Development of a nanoemulsion-adjuvanted prophylactic HSV-2 vaccine

Period of Performance: 03/01/2017 - 02/28/2018

$798K

Phase 2 SBIR

Recipient Firm

Nanobio Corporation
ANN ARBOR, MI 48105
Principal Investigator

Abstract

ABSTRACT Genital herpes simplex virus-2 (HSV-2) infections are a major public health problem affecting >40 million people in the United States and >500 million globally. HSV-2 infection causes recurring, genital sores that are painful and result in considerable psychological distress. Transmission can occur during sexual contact and from mother to child during birth with fatal consequences. There is no effective vaccine to prevent HSV-2. NanoBio Corporation is developing a novel, intranasal nanoemulsion (NE) vaccine that elicits serum neutralizing activity, a Th1 response, and Th17 cells for mucosal immunity, thereby offering protection systemically and at the site of HSV-2 entry through the mucosal surface. The proprietary oil-in-water NE has been shown to incorporate, deliver and adjuvant multiple different antigen types when administered by the intranasal route, thus enabling broad protection against both respiratory and sexually transmitted diseases. The NE adjuvant was formulated with protective gB2 and gD2 antigens for evaluation in the HSV-2 guinea pig challenge model. Data generated from two studies in this model demonstrated that: i. Intranasal immunization conferred favorable protection following HSV-2 challenge compared to intramuscular administration; ii. Robust protection was conferred even though intranasal immunization elicited lower serum antibody levels, indicating that additional mucosal immunity determinants are involved; iii. Incorporation of two glycoproteins, gB2 and gD2, into the NE vaccine was superior to gD2 antigen alone, a finding not observed with previous intramuscular vaccine candidates; and, iv. Intranasal immunization of the NE gB2/gD2 vaccine showed superior efficacy in the guinea pig model for prevention of infection, shedding, chronic recurrence, and viral latency, as compared to a conventional intramuscular gD2 vaccine formulated in alum and monophosphoryl lipid A (MPL). These data support the development of an intranasal NE gB2/gD2 vaccine to achieve protection against HSV- 2. In this Direct Phase II SBIR program, NanoBio will develop the research cell banks and the viral stock for production of gB2 and gD2 antigens, and develop upstream and downstream processes for antigen production, purification and scale-up to produce 10,000 vaccine doses (1 gram purified antigen). NanoBio simultaneously will develop the analytical methods required for final drug product release. A pre-IND meeting will be conducted with the FDA. After completion of this SBIR project, funding will be sought out to perform cGMP-compliant production of the vaccine, and an IND will be filed with the FDA to enable phase I/II clinical trials to assess safety, immunogenicity and preliminary efficacy of the NE vaccine to prevent HSV-2 infection in humans. A prophylactic NE gB2/gD2 genital herpes vaccine that induces both mucosal and systemic immunity will have great medical benefit in preventing HSV-2 infection in the United States and throughout the world.