The increased incidence of "allergic" symptomatology and clinical complications seen in non-endemic individuals with
loiasis, as compared to natives of endemic areas, is thought to reflect a heightened immune response to filarial
antigens. To identify
antigens involved in this hyperresponsiveness, a cDNA library constructed from adult female
RNA from the related filarial parasite, Onchocerca volvulus, was screened with serum from a North American who acquired
loiasis in West Africa. Sequence analysis of one of the identified clones, OvGalBP, revealed significant homology to the vertebrate
S-type lectins, a family of
thiol-dependent,
metal-independent galactoside binding
lectins, which includes an
IgE-binding protein thought to be involved in
IgE regulation. The 1100-bp insert of OvGalBP contains the entire protein coding region and has a 3'
poly(A) tail. The two
amino acid consensus sequences (WGxExR and HFNPRF) found in all of the
S-type lectins are present. Purified
recombinant protein expressed as a fusion with
glutathione-S-transferase (OvGalBP-GST) was recognized by sera from a majority of filaria-infected patients but not by putatively immune individuals from an endemic area or by unexposed endemic and non-endemic controls. Interestingly, OvGalBP-GST specifically bound
IgE (and not
IgG) in a
lactose-inhibitable manner, suggesting a potential role for this
protein in the pathophysiology of human filarial
infection.