期刊
FEBS JOURNAL
卷 274, 期 18, 页码 4680-4687出版社
BLACKWELL PUBLISHING
DOI: 10.1111/j.1742-4658.2007.05998.x
关键词
attenuated live parasite; malaria; MSP1; Plasmodium; protective immunity; RTS/S; severe disease; transmission-blocking antibodies; vaccine; var2CSA
Malaria vaccine discovery and development follow two principal strategies. Most subunit vaccines are designed to mimic naturally acquired immunity that develops over years upon continuous exposure to Plasmodium transmission. Experimental model vaccines, such as attenuated live parasites and transmission-blocking antigens, induce immune responses superior to naturally acquired immunity. The promises and hurdles of the different tracks towards an effective and affordable vaccine against malaria are discussed.
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