Literature DB >> 2672779

Comparative studies of three serologic methods for the measurement of Mycoplasma pneumoniae antibodies.

S H Lee1, S Charoenying, T Brennan, M Markowski, D R Mayo.   

Abstract

Antibodies against Mycoplasma pneumoniae in the sera of patients and normal adult controls were measured by a standard complement fixation (CF) test, a commercial immunofluorescence (IF) test (CROWNTITRE), and a commercial enzyme-linked immunosorbent assay (ELISA) (MYCOPLASMELISA). The findings showed that, in the control sera, 269 of 277 (97%) had negative results for CF antibodies. Of the 320 controls tested by the IF assay, all (100%) had negative results for IgM antibodies and 314 (98%) had negative results for IgG antibodies. Only 6 of the 201 (3%) controls by the ELISA were classified as negative/equivocal. Among the 450 patient sera, 105 (23%) had positive results for CF antibodies, and 158 (35%) had positive results for IgG and/or IgM membrane antibodies by the IF test; 424 of these patients' sera were also tested by the ELISA, and 397 (94%) of them were found to have positive results for anti-M. pneumoniae IgG antibodies. If the CF test were chosen as the standard for comparison, the IF test would have a sensitivity of 87% and a specificity of 81% and the ELISA would have a sensitivity of 71% and a specificity of 80%, provided an adjustment in the threshold ELISA-positive value was made. A single positive M. pneumoniae membrane IgM antibody titer appeared to be valuable for a presumptive diagnosis of an ongoing infection; 41 of 47 (87%) of the IgM-positive results in the paired sera were supported by a fourfold increase or a stable high level of CF antibody titer.

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Year:  1989        PMID: 2672779     DOI: 10.1093/ajcp/92.3.342

Source DB:  PubMed          Journal:  Am J Clin Pathol        ISSN: 0002-9173            Impact factor:   2.493


  5 in total

1.  Performance of Meridian ImmunoCard Mycoplasma test in a multicenter clinical trial.

Authors:  T S Alexander; L D Gray; J A Kraft; D S Leland; M T Nikaido; D H Willis
Journal:  J Clin Microbiol       Date:  1996-05       Impact factor: 5.948

2.  Clinical use of capillary PCR to diagnose Mycoplasma pneumonia.

Authors:  J Honda; T Yano; M Kusaba; J Yonemitsu; H Kitajima; M Masuoka; K Hamada; K Oizumi
Journal:  J Clin Microbiol       Date:  2000-04       Impact factor: 5.948

3.  Application of an indirect immunofluorescence test for detection of Mycoplasma pneumoniae in respiratory exudates.

Authors:  Y Hirai; J Shiode; T Masayoshi; Y Kanemasa
Journal:  J Clin Microbiol       Date:  1991-09       Impact factor: 5.948

4.  Microparticle agglutination versus antibody-capture enzyme immunoassay for diagnosis of community-acquired Mycoplasma pneumoniae pneumonia.

Authors:  D Lieberman; D Lieberman; S Horowitz; O Horovitz; F Schlaeffer; A Porath
Journal:  Eur J Clin Microbiol Infect Dis       Date:  1995-07       Impact factor: 3.267

5.  Comparison and evaluation of real-time PCR, real-time nucleic acid sequence-based amplification, conventional PCR, and serology for diagnosis of Mycoplasma pneumoniae.

Authors:  Kate E Templeton; Sitha A Scheltinga; A Willy Graffelman; Jolanda M Van Schie; Jantine W Crielaard; Peter Sillekens; Peterhans J Van Den Broek; Herman Goossens; Matthias F C Beersma; Eric C J Claas
Journal:  J Clin Microbiol       Date:  2003-09       Impact factor: 5.948

  5 in total

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