Literature DB >> 16305508

Microbicides for prevention of transmission of sexually transmitted diseases.

Mary K Howett1, Jeffrey P Kuhl.   

Abstract

In the last 50 years, changes in cultural and scientific realities and customs have resulted in a worldwide epidemic of sexually transmitted diseases (STD). This is a multi-factorial problem resulting in part from: 1) an increased permissiveness in sexual attitudes in the Western world that results in earlier onset of intercourse and increased numbers of partners and types of sex acts; 2) a global transportation network that facilitates contacts and interactions between urban and rural areas as well as between countries resulting in migration and spread of infections; 3) an emergence of new and mutated forms of pathogens with increased capabilities to cause infections and for which there are no available vaccines or therapies; and, 4) at risk populations in developing countries who are susceptible to these pathogens while having societal infrastructures that lack basic health education and proper access to healthcare. Overwhelming examples of increasing and emerging STD pathogens exist in the early twenty-first century. These include human immunodeficiency virus type 1 (HIV-1), the causative agent of acquired immunodeficiency syndrome (AIDS), with over 42 million current cases of infection, 20 million deaths to date, and an estimated 500,000 deaths per year; human papillomavirus (HPV) infections, the causative agents of genital warts and cervical cancer, with approximately 1 in 4 women harboring virus DNA in genital epithelium, 1-3 percent of women showing symptoms of infection and 250,000 deaths per year in women worldwide from cervical cancer; and numerous others. Topical microbicides have been proposed as agents to break the chain of transmission in these infections by providing chemical, biological, and/or physical barriers to infection by blocking and/or inactivating pathogens at the mucosal surface where infection can occur. For many sexually transmitted infections, vaccines do not exist, and therapeutic agents are only partially effective, expensive, and difficult to distribute. In addition, female partners in many relationships do not control pregnancy or STD risk and may benefit from discrete methods, other than condoms, that would provide protection. Thus, microbicides should be valuable additions to preventing these diseases if they can be shown effective. Currently, 62 microbicides are in development with 6 entering Phase III clinical trials, 11 entering Phase I clinical trials, and 44 in pre-clinical development. In this review, we will describe many of the principles of microbicide mechanisms and give examples of major types of microbicides and their actions. Space precludes a complete description of all of the agents and their mechanisms of action. We will also put forth the argument for alkyl sulfate microbicides, including sodium dodecyl sulfate (SDS), agents that are in active development in our laboratories.

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Year:  2005        PMID: 16305508     DOI: 10.2174/138161205774580633

Source DB:  PubMed          Journal:  Curr Pharm Des        ISSN: 1381-6128            Impact factor:   3.116


  12 in total

1.  Protection of mice from a Chlamydia trachomatis vaginal infection using a Salicylidene acylhydrazide, a potential microbicide.

Authors:  Anatoly Slepenkin; Hencelyn Chu; Mikael Elofsson; Pia Keyser; Ellena M Peterson
Journal:  J Infect Dis       Date:  2011-09-20       Impact factor: 5.226

2.  Adolescent girls' communication with "mothers" about topical microbicides.

Authors:  Punita K Sunder; Stephanie Ramos; Mary B Short; Susan L Rosenthal
Journal:  J Pediatr Adolesc Gynecol       Date:  2006-12       Impact factor: 1.814

3.  Enhanced removal of a human norovirus surrogate from fresh vegetables and fruits by a combination of surfactants and sanitizers.

Authors:  Ashley Predmore; Jianrong Li
Journal:  Appl Environ Microbiol       Date:  2011-05-27       Impact factor: 4.792

4.  Novel antivirals inhibit early steps in HPV infection.

Authors:  Hao-Shun Huang; Dohun Pyeon; Shane M Pearce; Simon M Lank; Laura M Griffin; Paul Ahlquist; Paul F Lambert
Journal:  Antiviral Res       Date:  2011-12-16       Impact factor: 5.970

5.  Candidate vaginal microbicides with activity against Chlamydia trachomatis and Neisseriagonorrhoeae.

Authors:  Hencelyn Chu; Anatoly Slepenkin; Mikael Elofsson; Pia Keyser; Luis M de la Maza; Ellena M Peterson
Journal:  Int J Antimicrob Agents       Date:  2010-06-01       Impact factor: 5.283

6.  Relationship context associated with microbicide-like product use.

Authors:  Mary B Short; Susan L Rosenthal; Beth A Auslander; Paul A Succop
Journal:  J Pediatr Adolesc Gynecol       Date:  2009-07-09       Impact factor: 1.814

7.  Carrageenan is a potent inhibitor of papillomavirus infection.

Authors:  Christopher B Buck; Cynthia D Thompson; Jeffrey N Roberts; Martin Müller; Douglas R Lowy; John T Schiller
Journal:  PLoS Pathog       Date:  2006-07       Impact factor: 6.823

8.  Microbicides and HIV: A Review and an update.

Authors:  Smriti Naswa; Y S Marfatia; T L N Prasad
Journal:  Indian J Sex Transm Dis AIDS       Date:  2012-07

9.  Multicompartmental pharmacokinetic model of tenofovir delivery by a vaginal gel.

Authors:  Yajing Gao; David F Katz
Journal:  PLoS One       Date:  2013-09-11       Impact factor: 3.240

10.  Establishment of human papillomavirus infection requires cell cycle progression.

Authors:  Dohun Pyeon; Shane M Pearce; Simon M Lank; Paul Ahlquist; Paul F Lambert
Journal:  PLoS Pathog       Date:  2009-02-27       Impact factor: 6.823

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