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用于区分可能的免疫介导的再生障碍性贫血与输血诱导的致敏反应的体外试验。

In vitro tests for distinguishing possible immune-mediated aplastic anemia from transfusion-induced sensitization.

作者信息

Torok-Storb B J, Sieff C, Storb R, Adamson J, Thomas E D

出版信息

Blood. 1980 Feb;55(2):211-5.

PMID:7353071
Abstract

Forty-two patients with aplastic anemia (AA) were studied to determine whether or not transfusion-induced sensitization is responsible for the in vitro inhibition by patient lymphocytes of HLA-identical erythroid burst-forming units (BFU-E). The results indicate that lymphocytes from 12 of 34 transfused patients inhibited normal colony growth. In contrast, lymphocytes from none of the 8 untransfused patients demonstrated inhibition. These data were interpreted to mean that coculture studies would not be useful for identifying immune-mediated AA in transfused patients. Therefore, in order to identify possible immune-related AA, we assayed BFU-E from patient blood before and after T-cell depletion. In all 32 patients studied, BFU-E failed to grow from peripheral blood cells before T-cell depletion, but in 8 cases, normal-appearing BFU-E grew after T cells had been removed. Growth of patient BFU-E colonies was inhibited in 6 cases when patient T cells were added back to the culture, indicating that in these 6 patients, an "autoimmune" mechanism may have been present.

摘要

对42例再生障碍性贫血(AA)患者进行了研究,以确定输血诱导的致敏是否是导致患者淋巴细胞对 HLA 相同的红系爆式集落形成单位(BFU-E)产生体外抑制的原因。结果表明,34例输血患者中有12例的淋巴细胞抑制了正常集落生长。相比之下,8例未输血患者的淋巴细胞均未表现出抑制作用。这些数据被解释为意味着共培养研究对于识别输血患者中的免疫介导性 AA 并无用处。因此,为了识别可能与免疫相关的 AA,我们检测了患者血液在 T 细胞清除前后的 BFU-E。在所有32例研究患者中,T 细胞清除前外周血细胞中的 BFU-E 均未生长,但在8例患者中,去除 T 细胞后出现了外观正常的 BFU-E 生长。当将患者的 T 细胞重新加入培养时,6例患者的 BFU-E 集落生长受到抑制,这表明在这6例患者中可能存在“自身免疫”机制。

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