Protective immunity evoked against anthrax lethal toxin after a single intramuscular administration of an adenovirus-based vaccine encoding humanized protective antigen.
| Publication Type | Academic Article |
| Authors | Tan Y, Hackett N, Boyer J, Crystal R |
| Journal | Hum Gene Ther |
| Volume | 14 |
| Issue | 17 |
| Pagination | 1673-82 |
| Date Published | 11/20/2003 |
| ISSN | 1043-0342 |
| Keywords | Adenoviridae, Anthrax Vaccines, Antibodies, Bacterial, Antigens, Bacterial, Bacterial Toxins |
| Abstract | Because of the need to develop a vaccine to rapidly protect the civilian population in response to a bioterrorism attack with Bacillus anthracis, we designed AdsechPA, a replication-deficient human serotype 5 adenovirus encoding B. anthracis protective antigen (PA) with codons optimized for expression in mammalian cells. With a single intramuscular administration to mice of 10(9) particle units of AdsechPA, a dose that can be scaled to human use, anti-PA antibodies were evoked more rapidly and at a higher level than with a single administration of the new U.S. military recombinant PA/Alhydrogel vaccine. Importantly, AdsechPA afforded approximately 2.7-fold more protection than the recombinant PA vaccine against B. anthracis lethal toxin challenge 4 weeks after a single vaccination. Even at 11 days postvaccination, AdsechPA provided some survival benefit, whereas the rPA/Alhydrogel vaccine provided none. In the context that equivalent human doses of Ad vectors have already been demonstrated to be safe in humans, a single administration of AdsechPA may provide the means to rapidly protect the civilian population against B. anthracis in response to a bioterrorism attack. |
| DOI | 10.1089/104303403322542310 |
| PubMed ID | 14633409 |
