权益分类	功能权益	普通用户	{{item.name}}会员
{{category.name}}	{{benefitItem.name}}

A novel cellular tumor vaccine strategy for mutant IDH1 glioma

针对突变 IDH1 神经胶质瘤的新型细胞肿瘤疫苗策略

基本信息

批准号：
10248330
负责人：
MICHAEL D GUNN
金额：
$ 16.09万
依托单位：
DUKE UNIVERSITY
依托单位国家：
美国
项目类别：
财政年份：
2014
资助国家：
美国
起止时间：
2014-09-24 至 2024-08-31
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/10248330
关键词：
2019-nCoV Address Adjuvant Advocate Animal Model Animals Antibodies Antibody Formation Antibody Response Antibody-Dependent Enhancement Antigen Targeting Antigens Autoantigens Award Back Blood Brain Neoplasms CD8-Positive T-Lymphocytes COVID-19 COVID-19 vaccine Cancer Vaccines Cells Cellular Immunity Chemistry Clinical Trials Cytotoxic T-Lymphocytes Data Dengue Development Disease Dose Elderly Electroporation GVAX Cancer Vaccine Generations Glioma Goals Health Health Personnel Human Humoral Immunities Immune response Immunity Immunotherapeutic agent In Situ In Vitro Infection Inflammation Intravenous infusion procedures Kinetics Leukapheresis Messenger RNA Modeling Mus Patients Performance Phase Phase I Clinical Trials Play Process Production Program Development Proteins RNA Viruses Reagent Recovery Resources Risk Factors Role SARS coronavirus Safety Sterility T cell response T memory cell T-Lymphocyte T-Lymphocyte Epitopes Testing Time Toxic effect Transfection Tumor Immunity Vaccinated Vaccination Vaccines Viral Virus Diseases efficacy testing high risk population immunogenic immunogenicity intravenous injection monocyte mortality mutant neutralizing antibody novel novel coronavirus preclinical study response tumor vaccination strategy vaccine development

项目摘要

Historically, stimulation of humoral immunity in the form of antibodies has been the most effective means to provide protection against most viral infections. For this reason, almost all SARS-CoV-2 vaccine efforts are focused on stimulating humoral immunity. At the same time, there is evidence to suggest that, as with other RNA viruses such as RSV and Dengue, stimulating protective humoral immune responses against SARS-CoV2 may not be feasible. The alternative, stimulating T cell immune responses to SARS-CoV-2, has been advocated as being the preferred means of inducing long term protective immunity. However, it is currently not known if T cell immunity by itself can protect against SARS-CoV-2 infection or the development of severe COVID-19. In addition, even if stimulating cellular immunity is the goal, it is not clear how this could best be achieved. Stimulating T cell responses, especially cytotoxic T cell responses, with vaccinations has proven to be difficult. We have developed a novel cellular vaccine strategy that induces very strong T cell, especially cytotoxic T cell, responses. In this strategy, circulating monocytes are purified from the blood, loaded with a target antigen, then given back by intravenous infusion. In animal models, this results in the development of much stronger T cell responses than we have been able to obtain with other vaccine strategies but no antibody responses. In the case of COVID-19, this monocyte vaccine platform provides an excellent opportunity to determine if T cell responses are sufficient to protect against SARS-CoV-2 infection or the development of severe COVID-19. In this supplement, we propose to perform critical preclinical studies that will be required by the FDA before a clinical trial of a COVID-19 monocyte vaccine can be approved. These studies include examining vaccine-induced immune responses to SARS-CoV-2 and the toxicity of monocyte vaccination in mice and demonstrating that we can formulate a human COVID-19 monocyte vaccine at a scale sufficient for a clinical trial.

从历史上看，以抗体形式刺激体液免疫一直是提供针对大多数病毒感染的保护的最有效手段。因此，几乎所有SARS-CoV-2疫苗的努力都集中在刺激体液免疫上。与此同时，有证据表明，与其他RNA病毒如RSV和登革热一样，刺激针对SARS-CoV 2的保护性体液免疫应答可能是不可行的。另一种方法是刺激T细胞对SARS-CoV-2的免疫应答，被认为是诱导长期保护性免疫的首选方法。然而，目前尚不清楚T细胞免疫本身是否可以防止SARS-CoV-2感染或严重COVID-19的发展。此外，即使刺激细胞免疫是目标，也不清楚如何才能最好地实现这一目标。用疫苗接种刺激T细胞应答，特别是细胞毒性T细胞应答已被证明是困难的。我们已经开发了一种新的细胞疫苗策略，诱导非常强的T细胞，特别是细胞毒性T细胞，反应。在这种策略中，从血液中纯化循环单核细胞，加载靶抗原，然后通过静脉输注返回。在动物模型中，这导致产生比我们用其他疫苗策略获得的更强的T细胞应答，但没有抗体应答。在COVID-19的情况下，这种单核细胞疫苗平台提供了一个很好的机会来确定T细胞应答是否足以防止SARS-CoV-2感染或严重COVID-19的发展。在本补充文件中，我们建议在COVID-19单核细胞疫苗的临床试验获得批准之前进行FDA要求的关键临床前研究。这些研究包括检查疫苗诱导的对SARS-CoV-2的免疫反应和小鼠单核细胞疫苗接种的毒性，并证明我们可以以足以进行临床试验的规模配制人COVID-19单核细胞疫苗。