Large-scale serological profiling of SARS-CoV-2 and related human CoVs with high-throughput microfluidic nano-immunoassays

  • Funded by Swiss National Science Foundation (SNSF)
  • Total publications:8 publications

Grant number: 198412

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Key facts

  • Disease

    COVID-19
  • Start & end year

    2020
    2023
  • Known Financial Commitments (USD)

    $1,070,847.66
  • Funder

    Swiss National Science Foundation (SNSF)
  • Principal Investigator

    Maerkl Sebastian
  • Research Location

    Switzerland
  • Lead Research Institution

    Laboratoire de caractérisation du réseau biologique - Institut de Bioingénierie EPFL STI IBI-STI LBNC
  • Research Priority Alignment

    N/A
  • Research Category

    Pathogen: natural history, transmission and diagnostics

  • Research Subcategory

    Diagnostics

  • Special Interest Tags

    Innovation

  • Study Type

    Non-Clinical

  • Clinical Trial Details

    N/A

  • Broad Policy Alignment

    Pending

  • Age Group

    Not Applicable

  • Vulnerable Population

    Not applicable

  • Occupations of Interest

    Not applicable

Abstract

During the current SARS-CoV-2 pandemic, it became increasingly clear that there is a lack of diagnostic innovation in the field of emerging viruses. New, sophisticated, high-throughput technologies are urgently needed, such as reliable and accurate immuno-assays that can measure previous exposure to SARS-CoV-2 in thousands of samples in parallel. Such assays could be used to: i) determine the seroprevalence in the general population and in high-risk groups such as health care workers, ii) estimate existing risk factors or identify risk groups for contracting COVID-19, and iii) monitor population-immunity after natural infection or after vaccination, once a vaccine is administered to large parts of the population. We recently developed an entire suite of microfluidic nano-immunoassay devices, including a device capable of analyzing 1,024 serum samples in parallel with limits of detection (LOD) similar or better than standard ELISAs. This method requires only minute amounts of reagents leading to a cost per assay of a fraction of a cent and assuring reagent supply. We propose to apply this technology to serve as a serological profiling assay to detect IgG antibodies against SARS-CoV-2 and other circulating human-pathogenic CoVs for epidemiological sero-monitoring.

Publicationslinked via Europe PMC

Evolving infectious disease dynamics shape school-based intervention effectiveness.

SARS-CoV-2 convalescence and hybrid immunity elicits mucosal immune responses.

Clinical sensitivity and specificity of a high-throughput microfluidic nano-immunoassay combined with capillary blood microsampling for the identification of anti-SARS-CoV-2 Spike IgG serostatus.

Clinical sensitivity and specificity of a high-throughput microfluidic nano-immunoassay combined with capillary blood microsampling for the identification of anti-SARS-CoV-2 Spike IgG serostatus

Neutralization capacity of antibodies elicited through homologous or heterologous infection or vaccination against SARS-CoV-2 VOCs.

Infectious viral load in unvaccinated and vaccinated individuals infected with ancestral, Delta or Omicron SARS-CoV-2.

A high-throughput microfluidic nanoimmunoassay for detecting anti-SARS-CoV-2 antibodies in serum or ultralow-volume blood samples.

A high-throughput microfluidic nano-immunoassay for detecting anti-SARS-CoV-2 antibodies in serum or ultra-low volume dried blood samples