The immunological impact of adenovirus early genes on vaccine-induced responses in mice and nonhuman primates

Kotou Sangare; Iskra Tuero; Mohammad Arif Rahman; Tanya Hoang; Leia K Miller-Novak; Diego A Vargas-Inchaustegui; David J Venzon; Celia LaBranche; David C Montefiori; Marjorie Robert-Guroff; Michael A Thomas

doi:10.1128/JVI.02253-20

The immunological impact of adenovirus early genes on vaccine-induced responses in mice and nonhuman primates

J Virol. 2021 Mar 10;95(7):e02253-20. doi: 10.1128/JVI.02253-20. Epub 2021 Jan 13.

Affiliations

¹ Department of Biology, Howard University, Washington, DC, USA.
² Section on Immune Biology of Retroviral Infection, Vaccine Branch, National Cancer Institute, National Institutes of Health, Bethesda, Maryland, USA.
³ Biostatistics and Data Management Section, National Cancer Institute, National Institutes of Health, Bethesda, Maryland, USA.
⁴ Duke University Medical Center, Durham, North Carolina, USA.
⁵ Department of Biology, Howard University, Washington, DC, USA michael.thomas1@howard.edu.

Abstract

Adenovirus (Ad) is being explored for use in the prevention and treatment of a variety of infectious diseases and cancers. Ad with a deletion in early region 3 (ΔE3) provokes a stronger immune response than Ad with deletions in early regions 1 and E3 (ΔE1/ΔE3). The ΔE1/ΔE3 Ads are more popular because they can carry a larger transgene and because of the deleted E1 (E1A and E1B), are perceived safer for clinical use. Ad with a deletion in E1B55K (ΔE1B55K) has been in phase III clinical trials for use in cancer therapy in the US and has been approved for use in head and neck tumor therapy in China, demonstrating that Ad containing E1A are safe for clinical use. We have shown previously that ΔE1B55K Ad, even while promoting lower levels of an inserted transgene, promoted similar levels of transgene-specific immune responses as a ΔE3 Ad. Products of the Ad early region 4 (E4) limit the ability of cells to mount an innate immune response. Using this knowledge, we deleted the Ad E4 open reading frames 1-4 (E4orf1-4) from the ΔE1B55K Ad. Here, we show that innate cytokine network genes are elevated in the ΔE4 Ad-infected cells beyond that of ΔE3 Ad-infected cells. Further, in immunized mice the IgG2a subclass was favored as was the IgG1 subclass in immunized nonhuman primates. Thus, Ad E4 impacts immune responses in cells, in immunized mice, and immunized nonhuman primates. These Ad may offer advantages that are beneficial for clinical use.Importance: Adenovirus (Ad) is being explored for use in the prevention and treatment of a variety of infectious diseases and cancers. Here we provide evidence in cells, mice, and nonhuman primates supporting the notion that Ad early gene-products limit specific immune responses. Ad constructed with deletions in early genes and expressing HIV envelope protein was shown to induce greater HIV-specific cellular immune responses and higher titer antibodies compared to the parental Ad with the early genes. In addition to eliciting enhanced immunity, the deleted Ad possesses more space for insertion of additional or larger transgenes needed for targeting other infectious agents or cancers.

Grants and funding

R00 AI114379/AI/NIAID NIH HHS/United States