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 |
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Hagerstown, MD
Lippincott Williams & Wilkins
19-02-2007
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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. |
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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 |
Author_xml | – sequence: 1 givenname: Marla J surname: KELLER fullname: KELLER, Marla J organization: Department of Medicine, Mount Sinai School of Medicine, New York, New York, United States – sequence: 2 givenname: Esmeralda surname: GUZMAN fullname: GUZMAN, Esmeralda organization: Department of Pediatrics, Mount Sinai School of Medicine, New York, New York, United States – sequence: 3 givenname: Kathleen surname: HOGARTY fullname: HOGARTY, Kathleen organization: Department of Medicine, Mount Sinai School of Medicine, New York, New York, United States – sequence: 4 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 – sequence: 6 givenname: Andrea surname: KASOWITZ fullname: KASOWITZ, Andrea organization: Department of Medicine, Mount Sinai School of Medicine, New York, New York, United States – sequence: 7 givenname: Natalia surname: CHESHENKO fullname: CHESHENKO, Natalia organization: Department of Pediatrics, Mount Sinai School of Medicine, New York, New York, United States – sequence: 8 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 – sequence: 11 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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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 |
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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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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 |
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