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Airway antibodies emerge according to COVID-19 severity and wane rapidly but reappear after SARS-CoV-2 vaccination
Alberto Cagigi, … , Karin Loré, Anna Smed-Sörensen
Alberto Cagigi, … , Karin Loré, Anna Smed-Sörensen
Published October 19, 2021
Citation Information: JCI Insight. 2021;6(22):e151463. https://doi.org/10.1172/jci.insight.151463.
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Research Article COVID-19 Immunology

Airway antibodies emerge according to COVID-19 severity and wane rapidly but reappear after SARS-CoV-2 vaccination

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Abstract

Understanding the presence and durability of antibodies against SARS-CoV-2 in the airways is required to provide insights into the ability of individuals to neutralize the virus locally and prevent viral spread. Here, we longitudinally assessed both systemic and airway immune responses upon SARS-CoV-2 infection in a clinically well-characterized cohort of 147 infected individuals representing the full spectrum of COVID-19 severity, from asymptomatic infection to fatal disease. In addition, we evaluated how SARS-CoV-2 vaccination influenced the antibody responses in a subset of these individuals during convalescence as compared with naive individuals. Not only systemic but also airway antibody responses correlated with the degree of COVID-19 disease severity. However, although systemic IgG levels were durable for up to 8 months, airway IgG and IgA declined significantly within 3 months. After vaccination, there was an increase in both systemic and airway antibodies, in particular IgG, often exceeding the levels found during acute disease. In contrast, naive individuals showed low airway antibodies after vaccination. In the former COVID-19 patients, airway antibody levels were significantly elevated after the boost vaccination, highlighting the importance of prime and boost vaccinations for previously infected individuals to obtain optimal mucosal protection.

Authors

Alberto Cagigi, Meng Yu, Björn Österberg, Julia Svensson, Sara Falck-Jones, Sindhu Vangeti, Eric Åhlberg, Lida Azizmohammadi, Anna Warnqvist, Ryan Falck-Jones, Pia C. Gubisch, Mert Ödemis, Farangies Ghafoor, Mona Eisele, Klara Lenart, Max Bell, Niclas Johansson, Jan Albert, Jörgen Sälde, Deleah D. Pettie, Michael P. Murphy, Lauren Carter, Neil P. King, Sebastian Ols, Johan Normark, Clas Ahlm, Mattias N. Forsell, Anna Färnert, Karin Loré, Anna Smed-Sörensen

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Figure 4

Longitudinal airway antibody responses to RBD across COVID-19 severity from acute disease up to 8 months from symptom onset.

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Longitudinal airway antibody responses to RBD across COVID-19 severity f...
Levels of IgG and IgA against RBD in (A) NSWs and (B) NPAs. The black lines indicate median values. Kruskal-Wallis with Dunn’s multiple comparisons was used to compare the groups and considered statistically significant at P < 0.05. *P < 0.05, **P < 0.01, ***P < 0.001, ****P < 0.0001. In A the line overlaps with not detected (ND) for IgG levels. (C) Heatmap generated grouping patients according to PDS showing acute and convalescent IgG and IgA titers against N, S, and RBD (plasma) and RBCs (NSWs, NPAs, and ETAs) for each patient. The heatmap includes data from patients (n = 147) and also data from PPHCs (n = 30) and PCR– individuals (n = 9) (indicated with PDS 0). Missing data and unavailable samples are shown in black. (D) Comparison of the levels of RBD IgG/A in patient-matched NSWs, NPAs, ETAs, and plasma collected at the same time point. The black lines connect data points from the same individuals. Friedman’s test with Dunn’s multiple comparisons test was used to compare the groups and considered statistically significant at P < 0.05. *P < 0.05, **P < 0.01. (E) Spearman correlation for NPAs (n = 34) versus plasma immunoglobulins against the RBD during acute disease.

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