PRO 2000 elicits a decline in genital tract immune mediators without compromising intrinsic antimicrobial activity

Vaginal microbicides should protect against infection without disrupting the mucosal environment or its mediators of host defense. The objective of this study was to examine the effect of 14 daily applications of 0.5% PRO 2000 or placebo gel on mediators of mucosal immunity and intrinsic antimicrobi...

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Published in:AIDS (London) Vol. 21; no. 4; pp. 467 - 476
Main Authors: KELLER, Marla J, GUZMAN, Esmeralda, HOGARTY, Kathleen, HEROLD, Betsy C, HAZRATI, Ehsan, KASOWITZ, Andrea, CHESHENKO, Natalia, WALLENSTEIN, Sylvan, COLE, Amy L, COLE, Alexander M, PROFY, Albert T, WIRA, Charles R
Format: Journal Article
Language:English
Published: Hagerstown, MD Lippincott Williams & Wilkins 19-02-2007
Subjects:
HIV
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Abstract Vaginal microbicides should protect against infection without disrupting the mucosal environment or its mediators of host defense. The objective of this study was to examine the effect of 14 daily applications of 0.5% PRO 2000 or placebo gel on mediators of mucosal immunity and intrinsic antimicrobial activity. A randomized, prospective, double-blind, placebo-controlled study was conducted among 24 healthy, abstinent women. Levels of cytokines, chemokines, defensins, and other protective factors and intrinsic antimicrobial activity were determined in cervicovaginal lavage samples collected on study days 0, 7, 14, and 21. No increase in pro-inflammatory cytokines was observed. Rather cytokines and protective factors including interleukin (IL)-1 receptor antagonist, immunoglobulins and human beta-defensin 2 were lower in the drug compared with the placebo group. All of the mediators returned towards baseline on day 21. Women who were cycling had lower levels of most proteins on study days 7 and/or 14 compared with women on oral contraceptives; however, the magnitude of decline was greater in women who received PRO 2000 compared with placebo gel. The reduction in protective factors was not associated with a loss in the intrinsic anti-viral (HIV or herpes simplex virus) activity or anti-bacterial activity (Escherichia coli or Staphylococcus aureus). In contrast to experience with nonoxynol-9, PRO 2000 did not trigger an inflammatory response in cervicovaginal secretions. There was a modest reduction in mucosal immune mediators, but this loss was not associated with a reduction in intrinsic antimicrobial activity.
AbstractList Vaginal microbicides should protect against infection without disrupting the mucosal environment or its mediators of host defense. The objective of this study was to examine the effect of 14 daily applications of 0.5% PRO 2000 or placebo gel on mediators of mucosal immunity and intrinsic antimicrobial activity. A randomized, prospective, double-blind, placebo-controlled study was conducted among 24 healthy, abstinent women. Levels of cytokines, chemokines, defensins, and other protective factors and intrinsic antimicrobial activity were determined in cervicovaginal lavage samples collected on study days 0, 7, 14, and 21. No increase in pro-inflammatory cytokines was observed. Rather cytokines and protective factors including interleukin (IL)-1 receptor antagonist, immunoglobulins and human beta-defensin 2 were lower in the drug compared with the placebo group. All of the mediators returned towards baseline on day 21. Women who were cycling had lower levels of most proteins on study days 7 and/or 14 compared with women on oral contraceptives; however, the magnitude of decline was greater in women who received PRO 2000 compared with placebo gel. The reduction in protective factors was not associated with a loss in the intrinsic anti-viral (HIV or herpes simplex virus) activity or anti-bacterial activity (Escherichia coli or Staphylococcus aureus). In contrast to experience with nonoxynol-9, PRO 2000 did not trigger an inflammatory response in cervicovaginal secretions. There was a modest reduction in mucosal immune mediators, but this loss was not associated with a reduction in intrinsic antimicrobial activity.
