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Treatment with Sotrovimab and Casirivimab/Imdevimab Enhances Serum SARS-CoV-2 S Antibody Levels in Patients Infected with the SARS-CoV-2 Delta, Omicron BA.1, and BA.5 Variants.
Fujimoto, Kana; Mutsuo, Satoru; Yasuda, Yuto; Arasawa, Soichi; Tashima, Noriyuki; Iwashima, Daisuke; Takahashi, Ken-Ichi.
  • Fujimoto K; Department of Respiratory Medicine, Kishiwada City Hospital, 1001 Gakuhara-cho, Kishiwada-shi 596-8501, Osaka, Japan.
  • Mutsuo S; Department of Central Clinical Laboratory, Kishiwada City Hospital, 1001 Gakuhara-cho, Kishiwada-shi 59-8501, Osaka, Japan.
  • Yasuda Y; Department of Respiratory Medicine, Kishiwada City Hospital, 1001 Gakuhara-cho, Kishiwada-shi 596-8501, Osaka, Japan.
  • Arasawa S; Department of Gastroenterology, Kishiwada City Hospital, 1001 Gakuhara-cho, Kishiwada-shi 596-8501, Osaka, Japan.
  • Tashima N; Department of Respiratory Medicine, Kishiwada City Hospital, 1001 Gakuhara-cho, Kishiwada-shi 596-8501, Osaka, Japan.
  • Iwashima D; Department of Respiratory Medicine, Kishiwada City Hospital, 1001 Gakuhara-cho, Kishiwada-shi 596-8501, Osaka, Japan.
  • Takahashi KI; Department of Respiratory Medicine, Kishiwada City Hospital, 1001 Gakuhara-cho, Kishiwada-shi 596-8501, Osaka, Japan.
Infect Dis Rep ; 14(6): 996-1003, 2022 Dec 09.
Article in English | MEDLINE | ID: covidwho-2154957
ABSTRACT

Background:

The neutralizing ability of sotrovimab and casirivimab/imdevimab against the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is attenuated in the subvariant BA.5. However, the efficacy of sotrovimab in the clinical setting remains to be investigated.

Methods:

Patients admitted to Kishiwada City Hospital with COVID-19 delta, omicron BA.1, or BA.5 subvariants were evaluated retrospectively for serum SARS-CoV-2 S and N antibody levels using the Elecsys Anti-SARS-CoV-2 assay.

Results:

In patients with COVID-19 during the BA.5 wave of the COVID-19 pandemic, anti-SARS-CoV-2 S antibody titers (median [interquartile range]) increased from 2154.0 (864.0−6669.3) U/mL on day 0 to 21,371.0 (19,656.3−32,225.0) U/mL on day 3 in the group treated with sotrovimab (N = 40) and were significantly higher than in the group treated with remdesivir plus dexamethasone plus baricitinib (p < 0.001).

Conclusion:

Treatment with sotrovimab could prevent severe disease in high-risk patients infected with SARS-CoV-2 subvariant BA.5.
Keywords

Full text: Available Collection: International databases Database: MEDLINE Type of study: Experimental Studies / Prognostic study Topics: Variants Language: English Journal: Infect Dis Rep Year: 2022 Document Type: Article Affiliation country: Idr14060099

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Full text: Available Collection: International databases Database: MEDLINE Type of study: Experimental Studies / Prognostic study Topics: Variants Language: English Journal: Infect Dis Rep Year: 2022 Document Type: Article Affiliation country: Idr14060099