Chlamydia Clinical Trial
Official title:
Chlamydia Trachomatis Immunology and Vaccinology Study: Determination of Protective T Cell Responses to Chlamydia Trachomatis Infection
The primary objective is to prospectively follow 200 women with or at risk of cervicitis to determine the chlamydia-specific cellular responses that correlate with protection against incident infection. The hypothesis is that a positive IFN-y response by peripheral CD4+ T cells responding to stimulation with HSP60 will be significantly associated with protection from incident C. trachomatis infection.
A total of 200 women with or at high risk of having cervicitis will be prospectively
followed for correlations between chlamydia-specific cellular responses and protection
against incident infection.
At enrollment participants will undergo a history and physical examination; blood draw; and
pelvic examination including collection of vaginal and cervical samples, STD testing and
endometrial biopsy.
Participants will have follow up visits conducted at 1, 4, 8 and 12 months following
enrollment. At the follow-up visits, participants will undergo a repeat history and
physical, blood draw and pelvic examination including collection of vaginal and cervical
samples and STD testing.
The study design will allow comprehensive identification of the antigen-specific cell
mediated immune responses most strongly associated with protection against C. trachomatis
infection.
The primary objective is to prospectively follow 200 women with or at risk for cervicitis to
determine the chlamydia-specific cellular responses that correlate with protection against
incident infection.
;
Observational Model: Case-Only, Time Perspective: Prospective
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