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Review
. 2018 Oct 2;6(4):70.
doi: 10.3390/vaccines6040070.

Assay Challenges for Emerging Infectious Diseases: The Zika Experience

Affiliations
Review

Assay Challenges for Emerging Infectious Diseases: The Zika Experience

Christine C Roberts et al. Vaccines (Basel). .

Abstract

From the perspective of vaccine development, it is imperative to accurately diagnose target infections in order to exclude subjects with prior exposure from evaluations of vaccine effectiveness, to track incident infection during the course of a clinical trial and to differentiate immune reactions due to natural infections from responses that are vaccine related. When vaccine development is accelerated to a rapid pace in response to emerging infectious disease threats, the challenges to develop such diagnostic tools is even greater. This was observed through the recent expansion of Zika virus infections into the Western Hemisphere in 2014⁻2017. When initial Zika vaccine clinical trials were being designed and launched in response to the outbreak, there were no standardized sets of viral and immunological assays, and no approved diagnostic tests for Zika virus infection. The diagnosis of Zika virus infection is still an area of active research and development on many fronts. Here we review emerging infectious disease vaccine clinical assay development and trial execution with a special focus on the state of Zika virus clinical assays and diagnostics.

Keywords: clinical trials; emerging infectious disease; flaviviruses; immune response; vaccines; virus detection; zika virus.

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Conflict of interest statement

Authors are employees of GeneOne Life Science, Inc.

References

    1. Kudchodkar S.B., Choi H., Reuschel E.L., Esquivel R., Jin-Ah Kwon J., Jeong M., Maslow J.N., Reed C.C., White S., Kim J.J., et al. Rapid response to an emerging infectious disease—lessons learned from development of a synthetic DNA vaccine targeting Zika virus. Microbes Infect. 2018 doi: 10.1016/j.micinf.2018.03.001. - DOI - PMC - PubMed
    1. Tebas P., Roberts C.C., Muthumani K., Reuschel E.L., Kudchodkar S.B., Zaidi F.I., White S., Khan A.S., Racine T., Choi H., et al. Safety and immunogenicity of an anti-zika virus DNA vaccine—Preliminary report. N. Engl. J. Med. 2017 doi: 10.1056/NEJMoa1708120. - DOI - PMC - PubMed
    1. Maslow J.N. Vaccines for emerging infectious diseases: Lessons from MERS coronavirus and Zika virus. Hum. Vaccinnes. Immunother. 2017;13:2918–2930. doi: 10.1080/21645515.2017.1358325. - DOI - PMC - PubMed
    1. Madore D.V., Meade B.D., Rubin F., Deal C., Lynn F., Meeting C. Utilization of serologic assays to support efficacy of vaccines in nonclinical and clinical trials: Meeting at the crossroads. Vaccine. 2010;28:4539–4547. doi: 10.1016/j.vaccine.2010.04.094. - DOI - PMC - PubMed
    1. Plotkin S.A., Gilbert P.B. Nomenclature for immune correlates of protection after vaccination. Clin. Infect. Dis. 2012;54:1615–1617. doi: 10.1093/cid/cis238. - DOI - PMC - PubMed

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