2018 Volume 81 Issue 1 Pages 16-23
We investigated whether mucosal and systemic antigen (Ag)specific immune re sponses were induced by nasal administration of synthetic hinokitiol (HNK). Mice in the experi mental groups were immunized under anesthesia three times at weekly intervals nasally with 100 μg of chicken ovalbumin (OVA) and 5 μg or 50 μg of HNK simultaneously. As a negative control, mice were given nasally 100 μg of OVA alone, and as a positive control, they were ad ministered nasally 100 μg of OVA and 50 μg of DNA plasmid expressing Flt3 ligand (pdF3L) as a mucosal adjuvant. Saliva, nasal washes (NWs), and plasma were collected on days 0, 7, 14 and 21, and we determined the Agspecific IgA antibodies (Abs) in each sample by Agspecific ELISA methods. In addition, mononuclear cells from submandibular glands (SMG), nasal pas sages (NPs), nasopharyngealassociated lymphoreticular tissues (NALT), cervical lymph nodes and spleen were supplied to antigenspecific ELISPOT assay in order to examine induction of OVAspecific IgA Abforming cells. Consequently, we found little induction of systemic or mu cosal IgA immune responses, compared with the positive control. These results suggest that HNK does not bear a mucosal adjuvanticity to provoke Agspecific IgA immune responses. Shika Igaku (J Osaka Odontol Soc) 2018 ;Mar ;81(1) : 16-23.