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T细胞受体α在人嗜T细胞病毒1型感染的T细胞中的多克隆应用。

Polyclonal use of T-cell receptor alpha for human T-cell lymphotropic virus type 1-infected T cells.

作者信息

Masuoka K, Sagawa K, Mochizuki M, Oizumi K, Itoh K

机构信息

Department of Immunology, Kurume University School of Medicine, Japan.

出版信息

Invest Ophthalmol Vis Sci. 1995 Jan;36(1):254-8.

PMID:7822155
Abstract

PURPOSE

To understand better the immunopathology of HTLV-I uveitis by investigating the clonality of HTLV-I-infected T-cell clones.

METHODS

Eleven T-cell clones were established from the aqueous humor (six clones) and the peripheral blood (five clones) of a patient with HTLV-I uveitis, and the clonality of the HTLV-I-infected T cells was investigated by sequencing the T-cell receptor (TCR) alpha gene after the amplification of TCR alpha cDNA using an adaptor-ligation method and reverse transcriptase-polymerase chain reaction (RT-PCR).

RESULTS

TCR alpha use was different for each of 11 T-cell clones, encompassing eight different HTLV-I-infected T-cell clones (four from the aqueous humor and four from peripheral blood) and three HTLV-I-negative T-cell clones.

CONCLUSIONS

This study demonstrated polyclonal use of TCR alpha for HTLV-I-infected T cells in the ocular lesion and the peripheral blood. Results suggested that these T cells are not precursors of the leukemic cells associated with malignant transformation. Instead, they might be randomly infected with HTLV-I in the process of HTLV-I uveitis.

摘要

目的

通过研究人类嗜T淋巴细胞病毒I型(HTLV-I)感染的T细胞克隆的克隆性,更好地理解HTLV-I葡萄膜炎的免疫病理学。

方法

从一名HTLV-I葡萄膜炎患者的房水(6个克隆)和外周血(5个克隆)中建立了11个T细胞克隆,并在使用衔接子连接法和逆转录聚合酶链反应(RT-PCR)扩增T细胞受体(TCR)α cDNA后,通过对TCRα基因进行测序来研究HTLV-I感染的T细胞的克隆性。

结果

11个T细胞克隆中的每一个克隆对TCRα的使用都不同,包括8个不同的HTLV-I感染的T细胞克隆(4个来自房水,4个来自外周血)和3个HTLV-I阴性T细胞克隆。

结论

本研究证明了在眼部病变和外周血中HTLV-I感染的T细胞对TCRα的多克隆使用。结果表明,这些T细胞不是与恶性转化相关的白血病细胞的前体。相反,它们可能在HTLV-I葡萄膜炎过程中被HTLV-I随机感染。

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引用本文的文献

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HTLV-1 in Ophthalmology.眼科中的人类嗜T淋巴细胞病毒1型
Front Microbiol. 2020 Mar 11;11:388. doi: 10.3389/fmicb.2020.00388. eCollection 2020.
2
HTLV-1 uveitis.人类嗜T淋巴细胞病毒1型葡萄膜炎
Front Microbiol. 2012 Jul 24;3:270. doi: 10.3389/fmicb.2012.00270. eCollection 2012.