Protective or pathogenic immune response to genital chlamydial infection in women-A possible role of cytokine secretion profile of cervical mucosal cells

被引:24
作者
Agrawal, T. [1 ]
Gupta, R. [1 ]
Dutta, R. [1 ]
Srivastava, P. [1 ]
Bhengraj, A. R. [1 ]
Sathan, S. [2 ]
Mittal, Aruna [1 ]
机构
[1] Inst Pathol ICMR, New Delhi 110029, India
[2] Safdarjang Hosp, Dept Obstet & Gynaecol, New Delhi, India
关键词
Chlamydia trachomatis; Mucosal immune response; Cytokines; Fertility disorders; Pathology; PELVIC INFLAMMATORY DISEASE; TRACHOMATIS INFECTION; GAMMA-INTERFERON; GENE-EXPRESSION; NEISSERIA-GONORRHOEAE; TRACT INFECTION; INTERLEUKIN-10; PNEUMONIAE; SEQUELAE; IL-10;
D O I
10.1016/j.clim.2008.10.004
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Little is known about genital mucosal immune response to chlamydial infection in women with or without sequelae (Chlamydia positive women with or without fertility disorders as infertility and multiple spontaneous abortions). Cervical lymphocytes were stimulated with chlamydial EBs and cytokine secretion was determined by ELISA, RT-PCR and ELISPOT assays. Stimulated cervical cells from women with fertility disorders (FD) secrete significantly (P<0.05) higher levels of IL-1 beta, IL-6, IL-8 and IL-10 and cells from fertile women secrete significantly higher levels of IL-12 and IFN-gamma compared to other groups. RT-PCR analysis showed similar results for IFN-gamma and IL-12. For IL-10 and IL-4, mRNA expression levels were significantly higher (P<0.05) in cells obtained from women with FD compared to other groups. Results for ELISPOT assay were similar as those of RT-PCR. The results suggest that cytokine secretion profile of cervical cells may decide whether infection does not hamper fertility or will develop fertility disorder. (C) 2008 Elsevier Inc. AR rights reserved.
引用
收藏
页码:347 / 354
页数:8
相关论文
共 42 条
  • [1] Mucosal and peripheral immune responses to chlamydial heat shock proteins in women infected with Chlamydia trachomatis
    Agrawal, T.
    Vats, V.
    Salhan, S.
    Mittal, A.
    [J]. CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 2007, 148 (03) : 461 - 468
  • [2] Local markers for prediction of women at higher risk of developing sequelae to Chlamydia trachomatis infection
    Agrawal, Tanvi
    Vats, Vikas
    Salhan, Sudha
    Mittal, Aruna
    [J]. AMERICAN JOURNAL OF REPRODUCTIVE IMMUNOLOGY, 2007, 57 (02) : 153 - 159
  • [3] Increased interleukin-10 in the endocervical secretions of women with non-ulcerative sexually transmitted diseases: a mechanism for enhanced HIV-1 transmission?
    Cohen, CR
    Plummer, FA
    Mugo, N
    Maclean, I
    Shen, CX
    Bukusi, EA
    Irungu, E
    Sinei, S
    Bwayo, J
    Brunham, RC
    [J]. AIDS, 1999, 13 (03) : 327 - 332
  • [4] IL-10, an inflammatory/inhibitory cytokine, but not always
    Conti, P
    Kempuraj, D
    Kandere, K
    Di Gioacchino, M
    Barbacane, RC
    Castellani, ML
    Felaco, M
    Boucher, W
    Letourneau, R
    Theoharides, TC
    [J]. IMMUNOLOGY LETTERS, 2003, 86 (02) : 123 - 129
  • [5] Toll-like receptor-2, but not toll-like receptor-4, is essential for development of oviduct pathology in chlamydial genital tract infection
    Darville, T
    O'Neill, JM
    Andrews, CW
    Nagarajan, UM
    Stahl, L
    Ojcius, DM
    [J]. JOURNAL OF IMMUNOLOGY, 2003, 171 (11) : 6187 - 6197
  • [6] Reduced levels of gamma-interferon secretion in response to chlamydial 60 kDa heat shock protein amongst women with pelvic inflammatory disease and a history of repeated Chlamydia trachomatis infections
    Debattista, J
    Timms, P
    Allan, J
    Allan, J
    [J]. IMMUNOLOGY LETTERS, 2002, 81 (03) : 205 - 210
  • [7] THE ROLE OF NEISSERIA-GONORRHOEAE AND CHLAMYDIA-TRACHOMATIS IN PELVIC INFLAMMATORY DISEASE AND ITS SEQUELAE IN ZIMBABWE
    DEMUYLDER, X
    LAGA, M
    TENNSTEDT, C
    VANDYCK, E
    AELBERS, GNM
    PIOT, P
    [J]. JOURNAL OF INFECTIOUS DISEASES, 1990, 162 (02) : 501 - 505
  • [8] ENK AH, 1993, J IMMUNOL, V151, P2390
  • [9] Temporal cytokine gene expression patterns in subjects with trachoma identify distinct conjunctival responses associated with infection
    Faal, N
    Bailey, RL
    Sarr, I
    Joof, H
    Mabey, DCW
    Holland, MJ
    [J]. CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 2005, 142 (02) : 347 - 353
  • [10] Gerard HC, 2002, J RHEUMATOL, V29, P1827