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Rethinking Immunological Risk: A Retrospective Cohort Study of Severe SARS-Cov-2 Infections in Individuals With Congenital Immunodeficiencies.
Nguyen, Alan A; Habiballah, Saddiq B; LaBere, Brenna; Day-Lewis, Megan; Elkins, Megan; Al-Musa, Amer; Chu, Anne; Jones, Jennifer; Fried, Ari J; McDonald, Douglas; Hoytema van Konijnenburg, David P; Rockowitz, Shira; Sliz, Piotr; Oettgen, Hans C; Schneider, Lynda C; MacGinnitie, Andrew; Bartnikas, Lisa M; Platt, Craig D; Ohsumi, Toshiro K; Chou, Janet.
Afiliação
  • Nguyen AA; Division of Immunology, Boston Children's Hospital and Harvard Medical School, Boston, Mass.
  • Habiballah SB; Division of Immunology, Boston Children's Hospital and Harvard Medical School, Boston, Mass.
  • LaBere B; Division of Immunology, Boston Children's Hospital and Harvard Medical School, Boston, Mass.
  • Day-Lewis M; Division of Immunology, Boston Children's Hospital and Harvard Medical School, Boston, Mass.
  • Elkins M; Division of Immunology, Boston Children's Hospital and Harvard Medical School, Boston, Mass.
  • Al-Musa A; Division of Immunology, Boston Children's Hospital and Harvard Medical School, Boston, Mass.
  • Chu A; Division of Immunology, Boston Children's Hospital and Harvard Medical School, Boston, Mass.
  • Jones J; Division of Immunology, Boston Children's Hospital and Harvard Medical School, Boston, Mass.
  • Fried AJ; Division of Immunology, Boston Children's Hospital and Harvard Medical School, Boston, Mass.
  • McDonald D; Division of Immunology, Boston Children's Hospital and Harvard Medical School, Boston, Mass.
  • Hoytema van Konijnenburg DP; Division of Immunology, Boston Children's Hospital and Harvard Medical School, Boston, Mass.
  • Rockowitz S; Research Computing, Information Technology, Boston Children's Hospital, Boston, Mass; The Manton Center for Orphan Disease Research, Boston Children's Hospital, Boston, Mass.
  • Sliz P; Research Computing, Information Technology, Boston Children's Hospital, Boston, Mass; The Manton Center for Orphan Disease Research, Boston Children's Hospital, Boston, Mass; Division of Molecular Medicine, Boston Children's Hospital, Boston, Massachusetts.
  • Oettgen HC; Division of Immunology, Boston Children's Hospital and Harvard Medical School, Boston, Mass.
  • Schneider LC; Division of Immunology, Boston Children's Hospital and Harvard Medical School, Boston, Mass.
  • MacGinnitie A; Division of Immunology, Boston Children's Hospital and Harvard Medical School, Boston, Mass.
  • Bartnikas LM; Division of Immunology, Boston Children's Hospital and Harvard Medical School, Boston, Mass.
  • Platt CD; Division of Immunology, Boston Children's Hospital and Harvard Medical School, Boston, Mass.
  • Ohsumi TK; Be Biopharma, Boston, Mass.
  • Chou J; Division of Immunology, Boston Children's Hospital and Harvard Medical School, Boston, Mass. Electronic address: Janet.Chou@childrens.harvard.edu.
J Allergy Clin Immunol Pract ; 11(11): 3391-3399.e3, 2023 11.
Article em En | MEDLINE | ID: mdl-37544429
ABSTRACT

BACKGROUND:

Debates on the allocation of medical resources during the coronavirus disease 2019 (COVID-19) pandemic revealed the need for a better understanding of immunological risk. Studies highlighted variable clinical outcomes of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infections in individuals with defects in both adaptive and innate immunity, suggesting additional contributions from other factors. Notably, none of these studies controlled for variables linked with social determinants of health.

OBJECTIVE:

To determine the contributions of determinants of health to risk of hospitalization for SARS-CoV-2 infection among individuals with inborn errors of immunodeficiencies.

METHODS:

This is a retrospective, single-center cohort study of 166 individuals with inborn errors of immunity, aged 2 months through 69 years, who developed SARS-CoV-2 infections from March 1, 2020, through March 31, 2022. Risks of hospitalization were assessed using a multivariable logistic regression analysis.

RESULTS:

The risk of SARS-CoV-2-related hospitalization was associated with underrepresented racial and ethnic populations (odds ratio [OR] 4.50; 95% confidence interval [95% CI] 1.57-13.4), a diagnosis of any genetically defined immunodeficiency (OR 3.32; 95% CI 1.24-9.43), obesity (OR 4.24; 95% CI 1.38-13.3), and neurological disease (OR 4.47; 95% CI 1.44-14.3). The COVID-19 vaccination was associated with reduced hospitalization risk (OR 0.52; 95% CI 0.31-0.81). Defects in T cell and innate immune function, immune-mediated organ dysfunction, and social vulnerability were not associated with increased risk of hospitalization after controlling for covariates.

CONCLUSIONS:

The associations between race, ethnicity, and obesity with increased risk of hospitalization for SARS-CoV-2 infection indicate the importance of variables linked with social determinants of health as immunological risk factors for individuals with inborn errors of immunity.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças da Imunodeficiência Primária / COVID-19 Tipo de estudo: Etiology_studies / Observational_studies / Risk_factors_studies Aspecto: Determinantes_sociais_saude / Equity_inequality Limite: Humans Idioma: En Revista: J Allergy Clin Immunol Pract Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças da Imunodeficiência Primária / COVID-19 Tipo de estudo: Etiology_studies / Observational_studies / Risk_factors_studies Aspecto: Determinantes_sociais_saude / Equity_inequality Limite: Humans Idioma: En Revista: J Allergy Clin Immunol Pract Ano de publicação: 2023 Tipo de documento: Article