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用单克隆抗体分离人T细胞的功能亚群

Separation of functional subsets of human T cells by a monoclonal antibody.

作者信息

Reinherz E L, Kung P C, Goldstein G, Schlossman S F

出版信息

Proc Natl Acad Sci U S A. 1979 Aug;76(8):4061-5. doi: 10.1073/pnas.76.8.4061.

DOI:10.1073/pnas.76.8.4061
PMID:315070
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC383977/
Abstract

A monoclonal antibody was produced to human peripheral blood T cells. This hybridoma antibody, termed OKT4, was reactive by indirect immunofluorescence with only 55-60% of the peripheral blood T cell population (OKT4+) and unreactive with normal B cells, null cells, and macrophages. The OKT4- T cell population contained the previously described TH2+ subset that has been shown to contain cytotoxic/suppressor cells. With cell-sorter separation of OKT4+ and OKT4- cells, it was shown that these T cell subsets were functionally discrete. Both gave proliferative responses with concanavalin A, alloantigens, and phytohemagglutinin although OKT4+ cells were much more responsive to the latter. OKT4+ cells alone responded to soluble antigens whereas OKT4- cells alone were cytotoxic after alloantigenic sensitization of unfractionated T cells. However, both OKT4+ and OKT4- cells were required during sensitization for optimal development of cytotoxicity. These data suggest that the OKT4+ subset represents a helper population and that the OKT4- subset contains the cytotoxic effector population. OKT4 could be a valuable reagent for determining alterations of these functional subsets in human diseases.

摘要

制备了一种针对人外周血T细胞的单克隆抗体。这种杂交瘤抗体称为OKT4,通过间接免疫荧光法,它仅与55%-60%的外周血T细胞群体(OKT4+)发生反应,而与正常B细胞、裸细胞和巨噬细胞不发生反应。OKT4-T细胞群体包含先前描述的TH2+亚群,该亚群已被证明含有细胞毒性/抑制性细胞。通过细胞分选仪分离OKT4+和OKT4-细胞,结果表明这些T细胞亚群在功能上是离散的。两者对刀豆球蛋白A、同种异体抗原和植物血凝素均有增殖反应,不过OKT4+细胞对后者的反应性更强。单独的OKT4+细胞对可溶性抗原有反应,而单独的OKT4-细胞在未分级T细胞经同种异体抗原致敏后具有细胞毒性。然而,在致敏过程中,为了使细胞毒性得到最佳发展,OKT4+和OKT4-细胞都需要。这些数据表明,OKT4+亚群代表辅助细胞群体,而OKT4-亚群包含细胞毒性效应细胞群体。OKT4可能是一种用于确定人类疾病中这些功能亚群变化的有价值试剂。

相似文献

1
Separation of functional subsets of human T cells by a monoclonal antibody.用单克隆抗体分离人T细胞的功能亚群
Proc Natl Acad Sci U S A. 1979 Aug;76(8):4061-5. doi: 10.1073/pnas.76.8.4061.
2
Functional analysis of human T cell subsets defined by monoclonal antibodies. II. Collaborative T-T interactions in the generation of TNP-altered-self-reactive cytotoxic T lymphocytes.单克隆抗体所定义的人T细胞亚群的功能分析。II. TNP改变自身反应性细胞毒性T淋巴细胞产生中的T-T协作相互作用。
J Immunol. 1981 May;126(5):1702-5.
3
Inhibition of specific cell-mediated cytotoxicity by monoclonal antibodies to human T cell antigens.抗人T细胞抗原单克隆抗体对特异性细胞介导细胞毒性的抑制作用。
Proc Natl Acad Sci U S A. 1981 Jul;78(7):4500-4. doi: 10.1073/pnas.78.7.4500.
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A monoclonal antibody reactive with the human cytotoxic/suppressor T cell subset previously defined by a heteroantiserum termed TH2.一种单克隆抗体,可与人细胞毒性/抑制性T细胞亚群发生反应,该亚群先前由一种名为TH2的异种抗血清所定义。
J Immunol. 1980 Mar;124(3):1301-7.
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Ia determinants on human T-cell subsets defined by monoclonal antibody. Activation stimuli required for expression.由单克隆抗体定义的人类T细胞亚群上的Ia决定簇。表达所需的激活刺激。
J Exp Med. 1979 Dec 1;150(6):1472-82. doi: 10.1084/jem.150.6.1472.
6
Human T lymphocyte subpopulations defined by Fc receptors and monoclonal antibodies. A comparison.由Fc受体和单克隆抗体定义的人T淋巴细胞亚群。一项比较。
J Exp Med. 1980 Apr 1;151(4):969-74. doi: 10.1084/jem.151.4.969.
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Defective expression of OKT4 antigen on the cell surface of helper T lymphocytes in a patient with systemic lupus erythematosus.系统性红斑狼疮患者辅助性T淋巴细胞细胞表面OKT4抗原表达缺陷。
Clin Exp Rheumatol. 1983 Oct-Dec;1(4):299-305.
8
Further dissection of the functional heterogeneity within the OKT4+ and OKT8+ human T cell subsets.对OKT4+和OKT8+人类T细胞亚群内功能异质性的进一步剖析。
J Clin Immunol. 1982 Jul;2(3 Suppl):8S-14S.
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Functional analysis of human T cell subsets defined by monoclonal antibodies. I. Collaborative T-T interactions in the immunoregulation of B cell differentiation.由单克隆抗体定义的人T细胞亚群的功能分析。I. B细胞分化免疫调节中的T-T协作相互作用。
J Immunol. 1980 Dec;125(6):2402-8.
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Functional analysis of human T cell subsets defined by monoclonal antibodies. VI. Distinct and opposing immunoregulatory functions within the OKT8+ population.由单克隆抗体定义的人T细胞亚群的功能分析。VI. OKT8+群体内不同且相反的免疫调节功能。
J Mol Cell Immunol. 1984;1(2):103-13.

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