Increased anti-nucleocapsid secretory IgA and consumption of complement component 3 in post-COVID syndrome patients - Report - MDSpire

Increased anti-nucleocapsid secretory IgA and consumption of complement component 3 in post-COVID syndrome patients

  • By

  • Zhiwen Hai

  • Weihua Yang

  • Azam Ghazi

  • Amalia Buitrago

  • Patricia Marín-García

  • Isabel G Azcárate

  • Alba González-Escalada

  • Nineth Rossi

  • Javier Benítez-Cruz

  • Iván Estévez-Benito

  • Agustín Tortajada

  • José R. Regueiro

  • José M. Bautista

  • Narcisa Martinez-Quiles

  • May 14, 2026

  • 0 min

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Clinical Report: Elevated Secretory IgA Against Nucleocapsid in Post-COVID Syndrome

Overview

This study identifies elevated levels of secretory IgA against the Nucleocapsid protein and reduced complement component C3 in patients with post-COVID syndrome. These findings suggest potential biomarkers for post-COVID syndrome and highlight the role of the complement system in its pathophysiology.

Background

Post-COVID syndrome poses a significant global health challenge, affecting millions with persistent symptoms following COVID-19 infection. Understanding the immune dysregulation, particularly the roles of antibodies and the complement system, is crucial for developing targeted therapies and improving patient outcomes. This study contributes to the growing body of evidence regarding immune responses in post-COVID syndrome.

Data Highlights

ParameterPost-COVID SyndromeCOVID-Recovered Controls
Anti-Nucleocapsid sIgAIncreasedNormal
C3 LevelsReducedNormal
C4 LevelsDecreasedNormal
CH50SimilarSimilar

Key Findings

  • Elevated anti-Nucleocapsid sIgA levels were observed in post-COVID syndrome patients.
  • Reduced C3 levels may indicate ongoing complement activation and consumption.
  • No significant differences were found in circulating immune complexes between groups.
  • Anti-Nucleocapsid IgG levels negatively correlated with factor H and CH50 in reinfected vaccinated patients.
  • Combining anti-Nucleocapsid sIgA and C3 levels improved discrimination between patients and controls.

Clinical Implications

The findings suggest that measuring salivary anti-Nucleocapsid IgA and complement component C3 may serve as useful biomarkers for diagnosing post-COVID syndrome. Clinicians should consider these parameters when evaluating patients with persistent symptoms following COVID-19 infection.

Conclusion

This study highlights the potential of salivary anti-Nucleocapsid IgA and complement dysregulation as biomarkers for post-COVID syndrome, warranting further investigation in larger cohorts.

Related Resources & Content

  1. Author(s)/Org, Infection, 2022 -- The relationship between micronutrient levels and SARS-CoV-2-specific antibody production in recovering patients
  2. Author(s)/Org, Acta Neuropathologica, 2026 -- Pathogenic IgG from long COVID patients with neurological sequelae triggers sensitive but not cognitive impairments upon transfer into mice
  3. Author(s)/Org, Frontiers in Immunology, 2026 -- Complement activation in patients with post-acute sequelae after SARS-CoV-2 infection
  4. Author(s)/Org, Open Forum Infectious Diseases -- Proteomic Analysis of Single Cells and Plasma Fails to Distinguish Between SARS-CoV-2 Antigenemia and Non-Antigenemia Patients During Convalescence in a Study of 100 Individuals
  5. CDC, Long COVID Clinical Guidance | Long COVID | CDC, 2026 -- Clinical Guidance for Long COVID Management
  6. Author(s)/Org, Nature Immunology -- Complement profile, 2024 -- Complement dysregulation in immune responses
  7. Author(s)/Org, Evaluation of Interventions for Cognitive Symptoms in Long COVID: A Randomized Clinical Trial - PubMed, 2026 -- Cognitive Symptoms in Long COVID
  8. Long COVID Clinical Guidance | Long COVID | CDC
  9. Complement profile | Nature Immunology
  10. Evaluation of Interventions for Cognitive Symptoms in Long COVID: A Randomized Clinical Trial - PubMed

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