Durable antibody response one year after hospitalization for COVID-19: A longitudinal cohort study


Por: Masia, M, Fernandez-Gonzalez, M, Telenti, G, Agullo, V, Garcia, J, Padilla, S, Garcia-Abellan, J, Galiana A, Gonzalo-Jimenez, N and Gutierrez, F

Publicada: 1 sep 2021 Ahead of Print: 1 jul 2021
Resumen:
Objectives: Durability of the humoral immune response to SARS-CoV-2 has yet to be defined. We longitudinally evaluated during a 12-month period the antibody responses to SARS-CoV-2, and analysed predictors of antibody titres decline and seroreversion. Methods: Prospective study conducted in a cohort of patients hospitalized for microbiologically-confirmed COVID-19. Blood and nasopharyngeal samples were sequentially obtained during hospital stay and at 1, 2, 6 and 12 months after patients' discharge for measuring anti-spike (S) and anti-nucleocapsid (N) IgG antibody levels and SARS-CoV-2 RNA, respectively. Results: 80 non-vaccinated patients were analysed. At month 12 after discharge, 73 (91.2%) patients exhibited detectable S-IgG and 35 (43.8%) N-IgG antibody titres. A gradual wane was observed in S-IgG and N-IgG antibody titres. Linear regression showed that S-IgG decline was positively associated with peak antibody titres (coefficient [95% CI] 0.059 [0.05-0.067], p < 0.001), inversely with WHO severity score (coefficient [95% CI]-0.042 [-0.079/-0.004], p = 0.033), and there was a trivial positive association with age (coefficient [95% CI] 0.002 [0-0.005], p = 0.10); N-IgG decline was positively associated with peak antibody titres (coefficient [95% CI] 0.091 [0.078-0.105], p < 0.001). Logistic regression showed that seroreversion for S-IgG was inversely associated with peak S-IgG (OR 0.19; 95% CI, 0.04-0.45; p = 0.004); seroreversion for N-IgG was inversely associated with peak N-IgG (OR 0.71; 95% 0.53-0.90; p = 0.009) and positively with cycle threshold of RT-PCR (OR 1.14; 95% CI, 1.00-1.33; p = 0.062). Conclusion: Anti-spike IgG antibodies remain detectable one year after hospitalization for COVID-19. Higher peak antibody titres and disease severity were associated with increased durability of detectable antibodies.

Filiaciones:
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 Hosp Gen Univ Elche, Infect Dis Unit, Alicante, Spain

 Univ Miguel Hernandez, Clin Med Dept, Alicante, Spain

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 Hosp Gen Univ Elche, Infect Dis Unit, Alicante, Spain

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 Hosp Gen Univ Elche, Infect Dis Unit, Alicante, Spain

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 Hosp Gen Univ Elche, Infect Dis Unit, Alicante, Spain

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 Hosp Gen Univ Elche, Infect Dis Unit, Alicante, Spain

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 Hosp Gen Univ Elche, Infect Dis Unit, Alicante, Spain

 Univ Miguel Hernandez, Clin Med Dept, Alicante, Spain

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 Hosp Gen Univ Elche, Infect Dis Unit, Alicante, Spain

Galiana A:
 Hosp Gen Univ Elche, Microbiol Serv, Alicante, Spain

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 Hosp Gen Univ Elche, Microbiol Serv, Alicante, Spain

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 Hosp Gen Univ Elche, Infect Dis Unit, Alicante, Spain

 Univ Miguel Hernandez, Clin Med Dept, Alicante, Spain
ISSN: 10959157





JOURNAL OF AUTOIMMUNITY
Editorial
Elsevier Inc., 24-28 OVAL RD, LONDON NW1 7DX, ENGLAND, Estados Unidos America
Tipo de documento: Article
Volumen: 123 Número:
Páginas: 102703-102703
WOS Id: 000685545200001
ID de PubMed: 34303083
imagen Bronze, Green Published

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