当社グループは 3,000 以上の世界的なカンファレンスシリーズ 米国、ヨーロッパ、世界中で毎年イベントが開催されます。 1,000 のより科学的な学会からの支援を受けたアジア および 700 以上の オープン アクセスを発行ジャーナルには 50,000 人以上の著名人が掲載されており、科学者が編集委員として名高い
。オープンアクセスジャーナルはより多くの読者と引用を獲得
700 ジャーナル と 15,000,000 人の読者 各ジャーナルは 25,000 人以上の読者を獲得
Amir S Khan, Kate E Broderick, Jian Yan, Matthew P Morrow and Niranjan Y Sardesai
Few viruses have elicited more fear of its potential as a tool of bioterrorism than smallpox. In the post-9/11
“Amerithrax” environment, the threat of an intentional release of smallpox has led to renewed efforts to develop a safer vaccine, with fewer side effects, that could be administered to the general public. DNA vaccines administered through the use of enhanced delivery using electroporation could provide a platform for delivering a smallpox vaccine. Previously published data have shown that an 8 plasmid combination vaccine consisting of VACV antigens (specifically, A4L, A27L, A33R, A56R, B5R, F9L, H3L, and L1R) delivered to rabbits and nonhuman primates followed by electroporation elicited robust humoral and cell-mediated immune responses. Furthermore, non-human primates were protected from lethal challenge with monkeypox, showing that this vaccine platform is effective. This review summarizes recent data supporting vaccine development using DNA and electroporation to protect the general public in the event of a bioterror incident using smallpox.