Cargando…

MABGEL 1: First Phase 1 Trial of the Anti-HIV-1 Monoclonal Antibodies 2F5, 4E10 and 2G12 as a Vaginal Microbicide

BACKGROUND: Monoclonal antibodies (mAbs) which potently neutralize a broad range of HIV isolates are potential microbicide candidates. To date, topical application of mAbs in humans and their stability in vaginal secretions has not been studied. OBJECTIVES: To assess the pharmacokinetics and safety...

Descripción completa

Detalles Bibliográficos
Autores principales: Morris, Georgina C., Wiggins, Rebecca C., Woodhall, Sarah C., Bland, J. Martin, Taylor, Carol R., Jespers, Vicky, Vcelar, Brigitta A., Lacey, Charles J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4278856/
https://www.ncbi.nlm.nih.gov/pubmed/25546420
http://dx.doi.org/10.1371/journal.pone.0116153
_version_ 1782350586958577664
author Morris, Georgina C.
Wiggins, Rebecca C.
Woodhall, Sarah C.
Bland, J. Martin
Taylor, Carol R.
Jespers, Vicky
Vcelar, Brigitta A.
Lacey, Charles J.
author_facet Morris, Georgina C.
Wiggins, Rebecca C.
Woodhall, Sarah C.
Bland, J. Martin
Taylor, Carol R.
Jespers, Vicky
Vcelar, Brigitta A.
Lacey, Charles J.
author_sort Morris, Georgina C.
collection PubMed
description BACKGROUND: Monoclonal antibodies (mAbs) which potently neutralize a broad range of HIV isolates are potential microbicide candidates. To date, topical application of mAbs in humans and their stability in vaginal secretions has not been studied. OBJECTIVES: To assess the pharmacokinetics and safety of the mAbs 2F5, 4E10 and 2G12 when applied vaginally in women. DESIGN: A randomized, double-blind, placebo-controlled phase 1 trial. METHODS: Twenty-eight healthy, sexually abstinent women administered 2.5 g of gel daily for 12 days containing either 10 or 20 mg/g of each mAb (MABGEL) or placebo. Main clinical evaluations and sampling occurred at baseline, 1, 8, and 24 hours post-1(st) dose and 12 and 36 hours post-12(th) dose. RESULTS: After adjustment for dilution factors, median levels of 2F5, 4E10 and 2G12 in vaginal secretions at 1 hour post high-dose MABGEL were 7.74, 5.28 and 7.48 mg/ml respectively. Levels of 2F5 and 4E10 declined exponentially thereafter with similar estimated half-lives (4.6 and 4.3 hours). In contrast, 2G12 levels declined more rapidly in the first 8 hours, with an estimated half-life of 1.4 hours during this period. There was no evidence of systemic absorption. There were no significant differences in local or systemic adverse event rates or vaginal flora changes (by qPCR) between active and placebo gel arms. Whilst at least 1 adverse event was recorded in 96% of participants, 95% were mild and none were serious. CONCLUSIONS: Vaginal application of 50 mg of each mAb daily was safe over a 12 day period. Median mAb concentrations detected at 8 hours post dose were potentially sufficient to block HIV transmission.2G12 exhibited more rapid elimination from the human vagina than 4E10 and 2F5, likely due to poor stability of 2G12 in acidic human vaginal secretions. Further research is needed to develop mAb-based vaginal microbicides and delivery systems. TRIAL REGISTRATION: ISRCTN 64808733 UK CRN Portfolio 6470
format Online
Article
Text
id pubmed-4278856
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-42788562015-01-05 MABGEL 1: First Phase 1 Trial of the Anti-HIV-1 Monoclonal Antibodies 2F5, 4E10 and 2G12 as a Vaginal Microbicide Morris, Georgina C. Wiggins, Rebecca C. Woodhall, Sarah C. Bland, J. Martin Taylor, Carol R. Jespers, Vicky Vcelar, Brigitta A. Lacey, Charles J. PLoS One Research Article BACKGROUND: Monoclonal antibodies (mAbs) which potently neutralize a broad range of HIV isolates are potential microbicide candidates. To date, topical application of mAbs in humans and their stability in vaginal secretions has not been studied. OBJECTIVES: To assess the pharmacokinetics and safety of the mAbs 2F5, 4E10 and 2G12 