Vaccines and Public Trust: Containing COVID-19 in Cuba.

IF 1.8 4区 医学 Q3 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH Medicc Review Pub Date : 2022-01-31 DOI:10.37757/MR2022.V24.N1.11
Conner Gorry
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引用次数: 3

Abstract

As 2021 drew to a close, Cuba struggled to contain the highly transmissible omicron variant of SARS-CoV-2, braced for a new wave of infections and kept a close eye on other variants of concern popping up around the world-a common experience to countries everywhere as we head into the second year of the pandemic. In Cuba, however, there is one marked difference making all the difference: by early January, 87% of the population was fully vaccinated using a three-dose schedule of vaccines developed and produced on the island.[1] This massive vaccination campaign is complemented by a rapid booster rollout-also using Cuban vaccines-that began in December 2021 and was ongoing as we finalized this issue. The island nation was able to achieve the third highest COVID-19 vaccination rate in the world[2] after decades of scientific investment, research, discovery and innovation; regulatory oversight and compliance; professional training; and increased production capacity. But a vaccine is only as effective as the health system charged with administering it-in a safe and timely manner, to as many people as possible. Here too, Cuba has decades of experience, including a national pediatric immunization program where 98% of children under 5 are immunized against 13 diseases,[3] an annual polio vaccination campaign (both launched in 1962 and uninterrupted since) and campaigns to contain epidemics such as H1N1. When the first COVID-19 cases were detected on the island in March 2020, Cuba harnessed this vaccine experience, making a hard tack towards developing its own vaccines. Two of the main protagonists in the country's biotechnology development, the Finlay Vaccine Institute (IFV) and the Genetic Engineering and Biotechnology Center (CIGB), both with several groundbreaking preventive and therapeutic vaccines in their portfolios, led the search for a vaccine. Today, Cuba has three vaccines authorized for emergency use-Soberana 02 and Soberana Plus developed by IFV, and Abdala, developed by CIGB. Schedules with these vaccines have demonstrated more than 90% efficacy in clinical trials,[4] and after regulatory approval for emergency use, became the backbone of Cuban COVID-19 vaccination efforts. A fourth vaccine, Mambisa (CIGB), administered nasally, and a fifth, Soberana 01 (IFV) are still in clinical trials. For this installment in MEDICC Review's series spotlighting leading women of Cuban science, we sat down with Dr Verena Muzio, Director of Clinical Research at CIGB. A pioneer of Cuba's biotechnology sector, she is an immunologist with a doctorate in biological sciences. Her professional trajectory began researching the genetically engineered hepatitis B surface antigen that led to the development of Cuba's recombinant hepatitis B vaccine in 1989. The same technological platform used in this vaccine was used to develop CIGB's Abdala vaccine against SARS-CoV-2-part of the reason Cuba was able to secure a vaccine so quickly. A phase 3 clinical trial determined a 92.28% efficacy rate for Abdala, with results to appear in forthcoming publications.

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疫苗和公众信任:在古巴遏制COVID-19。
随着2021年接近尾声,古巴努力控制高度传染性的SARS-CoV-2的基因组变体,为新一波感染做好准备,并密切关注世界各地出现的其他令人担忧的变体——在我们进入大流行的第二年之际,这是世界各国的共同经历。然而,在古巴,有一个显著的差异造成了一切不同:到1月初,87%的人口完全接种了岛上开发和生产的三剂疫苗。[1]在这一大规模疫苗接种运动的补充下,还迅速推出了助推器——也是使用古巴疫苗——从2021年12月开始,在我们完成本期问题时一直在进行。经过数十年的科学投入、研究、发现和创新,这个岛国能够实现世界第三高的COVID-19疫苗接种率[2];监管监督和合规;专业培训;提高了生产能力。但是,疫苗的有效性取决于负责接种疫苗的卫生系统以安全和及时的方式为尽可能多的人接种疫苗。在这方面,古巴也有几十年的经验,包括一项全国儿科免疫规划,98%的5岁以下儿童接种了13种疾病的疫苗[3],每年开展脊髓灰质炎疫苗接种运动(1962年启动,此后一直没有中断),以及控制H1N1等流行病的运动。当2020年3月在岛上发现第一例COVID-19病例时,古巴利用这一疫苗经验,采取强硬措施开发自己的疫苗。该国生物技术发展的两个主要参与者——芬利疫苗研究所(IFV)和基因工程和生物技术中心(CIGB)——在其投资组合中都有几种突破性的预防性和治疗性疫苗,它们领导了疫苗的研究。今天,古巴有三种获准用于紧急用途的疫苗:国际疫苗研究所开发的Soberana 02和Soberana Plus,以及CIGB开发的Abdala。这些疫苗的接种计划在临床试验中显示出90%以上的有效性[4],并在监管部门批准紧急使用后,成为古巴COVID-19疫苗接种工作的支柱。第四种疫苗Mambisa (CIGB)是鼻用疫苗,第五种疫苗Soberana 01 (IFV)仍处于临床试验阶段。在《医学评论》聚焦古巴科学界女性领军人物系列的本期节目中,我们采访了CIGB临床研究主任Verena Muzio博士。她是古巴生物技术领域的先驱,拥有生物科学博士学位的免疫学家。她的职业轨迹始于研究基因工程乙型肝炎表面抗原,该抗原导致古巴在1989年开发出重组乙型肝炎疫苗。这种疫苗使用的相同技术平台被用于开发CIGB针对sars - cov的Abdala疫苗-古巴能够如此迅速地获得疫苗的部分原因。一项3期临床试验确定Abdala的有效率为92.28%,结果将发表在即将发表的出版物中。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Medicc Review
Medicc Review PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH-
CiteScore
3.30
自引率
9.50%
发文量
49
审稿时长
>12 weeks
期刊介绍: Uphold the highest standards of ethics and excellence, publishing open-access articles in English relevant to global health equity that offer the best of medical, population health and social sciences research and perspectives by Cuban and other developing-country professionals.
期刊最新文献
Executive Summary: Insights from Cuba's COVID-19 Vaccine Enterprise: Report from a High Level Fact-Finding Delegation to Cuba. COVID-19, Viruses and Dementia. Full Technical Report: Insights from Cuba's COVID-19 Vaccine Enterprise: Report from a High Level Fact-Finding Delegation to Cuba. Health Care is a Right, Not a Commodity: The Legacy of Dr Paul Farmer MD PhD. Validation of a New Diagnostic Index to Determine Metabolic Obesity Phenotypes in Normal-Weight Women in Early Pregnancy.
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