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Serum IgG anti-SARS-CoV-2 Binding Antibody Level Is Strongly Associated With IgA and Functional Antibody Levels in Adults Infected With SARS-CoV-2.
Ye, Xunyan; Angelo, Laura S; Nicholson, Erin G; Iwuchukwu, Obinna P; Cabral de Rezende, Wanderson; Rajan, Anubama; Aideyan, Letisha O; McBride, Trevor J; Bond, Nanette; Santarcangelo, Patricia; Rayford, Yolanda J; Ferlic-Stark, Laura; Fragoso, Sonia; Momin, Zoha; Liu, Hongbing; Truong, Khanghy; Lopez, Brianna; Conner, Margaret E; Rice, Andrew P; Kimata, Jason T; Avadhanula, Vasanthi; Piedra, Pedro A.
  • Ye X; Department of Molecular Virology & Microbiology, Baylor College of Medicine, Houston, TX, United States.
  • Angelo LS; Department of Molecular Virology & Microbiology, Baylor College of Medicine, Houston, TX, United States.
  • Nicholson EG; Department of Molecular Virology & Microbiology, Baylor College of Medicine, Houston, TX, United States.
  • Iwuchukwu OP; Department of Molecular Virology & Microbiology, Baylor College of Medicine, Houston, TX, United States.
  • Cabral de Rezende W; Department of Molecular Virology & Microbiology, Baylor College of Medicine, Houston, TX, United States.
  • Rajan A; Department of Pharmacology, Baylor College of Medicine, Houston, TX, United States.
  • Aideyan LO; Department of Molecular Virology & Microbiology, Baylor College of Medicine, Houston, TX, United States.
  • McBride TJ; Department of Molecular Virology & Microbiology, Baylor College of Medicine, Houston, TX, United States.
  • Bond N; Department of Molecular Virology & Microbiology, Baylor College of Medicine, Houston, TX, United States.
  • Santarcangelo P; Department of Molecular Virology & Microbiology, Baylor College of Medicine, Houston, TX, United States.
  • Rayford YJ; Department of Molecular Virology & Microbiology, Baylor College of Medicine, Houston, TX, United States.
  • Ferlic-Stark L; Department of Molecular Virology & Microbiology, Baylor College of Medicine, Houston, TX, United States.
  • Fragoso S; Department of Molecular Virology & Microbiology, Baylor College of Medicine, Houston, TX, United States.
  • Momin Z; Department of Molecular Virology & Microbiology, Baylor College of Medicine, Houston, TX, United States.
  • Liu H; Department of Molecular Virology & Microbiology, Baylor College of Medicine, Houston, TX, United States.
  • Truong K; Department of Molecular Virology & Microbiology, Baylor College of Medicine, Houston, TX, United States.
  • Lopez B; Department of Molecular Virology & Microbiology, Baylor College of Medicine, Houston, TX, United States.
  • Conner ME; Department of Molecular Virology & Microbiology, Baylor College of Medicine, Houston, TX, United States.
  • Rice AP; Department of Molecular Virology & Microbiology, Baylor College of Medicine, Houston, TX, United States.
  • Kimata JT; Department of Molecular Virology & Microbiology, Baylor College of Medicine, Houston, TX, United States.
  • Avadhanula V; Department of Molecular Virology & Microbiology, Baylor College of Medicine, Houston, TX, United States.
  • Piedra PA; Department of Molecular Virology & Microbiology, Baylor College of Medicine, Houston, TX, United States.
Front Immunol ; 12: 693462, 2021.
Article in English | MEDLINE | ID: covidwho-1485053
ABSTRACT

Background:

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) was first reported in December 2019 in Wuhan, China, and then rapidly spread causing an unprecedented pandemic. A robust serological assay is needed to evaluate vaccine candidates and better understand the epidemiology of coronavirus disease (COVID-19).

Methods:

We used the full-length spike (S) protein of SARS-CoV-2 for the development of qualitative and quantitative IgG and IgA anti-S enzyme linked immunosorbent assays (ELISA). A total of 320 sera used for assay development were comprised of pandemic sera from SARS-CoV-2 infected adults (n=51) and pre-pandemic sera (n=269) including sera from endemic human coronavirus infected adults. Reverse cumulative curves and diagnostic test statistics were evaluated to define the optimal serum dilution and OD cutoff value for IgG anti-S and IgA anti-S ELISAs. The IgG and IgA anti-S, and three functional antibodies (ACE-2 receptor blocking antibody, lentipseudovirus-S neutralizing antibody, and SARS-CoV-2 neutralizing antibody) were measured using additional SARS-CoV-2 PCR positive sera (n=76) and surveillance sera (n=25). Lastly, the IgG and IgA anti-S levels were compared in different demographic groups.

Results:

The optimal serum dilution for the qualitative IgG anti-S ELISA was at 11024 yielding a 99.6% specificity, 92.2% sensitivity, 92.9% positive predictive value (PPV), and 99.6% negative predictive value (NPV) at a SARS-CoV-2 seroprevalence of 5%. The optimal serum dilution for the qualitative IgA anti-S ELISA was at 1128 yielding a 98.9% specificity, 76.5% sensitivity, 78.3% PPV, and 98.8% NPV at the same seroprevalence. Significant correlations were demonstrated between the IgG and IgA (r=0.833 for concentrations, r=0.840 for titers) as well as between IgG and three functional antibodies (r=0.811-0.924 for concentrations, r=0.795-0.917 for titers). The IgG and IgA anti-S levels were significantly higher in males than females (p<0.05), and in adults with moderate/severe symptoms than in adults with mild/moderate symptoms (p<0.001).

Conclusion:

We developed a highly specific and sensitive IgG anti-S ELISA assay to SARS-CoV-2 using full length S protein. The IgG anti-S antibody level was strongly associated with IgA and functional antibody levels in adults with SARS-CoV-2 infection. Gender and disease severity, rather than age, play an important role in antibody levels.
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Keywords

Full text: Available Collection: International databases Database: MEDLINE Main subject: Immunoglobulin A / Immunoglobulin G / SARS-CoV-2 / COVID-19 / Antibodies, Viral Type of study: Diagnostic study / Experimental Studies / Observational study / Prognostic study / Qualitative research / Randomized controlled trials Topics: Vaccines / Variants Limits: Adult / Female / Humans Language: English Journal: Front Immunol Year: 2021 Document Type: Article Affiliation country: Fimmu.2021.693462

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Immunoglobulin A / Immunoglobulin G / SARS-CoV-2 / COVID-19 / Antibodies, Viral Type of study: Diagnostic study / Experimental Studies / Observational study / Prognostic study / Qualitative research / Randomized controlled trials Topics: Vaccines / Variants Limits: Adult / Female / Humans Language: English Journal: Front Immunol Year: 2021 Document Type: Article Affiliation country: Fimmu.2021.693462