Topical estrogen protects against SIV vaginal transmission without evidence of systemic effect

Accumulating data suggest that the state of the vaginal epithelium affects a woman's risk of HIV vaginal transmission and several human and non-human primate studies have shown that the rate of HIV or SIV vaginal transmission is decreased when estrogen is dominant. Systemic estrogen can protect...

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Veröffentlicht in:AIDS (London) 2004-08, Vol.18 (12), p.1637-1643
Hauptverfasser: SMITH, Stephen M, MEFFORD, Megan, SODORA, Donald, KLASE, Zachary, SINGH, Mahender, ALEXANDER, Nancy, HESS, David, MARX, Preston A
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container_end_page 1643
container_issue 12
container_start_page 1637
container_title AIDS (London)
container_volume 18
creator SMITH, Stephen M
MEFFORD, Megan
SODORA, Donald
KLASE, Zachary
SINGH, Mahender
ALEXANDER, Nancy
HESS, David
MARX, Preston A
description Accumulating data suggest that the state of the vaginal epithelium affects a woman's risk of HIV vaginal transmission and several human and non-human primate studies have shown that the rate of HIV or SIV vaginal transmission is decreased when estrogen is dominant. Systemic estrogen can protect against SIV vaginal transmission. To determine the safety and efficacy of topical estrogen in preventing SIV vaginal transmission. The non-human primate model of HIV vaginal transmission was used to assess vaginal estriol cream in ovariectomized macaques. Twelve macaques were treated intravaginally with estriol and eight with placebo cream twice a week. The vaginal and systemic effects of estriol were determined by colposcopy and serum luteinizing hormone, levels of which would decline in the presence of systemic estrogen. After 5 weeks of therapy, the animals were challenged vaginally with pathogenic SIVmac251. Vaginal estriol resulted in minimal serum estriol levels and had no effect on serum luteinizing hormone levels. Vaginal epithelia cornified and thickened significantly in response to estriol therapy. One of the estriol-treated animals became infected after this single challenge, while six of the control animals became infected (P = 0.0044). These data demonstrate that topical vaginal estriol can strongly protect against SIV vaginal transmission, while having no detectable systemic effect. These results support the study of topical vaginal estriol in preventing HIV vaginal transmission in at-risk women.
doi_str_mv 10.1097/01.aids.0000131393.76221.cc
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Systemic estrogen can protect against SIV vaginal transmission. To determine the safety and efficacy of topical estrogen in preventing SIV vaginal transmission. The non-human primate model of HIV vaginal transmission was used to assess vaginal estriol cream in ovariectomized macaques. Twelve macaques were treated intravaginally with estriol and eight with placebo cream twice a week. The vaginal and systemic effects of estriol were determined by colposcopy and serum luteinizing hormone, levels of which would decline in the presence of systemic estrogen. After 5 weeks of therapy, the animals were challenged vaginally with pathogenic SIVmac251. Vaginal estriol resulted in minimal serum estriol levels and had no effect on serum luteinizing hormone levels. Vaginal epithelia cornified and thickened significantly in response to estriol therapy. One of the estriol-treated animals became infected after this single challenge, while six of the control animals became infected (P = 0.0044). These data demonstrate that topical vaginal estriol can strongly protect against SIV vaginal transmission, while having no detectable systemic effect. 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Systemic estrogen can protect against SIV vaginal transmission. To determine the safety and efficacy of topical estrogen in preventing SIV vaginal transmission. The non-human primate model of HIV vaginal transmission was used to assess vaginal estriol cream in ovariectomized macaques. Twelve macaques were treated intravaginally with estriol and eight with placebo cream twice a week. The vaginal and systemic effects of estriol were determined by colposcopy and serum luteinizing hormone, levels of which would decline in the presence of systemic estrogen. After 5 weeks of therapy, the animals were challenged vaginally with pathogenic SIVmac251. Vaginal estriol resulted in minimal serum estriol levels and had no effect on serum luteinizing hormone levels. Vaginal epithelia cornified and thickened significantly in response to estriol therapy. One of the estriol-treated animals became infected after this single challenge, while six of the control animals became infected (P = 0.0044). These data demonstrate that topical vaginal estriol can strongly protect against SIV vaginal transmission, while having no detectable systemic effect. 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Aids</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>SMITH, Stephen M</creatorcontrib><creatorcontrib>MEFFORD, Megan</creatorcontrib><creatorcontrib>SODORA, Donald</creatorcontrib><creatorcontrib>KLASE, Zachary</creatorcontrib><creatorcontrib>SINGH, Mahender</creatorcontrib><creatorcontrib>ALEXANDER, Nancy</creatorcontrib><creatorcontrib>HESS, David</creatorcontrib><creatorcontrib>MARX, Preston A</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>AIDS (London)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>SMITH, Stephen M</au><au>MEFFORD, Megan</au><au>SODORA, Donald</au><au>KLASE, Zachary</au><au>SINGH, Mahender</au><au>ALEXANDER, Nancy</au><au>HESS, David</au><au>MARX, Preston A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Topical estrogen protects against SIV vaginal transmission without evidence of systemic effect</atitle><jtitle>AIDS (London)</jtitle><addtitle>AIDS</addtitle><date>2004-08-20</date><risdate>2004</risdate><volume>18</volume><issue>12</issue><spage>1637</spage><epage>1643</epage><pages>1637-1643</pages><issn>0269-9370</issn><eissn>1473-5571</eissn><abstract>Accumulating data suggest that the state of the vaginal epithelium affects a woman's risk of HIV vaginal transmission and several human and non-human primate studies have shown that the rate of HIV or SIV vaginal transmission is decreased when estrogen is dominant. 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These data demonstrate that topical vaginal estriol can strongly protect against SIV vaginal transmission, while having no detectable systemic effect. These results support the study of topical vaginal estriol in preventing HIV vaginal transmission in at-risk women.</abstract><cop>Hagerstown, MD</cop><pub>Lippincott Williams &amp; Wilkins</pub><pmid>15280774</pmid><doi>10.1097/01.aids.0000131393.76221.cc</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record>
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source Journals@Ovid Complete - AutoHoldings; MEDLINE; EZB-FREE-00999 freely available EZB journals
subjects Administration, Topical
AIDS/HIV
Animals
Antibodies, Viral - analysis
Biological and medical sciences
CD4 Lymphocyte Count
Colposcopy - methods
Disease Transmission, Infectious - prevention & control
Epithelium - drug effects
Estradiol - blood
Estriol - administration & dosage
Estriol - blood
Female
Human immunodeficiency virus
Human viral diseases
Infectious diseases
Luteinizing Hormone - blood
Macaca mulatta
Medical sciences
Ovariectomy
RNA - blood
Simian Acquired Immunodeficiency Syndrome - immunology
Simian Acquired Immunodeficiency Syndrome - transmission
Simian immunodeficiency virus
Vagina - drug effects
Viral diseases
Viral diseases of the lymphoid tissue and the blood. Aids
title Topical estrogen protects against SIV vaginal transmission without evidence of systemic effect
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