High-throughput serological assay for detection of cytokines/chemokines in COVID-19 patients
High-throughput serological assay for detection of cytokines/chemokines in COVID-19 patients
批准号:
555017-2020
负责人:
Winnik, Mitchell
金额:
$3.64万
依托单位:
依托单位国家:
加拿大
项目类别:
Alliance Grants
财政年份:
2020
资助国家:
加拿大
项目状态:
已结题
起止时间:
2020-01-01 至 2021-12-31
中文摘要
COVID-19是一种新型病毒性疾病,具有从无症状到重症和死亡的广泛临床疾病。对病毒的免疫反应可能在最终的临床结果中起重要作用。据推测,炎症过度活跃或“细胞因子风暴”可能导致重症COVID-19的临床恶化。研究发现,炎症(或细胞因子)水平高的患者疾病更严重,死亡的可能性也更大。因此,我们必须弄清对COVID-19的炎症反应,既要确定有恶化风险的患者,又要确定启动针对免疫反应的治疗的潜在阈值。
英文摘要
COVID-19 is a novel viral illness, with a wide spectrum of clinical illness from asymptomatic to critical illness and death. The immune response to the virus may play an important role in the ultimate clinical outcome. It has been hypothesized that an inflammatory overactivity or "cytokine storm" may drive clinical deterioration in severe COVID-19. Patients with high levels of inflammation (or cytokines) have been found to have more severe disease and are more likely to die. It is therefore essential for us to unravel the inflammatory response to COVID-19, both to identify patients at-risk for deterioration and to define potential thresholds for initiation of therapies that target the immune response.
In order to do this, we need technologies to rapidly, efficiently, accurately measure cytokine levels. We aim to develop a technology, rooted in novel materials chemistry, to measure cytokine levels and as well antibodies against the SARS-CoV-2 antibody. This technology is based on the preparation of micrometre-sized plastic beads encoded with different metal atoms in which each encoded bead surface is coated with a capture biomolecule (antibody or antigen) to bind disease biomarkers from biological fluids collected from COVD-19 patients. In this way we can detecting 8 different cytokines in each patient sample. The technology can be expanded to detect 32 cytokines and antibodies in each sample. It also allows one to use secondary sample barcoding in order to analyze up to 20 patient samples in single test, where results can be acquired within a 1-hour timeframe. Upon development and deployment of this technology, we will use clinical samples from patients with COVID-19 to characterize the immune response and to conduct "serosurveillance" to identify and characterize patients who have been previously infected with COVID-19.
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