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2006DiPaolo Nelson; Ni Shaoheng; Gaggar Anuj; Strauss Robert; Tuve Sebastian; Li Zong Yi; Stone Daniel; Shayakhmetov Dmitry; Kiviat Nancy; Touré Papa; Sow Salif; Horvat Branka; Lieber André
Evaluation of adenovirus vectors containing serotype 35 fibers for vaccination.
Molecular therapy : the journal of the American Society of Gene Therapy 2006;13(4):756-65.
In contrast to commonly used serotype 5-based adenovirus (Ad) vectors, Ad's containing fibers derived from B-group serotype 35 (Ad5/35) efficiently transduce human DCs ex vivo and appear to target antigen-presenting cells after intravenous injection into baboons. Based on this, Ad5/35 vectors could be valuable tools for immunotherapy and vaccination. On the other hand, a number of studies indicate that signaling through the B-group Ad receptor, CD46, can cause tolerance or immunosuppression. Since mice do not express CD46 in a human-like pattern, we studied the in vivo properties of Ad5/35 in transgenic mice that express CD46 in a pattern and at a level similar to those of humans. Hypersensitivity assays and analyses of frequencies of regulatory T cells and T cell responses did not indicate that Ad5/35 injection exerts detrimental effects on the host's immune system. An Ad5/35 vector expressing a model antigen was able to trigger a strong T cell response against the test antigen after intramuscular injection. Overall, compared to Ad5 vectors, Ad5/35 vectors had a better safety profile, reflected by lower serum levels of proinflammatory cytokines.

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