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从2例表现出异常表型的大颗粒淋巴细胞增多症患者中建立长期细胞系。

Establishment of long term cell lines from 2 patients with large granular lymphocyte lymphocytosis displaying an unusual phenotype.

作者信息

Scott-Algara D, Vuillier F, Dauguet C, Dighiero G

机构信息

Unité d'Immunohématologie et d'Immunopathologie, Institut Pasteur, Paris, France.

出版信息

Nouv Rev Fr Hematol (1978). 1991;33(3):237-43.

PMID:1835534
Abstract

Two long-term cell lines obtained from two cases of large granular lymphocyte lymphocytosis (LGLL) displaying an unusual phenotype are reported here. Patient n. 1 was CD2+ CD3- CD16+ CD8+ CD56- CD57- CD29+ CD45RA+, whereas patient n. 2 was CD2-CD3+ CD8+ CD16+ CD56- CD57+ CD29+ CD45RA+. The cells were large granular lymphocytes by light and electron microscopic criteria and displayed strong antibody-dependent cell mediated cytotoxicity (ADCC) and NK activity. Northern blot analysis revealed aberrant transcripts of TCR beta chains for patient n. 1, and full length TCR alpha and beta transcripts for patient n. 2. In both cases, we were able to establish a long term cell line which functionally revealed strong ADCC and NK activity. Functional implications of these 2 subpopulations are discussed.

摘要

本文报道了从两例表现出异常表型的大颗粒淋巴细胞白血病(LGLL)患者中获得的两个长期细胞系。患者1的细胞表型为CD2+ CD3- CD16+ CD8+ CD56- CD57- CD29+ CD45RA+,而患者2的细胞表型为CD2-CD3+ CD8+ CD16+ CD56- CD57+ CD29+ CD45RA+。根据光镜和电镜标准,这些细胞为大颗粒淋巴细胞,并表现出强烈的抗体依赖性细胞介导的细胞毒性(ADCC)和NK活性。Northern印迹分析显示,患者1的TCRβ链转录本异常,患者2的TCRα和β链转录本全长。在这两种情况下,我们都能够建立一个长期细胞系,其功能上显示出强烈的ADCC和NK活性。本文讨论了这两个亚群的功能意义。

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