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简短通讯。糖原贮积病Ib型:由于磷酸己糖旁路受损导致的中性粒细胞杀菌缺陷。

Short communication. Glycogenosis Ib: neutrophil microbicidal defects due to impaired hexose monophosphate shunt.

作者信息

Seger R, Steinmann B, Tiefenauer L, Matsunaga T, Gitzelmann R

出版信息

Pediatr Res. 1984 Mar;18(3):297-9. doi: 10.1203/00006450-198403000-00019.

Abstract

We studied neutrophil microbicidal function and oxidative metabolic activity in a patient with glycogenosis Ib. The intracellular killing defect and the respiratory burst abnormality in gycogenosis Ib neutrophils were confirmed. The impaired oxygen-dependent microbicidal activity was shown to result from impaired hexose monophosphate shunt activity (impaired endogenous NADPH synthesis) and could be corrected by homogenization of the cells, followed by the addition of exogenous NADPH. Our data are thus consistent with a possible role for glucose-6-phosphate transport in neutrophil microbicidal function. We recommend a continuous prophylaxis with co-trimoxazole in patients with glycogen storage disease Ib.

摘要

我们研究了一名糖原贮积病Ib型患者的中性粒细胞杀菌功能和氧化代谢活性。糖原贮积病Ib型中性粒细胞的细胞内杀伤缺陷和呼吸爆发异常得到了证实。氧依赖性杀菌活性受损被证明是由于磷酸己糖旁路活性受损(内源性NADPH合成受损)所致,并且可以通过细胞匀浆,随后添加外源性NADPH来纠正。因此,我们的数据与磷酸葡萄糖转运在中性粒细胞杀菌功能中可能发挥的作用相一致。我们建议对糖原贮积病Ib型患者持续使用复方新诺明进行预防。

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