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Details

Autor(en) / Beteiligte
Titel
Generation and Characterization of ALX-0171, a Potent Novel Therapeutic Nanobody for the Treatment of Respiratory Syncytial Virus Infection
Ist Teil von
  • Antimicrobial agents and chemotherapy, 2016-01, Vol.60 (1), p.6-13
Ort / Verlag
United States: American Society for Microbiology
Erscheinungsjahr
2016
Link zum Volltext
Quelle
MEDLINE
Beschreibungen/Notizen
  • Respiratory syncytial virus (RSV) is an important causative agent of lower respiratory tract infections in infants and elderly individuals. Its fusion (F) protein is critical for virus infection. It is targeted by several investigational antivirals and by palivizumab, a humanized monoclonal antibody used prophylactically in infants considered at high risk of severe RSV disease. ALX-0171 is a trimeric Nanobody that binds the antigenic site II of RSV F protein with subnanomolar affinity. ALX-0171 demonstrated in vitro neutralization superior to that of palivizumab against prototypic RSV subtype A and B strains. Moreover, ALX-0171 completely blocked replication to below the limit of detection for 87% of the viruses tested, whereas palivizumab did so for 18% of the viruses tested at a fixed concentration. Importantly, ALX-0171 was highly effective in reducing both nasal and lung RSV titers when delivered prophylactically or therapeutically directly to the lungs of cotton rats. ALX-0171 represents a potent novel antiviral compound with significant potential to treat RSV-mediated disease.
Sprache
Englisch
Identifikatoren
ISSN: 0066-4804
eISSN: 1098-6596
DOI: 10.1128/aac.01802-15
Titel-ID: cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4704182
Format
Schlagworte
Administration, Inhalation, Animals, Antibodies, Neutralizing, Antibodies, Neutralizing - biosynthesis, Antibodies, Neutralizing - immunology, Antibodies, Neutralizing - pharmacology, Antibodies, Viral, Antibodies, Viral - biosynthesis, Antibodies, Viral - immunology, Antibodies, Viral - pharmacology, Antiviral Agents, Antiviral Agents - immunology, Antiviral Agents - metabolism, Antiviral Agents - pharmacology, Female, Gene Expression, Humans, Lung - drug effects, Lung - immunology, Lung - virology, Male, Models, Molecular, Nasal Cavity - drug effects, Nasal Cavity - immunology, Nasal Cavity - virology, Neutralization Tests, Palivizumab - biosynthesis, Palivizumab - immunology, Palivizumab - pharmacology, Pichia - genetics, Pichia - metabolism, Rats, Recombinant Proteins - chemistry, Recombinant Proteins - genetics, Recombinant Proteins - immunology, Respiratory syncytial virus, Respiratory Syncytial Virus Infections, Respiratory Syncytial Virus Infections - drug therapy, Respiratory Syncytial Virus Infections - immunology, Respiratory Syncytial Virus Infections - pathology, Respiratory Syncytial Virus Infections - virology, Respiratory Syncytial Viruses, Respiratory Syncytial Viruses - drug effects, Respiratory Syncytial Viruses - immunology, Respiratory Syncytial Viruses - pathogenicity, Sigmodontinae, Single-Domain Antibodies, Single-Domain Antibodies - biosynthesis, Single-Domain Antibodies - immunology, Single-Domain Antibodies - pharmacology, Viral Fusion Proteins, Viral Fusion Proteins - antagonists & inhibitors, Viral Fusion Proteins - chemistry, Viral Fusion Proteins - genetics, Viral Fusion Proteins - immunology, Viral Load - drug effects, Virus Replication - drug effects

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