Centrifugation enhances integrin-mediated transduction of dendritic cells by conventional and RGD-modified adenoviral vectors

• Published in: Journal of immunological methods 2006-05, Vol.312 (1), p.94-104
• Main Authors: Harui, Airi, Roth, Michael D., Sanghvi, Mihir, Vira, Darshni, Mizuguchi, Hiroyuki, Basak, Saroj K.
• Format: Article
• Language: English
• Subjects: Adenoviridae - genetics; Alpha-v; Animals; Antigens, Differentiation - analysis; Biological and medical sciences; Centrifugation; Coculture Techniques; Dendritic cells; Dendritic Cells - immunology; Fundamental and applied biological sciences. Psychology; Fundamental immunology; Gene therapy; Genetic Vectors - genetics; Green fluorescent protein; Green Fluorescent Proteins - analysis; Green Fluorescent Proteins - genetics; Histocompatibility Antigens Class I - analysis; Histocompatibility Antigens Class II - analysis; Integrin alpha Chains - metabolism; Lymphocyte Activation; Male; Mice; Mice, Inbred C57BL; Molecular immunology; Oligopeptides - genetics; OT-1; Ovalbumin; T-Lymphocytes - immunology; Techniques; Transduction, Genetic - methods; Transgenes
• ISSN: 0022-1759; 1872-7905
• DOI: 10.1016/j.jim.2006.02.014

The level of antigen loading can impact on the capacity for dendritic cells (DC) to activate T cell responses. Several different approaches to adenoviral (Ad)-based transduction were therefore assessed for their effect on both transgene expression and T cell activation. While a conventional E1(−)/E3Δ Ad vector (Ad/GFP) produced a concentration-dependent expression of GFP, a modified vector expressing Arginine–Glycine–Aspartic Acid (RGD) sequence on its fiber knob (Ad-RGD/GFP) enhanced transgene expression by 9–20-fold at each MOI. The addition of centrifugal force (2000× g) during DC transduction with Ad/GFP also increased expression up to 20-fold. However, combining centrifugation with the Ad-RGD/GFP vector produced no effect on transduction rate and only a 1.5- to 2-fold increase in GFP expression, suggesting overlapping mechanisms of action. Consistent with this, exogenous RGD peptide blocked transduction regardless of the vector used, or the addition of centrifugal force, and transduction was primarily limited to DC expressing the CD51 integrin receptor. Ad vectors expressing ovalbumin (OVA) were used to assess transduced DC for their capacity to activate OVA-specific T cells. We observed a significant relationship between transgene expression and the capacity for T cell activation regardless of whether transgene expression was increased by using a higher MOI, an RGD-modified vector, or by employing centrifugal force. Furthermore, combining these approaches produced synergistic effects on T cell activation. We conclude that RGD-modified vectors and centrifugation both enhance DC transduction by increasing entry via integrin receptors and that the capacity for T cell activation can be optimized by combining approaches to achieve the highest possible level of transgene expression.