Abstract 714: From cancer to COVID-19- development of a dendritic cell-targeted nano-vaccine for prevention and therapy of COVID-19

Daniella Vaskovich-Koubi, Ron Kleiner, Yulia Liubomirski, E. Yeini, G. Tiram, S. Pozzi, A. Eldar-Boock, H. Florindo, R. Satchi‐Fainaro
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引用次数: 1

Abstract

Dendritic cells (DC) are antigen-presenting cells with an important role in the initiation and regulation of the innate and adaptive arms of the immune system. By efficient presentation of antigens, DC elicit an antigen-specific immune response. Therefore, we previously established in our laboratory a melanoma-DC-targeted NP that was evaluated and validated against aggressive melanoma. Although DC-therapy is mainly exploited in the treatment of cancer, DC are becoming a key therapeutic target in other pathologies such as infectious diseases. Viral pathogens, similarly, to cancer, modulate the host defense mechanisms to their benefit. COVID-19, an ongoing pandemic, caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has spread globally and is already infecting tens of millions of people worldwide. Historically, vaccines are among therapies with the greatest impact in health and constitute an unmet medical need against coronavirus disease-19 (COVID-19) pandemic. To that end, we repurposed our recently published melanoma-targeted NP to co-deliver modulators of host immune response and SARS-CoV-2 specific antigen epitopes discovered by a computational approach integrating 3D information with large-scale statistical analysis. The immune response kinetics in patients infected with SARS-CoV-2 is poorly understood, but recent reports show that germinal B cells and active follicular T-helper cells, IgM/IgG SARS-CoV-2 antibodies, in addition to an enhanced cellular immunity, are found in patients with mild-to-moderate SARS-CoV-2 infection. Our preliminary data demonstrated that our nano-vaccine was able to activate specific immune cell response of effector T cells and B cells and decrease the regulatory activity of T cells, compared to controls. Moreover, we found that our DC-targeted SARS-CoV-2 NP successfully induced antigen-specific secretion of IgM and IgG antibodies with high binding affinity to the antigens. Importantly, our nano-vaccine elicited specific neutralization of Spike virus like particles (VLPs) by sera of immunized mice. We hypothesize that implementing our novel nano-vaccine platform for COVID-19 will lead to a safe and efficacious COVID-19 vaccine ready for first-in-human clinical trials. Citation Format: Daniella Vaskovich-Koubi, Ron Kleiner, Yulia Liubomirski, Eilam Yeini, Galia Tiram, Sabina Pozzi, Anat Eldar-Boock, Helena F. Florindo, Ronit Satchi-Fainaro. From cancer to COVID-19- development of a dendritic cell-targeted nano-vaccine for prevention and therapy of COVID-19 [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2021; 2021 Apr 10-15 and May 17-21. Philadelphia (PA): AACR; Cancer Res 2021;81(13_Suppl):Abstract nr 714.
从癌症到COVID-19——树突状细胞靶向纳米疫苗的研制
树突状细胞(DC)是抗原呈递细胞,在免疫系统固有臂和适应性臂的启动和调节中起重要作用。通过抗原的有效呈递,DC引起抗原特异性免疫反应。因此,我们之前在我们的实验室建立了黑色素瘤dc靶向NP,对侵袭性黑色素瘤进行了评估和验证。虽然DC治疗主要用于癌症的治疗,但DC也正在成为感染性疾病等其他疾病的关键治疗靶点。与癌症类似,病毒病原体也会调节宿主的防御机制,使其受益。COVID-19是一种由严重急性呼吸系统综合征冠状病毒2 (SARS-CoV-2)引起的持续大流行,已在全球蔓延,并已感染全球数千万人。从历史上看,疫苗是对健康影响最大的疗法之一,也是应对冠状病毒病-19 (COVID-19)大流行的一项未满足的医疗需求。为此,我们重新利用我们最近发表的黑素瘤靶向NP,共同递送宿主免疫反应调节剂和SARS-CoV-2特异性抗原表位,这些表位是通过将3D信息与大规模统计分析相结合的计算方法发现的。SARS-CoV-2感染患者的免疫反应动力学尚不清楚,但最近的报告显示,在轻度至中度SARS-CoV-2感染患者中,除了细胞免疫增强外,还发现生发B细胞和活性滤泡t辅助细胞、IgM/IgG SARS-CoV-2抗体。我们的初步数据表明,与对照组相比,我们的纳米疫苗能够激活效应T细胞和B细胞的特异性免疫细胞反应,并降低T细胞的调节活性。此外,我们发现我们的dc靶向SARS-CoV-2 NP成功诱导抗原特异性分泌IgM和IgG抗体,这些抗体与抗原具有高结合亲和力。重要的是,我们的纳米疫苗通过免疫小鼠的血清诱导特异性中和刺突病毒样颗粒(VLPs)。我们假设,实施我们的新型COVID-19纳米疫苗平台将导致安全有效的COVID-19疫苗准备进行首次人体临床试验。引用格式:Daniella Vaskovich-Koubi, Ron Kleiner, Yulia Liubomirski, Eilam Yeini, Galia Tiram, Sabina Pozzi, Anat eldar - book, Helena F. Florindo, Ronit Satchi-Fainaro。从癌症到COVID-19——树突状细胞靶向预防和治疗COVID-19纳米疫苗的研制[摘要]。见:美国癌症研究协会2021年年会论文集;2021年4月10日至15日和5月17日至21日。费城(PA): AACR;癌症杂志,2021;81(13 -增刊):摘要第714期。
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