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巴布亚新几内亚和澳大利亚儿童隐孢子虫病的血清流行病学

Seroepidemiology of cryptosporidiosis in children in Papua New Guinea and Australia.

作者信息

Groves V J, Lehmann D, Gilbert G L

机构信息

Department of Microbiology & Infectious Disease, Royal Children's Hospital, Victoria, Australia.

出版信息

Epidemiol Infect. 1994 Dec;113(3):491-9. doi: 10.1017/s0950268800068503.

Abstract

Enzyme immunoassays (EIA) were used to measure serum antibodies to Cryptosporidium in four immunocompetent adults with recent proven cryptosporidial infection, 379 healthy children and 73 adult volunteers in Melbourne, Australia, and 205 children in Papua New Guinea (PNG) (47 healthy children; 158 with pneumonia). Antibodies peaked 3-6 weeks after infection and fell to baseline within a few months. A high level (5000 EIA units/ml) or a significant change between paired sera, of IgG or IgM, were taken as evidence of recent infection and found in 24% of PNG children and in 8% of children and 5% of adults in Melbourne. Among PNG children with pneumonia who had high cryptosporidial antibody levels, those with measles (6/8) were significantly more likely (P = 0.002) to have diarrhoea than the remainder (4/28). Symptomatic cryptosporidiosis may be associated with transient immune suppression due to viral infection. This study indicates that serological surveys can contribute to an understanding of the epidemiology of cryptosporidosis.

摘要

酶免疫测定法(EIA)被用于检测澳大利亚墨尔本4名近期确诊隐孢子虫感染的免疫功能正常成年人、379名健康儿童和73名成年志愿者,以及巴布亚新几内亚(PNG)205名儿童(47名健康儿童;158名肺炎患儿)血清中的抗隐孢子虫抗体。抗体在感染后3至6周达到峰值,并在几个月内降至基线水平。IgG或IgM的高水平(5000 EIA单位/毫升)或配对血清之间的显著变化被视为近期感染的证据,在PNG儿童中占24%,在墨尔本儿童中占8%,在成年人中占5%。在隐孢子虫抗体水平高的PNG肺炎患儿中,患麻疹的患儿(6/8)比其余患儿(4/28)发生腹泻的可能性显著更高(P = 0.002)。有症状的隐孢子虫病可能与病毒感染导致的短暂免疫抑制有关。这项研究表明,血清学调查有助于了解隐孢子虫病的流行病学。

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Cryptosporidiosis in hospital patients with gastroenteritis.医院肠胃炎患者中的隐孢子虫病
Am J Trop Med Hyg. 1983 Sep;32(5):931-4. doi: 10.4269/ajtmh.1983.32.931.
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Human infection with Cryptosporidium spp.: results of a 24-month survey.
Med J Aust. 1987 Aug 17;147(4):175-7. doi: 10.5694/j.1326-5377.1987.tb133350.x.
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Quantitative differences among various proteins as blocking agents for ELISA microtiter plates.
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