Adenovirus type-35 vectors block human CD4⁺ T-cell activation via CD46 ligation

• Published in: Proceedings of the National Academy of Sciences - PNAS 2011-05, Vol.108 (18), p.7499-7504
• Main Authors: Adams, William C., Gujer, Cornelia, McInerney, Gerald, Gall, Jason G. D., Petrovas, Constantinos, Hedestam, Gunilla B. Karlsson, Koup, Richard A., Loré, Karin, Medzhitov, Ruslan
• Format: Article
• Language: English
• Subjects: Adenoviridae - genetics; Adenoviridae - metabolism; Adenovirus; Adenoviruses; Biological Sciences; Blood; Blotting, Western; CD28 antigen; CD4 antigen; CD4-Positive T-Lymphocytes - immunology; CD4-Positive T-Lymphocytes - metabolism; CD46 antigen; Cell activation; Cell proliferation; complement regulatory proteins; Coxsackie and Adenovirus Receptor-Like Membrane Protein; Cytometry; Dendritic cells; Dendritic Cells - metabolism; Down regulation; Epithelial cells; Expression vectors; Flow Cytometry; Genetic Vectors - metabolism; Humans; Immunological memory; Infection; Infections; Interleukin 2; Ligation; Lymphocyte Activation - physiology; Lymphocytes T; Medicin och hälsovetenskap; Membrane Cofactor Protein - metabolism; Memory cells; Monoclonal antibodies; NF- Kappa B protein; Nuclear transport; Pathogens; Receptors; Receptors, Virus - metabolism; T lymphocytes; Vaccination; Vaccines
• ISSN: 0027-8424; 1091-6490; 1091-6490
• DOI: 10.1073/pnas.1017146108

Recombinant adenoviruses (rAds) based on types 5 (rAd5) and 35 (rAd35) have emerged as important vaccine delivery vectors in clinical testing for a variety of pathogens. A major difference between these vectors is their binding to cellular receptors used for infection. Whereas rAd5 binds coxsackie-adenovirus receptor (CAR), rAd35 binds the complement regulatory protein CD46. Although rAd35 infected and phenotypically matured human blood dendritic cells (DCs) more efficiently than rAd5, we show here that rAd35 markedly suppressed DC-induced activation of naive CD4⁺ T cells. rAd35 specifically blocked both DCs and anti-CD3/CD28 mAb-induced naive T-cell proliferation and IL-2 production. This effect was also observed in CD4⁺ memory T cells but to a lesser extent. The suppression occurred by rAd35 binding to CD46 on T cells and was independent of infection. CD46 engagement with mAb mimicked the effects of rAd35 and also led to deficient NF-kB nuclear translocation. In contrast, rAd5 and rAd35 vectors with ablated CD46 binding did not inhibit T-cell activation. Our findings provide insights into the basic biology of adenoviruses and indicate that CD46 binding may have an impact on the generation of primary CD4⁺ T-cell responses by Ad35.