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先天性巨结肠症患者直肠免疫球蛋白模式异常。

Abnormal rectal immunoglobulin pattern in Hirschsprung's disease.

作者信息

Halpin T C, Gregoire R P, Izant R J

出版信息

Lancet. 1978 Sep 16;2(8090):606-8. doi: 10.1016/s0140-6736(78)92826-x.

Abstract

The immunoglobulin content of rectal biopsy tissue and secretions from twelve neonates in whom Hirschsprung's disease was suspected was determined by an organ-culture technique and radioimmunoassay. The immunoreactive IgG content of explanted rectal tissue and its secretions in those six children who proved to have Hirschsprung's disease was much higher than in those with other types of obstructive lower-intestinal disease. Increased amounts of IgG may represent maternally derived antibody associated with neonatal gut neural elements. This seems to be the first report of an immunological abnormality in Hirschsprung's disease.

摘要

采用器官培养技术和放射免疫分析法,测定了12例疑似先天性巨结肠症新生儿的直肠活检组织和分泌物中的免疫球蛋白含量。在确诊为先天性巨结肠症的6例患儿中,离体直肠组织及其分泌物的免疫反应性IgG含量明显高于其他类型的下消化道梗阻性疾病患儿。IgG含量增加可能代表与新生儿肠道神经元相关的母体来源抗体。这似乎是关于先天性巨结肠症免疫异常的首例报道。

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