TY - JOUR
T1 - Effectiveness of Monoclonal Antibodies in Preventing Severe COVID-19 With Emergence of the Delta Variant
AU - O'Horo, John C.
AU - Challener, Douglas W.
AU - Speicher, Leigh
AU - Bosch, Wendelyn
AU - Seville, Maria Teresa
AU - Bierle, Dennis M.
AU - Ganesh, Ravindra
AU - Wilker, Caroline G.
AU - Arndt, Richard F.
AU - Arndt, Lori L.
AU - Tulledge-Scheitel, Sidna M.
AU - Hanson, Sara N.
AU - Razonable, Raymund R.
N1 - Funding Information:
Grant Support: Mayo Clinic.Potential Competing Interests: J.C.O. has received consulting fees from Bates College and small grants from Nference, Inc outside of the present work. R.R.R. received research grants (funds given to the institution) from Gilead, Regeneron, and Roche, outside of the present work. R.R.R. is a member of the Data and Safety Monitoring Board of Novartis, outside of this work. R.R.R. received research internal funds from the Mayo Clinic on COVID-19 monoclonal antibody research. All other authors have no conflicts.
Publisher Copyright:
© 2021 Mayo Foundation for Medical Education and Research
PY - 2022/2
Y1 - 2022/2
N2 - Anti-spike monoclonal antibodies have proven invaluable in preventing severe outcomes from COVID-19, including hospitalization and death. The rise of the SARS-CoV-2 delta variant begs the question of whether monoclonal antibodies maintain similar efficacy now as they had when the alpha and beta variants predominated, when they were first assessed and approved. We used a retrospective cohort to compare rates of severe outcomes in an epoch in which alpha and beta were predominant compared with delta. A total of 5356 patients were infused during the alpha/beta variant–predominant (n=4874) and delta variant–predominant (n=482) era. Overall, odds of severe infection were 3.0% of patients in the alpha/beta-predominant era compared with 4.9% in the delta-predominant cohort. The unadjusted odds ratio (OR) was higher for severe disease in the delta era (OR, 1.67; 95% CI, 0.96 to 2.89), particularly when adjusted for Charlson Comorbidity Index (adjusted OR, 2.04; 95% CI, 1.30 to 3.08). The higher odds of severe infection could be due to a more virulent delta variant, although the possibility of decreased anti-spike monoclonal antibody effectiveness in the clinical setting cannot be excluded. Research into the most effective strategies for using and improving anti-spike monoclonals for the treatment of emerging variants is warranted.
AB - Anti-spike monoclonal antibodies have proven invaluable in preventing severe outcomes from COVID-19, including hospitalization and death. The rise of the SARS-CoV-2 delta variant begs the question of whether monoclonal antibodies maintain similar efficacy now as they had when the alpha and beta variants predominated, when they were first assessed and approved. We used a retrospective cohort to compare rates of severe outcomes in an epoch in which alpha and beta were predominant compared with delta. A total of 5356 patients were infused during the alpha/beta variant–predominant (n=4874) and delta variant–predominant (n=482) era. Overall, odds of severe infection were 3.0% of patients in the alpha/beta-predominant era compared with 4.9% in the delta-predominant cohort. The unadjusted odds ratio (OR) was higher for severe disease in the delta era (OR, 1.67; 95% CI, 0.96 to 2.89), particularly when adjusted for Charlson Comorbidity Index (adjusted OR, 2.04; 95% CI, 1.30 to 3.08). The higher odds of severe infection could be due to a more virulent delta variant, although the possibility of decreased anti-spike monoclonal antibody effectiveness in the clinical setting cannot be excluded. Research into the most effective strategies for using and improving anti-spike monoclonals for the treatment of emerging variants is warranted.
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U2 - 10.1016/j.mayocp.2021.12.002
DO - 10.1016/j.mayocp.2021.12.002
M3 - Article
C2 - 35120695
AN - SCOPUS:85123635387
SN - 0025-6196
VL - 97
SP - 327
EP - 332
JO - Mayo Clinic Proceedings
JF - Mayo Clinic Proceedings
IS - 2
ER -