Kulkarni Viraj, Valentin Antonio, Rosati Margherita, Alicea Candido, Singh Ashish K, Jalah Rashmi, Broderick Kate E, Sardesai Niranjan Y, Le Gall Sylvie, Mothe Beatriz, Brander Christian, Rolland Morgane, Mullins James I, Pavlakis George N, Felber Barbara K
Human Retrovirus Pathogenesis Section, Vaccine Branch, Center for Cancer Research, National Cancer Institute, Frederick, Maryland, United States of America.
Human Retrovirus Section, Vaccine Branch, Center for Cancer Research, National Cancer Institute, Frederick, Maryland, United States of America.
PLoS One. 2014 Jan 23;9(1):e86254. doi: 10.1371/journal.pone.0086254. eCollection 2014.
HIV sequence diversity and potential decoy epitopes are hurdles in the development of an effective AIDS vaccine. A DNA vaccine candidate comprising of highly conserved p24(gag) elements (CE) induced robust immunity in all 10 vaccinated macaques, whereas full-length gag DNA vaccination elicited responses to these conserved elements in only 5 of 11 animals, targeting fewer CE per animal. Importantly, boosting CE-primed macaques with DNA expressing full-length p55(gag) increased both magnitude of CE responses and breadth of Gag immunity, demonstrating alteration of the hierarchy of epitope recognition in the presence of pre-existing CE-specific responses. Inclusion of a conserved element immunogen provides a novel and effective strategy to broaden responses against highly diverse pathogens by avoiding decoy epitopes, while focusing responses to critical viral elements for which few escape pathways exist.
HIV序列多样性和潜在的诱饵表位是开发有效艾滋病疫苗的障碍。一种由高度保守的p24(gag)元件(CE)组成的候选DNA疫苗在所有10只接种疫苗的猕猴中均诱导出强大的免疫力,而全长gag DNA疫苗接种仅在11只动物中的5只中引发了对这些保守元件的反应,每只动物针对的CE较少。重要的是,用表达全长p55(gag)的DNA加强免疫CE预免疫的猕猴,可增加CE反应的强度和Gag免疫的广度,表明在存在预先存在的CE特异性反应的情况下,表位识别层次发生了改变。包含保守元件免疫原提供了一种新颖有效的策略,通过避免诱饵表位来拓宽针对高度多样化病原体的反应,同时将反应集中于几乎没有逃逸途径的关键病毒元件。