Human resistance and susceptibility to schistosomiasis is associated with a
ge and specific antibody isotype responses against worm (SWAP) and egg (SEA
) antigens. In a cross-sectional study of 176 individuals infected with Sch
istosoma japonicum in the Philippines, strikingly similar isotype response
patterns against SWAP and SEA was observed when compared to other endemic a
reas. Interestingly, IgA titres to SWAP correlated with older age among S.
japonicum-infected individuals (n = 176, P < 0.01), suggesting a role for t
his isotype in protective immunity. To identify the molecular targets of hu
man IgA, 17 high-IgA/SWAP responders were identified from the said populati
on. IgA antibodies from the majority (14/17) of these individuals recognize
d a band of 97 kDa (Sj97), comigrating in immunoblots with the myofibrillar
protein paramyosin. The antigen was confirmed as paramyosin by expressed s
equence tag (EST)-analysis of four clones obtained by screening an adult S.
japonicum cDNA library with pooled IgA antisera and mouse antiparamyosin p
olyclonal antibodies. The identification of paramyosin as a major target of
human IgA raises its potential as a vaccine candidate that targets mucosal
immune responses. Since this antigen is exposed on the parasite surface on
ly during the lung stages, we propose that human IgA contributes to parasit
e attrition during schistosome migration in the lungs.