Literature DB >> 10195045

Control of STDs--the role of prophylactic vaccines against herpes simplex virus.

L R Stanberry1.   

Abstract

OBJECTIVES: To summarise the current status of genital herpes simplex virus (HSV) vaccine development and provide a discussion of the potential benefits and limitations of genital herpes vaccines.
METHODS: Literature review.
RESULTS: Genital herpes simplex virus infection has a complex pathogenesis that has contributed to it becoming a serious worldwide problem. In an attempt to control the problem five different types of genital herpes vaccines have been developed. These include inactivated virion derived vaccines, adjuvanted subunit vaccines, vectored vaccines, replication limited live viral vaccines, genetically attenuated live viral vaccines, and nucleic acid vaccines. While available commercially in some parts of the world, inactivated virion derived vaccines have not been proved effective. Of the others, adjuvanted subunit vaccines, replication limited live viral vaccines, and nucleic acid vaccines are currently in clinical trials and vectored vaccines and genetically attenuated live viral vaccines are in preclinical development.
CONCLUSION: With regard to HSV vaccines in general, it is reasonable to expect that the newer vaccines may protect the individual from developing symptomatic genital herpes but may not protect against asymptomatic viral infection. With widespread use HSV vaccines might help to prevent the spread of genital herpes.

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Year:  1998        PMID: 10195045      PMCID: PMC1758161          DOI: 10.1136/sti.74.6.391

Source DB:  PubMed          Journal:  Sex Transm Infect        ISSN: 1368-4973            Impact factor:   3.519


  34 in total

1.  Report of twelve years experience in open study of Skinner herpes simplex vaccine towards prevention of herpes genitalis.

Authors:  G R Skinner; C Fink; J Melling; C Wiblin; B Thornton; J Hallworth; W Gardner; P McLeish; C Hartley; A Buchan
Journal:  Med Microbiol Immunol       Date:  1992       Impact factor: 3.402

2.  Preinfection prophylaxis with herpes simplex virus glycoprotein immunogens: factors influencing efficacy.

Authors:  L R Stanberry; M G Myers; D E Stephanopoulos; R L Burke
Journal:  J Gen Virol       Date:  1989-12       Impact factor: 3.891

3.  Thymidine kinase-deficient herpes simplex virus type 2 genital infection in guinea pigs.

Authors:  L R Stanberry; S Kit; M G Myers
Journal:  J Virol       Date:  1985-08       Impact factor: 5.103

4.  Efficacy of HSV-1 ISCOM vaccine in the guinea-pig model of HSV-2 infection.

Authors:  M Erturk; R J Phillpotts; M J Welch; R Jennings
Journal:  Vaccine       Date:  1991-10       Impact factor: 3.641

5.  Preparation and immunogenicity of vaccine Ac NFU1 (S-) MRC towards the prevention of herpes genitalis.

Authors:  G R Skinner; C B Woodman; C E Hartley; A Buchan; A Fuller; J Durham; M Synnott; J C Clay; J Melling; C Wiblin; J Wilkins
Journal:  Br J Vener Dis       Date:  1982-12

6.  Vaccination with recombinant herpes simplex virus glycoproteins: protection against initial and recurrent genital herpes.

Authors:  L R Stanberry; D I Bernstein; R L Burke; C Pachl; M G Myers
Journal:  J Infect Dis       Date:  1987-05       Impact factor: 5.226

7.  In vivo behavior of genetically engineered herpes simplex viruses R7017 and R7020: construction and evaluation in rodents.

Authors:  B Meignier; R Longnecker; B Roizman
Journal:  J Infect Dis       Date:  1988-09       Impact factor: 5.226

8.  Double-blind, placebo-controlled trial of a herpes simplex virus type 2 glycoprotein vaccine in persons at high risk for genital herpes infection.

Authors:  G J Mertz; R Ashley; R L Burke; J Benedetti; C Critchlow; C C Jones; L Corey
Journal:  J Infect Dis       Date:  1990-04       Impact factor: 5.226

9.  Genital herpes in guinea pigs: pathogenesis of the primary infection and description of recurrent disease.

Authors:  L R Stanberry; E R Kern; J T Richards; T M Abbott; J C Overall
Journal:  J Infect Dis       Date:  1982-09       Impact factor: 5.226

10.  T lymphocytes are required for protection of the vaginal mucosae and sensory ganglia of immune mice against reinfection with herpes simplex virus type 2.

Authors:  G N Milligan; D I Bernstein; N Bourne
Journal:  J Immunol       Date:  1998-06-15       Impact factor: 5.422

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