Zika purified inactivated virus (ZPIV) vaccine reduced vertical transmission in pregnant immunocompetent mice

Author:

Kim In-JeongORCID,Tighe Michael P.ORCID,Lanthier Paula A.,Clark Madeline J.,De La Barrera Rafael A.,Dussupt VincentORCID,Mendez-Rivera Letzibeth,Krebs Shelly J.ORCID,Travis Kelsey L.ORCID,Low-Beer Timothy C.ORCID,Cookenham Tres S.ORCID,Lanzer Kathleen G.ORCID,Bernacki Derek T.ORCID,Szaba Frank M.,Schneck Amanda A.ORCID,Ward JerroldORCID,Thomas Stephen J.ORCID,Modjarrad KayvonORCID,Blackman Marcia A.ORCID

Abstract

AbstractZika virus (ZIKV) is a significant threat to pregnant women and their fetuses as it can cause severe birth defects and congenital neurodevelopmental disorders, referred to as congenital Zika syndrome (CZS). Thus, a safe and effective ZIKV vaccine for pregnant women to prevent in utero ZIKV infection is of utmost importance. Murine models of ZIKV infection are limited by the fact that immunocompetent mice are resistant to ZIKV infection. As such, interferon-deficient mice have been used in some preclinical studies to test the efficacy of ZIKV vaccine candidates against lethal virus challenge. However, interferon-deficient mouse models have limitations in assessing the immunogenicity of vaccines, necessitating the use of immunocompetent mouse pregnancy models. Using the human stat2 knock-in (hSTAT2KI) mouse pregnancy model, we show that vaccination with a purified formalin-inactivated Zika virus (ZPIV) vaccine prior to pregnancy successfully prevented vertical transmission. In addition, maternal immunity protected offspring against postnatal challenge for up to 28 days. Furthermore, passive transfer of human IgG purified from hyper-immune sera of ZPIV vaccinees prevented maternal and fetal ZIKV infection, providing strong evidence that the neutralizing antibody response may serve as a meaningful correlate of protection.

Funder

U.S. Department of Defense

Trudeau Institute, Inc. Internal fund, TRN-UPSOO.

Publisher

Springer Science and Business Media LLC

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