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        <City>SAN DIEGO</City>
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        <BusinessNameLine1>Vaccine Research Institute of San Diego</BusinessNameLine1>
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        <AddressLine1>3030 Bunker Hill Street</AddressLine1>
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        <Description>MALARIA-HYBRID-WHCAG VLPS CARRYING 2 CS-REPEAT B CELL EPITOPES AND 4 CS-NONREPEAT B CELL EPITOPES WERE PRODUCED, PURIFIED AND USED TO IMMUNIZE MICE. ALL CONSTRUCTS ELICITED HIGH LEVES OF ANTI-INSERT ANTIBODIES.THE HYBRID-WHCAG VLPS CARRYING CS-REPEAT B CELL EPITOPES CONFERRED 98.7% PROTECTION AGAINST A 10,000 HYBRID SPOROZOITE CHALLENGE, WHEREAS THE NON-REPEAT B CELL EPITOPES WERE MINIMALLY TO NON-PROTECTIVE. ALTHOUGH ANTI-CS NON-REPEAT ANTIBODIES BOUND DRY SPOROZOITES, VIABLE SPOROZOITES WERE NOT RECOGNIZED BY ANTI-CS NON-REPEAT ANTIBODES. THE CRYPTIC NATURE OF CS-NONREPEAT EPITOMES ON VIABLE SPOROZOITES MAY EXPLAIN HE LACK OF PROTECTION. COMPARING CS-REPEAT B CELL EPITOPES, ANTI-NANP ANTIBODIES WERE MORE PROTECTIVE THAN ANTI-NVDP ANTIBODIES. HUM CD4+ / CD8+ T CELL RECOGNITION SITES WERE ALSO INSERTED ONTO HYBRID-WHCAG VLPS (I.E. UTC, TH.3R, CS.T3) AND A VLP CONSTRUCT CONTAINING ALL 3 WELL CHARACTERIZED T CELL DOMAINS PRIMED MURINE CS-SPECIFIC T CELLS AS WELL AS WHCAG-SPECIFIC T CELLS.</Description>
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        <Description>SALMONELLA GENES ASSOCIATED WITH COLOIZATION OF SPECIFIC HOSTS. THIS PROJECT HAS GENERATED A RESOURCE OF MUTANTS IN ALMOST EVERY PROTEIN CODING GENE IN THE PATHOGEN SALMONELLA. THIS RESOURCE IS BEING USED IN RESEARCH LABORATORIES WORLDWIDE TO UNDERSTAND HOW THIS ORGANISM INFECTS HUMANS AND DOMESTIC ANIMALS. BEYOND THE SCOPE OF THIS PROJECT, THE RESOURCE IS NOW ALSO BEING USED TO IMPROVE SALMONELLA AS A VECTOR FOR VACCINES AND FOR DELIVERING CANCER THERAPEUTICS.</Description>
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