Resistance mutations to nirsevimab are rare in respiratory syncytial virus (RSV)

Press release
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Nirsevimab is an antibody targeting the respiratory syncytial virus (RSV). Available in France since September 2023, it is indicated in neonates and infants for the prevention of bronchiolitis caused by RSV. However, its widespread use raises the question of the emergence of resistance mutations. The POLYRES study, the largest prospective surveillance study of nirsevimab breakthrough infections to date, has just delivered its conclusions. This work, coordinated by Prof. Slim Fourati and Prof. Marie-Anne Rameix-Welti1, was funded by the ANRS MIE with the support from the French Ministry of Higher Education and Research as part of the EMERGEN Consortium2. Scientists from AP-HP (including Henri Mondor University Hospitals), Inserm, Institut Pasteur and the Universities of Paris-Est-Créteil and Versailles-Saint-Quentin-en-Yvelines, members of the ANRS MIE virology network teams, have shown that nirsevimab resistance mutations in RSV are very rare. The results of this study have just been published in the Lancet Infectious Diseases on October 15th, 2024.

Respiratory syncytial virus (RSV) is the main cause of bronchiolitis, a lower respiratory tract infection in infants. Two groups of RSV (RSV-A and RSV-B) circulate alternately or together. Every year, RSV is responsible for more than 33 million cases of bronchiolitis worldwide, leading to the deaths of 100,000 children, mainly in low-income countries. In France, the disease is responsible for around 480,000 cases a year. It is by far the most common cause of hospitalisation in children, leading to more than 26,000 paediatric hospitalisations every year. Nirsevimab, a new neutralising antibody3 against the virus, became available in France in September 2023. This monoclonal antibody4 targets a specific antigenic site (the epitope5 Ø) of the RSV surface F protein, which is involved in viral multiplication, and blocks the virus. Due to the genetically variable forms of RSV, there is a theoretical risk of the emergence of variants carrying mutations resistant to neutralisation by nirsevimab, even in the absence of selection pressure. This risk could increase with the widespread preventive use of nirsevimab. During the phase IIb/III clinical trials, only 48 RSVs infecting children treated with nirsevimab could be studied, and escape mutations6 were found in two of them.  The aim of the POLYRES study was to assess the risk of viral escape from nirsevimab in a large cohort using a large, multicentre, real-life observational study conducted during the 2023-2024 winter season.

The study included 695 RSV infected infants, 349 of whom had received nirsevimab prophylaxis. RSV-A was the most dominant circulating virus this season and was found in 86.6% of infected children. The teams analysed the characteristics of RSV-A and RSV-B in nasopharyngeal swabs collected as part of the children's routine care. Full-length sequencing of the viral genome was conducted to identify potential mutations in the Ø site, the nirsevimab binding site (genotypic analysis7 ). The ability of nirsevimab to inhibit viral multiplication in cell culture was also investigated (phenotypic analysis8 ). Analysis of 472 RSV-A viruses (half from treated children) revealed no nirsevimab resistance mutation in the Ø site of the F protein. Of the 73 children infected with RSV-B, 24 had received nirsevimab prophylaxis. In these 24 children, two isolates of RSV-B had resistance mutations to the antibody. One mutation has been described before and the other is described here for the first time.

"This study is the largest surveillance study of nirsevimab virological failures to date. It was made possible thanks to collaborative synergy with the consortium of virologists at the ANRS MIE. It is a nationwide project that will help identify the resistance phenomenon associated with the widespread use of the drug. This type of study is essential for analysing the evolutionary dynamics of viruses, in the light of existing medical solutions" explains Prof Marie-Anne Rameix-Welti, head of the National Reference Centre for Respiratory Infection Viruses at the Institut Pasteur, and head of the M3P unit (Institut Pasteur, Inserm U1173).

"The low prevalence of nirsevimab resistance mutations in treated patients is reassuring. However, escape mutations have been observed in a few RSV-Bs from treated patients, prompting caution and highlighting the importance of active molecular surveillance in the context of future wider global use of nirsevimab. These results are essential in the fight against this disease and in anticipating any form of resistance", adds Prof Slim Fourati, Head of the Virology Unit-Respiratory Viruses, CHU Henri Mondor, Inserm U955.

In conclusion, the results of the POLYRES study support the continued use of nirsevimab for RSV prophylaxis in all newborns worldwide.

