Enhancing DNA vaccines using modified Cholera Toxin A1 Subunit as an adjuvant

Award Information
Agency:
Department of Health and Human Services
Branch
n/a
Amount:
$294,643.00
Award Year:
2007
Program:
SBIR
Phase:
Phase I
Contract:
1R43AI074334-01A1
Award Id:
85329
Agency Tracking Number:
AI074334
Solicitation Year:
n/a
Solicitation Topic Code:
n/a
Solicitation Number:
n/a
Small Business Information
TECHCENTER@UMBC, 1450 SOUTH ROLLING RD., BALTIMORE, MD, 21227
Hubzone Owned:
N
Minority Owned:
N
Woman Owned:
N
Duns:
185576639
Principal Investigator:
TIMOTHYFOUTS
(443) 543-5010
FOUTS@PROFECTUSBIOSCIENCES.COM
Business Contact:
JEFFREYMESHULAM
() -
meshulam@profectusbiosciences.com
Research Institute:
n/a
Abstract
DESCRIPTION (provided by applicant): Vaccination using plasmid DNA has the potential to provide enhanced safety and efficacy over conventional vaccines with increased stability, and accelerated product development. Unfortunately, vaccination of primates w ith DNA requires multiple inoculations using excessively large doses of plasmid. The A1 domains of cholera toxin (CTA1) and the related heat-labile enterotoxin (LTA1) have demonstrated particular promise as adjuvants that can enhance the immunogenicity of DNA vaccines in small animals and may provide a necessary dose sparing effect in primates. To maximally exploit this promise, however, the activity of CTA1 or LTA1 in vivo should be improved. Our objective is to identify modifications to CTA1 or LTA1 that will enhance their activity in vivo by pursuing the following aims: Aim 1: Identify mutations in the active site of either CTA1 or LTA1 that enhance enzymatic activity in vitro; Aim 2: Identify fusion constructs between CTA1 or LTA1 and human ARF6 that enhance enzymatic activity in vitro; and, Aim 3: Identify constructs from Aims 1, and 2 that optimally enhance the immunogenicity of a candidate SIMmac239-gag DNA vaccine in vivo. Candidate constructs that display a minimum of 10-fold enhanced adjuvanti city in vivo will be selected for evaluation in primate studies to be proposed in phase 2. Successful candidates in phase 2 will be incorporated into candidate HIV DNA vaccines intended for clinical evaluation.

* information listed above is at the time of submission.

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