OBJECTIVEVaginal microbicides should protect against infection without disrupting the mucosal environment or its mediators of host defense. The objective of this study was to examine the effect of 14 daily applications of 0.5% PRO 2000 or placebo gel on mediators of mucosal immunity and intrinsic antimicrobial activity.DESIGN AND METHODSA randomized, prospective, double-blind, placebo-controlled study was conducted among 24 healthy, abstinent women. Levels of cytokines, chemokines, defensins, and other protective factors and intrinsic antimicrobial activity were determined in cervicovaginal lavage samples collected on study days 0, 7, 14, and 21.RESULTSNo increase in pro-inflammatory cytokines was observed. Rather cytokines and protective factors including interleukin (IL)-1 receptor antagonist, immunoglobulins and human beta-defensin 2 were lower in the drug compared with the placebo group. All of the mediators returned towards baseline on day 21. Women who were cycling had lower levels of most proteins on study days 7 and/or 14 compared with women on oral contraceptives; however, the magnitude of decline was greater in women who received PRO 2000 compared with placebo gel. The reduction in protective factors was not associated with a loss in the intrinsic anti-viral (HIV or herpes simplex virus) activity or anti-bacterial activity (Escherichia coli or Staphylococcus aureus).CONCLUSIONIn contrast to experience with nonoxynol-9, PRO 2000 did not trigger an inflammatory response in cervicovaginal secretions. There was a modest reduction in mucosal immune mediators, but this loss was not associated with a reduction in intrinsic antimicrobial activity.
Objective: Vaginal microbicides should protect against infection without disrupting the mucosal environment or its mediators of host defense. The objective of this study was to examine the effect of 14 daily applications of 0.5% PRO 2000 or placebo gel on mediators of mucosal immunity and intrinsic antimicrobial activity. Design and methods: A randomized, prospective, double-blind, placebo-controlled study was conducted among 24 healthy, abstinent women. Levels of cytokines, chemokines, defensins, and other protective factors and intrinsic antimicrobial activity were determined in cervicovaginal lavage samples collected on study days 0, 7, 14, and 21. Results: No increase in pro-inflammatory cytokines was observed. Rather cytokines and protective factors including interleukin (IL)-1 receptor antagonist, immunoglobu-lins and human beta-defensin 2 were lower in the drug compared with the placebo group. All of the mediators returned towards baseline on day 21. Women who were cycling had lower levels of most proteins on study days 7 and/or 14 compared with women on oral contraceptives; however, the magnitude of decline was greater in women who received PRO 2000 compared with placebo gel. The reduction in protective factors was not associated with a loss in the intrinsic anti-viral (HIV or herpes simplex virus) activity or anti-bacterial activity (Escherichia coli or Staphylococcus aureus). Conclusion: In contrast to experience with nonoxynol-9, PRO 2000 did not trigger an inflammatory response in cervicovaginal secretions. There was a modest reduction in mucosal immune mediators, but this loss was not associated with a reduction in intrinsic antimicrobial activity.
