Tumor necrosis factor-alpha response to infection with Chlamydia trachomatis in human fallopian tube organ culture

被引:33
作者
Ault, KA
Tawfik, OW
SmithKing, MM
Gunter, J
Terranova, PT
机构
[1] UNIV KANSAS,MED CTR,DEPT OBSTET & GYNECOL,KANSAS CITY,KS 66103
[2] UNIV KANSAS,MED CTR,DEPT MED,KANSAS CITY,KS 66103
[3] UNIV KANSAS,MED CTR,DEPT PATHOL & LAB MED,KANSAS CITY,KS 66103
[4] UNIV KANSAS,MED CTR,DEPT PHYSIOL,KANSAS CITY,KS 66103
关键词
tumor necrosis factor; Chlamydia trachomatis; fallopian tube; cytokines;
D O I
10.1016/S0002-9378(96)70035-2
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
OBJECTIVE: Our purpose was to determine whether tumor necrosis factor-alpha is produced in response to infection with Chlamydia trachomatis in the fallopian tube. STUDY DESIGN: Fallopian tubes were harvested at the time of abdominal hysterectomy and processed by standard tissue culture techniques. Tubal segments were inoculated with Chlamydia trachomatis serotype E/UW-5/CX. At 48 hours of incubation supernatant fluid was assayed for tumor necrosis factor-alpha. Tubal segments were stained for chlamydial inclusions and tumor necrosis factor-alpha by use of immunohistochemical techniques. RESULTS: Mean tumor necrosis factor-alpha levels for infected segments were 92.1 +/- 21.3 pg/ml (mean +/- SEM) and for control segments were 61.9 +/- 13.9 pg/ml (p = 0.03 by paired t test). Tumor necrosis factor-alpha was predominantly localized in the tubal epithelium. CONCLUSIONS: Tumor necrosis factor-alpha is produced in response to chlamydial infection by the human fallopian tube. It is an important proinflammatory cytokine and may promote the production of other cytokines and immune-mediated damage of the fallopian tube.
引用
收藏
页码:1242 / 1245
页数:4
相关论文
共 18 条
[1]  
[Anonymous], 1995, Sex Transm Dis, V22, P71
[2]  
Beatty Wandy L., 1994, Trends in Microbiology, V2, P94, DOI 10.1016/0966-842X(94)90542-8
[3]   MORPHOLOGIC AND ANTIGENIC CHARACTERIZATION OF INTERFERON GAMMA-MEDIATED PERSISTENT CHLAMYDIA-TRACHOMATIS INFECTION INVITRO [J].
BEATTY, WL ;
BYRNE, GI ;
MORRISON, RP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (09) :3998-4002
[4]  
COOPER M, 1990, J GEN MICROBIOL, V36, P1109
[5]  
COSTE J, 1994, FERTIL STERIL, V62, P289
[6]   TUMOR-NECROSIS-FACTOR-ALPHA ACTIVITY IN GENITAL-TRACT SECRETIONS OF GUINEA-PIGS INFECTED WITH CHLAMYDIAE [J].
DARVILLE, T ;
LAFFOON, KK ;
KISHEN, LR ;
RANK, RG .
INFECTION AND IMMUNITY, 1995, 63 (12) :4675-4681
[7]   RELEASE OF TUMOR NECROSIS FACTOR-ALPHA BY HUMAN PERITONEAL-MACROPHAGES INVIVO AND INVITRO [J].
HALME, J .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1989, 161 (06) :1718-1725
[8]  
Herrera J. L., 1993, Morbidity and Mortality Weekly Report, V42, P1
[9]   CHLAMYDIA-TRACHOMATIS PNEUMONIA INDUCES INVIVO PRODUCTION OF INTERLEUKIN-1 AND INTERLEUKIN-6 [J].
MAGEE, DM ;
SMITH, JG ;
BLEICKER, CA ;
CARTER, CJ ;
BONEWALD, LF ;
SCHACHTER, J ;
WILLIAMS, DM .
INFECTION AND IMMUNITY, 1992, 60 (03) :1217-1220
[10]   LOCAL INDUCTION OF TUMOR-NECROSIS-FACTOR AS A MOLECULAR MECHANISM OF MUCOSAL DAMAGE BY GONOCOCCI [J].
MCGEE, ZA ;
CLEMENS, CM ;
JENSEN, RL ;
KLEIN, JJ ;
BARLEY, LR ;
GORBY, GL .
MICROBIAL PATHOGENESIS, 1992, 12 (05) :333-341