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两名先天性风疹婴儿的脱屑性间质性肺炎与抗原-抗体复合物

Desquamative interstitial pneumonia and antigen-antibody complexes in two infants with congenital rubella.

作者信息

Boner A, Wilmott R W, Dinwiddie R, Jeffries D J, Matthew D J, Marshall W C, Mowbray J F, Pincott J R, Rivers R P

出版信息

Pediatrics. 1983 Dec;72(6):835-9.

PMID:6646927
Abstract

Desquamative interstitial pneumonia was observed in two infants with the late-onset congenital rubella syndrome. In both infants this unusual lung disease was associated with circulating immunoglobulin M complexes and interstitial pulmonary deposits of IgM by immunofluorescence. Both infants had IgG deficiency. The first child recovered with a reduction in IgM complex levels and synthesis of rubella-specific IgG. The second infant died during the acute phase of his illness at which time there were high serum concentrations of IgM complexes and slightly increased levels of IgG complexes. Delayed maturation of the immune response in congenital rubella may predispose to persistent antigenemia and pulmonary deposition of rubella antigen-containing IgM complexes resulting in an acute form of interstitial pneumonia.

摘要

在两名迟发性先天性风疹综合征婴儿中观察到脱屑性间质性肺炎。通过免疫荧光法,在这两名婴儿中,这种不寻常的肺部疾病均与循环免疫球蛋白M复合物及肺部间质IgM沉积有关。两名婴儿均存在IgG缺乏。第一名儿童随着IgM复合物水平降低及风疹特异性IgG的合成而康复。第二名婴儿在疾病急性期死亡,当时血清中IgM复合物浓度很高,IgG复合物水平略有升高。先天性风疹中免疫反应的延迟成熟可能易导致持续性抗原血症及含风疹抗原的IgM复合物在肺部沉积,从而引发急性间质性肺炎。

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