Association between SARS-CoV-2 infection and anti-apolipoprotein A-1 antibody in children

Nicolas Vuilleumier1,2, Sabrina Pagano1,2, Elsa Lorthe3,4,5

  • 1Division of Laboratory Medicine, Diagnostics Department, Geneva University Hospitals, Geneva, Switzerland.

PubMed

Insights

Autoantibodies against apolipoprotein A-1 (AAA1) are elicited by SARS-CoV-2 infection in children. AAA1 seropositivity is linked to a two-fold increased risk of persistent COVID-19 symptoms lasting at least four weeks.

Area of Science:

  • Pediatrics
  • Immunology
  • Infectious Diseases

Background:

  • Autoantibodies against apolipoprotein A-1 (AAA1) are known to be triggered by SARS-CoV-2 infection in adults, correlating with persistent COVID-19 symptoms.
  • The prevalence and clinical significance of AAA1 in pediatric populations following SARS-CoV-2 infection remain largely unexplored.

Purpose of the Study:

  • To investigate the prevalence of AAA1 in children exposed to SARS-CoV-2.
  • To determine the association between AAA1 seropositivity and the persistence of COVID-19 symptoms in pediatric patients.

Main Methods:

  • A prospective cohort study (SEROCOV-KIDS) involving 1031 children (6 months to 17 years) was conducted.
  • Participants' serologies for anti-SARS-CoV-2 antibodies and AAA1 were analyzed.
  • Data on symptom persistence were collected via online questionnaires, and logistic regression was used for statistical analysis.

Main Results:

  • Overall AAA1 seropositivity was 5.8%, with higher rates observed in infected-unvaccinated children.
  • AAA1 seroconversion risk was doubled in infected-unvaccinated children compared to other groups (OR: 2.11).
  • AAA1 seropositivity was independently associated with a two-fold increased odds of symptom persistence for at least 4 weeks (p ≤ 0.03).

Conclusions:

  • SARS-CoV-2 infection can induce an AAA1 response in children.
  • AAA1 seropositivity in children is linked to a higher likelihood of short-term symptom persistence post-infection.
  • Further research is needed to understand the long-term implications of AAA1 in pediatric Long COVID.
Abstract