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系统性坏死性血管炎患者的T细胞受体(TCR)V基因使用情况。

T cell receptor (TCR) V gene usage in patients with systemic necrotizing vasculitis.

作者信息

Giscombe R, Grunewald J, Nityanand S, Lefvert A K

机构信息

Department of Medicine, Karolinska Hospital, Karolinska Institute, Stockholm, Sweden.

出版信息

Clin Exp Immunol. 1995 Aug;101(2):213-9. doi: 10.1111/j.1365-2249.1995.tb08341.x.

Abstract

Wegener's granulomatosis (WG) and polyarteritis nodosa (PAN) are systemic necrotizing vasculitides of unknown etiology. These disorders run a fatal course if untreated. T lymphocytes are implicated in the pathogenesis of WG, since they have been found to infiltrate affected organs, and sIL-2R correlates with disease activity. To elucidate further the role of T cells in necrotizing vasculitis, we have used a panel of 12 TCR V-specific MoAbs to investigate the number of cells expressing certain V alpha and V beta gene segments in the CD4+ and CD8+ subsets of altogether 11 patients with WG or PAN. In the group of patients, we found abnormal expansions of T cells using particular TCR V alpha or V beta gene products. These T cell expansions were more numerous, of a dramatically higher magnitude, and frequently more often found in the CD4 subset, compared with T cell expansions identified in healthy individuals. In long-term studies of the T cell expansions for up to 18 months, a heterogeneous pattern was revealed, with no obvious correlation to clinical features such as disease activity or treatment. Studies of TCR V gene usage in this group of patients may help in understanding the pathogenesis of necrotizing vasculitis, and in the identification of unknown antigens, and may open the possibility to a highly selective immunotherapy by targeting disease-mediating T cells.

摘要

韦格纳肉芽肿病(WG)和结节性多动脉炎(PAN)是病因不明的系统性坏死性血管炎。这些疾病若不治疗会导致致命后果。T淋巴细胞与WG的发病机制有关,因为已发现它们浸润受累器官,且可溶性白细胞介素-2受体(sIL-2R)与疾病活动相关。为进一步阐明T细胞在坏死性血管炎中的作用,我们使用了一组12种TCR V特异性单克隆抗体,来研究总共11例WG或PAN患者的CD4+和CD8+亚群中表达特定Vα和Vβ基因片段的细胞数量。在患者组中,我们发现使用特定TCR Vα或Vβ基因产物的T细胞出现异常扩增。与在健康个体中鉴定出的T细胞扩增相比,这些T细胞扩增数量更多、幅度显著更高,且在CD4亚群中更常出现。在对T细胞扩增长达18个月的长期研究中,发现了一种异质性模式,与疾病活动或治疗等临床特征无明显相关性。对该组患者TCR V基因使用情况的研究可能有助于理解坏死性血管炎的发病机制,识别未知抗原,并可能为通过靶向介导疾病的T细胞进行高度选择性免疫治疗开辟可能性。

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