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再生障碍性贫血中的淋巴细胞和淋巴因子:致病作用及对发病机制的影响

Lymphocytes and lymphokines in aplastic anemia: pathogenic role and implications for pathogenesis.

作者信息

Young N S, Leonard E, Platanias L

机构信息

Clinical Hematology Branch, National Heart, Lung, and Blood Institute, Bethesda, Maryland 20892.

出版信息

Blood Cells. 1987;13(1-2):87-100.

PMID:3311225
Abstract

Clinical observations first suggested an immune basis for aplastic anemia. Laboratory studies have implicated a suppressor T lymphocyte producing molecules like gamma-interferon that inhibit hematopoiesis. Extrapolation from in vitro studies is complicated by synergy and antagonism among lymphokines and interleukins, the presence of regulators of proliferation produced by bone marrow cells, and possible differences between endogenous and exogenously administered molecules on cell growth.

摘要

临床观察首先提示再生障碍性贫血存在免疫基础。实验室研究表明,一种抑制性T淋巴细胞可产生如γ干扰素等抑制造血的分子。体外研究的推断因淋巴因子和白细胞介素之间的协同作用和拮抗作用、骨髓细胞产生的增殖调节因子的存在,以及内源性和外源性给药分子对细胞生长可能存在的差异而变得复杂。

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