The prevalence of Chlamydia trachomatis and Mycoplasma genitalium tubal infections and their effects on the expression of IL-6 and leukaemia inhibitory factor in Fallopian tubes with and without an ectopic pregnancy

Author:

Refaat Bassem1,Ashshi Ahmed Mohamed1,Batwa Sarah Abdullah2,Ahmad Jawwad1,Idris Shakir1,Kutbi Seham Yahia2,Malibary Faizah Ahmed2,Kamfar Fadi Fayez3

Affiliation:

1. Laboratory Medicine Department, Faculty of Applied Medical Sciences, Umm Al-Qura University, Al Abdeyah, Makkah, KSA

2. Obstertics and Gynaecology Department, Maternity and Children Hospital, Al-Aziziyah, Ministry of Health, Jeddah, KSA

3. Pathology Department, Clinical Laboratories, Maternity and Children Hospital, Ministry of Health, Makkah, KSA

Abstract

This was a prospective case–control study that measured the prevalence of Chlamydia trachomatis (CT), Neisseria gonorrhoeae (NG) and Mycoplasma genitalium (MG) by an IVD CE multiplex PCR kit in fresh Fallopian tubes (FT) obtained from 96 ectopic pregnancies (EP) and 61 controls in the midluteal phase of the cycle. We later measured the expression profile of IL-6, leukaemia inhibitory factor (LIF) and their signalling molecules, in respect to the type and number of infections, by immunohistochemistry, ELISA and quantitative RT-PCR. The frequencies of CT, and MG mono- and co-infections were significantly higher in EP. IL-6, LIF, their receptors and intracellular mediators were significantly up-regulated at the gene and protein levels in positive compared with negative FTs within each group ( P < 0.05). EP tubal samples with co-infections showed the highest significant expression of the candidate cytokines by all techniques ( P < 0.05). CT and MG are frequent in EP and up-regulate the tubal expression of IL-6, LIF and their signalling molecules. Both cytokines could be involved in the tubal immune response against bacterial infections, as well as the pathogenesis of EP. Further studies are needed to explore the roles of IL-6 family in infection-induced tubal inflammation and EP.

Publisher

SAGE Publications

Subject

Infectious Diseases,Cell Biology,Molecular Biology,Immunology,Microbiology

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