Monoclonal Antibodies for Early Treatment of COVID-19 in a World of Evolving SARS-CoV-2 Mutations and Variants

被引:3
作者
Pogue, Jason M. [1 ]
Lauring, Adam S. [2 ]
Gandhi, Tejal N. [2 ]
Marshall, Vincent D. [1 ,3 ]
Eschenauer, Gregory A. [1 ]
Nagel, Jerod L. [3 ]
Baang, Ji Hoon [2 ]
Zhou, Shiwei [2 ]
Valesano, Andrew L. [4 ]
Petty, Lindsay A. [2 ]
机构
[1] Univ Michigan, Coll Pharm, 428 Church St, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Dept Internal Med, Div Infect Dis, Ann Arbor, MI 48109 USA
[3] Michigan Med, Dept Pharm, Ann Arbor, MI USA
[4] Univ Michigan, Sch Med, Ann Arbor, MI USA
关键词
bamlanivimab; bamlanivimab and etesevimab; casirivimab and imdevimab; COVID-19; SARS-CoV-2; variants;
D O I
10.1093/ofid/ofab268
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Monoclonal antibodies targeting the receptor binding domain (RBD) of severe acute respiratory syndrome coronavirus 2 spike protein are important outpatient treatment options in coronavirus disease 2019 to mitigate progression of disease and prevent hospitalization. The impact of different RBD mutations on the efficacy of the available monoclonal antibodies and processes for incorporating this impact into treatment algorithms are ill defined. Herein, we synthesize the data surrounding the impact of key RBD mutations on the efficacy of US Food and Drug Administration Emergency Use Authorized monoclonal antibodies and describe our approach at Michigan Medicine at monitoring mutation frequency in circulating virus and developing an algorithm that incorporates these data into outpatient treatment pathways.
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页数:5
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