Log on / register
BioMed Central home | Journals A-Z | Feedback | Support | My details
Open AccessResearch

Papanicolaou smears and cervical inflammatory cytokine responses

Jo-Ann S Passmore1 email, Chelsea Morroni2 email, Samual Shapiro3 email, Anna-Lise Williamson1,4 email and Margaret Hoffman2 email

Division of Medical Virology, Institute of Infectious Disease and Molecular Medicine, Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa

Women's Health Research Unit, School of Public Health and Family Medicine, Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa

Department Of Epidemiology, Mailman School of Public Health, New York, USA

National Health Laboratory Service, Groote Schuur Hospital, Observatory, Cape Town, South Africa

author email corresponding author email

Journal of Inflammation 2007, 4:8doi:10.1186/1476-9255-4-8

Published: 24 April 2007

Abstract

In a case-control study among 2064 South African women to investigate the risk of clinically invasive cancer of the cervix, we found a marked reduction in the risk of cervical cancer among women who gave a history of ever having undergone even a single Pap smear, and a statistically significant decline in the HPV positivity rate correlated with the lifetime number of Pap smears received. HPV infections and their associated low-grade lesions commonly regress, indicating that most often there is an effective host immune response against HPV infection. We hypothesized that act of performing a Pap smear is associated with inflammatory responses at the site of trauma, the cervix, and that this inflammatory signalling may be an immunological factor initiating these productive anti-HPV responses. In the present study, a randomized controlled trial, we enrolled 80 healthy young women to investigate the impact of performing a Pap smear on cervical inflammation. Forty one women, in the intervention group, received a Pap smear at enrollment and cervicovaginal lavages (CVLs) were collected at baseline and 2 weeks later. Thirty nine women received no intervention at enrollment (control group) but CVLs were collected at enrolment and 2 weeks later. We assessed various markers of inflammation including IL-12 p70, TNF-α, IL-8, IL-6, IL-10, and IL-1β in CVL specimens. While CVL levels of IL-8, IL-1β and IL-6 remained unchanged following a Pap smear, markers of cell mediated immunity (IL-12 p70 and TNF-α) and T cell regulation (IL-10) were significantly elevated.


© 1999-2010 BioMed Central Ltd unless otherwise stated. Part of Springer Science+Business Media.