Journal of Allergy and Clinical Immunology: Global (May 2024)

Altered COVID-19 immunity in children with asthma by atopic status

  • Sherry Tong, BS,
  • Jordan C. Scott, BS,
  • Enwono Eyoh, PhD,
  • Derek W. Werthmann, PhD,
  • Addison E. Stone, BS,
  • Amelie E. Murrell, BS,
  • Gilberto Sabino-Santos, PhD,
  • Ivy V. Trinh, BS,
  • Sruti Chandra, PhD,
  • Debra H. Elliott, BS,
  • Ashley R. Smira, BS,
  • Jalene V. Velazquez, BS,
  • John Schieffelin, MD,
  • Bo Ning, PhD,
  • Tony Hu, PhD,
  • Jay K. Kolls, MD,
  • Samuel J. Landry, PhD,
  • Kevin J. Zwezdaryk, PhD,
  • James E. Robinson, MD,
  • Bronwyn M. Gunn, PhD,
  • Felicia A. Rabito, PhD,
  • Elizabeth B. Norton, PhD

Journal volume & issue
Vol. 3, no. 2
p. 100236

Abstract

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Background: Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection causes a spectrum of clinical outcomes that may be complicated by severe asthma. Antiviral immunity is often compromised in patients with asthma; however, whether this is true for SARS-CoV-2 immunity and children is unknown. Objective: We aimed to evaluate SARS-CoV-2 immunity in children with asthma on the basis of infection or vaccination history and compared to respiratory syncytial viral or allergen (eg, cockroach, dust mite)-specific immunity. Methods: Fifty-three children from an urban asthma study were evaluated for medical history, lung function, and virus- or allergen-specific immunity using antibody or T-cell assays. Results: Polyclonal antibody responses to spike were observed in most children from infection and/or vaccination history. Children with atopic asthma or high allergen-specific IgE, particularly to dust mites, exhibited reduced seroconversion, antibody magnitude, and SARS-CoV-2 virus neutralization after SARS-CoV-2 infection or vaccination. TH1 responses to SARS-CoV-2 and respiratory syncytial virus correlated with antigen-respective IgG. Cockroach-specific T-cell activation as well as IL-17A and IL-21 cytokines negatively correlated with SARS-CoV-2 antibodies and effector functions, distinct from total and dust mite IgE. Allergen-specific IgE and lack of vaccination were associated with recent health care utilization. Reduced lung function (forced expiratory volume in 1 second ≤ 80%) was independently associated with (SARS-CoV-2) peptide-induced cytokines, including IL-31, whereas poor asthma control was associated with cockroach-specific cytokine responses. Conclusion: Mechanisms underpinning atopic and nonatopic asthma may complicate the development of memory to SARS-CoV-2 infection or vaccination and lead to a higher risk of repeated infection in these children.

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