Tendler Miriam, Simpson Andrew J G
Fundação Oswaldo Cruz, Laboratório de Esquistossomose Experimental, Av. Brasil, 4365, Manguinhos, Rio de Janeiro, RJ, CEP: 21-045-900, Brazil Institute FIOCRUZ, Brazil.
Acta Trop. 2008 Nov-Dec;108(2-3):263-6. doi: 10.1016/j.actatropica.2008.09.002. Epub 2008 Sep 11.
In the 1990s, WHO/TDR created a product development program and initiated collaborations with other major international donors to promote rapid vaccine development and other tools for the control of endemic diseases. This "push strategy" was chosen to achieve effective research projects fostering innovation in the context of rapid product development. In the field of vaccine development, the aim was to bring forth ways and means to immunize against the most important human parasite diseases. Although the malaria vaccine projects scored initial successes it has been difficult to move forward decidedly. With regard to schistosomiasis, more than 10 important antigens with strong potential as vaccines candidates emerged from the several 100 scientific projects supported by international donor agencies and national research programs over the last few decades. Among those still seriously pursued, the Fatty Acid-Binding Protein (FABP)-14 kDa Schistosoma mansoni (Sm14) antigen stands out, both due to its steady progress towards field trials and because it represents the sole vaccine candidate to emerge from an endemic country. Work has now progressed to the scale-up level and an industrial production process has successfully been put in place. The very special feature of Sm14 is its strong immunological reactivity with an antigen shared between two different important parasites, which give this vaccine candidate the potential to be used against more than one infection. It has been demonstrated that it has effect not only against S. mansoni in humans but also against Fasciola hepatica, a parasite that causes disease in cattle and sheep leading to annual losses over 3 $US billion to the food industry worldwide. The Sm14 patents, granted to Oswaldo Cruz Foundation (FIOCRUZ), a Brazilian scientific institution directly linked to the Brazilian Ministry of Health, have been licensed to a private company which has the intention to lead the Sm14 project to success, both in the veterinary and in the human field. The objective is to provide economic performance by fostering scientific and economic progress and thus reach the global market. Sm14 is at present at the stage of planning clinical trials under a private-public partnership (PPP) initiative in collaboration with FIOCRUZ which has recently received significant financial support from FINEP, a public Brazilian Financial Agency.
20世纪90年代,世界卫生组织/热带病研究与培训特别规划署(WHO/TDR)设立了一个产品开发项目,并与其他主要国际捐助方展开合作,以推动疫苗的快速研发以及控制地方病的其他工具的开发。选择这种“推动战略”是为了在快速产品开发的背景下促成有效的研究项目,推动创新。在疫苗研发领域,目标是找出针对最重要的人类寄生虫病进行免疫接种的方法和手段。尽管疟疾疫苗项目取得了初步成功,但要果断推进却很困难。关于血吸虫病,在过去几十年里,国际捐助机构和国家研究项目支持的数百个科研项目中,涌现出了10多种具有很强潜力的重要抗原,有望成为候选疫苗。在仍在大力推进的项目中,曼氏血吸虫14 kDa脂肪酸结合蛋白(FABP)(Sm14)抗原尤为突出,这既是因为它在迈向现场试验方面取得了稳步进展,也是因为它是唯一一个来自地方病流行国家的候选疫苗。目前工作已进展到扩大规模阶段,并且成功建立了工业化生产流程。Sm14的一个非常特殊的特点是,它与两种不同的重要寄生虫共有的一种抗原具有很强的免疫反应性,这使得这个候选疫苗有可能用于预防多种感染。已经证明,它不仅对人类的曼氏血吸虫有效,而且对肝片吸虫也有效,肝片吸虫是一种在牛和羊身上引发疾病的寄生虫,每年给全球食品行业造成超过30亿美元的损失。授予巴西一家与巴西卫生部直接相关的科研机构奥斯瓦尔多·克鲁兹基金会(FIOCRUZ)的Sm14专利,已授权给一家私营公司,该公司有意在兽医和人类领域带领Sm14项目取得成功。目标是通过促进科学和经济进步来实现经济效益,从而打入全球市场。目前,Sm14正处于与FIOCRUZ合作开展公私合营(PPP)倡议下的临床试验规划阶段,FIOCRUZ最近获得了巴西公共金融机构巴西国家科技发展基金会(FINEP)的大量资金支持。