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[日本干燥综合征患者唇唾液腺中与HTLV-I pXIV基因同源序列的表达及发病机制]

[Expression of sequences homologous to HTLV-I pXIV gene in the labial salivary glands of Japanese patients with Sjögren's syndrome and pathogenesis].

作者信息

Yonaha-Nagato F, Sumida T

机构信息

Division of Dermatology, Sakura Hospital, Toho University School of Medicine.

出版信息

Nihon Rinsho. 1995 Oct;53(10):2473-8.

PMID:8531358
Abstract

To address the question of whether the human T cell leukemia virus type I (HTLV-I) gene is associated with the etiology of Sjögren's syndrome (SS), RNA expression of HTLV-I gag, pol, env, and tax genes in labial salivary glands (LSGs) from SS patients who were seronegative for antibodies to HTLV-I was examined using RT-PCR method. The HTLV-I tax gene, but not the HTLV-I gag, pol, or env genes, was detected in LSG samples from 4 of 14 patients (29%). The nucleotide sequences of the HTLV-I pXIV region in these 4 patients' LSGs showed 100% homology to the HTLV-I pXIV gene from the MT-2 cell line. In conclusion, these findings suggest that products encoding sequences homologous to the HTLV-I pXIV gene in SS patients' LSGs might be candidates for self-antigen and/or lead to activation of autoreactive T lymphocytes through trans-acting transcriptional activation.

摘要

为了探讨人类I型嗜T细胞淋巴瘤病毒(HTLV-I)基因是否与干燥综合征(SS)的病因相关,我们采用逆转录聚合酶链反应(RT-PCR)方法检测了HTLV-I抗体血清学阴性的SS患者唇腺(LSG)中HTLV-I gag、pol、env和tax基因的RNA表达。在14例患者中的4例(29%)的LSG样本中检测到了HTLV-I tax基因,但未检测到HTLV-I gag、pol或env基因。这4例患者LSG中HTLV-I pXIV区域的核苷酸序列与MT-2细胞系的HTLV-I pXIV基因显示出100%的同源性。总之,这些发现表明,SS患者LSG中编码与HTLV-I pXIV基因同源序列的产物可能是自身抗原的候选物和/或通过反式转录激活导致自身反应性T淋巴细胞的激活。

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[Expression of sequences homologous to HTLV-I pXIV gene in the labial salivary glands of Japanese patients with Sjögren's syndrome and pathogenesis].[日本干燥综合征患者唇唾液腺中与HTLV-I pXIV基因同源序列的表达及发病机制]
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引用本文的文献

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Defective human T-cell lymphotropic virus type I (HTLV-I) provirus in 10 Chilean seronegative patients with tropical spastic paraparesis or HTLV-I-associated myelopathy.10例患有热带痉挛性截瘫或HTLV-I相关脊髓病的智利血清阴性患者中存在缺陷的人类嗜T淋巴细胞病毒I型(HTLV-I)前病毒。
J Clin Microbiol. 1998 Jun;36(6):1811-3. doi: 10.1128/JCM.36.6.1811-1813.1998.