Abstract

Women globally need access to multipurpose prevention technologies (MPTs) that prevent human immunodeficiency virus (HIV), sexually transmitted infections that increase HIV acquisition/transmission risk, and unintended pregnancy. Seeking an MPT with activity against HIV, herpes simplex virus-2 (HSV-2), and human papillomavirus (HPV), we developed a prototype intravaginal ring (IVR), the MZCL IVR, which released the antiviral agents MIV-150, zinc acetate, and carrageenan (MZC for short) and the contraceptive levonorgestrel (LNG). Previously, we showed that an MZC gel has potent activity against immunodeficiency viruses, HSV-2, and HPV and that the MZCL (MZC with LNG) IVR releases all four components in macaques in vivo at levels associated with efficacy. Vaginal fluid from treated macaques has in vitro activity against HIV, HSV-2, and HPV. Herein, we assessed the ability of the MZCL IVR to protect macaques against repeated co-challenge with HSV-2 and SHIV-RT (simian immunodeficiency virus [SIV] containing the reverse transcriptase gene from HIV) and prevent hormonal cycling. We evaluated in vivo drug release in co-challenged macaques by measuring drug levels in blood and vaginal fluid and residual drug levels in used IVRs. The MZCL IVR significantly prevented SHIV-RT infection, reduced HSV-2 vaginal shedding, and prevented cycling. No non-nucleoside HIV reverse transcriptase inhibitor (NNRTI)-resistant SHIV was detected in macaques that became infected after continuous exposure to MZC from the IVR. Macaques wearing the MZCL IVR also had carrageenan levels in vaginal fluid expected to protect from HPV (extrapolated from mice) and LNG levels in blood associated with contraceptive efficacy. The MZCL IVR is a promising MPT candidate that warrants further development.

Highlights

  • The non-curable sexually transmitted infections (STIs) caused by human immunodeficiency virus (HIV), herpes simplex virus type 2 (HSV-2), and human papillomavirusDrug Deliv. and Transl

  • We provide the first evidence that an intravaginal ring (IVR) delivering the unique broad-spectrum MZC combination microbicide and the contraceptive LNG significantly protects macaques against repeated vaginal challenge with SHIV-RT without leading to nucleoside HIV reverse transcriptase inhibitor (NNRTI) resistance in breakthrough infections, significantly reduces HSV-2 shedding, produces vaginal levels of CG associated with protection from human papillomavirus (HPV), and suppresses macaque menstrual cycles

  • multipurpose prevention technologies (MPTs) IVR development requires a multipronged approach that aims to correlate in vivo biological effects in animal models with PK/PD and with IVR performance measures like in vitro and in vivo release profiles

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Summary

Introduction

The non-curable sexually transmitted infections (STIs) caused by human immunodeficiency virus (HIV), herpes simplex virus type 2 (HSV-2), and human papillomavirusDrug Deliv. and Transl. A safe, acceptable, affordable, and accessible self-initiated multipurpose prevention technology (MPT) that protects women against these four indications could significantly improve the health of women globally. A large number of topically applied vaginal formulations have been developed to meet end-user preferences for HIV prevention [2, 3]. These formulations can be broadly categorized as short-acting/on-demand (e.g., douches, films, gels, inserts, nanofibers) and long-acting/sustained release (e.g., intravaginal rings [IVRs]). Several gels and IVRs that release one or more anti-HIV drugs have demonstrated their potential utility by blocking immunodeficiency virus infection in preclinical models [2, 3] and have advanced beyond Phase 1 clinical testing

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