Prevalence of Chlamydia pneumoniae and Mycoplasma pneumoniae immunoglobulin G and A antibodies in a healthy Finnish population as analyzed by quantitative enzyme immunoassays

被引:60
作者
Tuuminen, T
Varjo, S
Ingman, H
Weber, T
Oksi, J
Viljanen, M
机构
[1] Labsyst OY, Labsyst Res Labs, Helsinki 00811, Finland
[2] Laakso City Hosp, Helsinki 00250, Finland
[3] Turku Univ, Dept Med Microbiol, FIN-20520 Turku, Finland
[4] Natl Publ Hlth Inst, Turku 20520, Finland
关键词
D O I
10.1128/CDLI.7.5.734-738.2000
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Chlamydia pneumoniae and Mycoplasma pneumoniae immunoglobulin G (IgG) and IgA antibody seroprevalence rates and antibody levels related to age and gender were studied. The samples (n = 742) were collected during a nonepidemic period and analyzed by quantitative enzyme immunoassays (EIAs), Seroprevalence to C. pneumoniae was found to increase sharply in young children, and in the 15- to 19-year old group it reached levels as high as 70 and 60% for IgG and IgA, respectively. After adolescence, seroprevalence showed a transient decrease and then continued to increase, although less dramatically than in early childhood. In the elderly the seroprevalence of IgG antibodies reached 75 and 100% in women and men, respectively. The corresponding rates of IgA antibodies were 73 and 100%. When a randomly selected subgroup of samples (II = 66) was analyzed in parallel by a microimmunofluorescence test and an EIA for C, pneumoniae! IgA antibodies, similar seroprevalence rates were obtained (36 versus 35%), Seroprevalence to M. pneumoniae was already found to increase very sharply in 2- to 4-year-old children, reaching 16% for IgG and 8% for IgA, Seroprevalence to M. pneumoniae also continued to increase in adolescence, but in contrast to that to C, pneumoniae, the increase leveled off at about 40 to 50% in adulthood. In subjects aged over 65 years, prevalence did not exceed 60% for IgG or 35% for IgA, The seroprevalence patterns as well as the medians and variations of levels of C. pneumoniae and M. pneumoniae IgG antibodies mere similar to those of corresponding IgA antibodies. Com pared to IgG antibodies, IgA antibodies do not seem to be of additional value in the diagnosis of infections caused by these pathogens when single serum specimens are studied.
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页码:734 / 738
页数:5
相关论文
共 13 条
[1]  
FOY HM, 1993, CLIN INFECT DIS S1, V17, P37
[2]   A NEW RESPIRATORY-TRACT PATHOGEN - CHLAMYDIA-PNEUMONIAE STRAIN TWAR [J].
GRAYSTON, JT ;
CAMPBELL, LA ;
KUO, CC ;
MORDHORST, CH ;
SAIKKU, P ;
THOM, DH ;
WANG, SP .
JOURNAL OF INFECTIOUS DISEASES, 1990, 161 (04) :618-625
[3]   CHLAMYDIA-PNEUMONIAE IGG ANTIBODY PREVALENCE IN SOUTH-WESTERN AND EASTERN FINLAND IN 1982 AND 1987 [J].
KARVONEN, M ;
TUOMILEHTO, J ;
PITKANIEMI, J ;
NAUKKARINEN, A ;
SAIKKU, P .
INTERNATIONAL JOURNAL OF EPIDEMIOLOGY, 1994, 23 (01) :176-184
[4]   CHLAMYDIA-PNEUMONIAE (TWAR) [J].
KUO, CC ;
JACKSON, LA ;
CAMPBELL, LA ;
GRAYSTON, JT .
CLINICAL MICROBIOLOGY REVIEWS, 1995, 8 (04) :451-&
[5]   Pneumonia with serological evidence of acute infection with the chlamydia-like microorganism ''Z'' [J].
Lieberman, D ;
Kahane, S ;
Lieberman, D ;
Friedman, MG .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1997, 156 (02) :578-582
[6]   Molecular evidence for the existence of additional members of the order Chlamydiales [J].
Ossewaarde, JM ;
Meijer, A .
MICROBIOLOGY-SGM, 1999, 145 :411-417
[7]  
PEELING RW, CHLAMYDIAL INFECTION, P159
[8]   Comparison of five serologic tests for diagnosis of acute infections by Chlamydia pneumoniae [J].
Persson, K ;
Boman, J .
CLINICAL AND DIAGNOSTIC LABORATORY IMMUNOLOGY, 2000, 7 (05) :739-744
[9]   Detection of antibodies to Mycoplasma pneumoniae adhesin P1 in serum specimens from infected and non-infected subjects by immunoblotting [J].
Rastawicki, W ;
Raty, R ;
Kleemola, M .
DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE, 1996, 26 (3-4) :141-143
[10]   SEROLOGICAL EVIDENCE OF AN ASSOCIATION OF A NOVEL CHLAMYDIA, TWAR, WITH CHRONIC CORONARY HEART-DISEASE AND ACUTE MYOCARDIAL-INFARCTION [J].
SAIKKU, P ;
MATTILA, K ;
NIEMINEN, MS ;
HUTTUNEN, JK ;
LEINONEN, M ;
EKMAN, MR ;
MAKELA, PH ;
VALTONEN, V .
LANCET, 1988, 2 (8618) :983-986