The Landscape of Neutralizing Monoclonal Antibodies (nAbs) for Treatment and Prevention of COVID-19

2019年冠状病毒病(COVID-19) 大流行 严重急性呼吸综合征冠状病毒2型(SARS-CoV-2) 未来研究 单克隆抗体 2019-20冠状病毒爆发 医学 接种疫苗 业务 重症监护医学 风险分析(工程) 病毒学 爆发 抗体 免疫学 计算机科学 疾病 传染病(医学专业) 人工智能 病理
作者
Aline Almeida-Oliveira,Diana Freire,A. Andrade,Amanda de Miranda Marques,Luciana da Silva Madeira,José Senna,Ivna Silveira,Beatriz de Castro Fialho
出处
期刊:Journal of Pharmaceutical Innovation [Springer Science+Business Media]
卷期号:18 (3): 1194-1212 被引量:10
标识
DOI:10.1007/s12247-023-09713-w
摘要

Abstract Purpose After nearly 3 years of the COVID-19 pandemic, even though a vast body of knowledge and products (including vaccines and treatments) have been developed and disseminated, the virus is still evolving and new variants arising. Consequently, thousands of lives continue to be lost. Neutralizing monoclonal antibodies (nAbs) are promising drugs that emerged to treat SARS-CoV-2. In the uncertainty of the current situation, there is the question of whether organizations should continue to invest in this technology. To help decision-making in scientifical and pharmaceutical organizations, it is of major importance to monitor the development of products and technologies. Therefore, the aim of this study is analyze the landscape of nAbs for COVID-19. Methods The scenario of 473 biotherapeutics focusing on nAbs was evaluated using foresight techniques and a review of literature. Data were obtained from structured and semi-structured databases and processed for treatment, cleaning, consistency, validation, and enrichment. Results We identified 227 nAbs and performed an extensive literature review of 16 nAbs in late clinical development, including development technologies, responses to variants of concern (VOCs), manufacturing, and clinical aspects. Conclusions Even though the emergence of new VOCs is a threat to the effectiveness of this treatment, demanding constant genomic surveillance, the use of nAbs to treat and prevent COVID-19 will probably continue to be relevant due to excellent safety profiles and the possibility of immediate immunity transfer, especially in patients showing inadequate immunological response to vaccination. Therefore, we suggest that organizations should keep investing in improvements in this technology.

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