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具有γ/δ和α/β受体的人T细胞克隆受到抗CD2单克隆抗体的不同刺激。

Human T cell clones with gamma/delta and alpha/beta receptors are differently stimulated by monoclonal antibodies to CD2.

作者信息

Pawelec G, Schaudt K, Rehbein A, Olive D, Bühring H J

机构信息

Second Department of Internal Medicine, University Medical Clinic, Tübingen, Federal Republic of Germany.

出版信息

Cell Immunol. 1990 Sep;129(2):385-93. doi: 10.1016/0008-8749(90)90214-c.

DOI:10.1016/0008-8749(90)90214-c
PMID:1974482
Abstract

Requirements for stimulating autocrine proliferation of human T cell clones expressing either alpha/beta or gamma/delta antigen receptors via the "alternative" CD2 pathway have been examined using a large set of monoclonal antibodies (mAb). In the presence of autologous accessory cells (AC, B-lymphoblastoid cell lines) 2 of 13 single CD2 mAb (CLB-T11.1/1 and 6F10.3) stimulated proliferation of gamma/delta but not alpha/beta cells. Interleukin (IL) 1 or IL 6 did not substitute for AC in stimulating gamma/delta clones. Addition of CD28 mAb YTH 913.12 with the CD2 mAb did not result in stimulation of any alpha/beta clones. In the absence of AC, none of the CD2 mAb singly could stimulate any T cell clones, but pairs of mAb directed to different epitopes of CD2 (CLB-T11.1/1 + CLB- T11.2/1 or 6F10.3 + 39C1.5) stimulated both alpha/beta and gamma/delta clones. In both cases, stimulation was reduced by the presence of CD3 mAb. These results confirm that the established AC-independent alternative pathway of T cell activation, which requires binding of two separate epitopes of CD2, operates in both gamma/delta and alpha/beta T cells, and further suggest that an additional pathway initiated by binding of a single CD2 epitope in the presence of AC is exclusively operational in gamma/delta cells.

摘要

通过“替代”CD2途径刺激表达α/β或γ/δ抗原受体的人T细胞克隆自分泌增殖的要求,已使用大量单克隆抗体(mAb)进行了研究。在自体辅助细胞(AC,B淋巴细胞系)存在的情况下,13种单一CD2 mAb中的2种(CLB-T11.1/1和6F10.3)刺激了γ/δ细胞的增殖,但未刺激α/β细胞。白细胞介素(IL)1或IL 6在刺激γ/δ克隆时不能替代AC。将CD28 mAb YTH 913.12与CD2 mAb一起添加不会刺激任何α/β克隆。在没有AC的情况下,没有一种CD2 mAb能单独刺激任何T细胞克隆,但针对CD2不同表位的mAb对(CLB-T11.1/1 + CLB-T11.2/1或6F10.3 + 39C1.5)刺激了α/β和γ/δ克隆。在这两种情况下,CD3 mAb的存在都会降低刺激作用。这些结果证实,已确立的不依赖AC的T细胞激活替代途径,需要CD2的两个单独表位结合,在γ/δ和α/β T细胞中均起作用,并且进一步表明,在AC存在下由单个CD2表位结合引发的另一条途径仅在γ/δ细胞中起作用。

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Human T cell clones with gamma/delta and alpha/beta receptors are differently stimulated by monoclonal antibodies to CD2.具有γ/δ和α/β受体的人T细胞克隆受到抗CD2单克隆抗体的不同刺激。
Cell Immunol. 1990 Sep;129(2):385-93. doi: 10.1016/0008-8749(90)90214-c.
2
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CD3Ti+ human thymocyte-derived clones displaying a differential response to activation via CD3Ti and CD2.CD3Ti+人胸腺细胞衍生克隆对通过CD3Ti和CD2激活表现出不同反应。
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Induction of lysis by T cell receptor gamma delta+/CD3+ T lymphocytes via CD2 requires triggering via the T11.1 epitope only.T细胞受体γδ⁺/CD3⁺ T淋巴细胞通过CD2诱导细胞溶解仅需通过T11.1表位触发。
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"CD3low" human thymocyte populations can readily be triggered via the CD2 and/or CD28 activation pathways whereas the CD3 pathway remains nonfunctional.“CD3低表达”的人类胸腺细胞群体可通过CD2和/或CD28激活途径轻易被触发,而CD3途径仍无功能。
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Human resting B lymphocytes can serve as accessory cells for anti-CD2-induced T cell activation.人类静息B淋巴细胞可作为抗CD2诱导的T细胞活化的辅助细胞。
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A novel subset of CD2-, CD3/T cell receptor alpha/beta+ human peripheral blood T cells. Phenotypic and functional characterization of interleukin 2-dependent CD2-CD3+ T cell clones.一类新型的CD2阴性、CD3/T细胞受体α/β阳性人外周血T细胞。白细胞介素2依赖性CD2阴性CD3阳性T细胞克隆的表型和功能特征。
J Exp Med. 1989 Aug 1;170(2):559-69. doi: 10.1084/jem.170.2.559.

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