A practical approach for adoption of a hub and spoke model for cell and gene therapies in low- and middle-income countries: framework and case studies

IF 4.6 3区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Shadi Saleh, Omar Dabbous, Sean D. Sullivan, Dipen Ankleshwaria, Daiane Trombini, Mondher Toumi, Mahmoud Diaa, Anish Patel, Burcu Kazazoglu Taylor, Sean Tunis
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引用次数: 0

Abstract

In the rapidly evolving landscape of biotechnologies, cell and gene therapies are being developed and adopted at an unprecedented pace. However, their access and adoption remain limited, particularly in low- and middle-income countries (LMICs). This study aims to address this critical gap by exploring the potential of applying a hub and spoke model for cell and gene therapy delivery in LMICs. We establish the identity and roles of relevant stakeholders, propose a hub and spoke model for cell and gene therapy delivery, and simulate its application in Brazil and the Middle East and North Africa. The development and simulation of this model were informed by a comprehensive review of academic articles, grey literature, relevant websites, and publicly available data sets. The proposed hub and spoke model is expected to expand availability of and access to cell and gene therapy in LMICs and presents a comprehensive framework for the roles of core stakeholders, laying the groundwork for more equitable access to these lifesaving therapies. More research is needed to explore the practical adoption and implications of this model.

Abstract Image

Abstract Image

在低收入和中等收入国家采用细胞和基因治疗中心辐射模型的实用方法:框架和案例研究。
在快速发展的生物技术领域,细胞和基因疗法正以前所未有的速度被开发和采用。然而,它们的获取和采用仍然有限,特别是在中低收入国家。本研究旨在通过探索在LMIC中应用中枢辐射模型进行细胞和基因治疗的潜力来解决这一关键差距。我们确定了相关利益相关者的身份和角色,提出了一个细胞和基因治疗交付的轮辐模型,并模拟了其在巴西、中东和北非的应用。该模型的开发和模拟是通过对学术文章、灰色文献、相关网站和公开数据集的全面审查来进行的。拟议的轮辐式模式预计将扩大LMIC中细胞和基因治疗的可用性和可及性,并为核心利益相关者的角色提供一个全面的框架,为更公平地获得这些救命疗法奠定基础。需要更多的研究来探索这种模式的实际采用和影响。
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来源期刊
Gene Therapy
Gene Therapy 医学-生化与分子生物学
CiteScore
9.70
自引率
2.00%
发文量
67
审稿时长
4-8 weeks
期刊介绍: Gene Therapy covers both the research and clinical applications of novel therapeutic techniques based on a genetic component. Over the last few decades, significant advances in technologies ranging from identifying novel genetic targets that cause disease through to clinical studies, which show therapeutic benefit, have elevated this multidisciplinary field to the forefront of modern medicine.
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