Passive immunisation of convalescent human anti-Zika plasma protects against challenge with New World Zika virus in cynomolgus macaques

Neil Berry*, Sarah Kempster, Claire Ham, Adrian Jenkins, Jo Hall, Mark Page, Giada Mattiuzzo, Yemisi Adedeji, Roger Hewson, Elaine Giles, Debbie Ferguson, Neil Almond

*Corresponding author for this work

    Research output: Contribution to journalArticlepeer-review

    8 Citations (Scopus)

    Abstract

    Zika virus (ZIKV) causes neurological complications in susceptible individuals, highlighted in the recent South American epidemic. Natural ZIKV infection elicits host responses capable of preventing subsequent re-infection, raising expectations for effective vaccination. Defining protective immune correlates will inform viral intervention strategies, particularly vaccine development. Non-human primate (NHP) species are susceptible to ZIKV and represent models for vaccine development. The protective efficacy of a human anti-ZIKV convalescent plasma pool (16/320-14) developed as a candidate reference material for a WHO International Standard was evaluated in macaques. Convalescent plasma administered to four cynomolgus macaques (Macaca fascicularis) intra-peritoneally 24 hrs prior to sub-cutaneous challenge with 103 pfu ZIKVPRVABC59 protected against detectable infection, with absence of detectable ZIKV RNA in blood and lymphoid tissues. Passively immunised anti-ZIKV immunoglobulin administered prior to time of challenge remained present only at very low levels 42 days post-challenge. Absence of de novo antibody responses in passively immunised macaques indicate sterilising immunity compared with naïve challenge controls that exhibited active ZIKV-specific IgM and IgG responses post-challenge. Demonstration that the presence of convalescent anti-ZIKV at levels of 400 IU/mL neutralising antibody protects against virus challenge provides a scientific framework for development of anti-ZIKV vaccines and facilitates regulatory approval.

    Original languageEnglish
    Article number86
    Journalnpj Vaccines
    Volume5
    Issue number1
    DOIs
    Publication statusPublished - 1 Dec 2020

    Bibliographical note

    Funding Information:
    We thank staff of NIBSC Biological Services Division for their support and expertise. This paper is based on independent research commissioned and funded by the NIHR Policy Research Programme (NIBSC Regulatory Science Research Unit). The views expressed in the publication are those of the authors and not necessarily those of the NHS, the NIHR, the Department of Health, “arms” length bodies, or other government departments. This study was funded in part by a grant from Innovate UK, Serological Vaccines Standards for Emerging Diseases, Grant No: 97163.

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