The microimmunofluorescence test for Chlamydia pneumoniae infection: Technique and interpretation

Authors
Citation
Sp. Wang, The microimmunofluorescence test for Chlamydia pneumoniae infection: Technique and interpretation, J INFEC DIS, 181, 2000, pp. S421-S425
Citations number
19
Categorie Soggetti
Clinical Immunolgy & Infectious Disease",Immunology
Journal title
JOURNAL OF INFECTIOUS DISEASES
ISSN journal
00221899 → ACNP
Volume
181
Year of publication
2000
Supplement
3
Pages
S421 - S425
Database
ISI
SICI code
0022-1899(200006)181:<S421:TMTFCP>2.0.ZU;2-E
Abstract
A brief description of current procedures for the Chlamydia microimmunofluo rescence (MIF) test is presented. To date, use of MIF serology with Chlamyd ia pneumoniae (TWAR) antigen has provided the most sensitive and specific m ethod for diagnosis of acute TWAR infection. In primary infections, the TWA R IgM antibody response is longer lasting and IgG antibody is slower to dev elop compared with Chlamydia trachomatis infection. Unlike other Chlamydia species, only a single serovar for C. pneumoniae has been recognized in the MIF system and cross-reaction with other species is negligible. While IgM antibody response is an important marker for serodiagnosis of acute infecti on, rheumatoid factor often causes false-positive reactions. Persistent TWA R IgG antibody has been useful for seroepidemiologic studies and an associa tion of TWAR IgG antibody and atherosclerotic diseases has been observed. I gA antibody may not be a useful marker for chronic TWAR infection or for ac ute infection.