Drug (ID: DG00524) and It's Reported Resistant Information
Name
Bamlanivimab
Synonyms
LY-CoV555; LY3819253
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Drug Resistance Disease(s)
Disease(s) with Resistance Information Discovered by Cell Line Test for This Drug (1 diseases)
COVID-19 [ICD-11: 1D92]
[1]
Disease(s) with Clinically Reported Resistance for This Drug (1 diseases)
Severe Acute Respiratory Syndrome coronavirus [ICD-11: XN1V8]
[2]
Click to Show/Hide the Molecular Information and External Link(s) of This Drug
Formula
C6498H10068N1732O2032S46
DrugBank ID
DB15718
Type(s) of Resistant Mechanism of This Drug
  ADTT: Aberration of the Drug's Therapeutic Target
  EADR: Epigenetic Alteration of DNA, RNA or Protein
Drug Resistance Data Categorized by Their Corresponding Diseases
ICD-01: Infectious/parasitic diseases
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COVID-19 [ICD-11: 1D92]
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Drug Resistance Data Categorized by Their Corresponding Mechanisms
  Aberration of the Drug's Therapeutic Target (ADTT) Click to Show/Hide
Key Molecule: Moesin (MSN) [1]
Resistant Disease Corona Virus Disease 2019 [ICD-11: 1D92.0]
Molecule Alteration Mutations
E340K
Experimental Note Revealed Based on the Cell Line Data
In Vitro Model Hela cells Cervix uteri Homo sapiens (Human) CVCL_0030
Vero E6 cells Kideny Homo sapiens (Human) N.A.
BHKG43 cells Kideny Homo sapiens (Human) N.A.
HEK 293T cells Kidney Homo sapiens (Human) CVCL_0063
Experiment for
Molecule Alteration
qRT-PCR; Deep sequencing assay
Experiment for
Drug Resistance
Immunofluorescence assay
Mechanism Description Monoclonal antibodies targeting the Spike protein of SARS-CoV-2 are effective against COVID-19 and might mitigate future pandemics. However, their efficacy is challenged by the emergence of antibody-resistant virus variants.
ICD-X: Extension Codes
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Severe Acute Respiratory Syndrome coronavirus [ICD-11: XN1V8]
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Drug Resistance Data Categorized by Their Corresponding Mechanisms
  Epigenetic Alteration of DNA, RNA or Protein (EADR) Click to Show/Hide
Key Molecule: Spike glycoprotein (S) [2]
Resistant Disease severe acute respiratory syndrome coronavirus 2 [ICD-11: XN1V8]
Molecule Alteration Mutation
.
Experimental Note Identified from the Human Clinical Data
In Vivo Model Patient-derived allogeneic stem cell transplant model Homo sapiens
Mechanism Description We report the case of an allogeneic stem cell transplant recipient with nosocomial acquisition of SARS-CoV-2 infection who received antispike neutralizing monoclonal antibody bamlanivimab 2 days after diagnosis of SARS-CoV-2 infection but progressed to severe COVID-19 pneumonia and died with the selection of E484K/Q resistance mutations to bamlanivimab.
References
Ref 1 Identification of antibody-resistant SARS-CoV-2 mutants via N4-Hydroxycytidine mutagenesis. Antiviral Res. 2024 Nov;231:106006.
Ref 2 Failure of bamlanivimab with selection of E484K mutation in an allogeneic stem cell transplant recipient with nosocomial SARS-CoV-2 infection. Antivir Ther. 2024 Feb;29(1):13596535221097495.

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