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Comparison between the Enzyme-linked Immunosorbent Assay (ELISA) and the Micro-immunofluorescence (MIF) Method for Detection of Chlamydia pneumoniae Antibodies Kazuhiko Ikeda 1 , Kazuhira Maehara 2 , Masayuki Mita 3 , Tokuo Yui 1 , Yukio Maruyama 2 1Department of Internal Medicine, Kitakata Hospital 2First Department of Internal Medicine, Fukushima Medical University 3Department of Internal Medicine, Hoshi General Hospital Keyword: 肺炎クラミジア , ELISA法 , MIF法 , Chlamydia pneumoniae , ELISA , microimmunofluorescence method pp.725-729
Published Date 2000/7/15
DOI https://doi.org/10.11477/mf.1404902128
  • Abstract
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Chlamydia pneumoniae (C. pneumoniae) is a commonrespiratory tract pathogen. Detection of C. pneumoniaeantibody is useful for diagnosis, and the microimmuno-fluorescence (MIF) method has also been used. Recentlythe enzyme-linked immunosorbent assay (ELISA) hasbeen newly developed, however, it has not been fullyevaluated. With this in mind, we made a comparativestudy of the accuracy of detection of C. pneumoniaeantibody by MIF and that by ELISA methods, withreference to the Western Blotting (WB) method. Thirty-six sera from twenty-eight patients with suspected C.pneumoniae respiratory tract infection were examined. IgG antibody against C. pneumoniae was positive in 35of 36 specimens examined by the WB method. Therewas no significant difference in sensitivity between MIF(97 %) and ELISA (91 %, p=0.16). IgA antibodyagainst C. pneumoniae was positive in 33 of 36 speci-mens. The sensitivity of ELISA (94 %) was significantlyhigher than MIF (76 %, p<0.05). In conclusion, theELISA method could be said to be more sensitive for thedetection of serum IgA antibody and, thus, more usefulfor the diagnosis of C. pneumoniae infection.


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電子版ISSN 1882-1200 印刷版ISSN 0452-3458 医学書院

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