4.7 Article

Expanding COVID-19 Vaccine Availability: Role for Combined Orthogonal Serology Testing (COST)

期刊

VACCINES
卷 9, 期 4, 页码 -

出版社

MDPI
DOI: 10.3390/vaccines9040376

关键词

COVID-19; SARS-CoV-2; IgG; IgM; spike; nucleocapsid; orthogonal antibody testing; vaccine; vaccine prioritization

资金

  1. State of Texas
  2. Tarrant County
  3. Dallas County
  4. City of FortWorth
  5. City of Dallas
  6. Lyda Hill Philanthropies
  7. Communities Foundation of Texas

向作者/读者索取更多资源

The study evaluated the utility of a combination orthogonal serological testing (COST) algorithm alongside RT-PCR to quantify infection prevalence, with the aim of identifying patient clusters for single dose and/or delayed vaccination. The results showed that IgG(NC) serology could identify twice the number of COVID-positive cases compared to RT-PCR alone, and COST further increased the number of detected positive cases, demonstrating its potential as an effective tool for vaccination prioritization.
Background: The persisting Coronavirus disease 2019 (COVID-19) pandemic and limited vaccine supply has led to a shift in global health priorities to expand vaccine coverage. Relying on severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) molecular testing alone cannot reveal the infection proportion, which could play a critical role in vaccination prioritization. We evaluated the utility of a combination orthogonal serological testing (COST) algorithm alongside RT-PCR to quantify prevalence with the aim of identifying candidate patient clusters to receive single and/or delayed vaccination. Methods: We utilized 108,505 patients with suspected COVID-19 in a retrospective analysis of SARS-CoV-2 RT-PCR vs. IgG-nucleocapsid (IgG(NC)) antibody testing coverage in routine practice for the estimation of prevalence. Prospectively, an independent cohort of 21,388 subjects was simultaneously tested by SARS-CoV-2 RT-PCR and IgG(NC) to determine the prevalence. We used 614 prospective study subjects to assess the utility of COST (IgG(NC), IgM-spike (IgM(SP)), and IgG-spike (IgG(SP))) in establishing the infection proportion to identify a single-dose vaccination cohort. Results: Retrospectively, we observed a 6.3% (6871/108,505) positivity for SARS-CoV-2 RT-PCR, and only 2.3% (2533/108,505) of cases had paired IgG(NC) serology performed. Prospectively, IgG(NC) serology identified twice the number of COVID-positive cases in relation to RT-PCR alone. COST further increased the number of detected positive cases: IgG(NC)+ or IgM(SP)+ (18.0%); IgG(NC)+ or IgG(SP)+ (23.5%); IgM(SP)+ or IgG(SP)+ (23.8%); and IgG(NC)+ or IgM(SP)+ or IgG(SP)+ (141/584 = 24.1%). Conclusion: COST may be an effective tool for the evaluation of infection proportion and thus could define a cohort for a single dose and/or delayed vaccination.

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