Skip to main content
Oxford University Press - PMC COVID-19 Collection logoLink to Oxford University Press - PMC COVID-19 Collection
. 2022 Jan 25:jiac016. doi: 10.1093/infdis/jiac016

SARS-CoV-2 DNA Vaccine INO-4800 Induces Durable Immune Responses Capable of Being Boosted in a Phase 1 Open-Label Trial

Kimberly A Kraynyak 1,1,, Elliott Blackwood 2,1, Joseph Agnes 3,1, Pablo Tebas 4, Mary Giffear 5, Dinah Amante 6, Emma L Reuschel 7, Mansi Purwar 8, Aaron Christensen-Quick 9, Neiman Liu 10, Viviane M Andrade 11, Malissa C Diehl 12, Snehal Wani 13, Martyna Lupicka 14, Albert Sylvester 15, Matthew P Morrow 16, Patrick Pezzoli 17, Trevor McMullan 18, Abhijeet J Kulkarni 19, Faraz I Zaidi 20, Drew Frase 21, Kevin Liaw 22, Trevor R F Smith 23, Stephanie J Ramos 24, John Ervin 25, Mark Adams 26, Jessica Lee 27, Michael Dallas 28, Ami Shah Brown 29, Jacqueline E Shea 30, J Joseph Kim 31, David B Weiner 32, Kate E Broderick 33, Laurent M Humeau 34,, Jean D Boyer 35, Mammen P Mammen 36
PMCID: PMC8807286  PMID: 35079784

Abstract

Background

Additional SARS-CoV-2 vaccines that are safe and effective as primary vaccines and boosters remain urgently needed to combat the COVID-19 pandemic. We describe the safety and durability of the immune responses following two primary doses and a homologous booster dose of an investigational DNA vaccine (INO-4800) targeting the full-length spike antigen.

Methods

Three dosage strengths of INO-4800 (0.5 mg, 1.0 mg, and 2.0 mg) were evaluated in 120 age-stratified healthy adults. Intradermal injection of INO-4800 followed by electroporation at 0 and 4 weeks preceded an optional booster 6-10.5 months after the second dose.

Results

INO-4800 appeared well tolerated, with no treatment-related serious adverse events. Most adverse events were mild and did not increase in frequency with age and subsequent dosing. A durable antibody response was observed 6 months following the second dose; a homologous booster dose significantly increased immune responses. Cytokine producing T cells and activated CD8+ T cells with lytic potential were significantly increased in the 2.0 mg dose group.

Conclusion

INO-4800 was well tolerated in a 2-dose primary series and as a homologous booster in all adults, including the elderly. These results support further development of INO-4800 for use as a primary vaccine and as a booster.

Keywords: SARS-CoV-2, Clinical trial, DNA Vaccine, INO-4800, COVID-19, Safety, Immunogenicity, Booster

Contributor Information

Kimberly A Kraynyak, Inovio Pharmaceuticals, Plymouth Meeting, PA, USA.

Elliott Blackwood, Inovio Pharmaceuticals, Plymouth Meeting, PA, USA.

Joseph Agnes, Inovio Pharmaceuticals, Plymouth Meeting, PA, USA.

Pablo Tebas, Hospital of the University of Pennsylvania, Philadelphia, PA, USA.

Mary Giffear, Inovio Pharmaceuticals, Plymouth Meeting, PA, USA.

Dinah Amante, Inovio Pharmaceuticals, Plymouth Meeting, PA, USA.

Emma L Reuschel, Vaccine and Immunotherapy Center, Wistar Institute, Philadelphia, PA, USA.

Mansi Purwar, Vaccine and Immunotherapy Center, Wistar Institute, Philadelphia, PA, USA.

Aaron Christensen-Quick, Inovio Pharmaceuticals, Plymouth Meeting, PA, USA.

Neiman Liu, Inovio Pharmaceuticals, Plymouth Meeting, PA, USA.

Viviane M Andrade, Inovio Pharmaceuticals, Plymouth Meeting, PA, USA.

Malissa C Diehl, Inovio Pharmaceuticals, Plymouth Meeting, PA, USA.

Snehal Wani, Inovio Pharmaceuticals, Plymouth Meeting, PA, USA.

Martyna Lupicka, Inovio Pharmaceuticals, Plymouth Meeting, PA, USA.

Albert Sylvester, Inovio Pharmaceuticals, Plymouth Meeting, PA, USA.

Matthew P Morrow, Inovio Pharmaceuticals, Plymouth Meeting, PA, USA.

Patrick Pezzoli, Inovio Pharmaceuticals, Plymouth Meeting, PA, USA.

Trevor McMullan, Inovio Pharmaceuticals, Plymouth Meeting, PA, USA.

Abhijeet J Kulkarni, Vaccine and Immunotherapy Center, Wistar Institute, Philadelphia, PA, USA.

Faraz I Zaidi, Vaccine and Immunotherapy Center, Wistar Institute, Philadelphia, PA, USA.

Drew Frase, Vaccine and Immunotherapy Center, Wistar Institute, Philadelphia, PA, USA.

Kevin Liaw, Vaccine and Immunotherapy Center, Wistar Institute, Philadelphia, PA, USA.

Trevor R F Smith, Inovio Pharmaceuticals, Plymouth Meeting, PA, USA.

Stephanie J Ramos, Inovio Pharmaceuticals, Plymouth Meeting, PA, USA.

John Ervin, Alliance for Multispecialty Research, Kansas City, MO, USA.

Mark Adams, Alliance for Multispecialty Research, Lexington, KY, USA.

Jessica Lee, Inovio Pharmaceuticals, Plymouth Meeting, PA, USA.

Michael Dallas, Inovio Pharmaceuticals, Plymouth Meeting, PA, USA.

Ami Shah Brown, Inovio Pharmaceuticals, Plymouth Meeting, PA, USA.

Jacqueline E Shea, Inovio Pharmaceuticals, Plymouth Meeting, PA, USA.

J Joseph Kim, Inovio Pharmaceuticals, Plymouth Meeting, PA, USA.

David B Weiner, Vaccine and Immunotherapy Center, Wistar Institute, Philadelphia, PA, USA.

Kate E Broderick, Inovio Pharmaceuticals, Plymouth Meeting, PA, USA.

Laurent M Humeau, Inovio Pharmaceuticals, Plymouth Meeting, PA, USA.

Jean D Boyer, Inovio Pharmaceuticals, Plymouth Meeting, PA, USA.

Jr. Mammen P Mammen, Inovio Pharmaceuticals, Plymouth Meeting, PA, USA.

Supplementary Material

jiac016_suppl_Supplementary_Data
jiac016_suppl_Supplementary_Methods

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

jiac016_suppl_Supplementary_Data
jiac016_suppl_Supplementary_Methods

Articles from The Journal of Infectious Diseases are provided here courtesy of Oxford University Press

RESOURCES