Salivary gland genetic vaccination: a scalable technology for promoting distal mucosal immunity and heightened systemic immune responses
- PMID: 15193415
- DOI: 10.1016/j.vaccine.2003.12.034
Salivary gland genetic vaccination: a scalable technology for promoting distal mucosal immunity and heightened systemic immune responses
Abstract
Use of plasmid DNA for vaccination has been demonstrated quite successfully in small rodents. However, some of the many challenges of DNA vaccine development are the relatively low performance obtained in larger animals and a generally weak mucosal immune response. Vaccination through salivary gland (SG) cannulation and delivery of aqueous solutions of DNA is one potential solution. The scalability of SG DNA vaccination was tested in multiple animal models; antigen specific titers above 10,000 were demonstrated in dogs and rats. Immune responses were also present at a variety of mucosal sites. In conclusion, our data demonstrate that DNA vaccination to the SG presents a unique and advantageous method for eliciting systemic and mucosal immune responses.
Similar articles
-
Mucosal priming with replicative Tiantan vaccinia and systemic boosting with DNA vaccine raised strong mucosal and systemic HIV-specific immune responses.Vaccine. 2007 Dec 17;25(52):8874-84. doi: 10.1016/j.vaccine.2007.08.066. Epub 2007 Sep 24. Vaccine. 2007. PMID: 18061316
-
Mucosal immune responses associated with polynucleotide vaccination.Behring Inst Mitt. 1997 Feb;(98):63-72. Behring Inst Mitt. 1997. PMID: 9382771 Review.
-
Induction of gp120-specific protective immune responses by genetic vaccination with linear polyethylenimine-plasmid complex.Vaccine. 2005 Feb 3;23(11):1384-92. doi: 10.1016/j.vaccine.2004.09.009. Vaccine. 2005. PMID: 15661387
-
Intramuscular delivery of a cholera DNA vaccine primes both systemic and mucosal protective antibody responses against cholera.Vaccine. 2009 Jun 12;27(29):3821-30. doi: 10.1016/j.vaccine.2009.04.008. Epub 2009 Apr 23. Vaccine. 2009. PMID: 19443090
-
[Novel vaccines against M. tuberculosis].Kekkaku. 2006 Dec;81(12):745-51. Kekkaku. 2006. PMID: 17240920 Review. Japanese.
Cited by
-
Salivary glands act as mucosal inductive sites via the formation of ectopic germinal centers after site-restricted MCMV infection.FASEB J. 2011 May;25(5):1680-96. doi: 10.1096/fj.10-174656. Epub 2011 Feb 9. FASEB J. 2011. PMID: 21307334 Free PMC article.
-
The salivary gland as a target for enhancing immunization response.Trop Dis Travel Med Vaccines. 2017 Feb 17;3:4. doi: 10.1186/s40794-017-0047-z. eCollection 2017. Trop Dis Travel Med Vaccines. 2017. PMID: 28883974 Free PMC article. Review.
-
A focused salivary gland infection with attenuated MCMV: an animal model with prevention of pathology associated with systemic MCMV infection.Exp Mol Pathol. 2007 Jun;82(3):269-79. doi: 10.1016/j.yexmp.2006.12.010. Epub 2007 Jan 12. Exp Mol Pathol. 2007. PMID: 17320076 Free PMC article.
-
Protective MCMV immunity by vaccination of the salivary gland via Wharton's duct: replication-deficient recombinant adenovirus expressing individual MCMV genes elicits protection similar to that of MCMV.FASEB J. 2014 Apr;28(4):1698-710. doi: 10.1096/fj.13-244178. Epub 2014 Jan 3. FASEB J. 2014. PMID: 24391133 Free PMC article.
-
Tetravalent dengue DNA vaccine is not immunogenic when delivered by retrograde infusion into salivary glands.Trop Dis Travel Med Vaccines. 2020 Jun 3;6:10. doi: 10.1186/s40794-020-00111-5. eCollection 2020. Trop Dis Travel Med Vaccines. 2020. PMID: 32518668 Free PMC article.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical