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肺炎衣原体肺炎的抗体反应:为何肺炎衣原体肺炎难以诊断?

Antibody responses of Chlamydophila pneumoniae pneumonia: Why is the diagnosis of C. pneumoniae pneumonia difficult?

作者信息

Miyashita Naoyuki, Kawai Yasuhiro, Tanaka Takaaki, Akaike Hiroto, Teranishi Hideto, Wakabayashi Tokio, Nakano Takashi, Ouchi Kazunobu, Okimoto Niro

机构信息

Department of Internal Medicine I, Kawasaki Medical School, Okayama, Japan.

Department of Internal Medicine I, Kawasaki Medical School, Okayama, Japan.

出版信息

J Infect Chemother. 2015 Jul;21(7):497-501. doi: 10.1016/j.jiac.2015.03.003. Epub 2015 Mar 12.

Abstract

The ELNAS Plate Chlamydophila pneumoniae commercial test kit for the detection of anti-C. pneumoniae-specific immunoglobulin M (IgM), IgA and IgG antibodies has become available in Japan recently. To determine the optimum serum collection point for the ELNAS plate in the diagnosis of C. pneumoniae pneumonia, we analyzed the kinetics of the antibody response in patients with laboratory-confirmed C. pneumoniae pneumonia. We enrolled five C. pneumoniae pneumonia cases and collected sera from patients for several months. The kinetics of the IgM and IgG antibody responses were similar among the five patients. Significant increases in IgM and IgG antibody titer between paired sera were observed in all patients. IgM antibodies appeared approximately 2-3 weeks after the onset of illness, reached a peak after 4-5 weeks, and were generally undetectable after 3-5 months. IgG antibodies developed slowly for the first 30 days and reached a plateau approximately 3-4 months after the onset of illness. The kinetics of IgA antibody responses were different among the five patients, and significant increases in IgA antibody titer between paired sera were observed in only two patients. Although the sample size was small, the best serum collection time seemed to be approximately 3-6 weeks after onset of illness when using a single serum sample for the detection of IgM antibodies. Paired sera samples should be obtained at least 4 weeks apart. IgA antibody analysis using ELNAS may not be a useful marker for acute C. pneumoniae pneumonia.

摘要

用于检测抗肺炎衣原体特异性免疫球蛋白M(IgM)、IgA和IgG抗体的ELNAS平板肺炎衣原体商业检测试剂盒最近已在日本上市。为确定ELNAS平板在肺炎衣原体肺炎诊断中的最佳血清采集时间点,我们分析了实验室确诊的肺炎衣原体肺炎患者抗体反应的动力学。我们纳入了5例肺炎衣原体肺炎病例,并在数月内收集患者血清。5例患者中IgM和IgG抗体反应的动力学相似。所有患者配对血清之间的IgM和IgG抗体滴度均显著升高。IgM抗体在发病后约2 - 3周出现,4 - 5周后达到峰值,3 - 5个月后通常检测不到。IgG抗体在发病后的前30天内缓慢产生,发病后约3 - 4个月达到平台期。5例患者中IgA抗体反应的动力学不同,仅在2例患者中观察到配对血清之间的IgA抗体滴度显著升高。尽管样本量较小,但使用单一血清样本检测IgM抗体时,最佳血清采集时间似乎是发病后约3 - 6周。配对血清样本应至少间隔4周采集。使用ELNAS进行IgA抗体分析可能不是急性肺炎衣原体肺炎的有用标志物。

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