Site-directed immune responses in DNA vaccines encoding ligand-antigen fusions
Details
Publication Year 2000-02-25,Volume 18,Issue #16,Page 1681-1685
Journal Title
VACCINE
Publication Type
Journal Article
Abstract
One of the key limitations to DNA vaccines is lack of efficacy. We found that the spleen was a superior injection site to the dermis or muscle for inducing immune responses. To target sites of immune induction more practicably, antigen (human IgG1) was fused with two ligands, L-selectin (L-SEL-hIg) or CTLA4 (CTLA4-hIg) the receptors of which are found on high endothelial venule cells in lymph nodes and antigen presenting cells, respectively. Antibody and lymphocyte proliferative responses were increased. We now show that dimerization is critical for this enhancement, presumably because of avidity considerations. The hinge of hIgG3 can replace that of hIgG1 as a dimerization moiety. Fusion of other antigens e.g, ovalbumin and a malaria antigen AMA-1 have confirmed that CTLA4 induces an enhanced antibody response. Notably, in a challenge model, we have shown that CTLA4 also improves efficacy. (C) 2000 Elsevier Science Ltd. All rights reserved.
Publisher
ELSEVIER SCI LTD
Keywords
PLASMID DNA; IMMUNIZATION; INDUCTION; ROUTE
Terms of Use/Rights Notice
Refer to copyright notice on published article.


Creation Date: 2000-02-25 12:00:00
An error has occurred. This application may no longer respond until reloaded. Reload 🗙