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PMID: 9009296 Published · ppublish English Clinical Trial Journal Article Randomized Controlled Trial Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Safety of live oral Salmonella typhi vaccine strains with deletions in htrA and aroC aroD and immune response in humans.

Infection and immunity ·Vol. 65 ·No. 2 ·1997-02-00 ·Pages 452-6

Tacket CO, Sztein MB, Losonsky GA, Wasserman SS, Nataro JP, Edelman R, Pickard D, Dougan G, Chatfield SN, Levine MM

Abstract

A single-dose, oral Salmonella typhi vaccine strain has been sought as a carrier or vector of cloned genes encoding protective antigens of other pathogens. Such a hybrid vaccine, administered orally, would stimulate immune responses both at the mucosal surface and in the systemic compartment and would potentially provide protection against multiple pathogens. S. typhi CVD 908 and CVD 906, which harbor deletions in aroC and aroD, were further engineered by deletion in htrA to produce strains CVD 908-htrA and CVD 906-htrA, which are unable to sustain growth and are severely impaired in their ability to survive in host tissues. These strains were fed to humans at doses of 5 x 10(7) to 5 x 10(9) CFU with buffer, and safety and immune responses were assessed. CVD 908-htrA and CVD 906-htrA were well tolerated in volunteers; mild diarrhea in 3 of 36 volunteers and mild fever in 1 volunteer were the only notable adverse responses. The vaccine strains were not detected in blood cultures and only transiently detected in stool. Serum immune responses to S. typhi lipopolysaccharide and H antigens were observed in 75 to 100% of volunteers who received 5 x 10(8) to 5 x 10(9) CFU, and cells secreting S. typhi-specific antibodies were found in all volunteers after ingestion of either strain. Sixty-three percent to 83% of volunteers developed lymphoproliferative responses to S. typhi flagellar and particulate antigens after the higher doses. These studies demonstrate the potential of CVD 908-htrA as a live vector for the delivery of heterologous genes, and a clinical trial of such a construct is planned.

MeSH Terms
Administration, Oral Adolescent Adult Antibodies, Bacterial/biosynthesis Bacterial Proteins/genetics,immunology Bacterial Vaccines/adverse effects,genetics,immunology Dose-Response Relationship, Immunologic Double-Blind Method Gene Deletion Heat-Shock Proteins Humans Immunity, Cellular Periplasmic Proteins Salmonella typhi/immunology Serine Endopeptidases/genetics,immunology
Chemicals
Antibodies, Bacterial Bacterial Proteins Bacterial Vaccines Heat-Shock Proteins Periplasmic Proteins DegP protease Serine Endopeptidases
Authors & Affiliations
10 authors, click to expand affiliations / ORCID
Tacket C O
Department of Medicine, University of Maryland School of Medicine, Baltimore 21201, USA. ctacket@umppa1.ab.umd.edu
Sztein M B
Losonsky G A
Wasserman S S
Nataro J P
Edelman R
Pickard D
Dougan G
Chatfield S N
Levine M M
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20 references, click to expand
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Article Info
Journal
Infection and immunity
Abbr.
Infect Immun
ISSN
0019-9567
Published
1997-02-00
Pages
452-6
Language
English
Region
United States
NLM ID
0246127
PMCID
PMC174616
Subset
IM
Grants
NIAID NIH HHS · N01 AI45251 · United States
NIAID NIH HHS · R01 AI29471-06 · United States
NIAID NIH HHS · R01 AI36525 · United States
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