S. Ghaemmaghami et al., CHARACTERIZATION OF B-CELL RESPONSES TO CHLAMYDIA-TRACHOMATIS ANTIGENS IN HUMANS WITH TRACHOMA, Infection and immunity, 65(12), 1997, pp. 4958-4964
The circulating B-cell responses to Chlamydia trachomatis of 60 childr
en and 34 adults in The Gambia were characterized in a cross-sectional
study of different grades of trachoma, using the enzyme-linked immuno
spot (ELISPOT) assay, Antibody-secreting cells (ASCs) specific to chla
mydial major outer membrane protein (MOMP), heat shock protein 60, and
whole elementary bodies were detected in children with no evidence of
ocular disease, and the immunoglobulin (IgA) response was significant
ly increased in those with follicular trachoma, In marked contrast, ch
ildren with the most intense ocular inflammation paradoxically had an
almost completely absent B-cell response of all isotypes and to all ch
lamydial antigens, but with normal serum IgG and IgA responses, which
was even lower than in the group with no ocular inflammation, Adults w
ith or without evidence of trachomatous scarring had equivalent number
s of circulating B cells, principally IgA, to all chlamydial antigens.
Plasmablasts secreting antibodies to MOMP were present in the urine o
f children in the absence of urogenital infection detectable by PCR, a
nd relative numbers were 8 to 25 times higher than in blood, suggestin
g site-specific homing within a common mucosal immune system, These re
sults suggest that ELISPOT assay of ongoing B-cell responses detects s
uppression of chlamydia-specific IgA ASCs during the proinflammatory r
esponse to ocular chlamydial infection seen in intense trachoma, which
may play a role in tissue damage leading to trachomatous scarring.