Literature DB >> 31607605

Capsid containing virus like particle vaccine against Zika virus made from a stable cell line.

Himanshu Garg1, Tugba Mehmetoglu-Gurbuz2, Gregory M Ruddy2, Anjali Joshi3.   

Abstract

Zika virus infection during pregnancy is associated with severe birth defects including microcephaly in the new born. The lack of specific treatment calls for the development of a safe and effective vaccine for use in pregnant women. We recently tested the efficacy of a Virus Like Particle (VLP) vaccine for Zika virus in mice and found that Capsid-preMembrane-Env (CprME) VLPs generated a better neutralizing antibody response than preMembrane-Env (prME) VLPs. The superiority of CprME VLPs suggested that inclusion of capsid in the vaccine may enhance the immune response. However, production of CprME VLPs requires co-expression of NS2B-3 protease, which creates a major hurdle for generation of stable cell lines. To overcome this limitation, we generated a bicistronic vector that expresses CprME and NS2B-3 using an IRES sequence. This bicistronic expression cassette, in a lentiviral vector, was used to create a stable cell line that constitutively secretes CprME VLPs. The expression of NS2B-3, presence of capsid in the secreted VLPs, efficiency of VLP release, and stability of the cell line was extensively tested. Antigen sparing studies in mice using prME and CprME VLPs, both derived from stable cell lines, confirmed the superiority of CprME VLPs in generation of neutralizing antibody response. Capsid specific antibodies were detected in CprME VLP immunized mice providing mechanistic insights into the superiority of these VLPs. Challenge of CprME VLP immunized mice with Zika PRVABC59 showed complete protection against day 3 viremia further validating the efficacy of the vaccine. Our study is the first to generate a stable cell line secreting Zika CprME VLPs via natural NS2B-3 cleavage, demonstrate incorporation of capsid in CprME VLPs and complete protection in challenge studies. This is a major advancement for the Zika vaccine platform that is safe for use in pregnant women and readily scalable for use in developing countries.
Copyright © 2019 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  CprME; NS2B-3; Vaccine; Virus like particle; Zika; prME

Year:  2019        PMID: 31607605     DOI: 10.1016/j.vaccine.2019.09.093

Source DB:  PubMed          Journal:  Vaccine        ISSN: 0264-410X            Impact factor:   3.641


  5 in total

1.  Enhancement of Zika virus infection by antibodies from West Nile virus seropositive individuals with no history of clinical infection.

Authors:  Himanshu Garg; Rose Yeh; Douglas M Watts; Tugba Mehmetoglu-Gurbuz; Robert Resendes; Bruce Parsons; Fernando Gonzales; Anjali Joshi
Journal:  BMC Immunol       Date:  2021-01-09       Impact factor: 3.615

2.  Single dose of a replication-defective vaccinia virus expressing Zika virus-like particles is protective in mice.

Authors:  Brittany Jasperse; Caitlin M O'Connell; Yuxiang Wang; Paulo H Verardi
Journal:  Sci Rep       Date:  2021-03-22       Impact factor: 4.379

3.  Zika virus-like particle vaccine protects AG129 mice and rhesus macaques against Zika virus.

Authors:  Lo Vang; Christopher S Morello; Jason Mendy; Danielle Thompson; Darly Manayani; Ben Guenther; Justin Julander; Daniel Sanford; Amit Jain; Amish Patel; Paul Shabram; Jonathan Smith; Jeff Alexander
Journal:  PLoS Negl Trop Dis       Date:  2021-03-12

Review 4.  Virus-Like Particles: Revolutionary Platforms for Developing Vaccines Against Emerging Infectious Diseases.

Authors:  Hasnat Tariq; Sannia Batool; Saaim Asif; Mohammad Ali; Bilal Haider Abbasi
Journal:  Front Microbiol       Date:  2022-01-03       Impact factor: 5.640

5.  Humoral immune response induced with dengue virus-like particles serotypes 1 and 4 produced in silkworm.

Authors:  Doddy Irawan Setyo Utomo; Sabar Pambudi; Enoch Y Park
Journal:  AMB Express       Date:  2022-01-31       Impact factor: 3.298

  5 in total

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