Chlamydia trachomatis-associated tubal factor subfertility:: immunogenetic aspects and serological screening

被引:63
作者
den Hartog, J. E.
Morre, S. A.
Land, J. A.
机构
[1] Acad Hosp Maastricht, Res Inst Growth & Dev, NL-6202 AZ Maastricht, Netherlands
[2] Acad Hosp Maastricht, Dept Obstet & Gynaecol, NL-6202 AZ Maastricht, Netherlands
[3] Vrije Univ Amsterdam, Med Ctr, Immunogenet Lab, Dept Pathol,Sect Immunogenet Infect Dis, NL-1081 HV Amsterdam, Netherlands
[4] Vrije Univ Amsterdam, Med Ctr, Dept Internal Med, Infect Dis Sect, NL-1081 HV Amsterdam, Netherlands
关键词
Chlamydia trachomatis; immunogenetics; serological markers; tubal factor subfertility;
D O I
10.1093/humupd/dml030
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Chlamydia (C.) trachomatis female genital tract infections usually remain asymptomatic and untreated. Therefore, an adequate immune response, rather than antibiotic treatment, is essential to clear the pathogen. Most women will effectively clear C. trachomatis infections, but some will have persistent C. trachomatis infections, which may ascend to the upper genital tract and increase the risk of tubal factor subfertility. Pattern recognition receptors (PRRs) of the toll-like receptor (TLR) and nucleotide-binding oligomerization domain (NOD) families recognize C. trachomatis and initiate the immune response. Host immune factors are determinants of the course of C. trachomatis infections. Genetic variations in TLR and NOD genes may affect receptor function, leading to inadequate recognition of C. trachomatis, an inadequate immune response, and consequently an increased risk of persistence and late sequelae. For the risk assessment of tubal pathology in subfertile women, C. trachomatis immunoglobulin (Ig) G antibody testing (CAT) in serum is widely used. A positive CAT is indicative of a previous infection but not of a persistent infection. Measuring serological markers of persistence, of which C-reactive protein (CRP) seems promising, in CAT-positive women may identify a subgroup of subfertile women with persistent C. trachomatis infections and the highest risk of tubal pathology.
引用
收藏
页码:719 / 730
页数:12
相关论文
共 111 条
[1]   The chlamydial developmental cycle [J].
AbdelRahman, YM ;
Belland, RJ .
FEMS MICROBIOLOGY REVIEWS, 2005, 29 (05) :949-959
[2]   Tubal damage in infertile women: prediction using chlamydia serology [J].
Akande, VA ;
Hunt, LP ;
Cahill, DJ ;
Caul, EO ;
Ford, WCL ;
Jenkins, JM .
HUMAN REPRODUCTION, 2003, 18 (09) :1841-1847
[3]   Toll-like receptor signalling [J].
Akira, S ;
Takeda, K .
NATURE REVIEWS IMMUNOLOGY, 2004, 4 (07) :499-511
[4]   Ectopic pregnancies and reproductive capacity after chlamydia trachomatis positive and negative test results: A historical follow-up study [J].
Andersen, B ;
Ostergaard, L ;
Puho, E ;
Skriver, MV ;
Schonheyder, HC .
SEXUALLY TRANSMITTED DISEASES, 2005, 32 (06) :377-381
[5]   Serotypes of Chlamydia trachomatis and risk for development of cervical squamous cell carcinoma [J].
Anttila, T ;
Saikku, P ;
Koskela, P ;
Bloigu, A ;
Dillner, J ;
Ikäheimo, I ;
Jellum, E ;
Lehtinen, M ;
Lenner, P ;
Hakulinen, T ;
Närvänen, A ;
Pukkala, E ;
Thoresen, S ;
Youngman, L ;
Paavonen, J .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2001, 285 (01) :47-51
[6]   SEROLOGIC RESPONSES OF INFERTILE WOMEN TO THE 60-KD CHLAMYDIAL HEAT-SHOCK PROTEIN (HSP60) [J].
ARNO, JN ;
YUAN, Y ;
CLEARY, RE ;
MORRISON, RP .
FERTILITY AND STERILITY, 1995, 64 (04) :730-735
[7]   SUBJECTS RECOVERING FROM HUMAN OCULAR CHLAMYDIAL INFECTION HAVE ENHANCED LYMPHOPROLIFERATIVE RESPONSES TO CHLAMYDIAL ANTIGENS COMPARED WITH THOSE OF PERSISTENTLY DISEASED CONTROLS [J].
BAILEY, RL ;
HOLLAND, MJ ;
WHITTLE, HC ;
MABEY, DCW .
INFECTION AND IMMUNITY, 1995, 63 (02) :389-392
[8]  
BAILEY RL, 1998, P 9 INT S HUM CHLAM, P474
[9]   Electron microscopic evidence of persistent chlamydial infection following treatment [J].
Bragina, EY ;
Gomberg, MA ;
Dmitriev, GA .
JOURNAL OF THE EUROPEAN ACADEMY OF DERMATOLOGY AND VENEREOLOGY, 2001, 15 (05) :405-409
[10]   Polymorphisms in the Chlamydia trachomatis cytotoxin locus associated with ocular and genital isolates [J].
Carlson, JH ;
Hughes, S ;
Hogan, D ;
Cieplak, G ;
Sturdevant, DE ;
McClarty, G ;
Caldwell, HD ;
Belland, RJ .
INFECTION AND IMMUNITY, 2004, 72 (12) :7063-7072