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Clinical outcomes and immunological features of COVID-19 patients receiving B-cell depletion therapy during the Omicron era

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Authors

Lee, Chan Mi; Kim, Minji; Park, Seong-wook; Kang, Chang Kyung; Choe, Pyoeng Gyun; Kim, Nam Joong; Jo, Hyeon Jae; Shin, Hyun Mu; Lee, Chang-Han; Kim, Hang-Rae; Park, Wan Beom; Oh, Myoung-don

Issue Date
2024-02
Publisher
Taylor and Francis Ltd.
Citation
Infectious Diseases, Vol.56 No.2, pp.116-127
Abstract
Background: The clinical outcomes and immunological features of coronavirus disease 2019 (COVID-19) patients receiving B-cell depletion therapy (BCDT), especially in Omicron variant era, have not been fully elucidated. We aimed to investigate the outcomes and immune responses of COVID-19 patients receiving BCDT during the Omicron period.Methods: We retrospectively compared clinical outcomes between COVID-19 patients treated with BCDT (the BCDT group) and those with the same underlying diseases not treated with BCDT (the non-BCDT group). For immunological analyses, we prospectively enrolled COVID-19 patients receiving BCDT and immunocompetent COVID-19 patients as controls. We measured humoral and cellular immune responses using the enzyme-linked immunosorbent assay and flow cytometry.Results: Severe to critical COVID-19 was more frequent in the BCDT group than in the non-BCDT group (41.9% vs. 28.3%, p = .030). BCDT was an independent risk factor for severe to critical COVID-19 (adjusted odds ratio [aOR] 2.21, 95% confidence interval [CI] 1.21-4.04, p = .010) as well as for COVID-19-related mortality (aOR 4.03, 95% CI 1.17-13.86, p = .027). Immunological analyses revealed that patients receiving BCDT had lower anti-S1 IgG titres and a tendency to higher proportions of activated CD4+ T-cells than the controls.Conclusions: BCDT was associated with worse COVID-19 outcomes in the Omicron period. Humoral immune response impairment and T-cell hyperactivation were the main immunological features of COVID-19 patients treated with BCDT, which may have contributed to the worse outcomes of COVID-19 in this population.
ISSN
2374-4235
URI
https://hdl.handle.net/10371/199558
DOI
https://doi.org/10.1080/23744235.2023.2276784
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  • College of Medicine
  • Department of Medicine
Research Area Immunology, Infectious Diseases, Vaccination

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