The circulating and cervical B cell responses to Chlamydia trachomatis plasmid
protein pgp3 were characterized in children and adults with ocular or genital chlamydial
infection using the
enzyme-linked immunospot assay (ELISPOT) and ELISA. No pgp3-specific ASCs were detected in healthy controls, but predominantly
IgA ASCs were detected in UK adults with uncomplicated
cervicitis or
urethritis (P = 0.03, 0.019). In patients with extragenital complications or
pelvic inflammatory disease a mixed response with more
IgG and
IgM ASCs was evident, suggesting a breach of mucosal immune compartmentalization with more extensive
infection. In women with chlamydial
cervicitis, ASCs secreting predominantly
IgA, but also
IgG, to pgp3 were present in cervix at presentation, with a frequency 30-50 times higher than blood. Cervical ASC numbers, especially
IgG, fell markedly six weeks after
antibiotic treatment. We detected principally
IgA pgp3-specific antibody secreting cells (ASCs) in children resident in a Gambian endemic area, with a trend towards suppression of
IgA responses during intense trachomatous
inflammation (P = 0.06), as previously reported for other chlamydial
antigens, and in keeping with the findings in
genital disease. These data provide a rationale for further studies of immune responses to pgp3 in humans and animal models of chlamydia-induced disease, and its potential use in diagnostic assays and protective immunization strategies.