B. Baras et al., Single-dose mucosal immunization with biodegradable microparticles containing a Schistosoma mansoni antigen, INFEC IMMUN, 67(5), 1999, pp. 2643-2648
The purpose of this work was to assess the immunogenicity of a single nasal
or oral administration of recombinant 28-kDa glutathione S-transferase of
Schistosoma mansoni (rSm28GST) entrapped by poly(lactide-co-glycolide) (PLG
)- or polycaprolactone (PCL)-biodegradable microparticles. Whatever the pol
ymer and the route of administration used, the equivalent of 100 mu g of en
trapped rSm28GST induced a long-lasting and stable antigen specific serum a
ntibody response, with a peak at 9 to 10 weeks following immunization. Isot
ype profiles were comparable, with immunoglobulin G1 being the predominant
isotype produced. The abilities of specific antisera to neutralize the rSm2
8GST enzymatic activity have been used as criteria of immune response quali
ty. Pooled 10-week sera from mice receiving PLG microparticles by the nasal
or oral route neutralized the rSm28GST enzymatic activity, whereas sera of
mice receiving either PCL microparticles, free rSm28GST, or empty micropar
ticles inefficiently neutralized this enzymatic activity. Finally, this stu
dy shows that a single administration of these microparticles could provide
distinct and timely release pulses of microencapsulated antigen, which mig
ht greatly facilitate future vaccine development.