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Author Spotlight: Advancements in Multiplex Detection of Respiratory Viruses
Published on: November 10, 2023
COVID-19 in Russia: Clinical and Immunological Features of the First-Wave Patients
T V Bobik1, N N Kostin1, G A Skryabin1
1Shemyakin-Ovchinnikov Institute of Bioorganic Chemistry, Russian Academy of Sciences, Moscow, 117997 Russia.
Insights
Immunoglobulin A (IgA) is the earliest marker for SARS-CoV-2 infection, showing higher diagnostic value than Immunoglobulin M (IgM). Evaluating both RBD- and N-specific antibodies improves ELISA sensitivity for COVID-19 detection.
Area of Science:
- Immunology
- Virology
- Infectious Diseases
Background:
- The COVID-19 pandemic, caused by SARS-CoV-2, has led to millions of deaths globally.
- Understanding the immune response, particularly antibody kinetics and diagnostic markers, is crucial for managing the pandemic.
- Previous studies have focused on various SARS-CoV-2 antigens, but a comprehensive analysis of immunoglobulin classes and subclasses in relation to clinical outcomes is needed.
Purpose of the Study:
- To analyze the functional and immunological status of COVID-19 patients in the Moscow Region during the first wave of the pandemic.
- To evaluate the diagnostic significance of different immunoglobulin classes (IgM, IgA, IgG) and antibody specificities (N-protein, RBD, NTD) in SARS-CoV-2 infection.
- To correlate immunological findings with clinical outcomes, including mechanical ventilation and mortality.
Main Methods:
- Functional analysis of 155 COVID-19 patients with confirmed PCR and CT findings.
- Clinical correlation analysis across four groups: non-ventilated, ventilated, recovered, and deceased patients.
- Immunological assessment using an original ELISA kit detecting SARS-CoV-2 specific antibodies (IgM, IgA, IgG) against linear and conformational epitopes of N-protein, RBD, and NTD.
Main Results:
- Immunoglobulin A (IgA) was identified as the earliest serological marker for SARS-CoV-2 infection, demonstrating superior sensitivity and diagnostic significance compared to Immunoglobulin M (IgM).
- Seroconversion rates for early N-protein-specific IgM and IgA antibodies were comparable to those for antibodies targeting conformational RBD epitopes.
- SARS-CoV-2 N-protein-specific IgG seroconversion was significantly faster than for other specific antibodies, and evaluating RBD- and N-specific antibodies in parallel enhances ELISA sensitivity.
Conclusions:
- Immunoglobulin A serves as a critical early diagnostic marker for SARS-CoV-2 infection.
- Conformational epitopes of the RBD fragment are the primary drivers of strong immunogenicity, while linear RBD and NTD epitopes exhibit lower immunogenicity.
- Parallel assessment of RBD- and N-specific antibodies, alongside analysis of immunoglobulin subclass distribution (IgG1-4, IgA1-2), provides a more comprehensive understanding of the immune response to SARS-CoV-2.
Abstract:
The coronavirus disease outbreak in 2019 (COVID-19) has now achieved the level of a global pandemic and affected more than 100 million people on all five continents and caused over 2 million deaths. Russia is, needless to say, among the countries affected by SARS-CoV-2, and its health authorities have mobilized significant efforts and resources to fight the disease. The paper presents the result of a functional analysis of 155 patients in the Moscow Region who were examined at the Central Clinical Hospital of the Russian Academy of Sciences during the first wave of the pandemic (February-July, 2020). The inclusion criteria were a positive PCR test and typical, computed tomographic findings of viral pneumonia in the form of ground-glass opacities. A clinical correlation analysis was performed in four groups of patients: (1) those who were not on mechanical ventilation, (2) those who were on mechanical ventilation, and (3) those who subsequently recovered or (4) died. The correlation analysis also considered confounding comorbidities (diabetes, metabolic syndrome, hypertension, etc.). The immunological status of the patients was examined (levels of immunoglobulins of the M, A, G classes and their subclasses, as well as the total immunoglobulin level) using an original SARS-CoV-2 antibody ELISA kit. The ELISA kit was developed using linear S-protein RBD-SD1 and NTD fragments, as well as the N-protein, as antigens. These antigens were produced in the prokaryotic E. coli system. Recombinant RBD produced in the eukaryotic CHO system (RBD CHO) was used as an antigen representing conformational RBD epitopes. The immunoglobulin A level was found to be the earliest serological criterion for the development of a SARS-CoV-2 infection and it yielded the best sensitivity and diagnostic significance of ELISA compared to that of class M immunoglobulin. We demonstrated that the seroconversion rate of "early" N-protein-specific IgM and IgA antibodies is comparable to that of antibodies specific to RBD conformational epitopes. At the same time, seroconversion of SARS-CoV-2 N-protein-specific class G immunoglobulins was significantly faster compared to that of other specific antibodies. Our findings suggest that the strong immunogenicity of the RBD fragment is for the most part associated with its conformational epitopes, while the linear RBD and NTD epitopes have the least immunogenicity. An analysis of the occurrence rate of SARS-CoV-2-specific immunoglobulins of different classes revealed that RBD- and N-specific antibodies should be evaluated in parallel to improve the sensitivity of ELISA. An analysis of the immunoglobulin subclass distribution in sera of seropositive patients revealed uniform induction of N-protein-specific IgG subclasses G1-G4 and IgA subclasses A1-A2 in groups of patients with varying severity of COVID-19. In the case of the S-protein, G1, G3, and A1 were the main subclasses of antibodies involved in the immune response.
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