非洲基因工程生物安全监管框架导航:聚焦基因组编辑和基因驱动技术。

IF 4.3 3区 工程技术 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Frontiers in Bioengineering and Biotechnology Pub Date : 2024-10-24 eCollection Date: 2024-01-01 DOI:10.3389/fbioe.2024.1483279
Tilahun Rabuma, Felix Moronta-Barrios, Wendy Craig
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引用次数: 0

摘要

基因组编辑和基因驱动技术在非洲的吸引力与日俱增,研究人员正在探索这些技术在农业、卫生和环境领域的潜在应用。虽然健全的监管框架对促进这些技术的开发和利用至关重要,但非洲大陆监管机构信息零散、准备不足,阻碍了知情决策:本研究调查了非洲国家基因组编辑和基因驱动技术的监管框架,确定了常见的监管挑战,并提出了可行的解决方案:方法:通过问卷调查收集原始数据,并对在线数据库和科学文献中的现有生物安全法规进行分析:我们的研究结果表明,虽然一些非洲国家最近更新了监管框架,但许多国家仍在讨论之中。制定和实施过程中面临的挑战包括资源、专业知识、意识和公众抵制等方面的限制:结论:研究结果突出表明,迫切需要进一步提高监管能力。通过揭示这些挑战,我们的研究可以为非洲监管机构提供宝贵的见解,指导制定有效的监管框架。这些框架对于利用基因组编辑和基因驱动技术的潜力,同时保护非洲的人类健康和环境至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Navigating biosafety regulatory frameworks for genetic engineering in Africa: a focus on genome editing and gene drive technologies.

Genome editing and gene drive technologies are increasingly gaining attraction in Africa, with researchers exploring their potential applications in agriculture, health and the environment. Acknowledging that robust regulatory frameworks are crucial in facilitating the development and utilization of these technologies, informed decision-making is, however, being impeded by the fragmented information availability and readiness of regulatory authorities on the continent.

Objectives: This study investigates the regulatory frameworks governing genome editing and gene drive technologies in African countries, identifies common regulatory challenges and proposes actionable solutions.

Methods: Primary data were collected through questionnaires and complemented by analysing existing biosafety regulations from online databases and scientific literature.

Results: Our findings suggest that while a few African countries have recently updated their regulatory frameworks, many are still under discussion. Challenges to development and implementation include limited resources, expertise, awareness, and public resistance.

Conclusion: The findings underscore the urgent need for further development in regulatory capacities. By shedding light on these challenges, our study could provide African regulators with valuable insights to guide the formulation of effective regulatory frameworks. Such frameworks are essential for harnessing the potential of genome editing and gene drive technologies while safeguarding human health and the environment in Africa.

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来源期刊
Frontiers in Bioengineering and Biotechnology
Frontiers in Bioengineering and Biotechnology Chemical Engineering-Bioengineering
CiteScore
8.30
自引率
5.30%
发文量
2270
审稿时长
12 weeks
期刊介绍: The translation of new discoveries in medicine to clinical routine has never been easy. During the second half of the last century, thanks to the progress in chemistry, biochemistry and pharmacology, we have seen the development and the application of a large number of drugs and devices aimed at the treatment of symptoms, blocking unwanted pathways and, in the case of infectious diseases, fighting the micro-organisms responsible. However, we are facing, today, a dramatic change in the therapeutic approach to pathologies and diseases. Indeed, the challenge of the present and the next decade is to fully restore the physiological status of the diseased organism and to completely regenerate tissue and organs when they are so seriously affected that treatments cannot be limited to the repression of symptoms or to the repair of damage. This is being made possible thanks to the major developments made in basic cell and molecular biology, including stem cell science, growth factor delivery, gene isolation and transfection, the advances in bioengineering and nanotechnology, including development of new biomaterials, biofabrication technologies and use of bioreactors, and the big improvements in diagnostic tools and imaging of cells, tissues and organs. In today`s world, an enhancement of communication between multidisciplinary experts, together with the promotion of joint projects and close collaborations among scientists, engineers, industry people, regulatory agencies and physicians are absolute requirements for the success of any attempt to develop and clinically apply a new biological therapy or an innovative device involving the collective use of biomaterials, cells and/or bioactive molecules. “Frontiers in Bioengineering and Biotechnology” aspires to be a forum for all people involved in the process by bridging the gap too often existing between a discovery in the basic sciences and its clinical application.
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