4.4 Article

A High-throughput Multiplexed Screening for Type 1 Diabetes, Celiac Diseases, and COVID-19

Journal

JOVE-JOURNAL OF VISUALIZED EXPERIMENTS
Volume -, Issue 185, Pages -

Publisher

JOURNAL OF VISUALIZED EXPERIMENTS
DOI: 10.3791/63787

Keywords

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Funding

  1. JDRF [2-SRA-2019-695-S-B, 2-SRA-2020-965-S-B, 1-SRA-2017-564-M_N]
  2. NIH [DK32083]
  3. Diabetes Research Center (DRC) [P30 DK116073]

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The ongoing clinical trial, Autoimmunity Screening for Kids (ASK), is the first study in the general population in the United States to screen for type 1 diabetes (T1D) and celiac disease. In response to the COVID-19 pandemic, there is an urgent need to understand the epidemiology of COVID-19 in the general population and its association with T1D development. A novel 6-Plex electrochemiluminescence (ECL) assay has been developed and validated as the primary screening tool for the ASK study, offering high efficiency, low cost, and low serum volume for the detection of T1D, celiac disease, and COVID-19.
An ongoing clinical trial, Autoimmunity Screening for Kids (ASK), is the first screening study in the general population for type 1 diabetes (T1D) and celiac disease in the United States. With the coronavirus disease 2019 (COVID-19) pandemic, the epidemiology of COVID-19 in the general population and knowledge about the association between COVID-19 infection and T1D development are urgently needed. The currently standard screening method of the radio-binding assay (RBA) has met two great challenges: low efficiency with a single assay format and low disease specificity with a large proportion of low-affinity antibodies generated in screening. With the platform of the multiplex electrochemiluminescence (ECL) assay we established previously, a novel 6-Plex ECL assay was developed that combines, in a single well, all four islet autoantibodies (IAbs) to insulin, glutamic acid decarboxylase (GAD65), insulinoma antigen 2 (IA-2), and Zinc transporter 8 (ZnT8) for T1D, transglutaminase autoantibodies (TGA) for celiac disease, and severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) receptor-binding domain (RBD) antibodies for COVID-19. The assay was validated in blind using 880 samples from the ASK study, including 325 positive samples and 555 all antibody-negative samples, and compared with the standard RBAs and a single ECL assay. With the advantages of high efficiency, low cost, and low serum volume, this assay has been accepted as the primary screening tool for the ASK study.

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