2013
DOI: 10.1016/j.vaccine.2013.03.020
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Clinical development of Modified Vaccinia virus Ankara vaccines

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Cited by 136 publications
(106 citation statements)
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“…Our data with ChAd63 RH5 add to the growing body of evidence that this simian adenovirus vector is safe for clinical use. Likewise, the clinical safety of MVA as a recombinant vaccine vector for many infectious diseases and cancer is now well documented (57). MVA RH5 appeared to be more reactogenic than the ChAd63 vector at the higher dose, consistent with previous vaccine trials using this orthopoxvirus vector (38,39,43,44,46,58).…”
Section: Discussionsupporting
confidence: 71%
“…Our data with ChAd63 RH5 add to the growing body of evidence that this simian adenovirus vector is safe for clinical use. Likewise, the clinical safety of MVA as a recombinant vaccine vector for many infectious diseases and cancer is now well documented (57). MVA RH5 appeared to be more reactogenic than the ChAd63 vector at the higher dose, consistent with previous vaccine trials using this orthopoxvirus vector (38,39,43,44,46,58).…”
Section: Discussionsupporting
confidence: 71%
“…At present, MVA serves as one of the most advanced recombinant poxvirus vectors in preclinical research and human clinical trials for developing new vaccines against infectious disease and cancer (12,13,14).…”
mentioning
confidence: 99%
“…Thus the use of MVA in humans is completely safe. Other advantages of MVA are that it is genetically stable, very immunogenic, and easy to manufacture [113,114]. The MVA immunogenic potential for cytotoxic responses is due in part to uptake of dying vaccinia virus-infected cells by antigenpresenting cells and cross-presentation of antigens to CD8+ T cells [115].…”
Section: Recombinant Virusmentioning
confidence: 99%