| Literature DB >> 24120457 |
Azra Blazevic1, Christopher S Eickhoff1, Jaime Stanley1, Mark R Buller2, Jill Schriewer2, Eric M Kettelson2, Daniel F Hoft3.
Abstract
A better understanding of mucosal immunity is required to develop more protective vaccines against Mycobacterium tuberculosis. We developed a murine aerosol challenge model to investigate responses capable of protecting against mucosal infection. Mice received vaccinations intranasally with CpG-adjuvanted antigen 85B (Ag85B/CpG) and/or Bacillus Calmette-Guerin (BCG). Protection against aerosol challenge with a recombinant GFP-expressing BCG was assessed. Mucosal prime/boost vaccinations with Ag85B/CpG and BCG were protective, but did not prevent lung infection indicating more efficacious mucosal vaccines are needed. Our novel finding that protection correlated with increased airway dendritic cells early post-challenge could help guide the development of enhanced mucosal vaccines.Entities:
Keywords: BCG; Mucosal specific immunity; Mycobacterium tuberculosis (Mtb); Vaccination
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Year: 2013 PMID: 24120457 PMCID: PMC3947004 DOI: 10.1016/j.micinf.2013.09.006
Source DB: PubMed Journal: Microbes Infect ISSN: 1286-4579 Impact factor: 2.700