Literature DB >> 1664123

Introduction: objectives of herpes simplex virus vaccines seen from a historical perspective.

B Roizman1.   

Abstract

Herpes simplex virus (HSV) types 1 and 2 cause a variety of severe manifestations in humans. A major characteristic of HSVs is their ability to establish latent infection in sensory ganglia, where these viruses are shielded from the immune system and are impervious to the action of antiviral drugs known to date. Ideally, HSV-induced clinical syndromes should be prevented by vaccination, but two major problems arise. First, although many antiviral vaccines have successfully prevented disease, none have prevented infection. Once the virus infects cells at the portal of entry of the infection, it can establish latent infection in sensory neurons that innervate the cell. Second, while HSV disease primarily affects adults greater than 18 years of age, mass immunization in the United States is effectively carried out in the interval between nursery school and high school, and yet the vaccines must confer protection for a long time after vaccination. The central issues involved in the development of an anti-HSV vaccine include what type of vaccine should be developed, what we should expect from an HSV vaccine, and how we should monitor the effectiveness of the vaccine.

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Year:  1991        PMID: 1664123     DOI: 10.1093/clind/13.supplement_11.s892

Source DB:  PubMed          Journal:  Rev Infect Dis        ISSN: 0162-0886


  8 in total

1.  HSV Recombinant Vectors for Gene Therapy.

Authors:  Roberto Manservigi; Rafaela Argnani; Peggy Marconi
Journal:  Open Virol J       Date:  2010-06-18

2.  Immunization with DNA vaccines encoding glycoprotein D or glycoprotein B, alone or in combination, induces protective immunity in animal models of herpes simplex virus-2 disease.

Authors:  W L McClements; M E Armstrong; R D Keys; M A Liu
Journal:  Proc Natl Acad Sci U S A       Date:  1996-10-15       Impact factor: 11.205

3.  Immunization with an acellular vaccine consisting of the outer membrane complex of Chlamydia trachomatis induces protection against a genital challenge.

Authors:  S Pal; I Theodor; E M Peterson; L M de la Maza
Journal:  Infect Immun       Date:  1997-08       Impact factor: 3.441

4.  Intranasal immunization induces long-term protection in mice against a Chlamydia trachomatis genital challenge.

Authors:  S Pal; E M Peterson; L M de la Maza
Journal:  Infect Immun       Date:  1996-12       Impact factor: 3.441

5.  Protection against infertility in a BALB/c mouse salpingitis model by intranasal immunization with the mouse pneumonitis biovar of Chlamydia trachomatis.

Authors:  S Pal; T J Fielder; E M Peterson; L M de la Maza
Journal:  Infect Immun       Date:  1994-08       Impact factor: 3.441

6.  Correlation between precolonization of trigeminal ganglia by attenuated strains of pseudorabies virus and resistance to wild-type virus latency.

Authors:  L M Schang; G F Kutish; F A Osorio
Journal:  J Virol       Date:  1994-12       Impact factor: 5.103

7.  Induction of protective immunity against a Chlamydia trachomatis genital infection in three genetically distinct strains of mice.

Authors:  Sukumar Pal; Ellena M Peterson; Luis M de la Maza
Journal:  Immunology       Date:  2003-11       Impact factor: 7.397

8.  Immunization with replication-defective mutants of herpes simplex virus type 1: sites of immune intervention in pathogenesis of challenge virus infection.

Authors:  L A Morrison; D M Knipe
Journal:  J Virol       Date:  1994-02       Impact factor: 5.103

  8 in total

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