when applied vaginally in women. DESIGN: A randomized, double-blind, placebo-controlled phase 1 trial. METHODS: Twenty-eight healthy, sexually abstinent women administered 2.5 g of gel daily for 12 days containing either 10 or 20 mg/g of each mAb (MABGEL) or placebo. Main clinical evaluations and sampling occurred at baseline, 1, 8, and 24 hours post-1(st) dose and 12 and 36 hours post-12(th) dose. RESULTS: After adjustment for dilution factors, median levels of 2F5, 4E10 and 2G12 in vaginal secretions at 1 hour post high-dose MABGEL were 7.74, 5.28 and 7.48 mg/ml respectively. Levels of 2F5 and 4E10 declined exponentially thereafter with similar estimated half-lives (4.6 and 4.3 hours). In contrast, 2G12 levels declined more rapidly in the first 8 hours, with an estimated half-life of 1.4 hours during this period. There was no evidence of systemic absorption. There were no significant differences in local or systemic adverse event rates or vaginal flora changes (by qPCR) between active and placebo gel arms. Whilst at least 1 adverse event was recorded in 96% of participants, 95% were mild and none were serious. CONCLUSIONS: Vaginal application of 50 mg of each mAb daily was safe over a 12 day period. Median mAb concentrations detected at 8 hours post dose were potentially sufficient to block HIV transmission.2G12 exhibited more rapid elimination from the human vagina than 4E10 and 2F5, likely due to poor stability of 2G12 in acidic human vaginal secretions. Further research is needed to develop mAb-based vaginal microbicides and delivery systems. TRIAL REGISTRATION: ISRCTN 64808733 UK CRN Portfolio 6470 Public Library of Science 2014-12-29 /pmc/articles/PMC4278856/ /pubmed/25546420 http://dx.doi.org/10.1371/journal.pone.0116153 Text en © 2014 Morris et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Morris, Georgina C.
Wiggins, Rebecca C.
Woodhall, Sarah C.
Bland, J. Martin
Taylor, Carol R.
Jespers, Vicky
Vcelar, Brigitta A.
Lacey, Charles J.
MABGEL 1: First Phase 1 Trial of the Anti-HIV-1 Monoclonal Antibodies 2F5, 4E10 and 2G12 as a Vaginal Microbicide
title MABGEL 1: First Phase 1 Trial of the Anti-HIV-1 Monoclonal Antibodies 2F5, 4E10 and 2G12 as a Vaginal Microbicide
title_full MABGEL 1: First Phase 1 Trial of the Anti-HIV-1 Monoclonal Antibodies 2F5, 4E10 and 2G12 as a Vaginal Microbicide
title_fullStr MABGEL 1: First Phase 1 Trial of the Anti-HIV-1 Monoclonal Antibodies 2F5, 4E10 and 2G12 as a Vaginal Microbicide
title_full_unstemmed MABGEL 1: First Phase 1 Trial of the Anti-HIV-1 Monoclonal Antibodies 2F5, 4E10 and 2G12 as a Vaginal Microbicide
title_short MABGEL 1: First Phase 1 Trial of the Anti-HIV-1 Monoclonal Antibodies 2F5, 4E10 and 2G12 as a Vaginal Microbicide
title_sort mabgel 1: first phase 1 trial of the anti-hiv-1 monoclonal antibodies 2f5, 4e10 and 2g12 as a vaginal microbicide
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4278856/
https://www.ncbi.nlm.nih.gov/pubmed/25546420
http://dx.doi.org/10.1371/journal.pone.0116153
work_keys_str_mv AT morrisgeorginac mabgel1firstphase1trialoftheantihiv1monoclonalantibodies2f54e10and2g12asavaginalmicrobicide
AT wigginsrebeccac mabgel1firstphase1trialoftheantihiv1monoclonalantibodies2f54e10and2g12asavaginalmicrobicide
AT woodhallsarahc mabgel1firstphase1trialoftheantihiv1monoclonalantibodies2f54e10and2g12asavaginalmicrobicide
AT blandjmartin mabgel1firstphase1trialoftheantihiv1monoclonalantibodies2f54e10and2g12asavaginalmicrobicide
AT taylorcarolr mabgel1firstphase1trialoftheantihiv1monoclonalantibodies2f54e10and2g12asavaginalmicrobicide
AT jespersvicky mabgel1firstphase1trialoftheantihiv1monoclonalantibodies2f54e10and2g12asavaginalmicrobicide
AT vcelarbrigittaa mabgel1firstphase1trialoftheantihiv1monoclonalantibodies2f54e10and2g12asavaginalmicrobicide
AT laceycharlesj mabgel1firstphase1trialoftheantihiv1monoclonalantibodies2f54e10and2g12asavaginalmicrobicide