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基于基因组的疫苗设计:对疟疾和其他传染病的前景

Genome-based vaccine design: the promise for malaria and other infectious diseases.

作者信息

Doolan Denise L, Apte Simon H, Proietti Carla

机构信息

Infectious Diseases Programme, QIMR Berghofer Medical Research Institute, Brisbane, QLD 4029, Australia.

Infectious Diseases Programme, QIMR Berghofer Medical Research Institute, Brisbane, QLD 4029, Australia.

出版信息

Int J Parasitol. 2014 Oct 15;44(12):901-13. doi: 10.1016/j.ijpara.2014.07.010. Epub 2014 Sep 6.

Abstract

Vaccines are one of the most effective interventions to improve public health, however, the generation of highly effective vaccines for many diseases has remained difficult. Three chronic diseases that characterise these difficulties include malaria, tuberculosis and HIV, and they alone account for half of the global infectious disease burden. The whole organism vaccine approach pioneered by Jenner in 1796 and refined by Pasteur in 1857 with the "isolate, inactivate and inject" paradigm has proved highly successful for many viral and bacterial pathogens causing acute disease but has failed with respect to malaria, tuberculosis and HIV as well as many other diseases. A significant advance of the past decade has been the elucidation of the genomes, proteomes and transcriptomes of many pathogens. This information provides the foundation for new 21st Century approaches to identify target antigens for the development of vaccines, drugs and diagnostic tests. Innovative genome-based vaccine strategies have shown potential for a number of challenging pathogens, including malaria. We advocate that genome-based rational vaccine design will overcome the problem of poorly immunogenic, poorly protective vaccines that has plagued vaccine developers for many years.

摘要

疫苗是改善公众健康最有效的干预措施之一,然而,针对许多疾病研发高效疫苗仍然困难重重。体现这些困难的三种慢性疾病包括疟疾、结核病和艾滋病病毒,它们单独就占了全球传染病负担的一半。1796年詹纳开创并于1857年由巴斯德以“分离、灭活和注射”模式完善的全生物体疫苗方法,已被证明对许多导致急性疾病的病毒和细菌病原体非常成功,但在疟疾、结核病和艾滋病病毒以及许多其他疾病方面却失败了。过去十年的一项重大进展是阐明了许多病原体的基因组、蛋白质组和转录组。这些信息为21世纪识别用于疫苗、药物和诊断测试开发的靶抗原的新方法奠定了基础。基于创新基因组的疫苗策略已显示出对包括疟疾在内的许多具有挑战性的病原体的潜力。我们主张基于基因组的合理疫苗设计将克服多年来困扰疫苗开发者的免疫原性差、保护性差的疫苗问题。

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