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TAP1缺陷患者(I型裸淋巴细胞综合征)中自然杀伤细胞(NK)和淋巴因子激活的杀伤细胞(LAK)活性对HLA I类缺陷靶标的耐受性

Tolerance of NK and LAK activity for HLA class I-deficient targets in a TAP1-deficient patient (bare lymphocyte syndrome type I).

作者信息

Furukawa H, Yabe T, Watanabe K, Miyamoto R, Miki A, Akaza T, Tadokoro K, Tohma S, Inoue T, Yamamoto K, Juji T

机构信息

Department of Research, Japanese Red Cross Central Blood Center, Tokyo.

出版信息

Hum Immunol. 1999 Jan;60(1):32-40. doi: 10.1016/s0198-8859(98)00097-4.

Abstract

NK cells recognize target cells that lack HLA class I molecules and lyse them, according to the 'missing self' hypothesis. It was previously reported that a TAP2-deficient patient with an HLA class I-deficiency, had a normal number of NK cells but that the lymphocytes of this patient had lost their NK activity against K562 cells. In this study, we investigated the HLA class I-recognizing NK receptor expressions and the NK and LAK activities of the lymphocytes of a TAP1-deficient patient. The patient had a normal number of NK cells. Although the lymphocytes showed LAK activity against class I expressing targets following IL-2, IL-12 and IL-15 stimulation for 3 days, neither NK nor LAK activity against targets lacking class I molecules was induced. The NK cells of the patient expressed class I-recognizing NK receptors, although the percentages of such cells were low. However, no differences were observed in the expression levels of inhibitory and activating NK receptors between lymphocytes of the patient and those of healthy controls, suggesting that the modulation of the NK receptor expression is not primarily responsible for this tolerance. These results also suggest that the lymphocytes of the patient are defective in the recognition of class I-deficient target cells in order to promote the induction of self tolerance.

摘要

根据“缺失自我”假说,自然杀伤(NK)细胞识别缺乏HLA I类分子的靶细胞并将其裂解。此前有报道称,一名患有HLA I类缺陷的TAP2缺陷患者,其NK细胞数量正常,但该患者的淋巴细胞对K562细胞失去了NK活性。在本研究中,我们调查了一名TAP1缺陷患者淋巴细胞的HLA I类识别NK受体表达以及NK和LAK活性。该患者的NK细胞数量正常。尽管淋巴细胞在经白细胞介素-2(IL-2)、白细胞介素-12(IL-12)和白细胞介素-15(IL-15)刺激3天后,对表达I类分子的靶细胞显示出LAK活性,但未诱导出针对缺乏I类分子靶细胞的NK或LAK活性。该患者的NK细胞表达I类识别NK受体,尽管此类细胞的百分比很低。然而,在患者淋巴细胞与健康对照淋巴细胞之间,抑制性和激活性NK受体的表达水平未观察到差异,这表明NK受体表达的调节并非这种耐受性的主要原因。这些结果还表明,该患者的淋巴细胞在识别缺乏I类分子的靶细胞方面存在缺陷,从而促进了自身耐受性的诱导。

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