It appears you don't have support to open PDFs in this web browser. To view this file, Open with your PDF reader
Abstract
Zika virus (ZIKV) is a mosquito-borne arbovirus that can cause severe congenital birth defects. The utmost goal of ZIKV vaccines is to prevent both maternal-fetal infection and congenital Zika syndrome. A Zika purified inactivated virus (ZPIV) was previously shown to be protective in non-pregnant mice and rhesus macaques. In this study, we further examined the efficacy of ZPIV against ZIKV infection during pregnancy in immunocompetent C57BL6 mice and common marmoset monkeys (Callithrix jacchus). We showed that, in C57BL/6 mice, ZPIV significantly reduced ZIKV-induced fetal malformations. Protection of fetuses was positively correlated with virus-neutralizing antibody levels. In marmosets, the vaccine prevented vertical transmission of ZIKV and elicited neutralizing antibodies that remained above a previously determined threshold of protection for up to 18 months. These proof-of-concept studies demonstrate ZPIV’s protective efficacy is both potent and durable and has the potential to prevent the harmful consequence of ZIKV infection during pregnancy.
You have requested "on-the-fly" machine translation of selected content from our databases. This functionality is provided solely for your convenience and is in no way intended to replace human translation. Show full disclaimer
Neither ProQuest nor its licensors make any representations or warranties with respect to the translations. The translations are automatically generated "AS IS" and "AS AVAILABLE" and are not retained in our systems. PROQUEST AND ITS LICENSORS SPECIFICALLY DISCLAIM ANY AND ALL EXPRESS OR IMPLIED WARRANTIES, INCLUDING WITHOUT LIMITATION, ANY WARRANTIES FOR AVAILABILITY, ACCURACY, TIMELINESS, COMPLETENESS, NON-INFRINGMENT, MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE. Your use of the translations is subject to all use restrictions contained in your Electronic Products License Agreement and by using the translation functionality you agree to forgo any and all claims against ProQuest or its licensors for your use of the translation functionality and any output derived there from. Hide full disclaimer
Details

















1 Trudeau Institute, Inc., Saranac Lake, USA (GRID:grid.250945.f) (ISNI:0000 0004 0462 7513)
2 Walter Reed Army Institute of Research, Pilot Bioproduction Facility, Center for Enabling Capabilities, Silver Spring, USA (GRID:grid.507680.c) (ISNI:0000 0001 2230 3166)
3 Texas Biomedical Research Institute, Southwest National Primate Center, San Antonio, USA (GRID:grid.250889.e) (ISNI:0000 0001 2215 0219)
4 University of Illinois Chicago, Department of Human Development Nursing Science, College of Nursing, Chicago, USA (GRID:grid.185648.6) (ISNI:0000 0001 2175 0319)
5 University of California, Department of Pathology, Microbiology and Immunology, School of Veterinary Medicine, Davis, USA (GRID:grid.27860.3b) (ISNI:0000 0004 1936 9684)
6 University of California at San Francisco, Department of Laboratory Medicine, School of Medicine, San Francisco, USA (GRID:grid.266102.1) (ISNI:0000 0001 2297 6811); University of California at Berkeley, Division of Infectious Diseases and Vaccinology, School of Public Health, Berkeley, USA (GRID:grid.47840.3f) (ISNI:0000 0001 2181 7878)
7 University of California at San Francisco, Department of Laboratory Medicine, School of Medicine, San Francisco, USA (GRID:grid.266102.1) (ISNI:0000 0001 2297 6811)
8 State University of New York, Upstate Medical University, Division of Infectious Diseases, Institute for Global Health and Translational Sciences, Syracuse, USA (GRID:grid.411023.5) (ISNI:0000 0000 9159 4457)
9 Walter Reed Army Institute of Research, Emerging Infectious Diseases Branch, Silver Spring, USA (GRID:grid.507680.c) (ISNI:0000 0001 2230 3166)