Towards the spanish vaccine against SARS-CoV-2, responsible for the pandemic Covid-19

M. Esteban, J. G. Arriaza
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Abstract

There is a general consensus that the only way to stop the pandemic caused by the coronavirus SARS-CoV-2 is through the development of an effective and safe vaccine. Various countries have move forward to develop a vaccine, and currently a number of preclinical and clinical trials phase I/II revealed that some of the vaccines triggered activation of humoral and cellular immune responses that could be relevant in protection against the coronavirus, but it remains yet to demonstrated efficacy in the population of any of the vaccines. Our group of Poxvirus and Vaccines at the CNB-CSIC started with the development of a vaccine immediately after the full genome (30.000 nucleotides) sequence of the SARS-CoV-2 was published in January 10, 2020. In this article we describe the steps that we have follow up to develop a vaccine candidate using as a vector (vehicle) an attenuated strain of modified vaccinia virus strain (MVA) expressing the full-length S (Spike) protein of SARS-CoV-2. We have demonstrated in cultured cells and in animals (mice) that the vaccine fulfills relevant criteria to be considered a candidate against COVID-19, like expression of the entire protein at the cell membrane, formation of oligomers (trimers), high stability and ability to induce neutralizing antibodies, a type of Th1 response and induction of a wide spectrum of SARS-CoV-2 specific T cells, like CD4+, CD8+, Tfh, Tregs and memory cells. We have programmed efficacy studies in animals (humanized mice and macaques) and phase I/II and III clinical trials. The GMP lot is under production by an Spanish company and a patent has been presented.
对导致Covid-19大流行的西班牙SARS-CoV-2疫苗
人们普遍认为,阻止由冠状病毒SARS-CoV-2引起的大流行的唯一途径是开发有效和安全的疫苗。各国已在开发疫苗方面取得进展,目前一些I/II期临床前和临床试验表明,一些疫苗触发了体液和细胞免疫反应的激活,这可能与预防冠状病毒有关,但仍未证明任何疫苗在人群中的有效性。我们在CNB-CSIC的痘病毒和疫苗小组在2020年1月10日公布了SARS-CoV-2的全基因组(30,000个核苷酸)序列后立即开始开发疫苗。在本文中,我们描述了我们使用表达SARS-CoV-2全长S (Spike)蛋白的修饰痘苗病毒(MVA)减毒株作为载体(载体)开发候选疫苗的后续步骤。我们已经在培养细胞和动物(小鼠)中证明,该疫苗符合被认为是COVID-19候选疫苗的相关标准,如在细胞膜上表达整个蛋白质,形成寡聚物(三聚体),高稳定性和诱导中和抗体的能力,一种Th1反应和诱导广泛的SARS-CoV-2特异性T细胞,如CD4+, CD8+, Tfh, Tregs和记忆细胞。我们已经在动物(人源化小鼠和猕猴)和I/II和III期临床试验中进行了疗效研究。西班牙一家公司正在生产GMP批号,并已申请专利。
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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