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全身性淋巴结病综合征中淋巴结淋巴细胞的免疫学研究。

Immunologic studies of lymph node lymphocytes in the generalized lymphadenopathy syndrome.

作者信息

Kohn D B, Trigg M E, Borcherding W, Hong R

出版信息

Am J Pediatr Hematol Oncol. 1987 Spring;9(1):1-7. doi: 10.1097/00043426-198721000-00001.

Abstract

A generalized lymphadenopathy syndrome (GLS) occurs in persons at high risk for development of acquired immunodeficiency syndrome (AIDS). The natural history and immunologic status of patients with GLS are not fully known, although in some persons GLS may progress to full AIDS. We present the clinical and immunologic findings in two children with severe hemophilia A with nonprogressive GLS for 18-24 months. The functional activity in vitro of lymphocytes from both peripheral blood and biopsied lymph nodes were compared. The peripheral blood lymphocytes responded normally to both mitogens and antigens; lymph node lymphocytes failed to respond to antigens, but did respond to mitogens. The implications of these abnormalities for understanding the pathogenesis of GLS are discussed.

摘要

一种全身性淋巴结病综合征(GLS)发生于获得性免疫缺陷综合征(AIDS)高发人群中。尽管在某些人身上GLS可能进展为完全型AIDS,但GLS患者的自然病史和免疫状态尚未完全明确。我们报告了两名重度甲型血友病患儿的临床和免疫学表现,他们患有非进行性GLS达18 - 24个月。对来自外周血和活检淋巴结的淋巴细胞的体外功能活性进行了比较。外周血淋巴细胞对丝裂原和抗原均有正常反应;淋巴结淋巴细胞对抗原无反应,但对丝裂原有反应。讨论了这些异常对于理解GLS发病机制的意义。

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