克隆对某些靶细胞(如Daudi和Molt 4)的细胞毒性可被针对TCR-γ/δ的单克隆抗体特异性抑制。因此,这些克隆上的TCR-γ/δ要么直接识别某些肿瘤靶标上的靶表位,要么参与其细胞毒性功能的调节。与BB3和TiγA单克隆抗体反应的TCR-γ/δ产物的表达反映了相同TCR-γ/δ V区基因的使用情况,这些基因似乎与人类外周血γ/δ细胞这一主要亚群所显示的非MHC限制细胞毒性的特征模式相关。