Literature DB >> 25056362

A novel live vector group A streptococcal emm type 9 vaccine delivered intranasally protects mice against challenge infection with emm type 9 group A streptococci.

Aniela Wozniak1, Patricia García2, Enrique A Geoffroy2, Daniel B Aguirre2, Samantha A González2, Victoria A Sarno2, James B Dale3, Francisco J Salazar-Echegarai4, Andrea Vera2, Susan M Bueno4, Alexis M Kalergis5.   

Abstract

The availability of a protective vaccine against Streptococcus pyogenes (group A Streptococcus [GAS]) is a priority for public health worldwide. Here, we have generated six live vaccine strains, each engineered to express an N-terminal M protein peptide from one of six of the most prevalent emm types of GAS (M1, M2, M4, M9, M12, and M28). The vaccine strains are based on a food-grade Lactococcus lactis strain and do not bear any antibiotic resistance. Mice immunized with the vaccine strain expressing the M9 peptide (termed here the L. lactis M9 strain) showed high titers of serum antibodies when delivered intranasally. Mice immunized with the L. lactis M9 strain were protected against infection after intranasal challenge with type 9 streptococci. Several parameters of disease, such as weight loss, body temperature, colony counts in mouth washes, and lung histology, were significantly improved in immunized mice compared to naive control mice. Our results indicate that intranasal delivery of the L. lactis M9 strain live bacterial vaccine induced GAS-specific IgG titers, prevented pharyngeal colonization of GAS, and protected mice from disease upon challenge. The design of this vaccine prototype may provide a lower cost alternative to vaccines comprised of purified recombinant proteins.
Copyright © 2014, American Society for Microbiology. All Rights Reserved.

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Year:  2014        PMID: 25056362      PMCID: PMC4178559          DOI: 10.1128/CVI.00330-14

Source DB:  PubMed          Journal:  Clin Vaccine Immunol        ISSN: 1556-679X


  26 in total

1.  Intranasal immunization with multivalent group A streptococcal vaccines protects mice against intranasal challenge infections.

Authors:  Mary A Hall; Steven D Stroop; Mary C Hu; Michael A Walls; Mark A Reddish; David S Burt; George H Lowell; James B Dale
Journal:  Infect Immun       Date:  2004-05       Impact factor: 3.441

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Authors:  Oliver Goldmann; Manfred Rohde; Gursharan Singh Chhatwal; Eva Medina
Journal:  Infect Immun       Date:  2004-05       Impact factor: 3.441

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Authors:  D Bessen; V A Fischetti
Journal:  Infect Immun       Date:  1988-10       Impact factor: 3.441

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Journal:  Proc Natl Acad Sci U S A       Date:  1995-07-18       Impact factor: 11.205

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Journal:  J Exp Med       Date:  1986-05-01       Impact factor: 14.307

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Journal:  J Exp Med       Date:  1986-06-01       Impact factor: 14.307

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Authors:  K F Jones; V A Fischetti
Journal:  J Exp Med       Date:  1988-03-01       Impact factor: 14.307

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Journal:  J Exp Med       Date:  1983-11-01       Impact factor: 14.307

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  1 in total

1.  Protective immunity induced by an intranasal multivalent vaccine comprising 10 Lactococcus lactis strains expressing highly prevalent M-protein antigens derived from Group A Streptococcus.

Authors:  Aniela Wozniak; Natalia Scioscia; Patricia C García; James B Dale; Braulio A Paillavil; Paulette Legarraga; Francisco J Salazar-Echegarai; Susan M Bueno; Alexis M Kalergis
Journal:  Microbiol Immunol       Date:  2018-06-11       Impact factor: 1.955

  1 in total

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