Author HEROLD, Betsy C
HAZRATI, Ehsan
PROFY, Albert T
COLE, Alexander M
CHESHENKO, Natalia
WALLENSTEIN, Sylvan
KELLER, Marla J
GUZMAN, Esmeralda
WIRA, Charles R
COLE, Amy L
KASOWITZ, Andrea
HOGARTY, Kathleen
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  fullname: GUZMAN, Esmeralda
  organization: Department of Pediatrics, Mount Sinai School of Medicine, New York, New York, United States
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  givenname: Kathleen
  surname: HOGARTY
  fullname: HOGARTY, Kathleen
  organization: Department of Medicine, Mount Sinai School of Medicine, New York, New York, United States
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  givenname: Betsy C
  surname: HEROLD
  fullname: HEROLD, Betsy C
  organization: Department of Pediatrics, Mount Sinai School of Medicine, New York, New York, United States
– sequence: 5
  givenname: Ehsan
  surname: HAZRATI
  fullname: HAZRATI, Ehsan
  organization: Department of Pediatrics, Mount Sinai School of Medicine, New York, New York, United States
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  givenname: Andrea
  surname: KASOWITZ
  fullname: KASOWITZ, Andrea
  organization: Department of Medicine, Mount Sinai School of Medicine, New York, New York, United States
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  givenname: Natalia
  surname: CHESHENKO
  fullname: CHESHENKO, Natalia
  organization: Department of Pediatrics, Mount Sinai School of Medicine, New York, New York, United States
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  givenname: Sylvan
  surname: WALLENSTEIN
  fullname: WALLENSTEIN, Sylvan
  organization: Department of community Medicine, Mount Sinai School of Medicine, New York, New York, United States
– sequence: 9
  givenname: Amy L
  surname: COLE
  fullname: COLE, Amy L
  organization: Department of Molecular Biology and Microbiology, University of Central Florida, Orlando, Florida, United States
– sequence: 10
  givenname: Alexander M
  surname: COLE
  fullname: COLE, Alexander M
  organization: Department of Molecular Biology and Microbiology, University of Central Florida, Orlando, Florida, United States
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  givenname: Albert T
  surname: PROFY
  fullname: PROFY, Albert T
  organization: Indevus Pharmaceuticals Inc, Lexington, Massachusetts, United States
– sequence: 12
  givenname: Charles R
  surname: WIRA
  fullname: WIRA, Charles R
  organization: Department of Physiology, Dartmouth Medical School, Lebanon, New Hampshire, United States
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IsPeerReviewed true
IsScholarly true
Issue 4
Keywords Escherichia coli
Mucosa
Uterine cervix
Genital herpes
Antimicrobial agent
innate immunity
Bacteria
Micrococcales
Micrococcaceae
cytokines
Staphylococcus aureus
Enterobacteriaceae
Immunopathology
defensins
microbicides
Genital system
Cytokine
Vagina
AIDS
Immune deficiency
Infection
Virus
Sexually transmitted disease
HIV
Viral disease
Bacteriosis
Mediator
Defensin
Language English
License CC BY 4.0
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PublicationTitle AIDS (London)
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Snippet Vaginal microbicides should protect against infection without disrupting the mucosal environment or its mediators of host defense. The objective of this study...
Objective: Vaginal microbicides should protect against infection without disrupting the mucosal environment or its mediators of host defense. The objective of...
OBJECTIVEVaginal microbicides should protect against infection without disrupting the mucosal environment or its mediators of host defense. The objective of...
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StartPage 467
SubjectTerms Administration, Intravaginal
Adolescent
Adult
AIDS/HIV
Anti-Infective Agents, Local - administration & dosage
Anti-Infective Agents, Local - pharmacology
Antiviral Agents - administration & dosage
Antiviral Agents - pharmacology
Biological and medical sciences
Chemokines - biosynthesis
Cytokines - biosynthesis
Defensins - biosynthesis
Double-Blind Method
Drug Administration Schedule
Escherichia coli
Female
Herpes Genitalis - prevention & control
Herpes simplex virus
HIV Infections - prevention & control
Human immunodeficiency virus
Human viral diseases
Humans
Immunity, Mucosal - drug effects
Immunodeficiencies
Immunodeficiencies. Immunoglobulinopathies
Immunopathology
Infectious diseases
Inflammation Mediators - metabolism
Medical sciences
Middle Aged
Naphthalenesulfonates - administration & dosage
Naphthalenesulfonates - pharmacology
Polymers - administration & dosage
Polymers - pharmacology
Staphylococcus aureus
Therapeutic Irrigation
Vagina - immunology
Vagina - metabolism
Vaginal Creams, Foams, and Jellies
Viral diseases
Viral diseases of the genital and urinary system
Viral diseases of the lymphoid tissue and the blood. Aids
Title PRO 2000 elicits a decline in genital tract immune mediators without compromising intrinsic antimicrobial activity
URI https://www.ncbi.nlm.nih.gov/pubmed/17301565
https://search.proquest.com/docview/19776025
https://search.proquest.com/docview/69003987
Volume 21
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