 


1 Head of the National Reference Centre for Respiratory Infection Viruses at the Institut Pasteur and head of the M3P unit (Institut Pasteur, Inserm U1173)

2 Coordinated by Santé publique France and ANRS MIE

3 Neutralising antibodies are specific antibodies that prevent infection by blocking the virus from entering the target cells. They do this by forming an antigen-antibody complex which inhibits the biological activity of the antigen (a substance foreign to the body capable of triggering an immune response aimed at eliminating it)

4 Monoclonal antibodies consist of a single type of antibody (polyclonal antibodies have several types). They are used in medicine.

5 Monoclonal antibodies consist of a single type of antibody (polyclonal antibodies have several types). They are used in medicine.

6 Escape mutations enable the virus to thwart the action of antibodies in the human immune system.

7 Genotypic tests are based on the identification of mutations that confer resistance to the virus.

8 Phenotyping, carried out using phenotypic tests, makes it possible to define the sensitive or resistant nature of the virus. This is done by culturing the virus in the presence of the antiviral being studied.

 


Source

Genotypic and Phenotypic Characterisation of RSV after Nirsevimab Breakthrough Infections in a Large Multicentre Observational Real-world Study. Lancet Infectious Diseases. 15th October 2024.

Fourati S1,2,3, Reslan A4,5, Bourret J5, Casalegno J6 , Rahou Y4,5, Chollet L7, Pillet S8, Tremeaux P9, Dossou NC10, Gault E4,11, Salmona M12, Imbert-Marcille B13, Mirand A14, Larrat S15, Moisan A16, Marot S17, Schnuriger A18, Veyrenche N19, Engelmann I20, Handala L21, Henry A22, Stephan V23, Brichler S24, Avettand-Fenoel V25, Zemali N26, Lefeuvre C27, Pronier C28, Deroche L29, Jaffar-Bandjee M30, Mouna L31, Francois C32, Regueme A33, Hartard C34, Rogez S35, Gallais F36, Boschi C37, Ly A1, Rodriguez C1,2,3, Dos Santos G38, Simon-Loriere E39, Schwartz O40, Buchrieser J40, Pawlotsky J-M1,2,3, Lemoine F5,41, Audureau E2,42, Rameix Welti MA4,5,11 on behalf of the POLYRES investigators.

  1. Department of Virology, Hôpitaux Universitaires Henri Mondor, AP-HP, Créteil, France
  2. Université Paris-Est-Créteil (UPEC), Créteil, France
  3. INSERM U955, Team « Viruses, Hepatology, Cancer », Créteil, France
  4. M3P, UMR 1173 (2I), INSERM, université de Versailles St. Quentin, Université Paris Saclay, Paris, France
  5. M3P Centre National de Référence Virus des Infections Respiratoire (CNR VIR) Institut Pasteur Université Paris Cité, 75015 Paris, France
  6. Laboratoire de virologie, Institut des Agents Infectieux, Centre de Biologie et Pathologie Nord, Hôpital de la Croix-Rousse, Hospices Civils de Lyon, Lyon France, France
  7. Laboratoire de Biologie Médicale Centre Hospitalier Intercommunal de Toulon La Seyne sur Mer, rue Henri Sainte Claire Deville - CS 31412 - 83056 TOULON Cedex
  8. Service des agents infectieux et d’hygiène-Plateau de biologie Hôpital Nord-CHU de Saint-Etienne, France, Saint-Etienne, France
  9. Laboratoire de Virologie, CHU Toulouse, France, Toulouse France, France
  10. Normandie, INSERM, Normandie Univ, DYNAMICURE UMR1311, CHU Caen, Department of Virology, F-14000 Caen, France, Caen Normandie, France
  11. Virology Department, Hôpital Ambroise Paré (AP-HP), Paris, France
  12. Virology Department, Hôpital Saint Louis (AP-HP), INSIGHT U976, INSERM, Université Paris-Cité Paris, France
  13. Virology department, CHU de Nantes, Nantes, France
  14. Virology department, CHU de Clermont-Ferrand, Clermond-Ferrand, France
  15. Univ. Grenoble Alpes, Laboratoire de Virologie, Institut de Biologie-Pathologie, Centre Hospitalier Universitaire Grenoble Alpes, 38000, Grenoble France, France
  16. Univ Rouen Normandie, Université de Caen Normandie, INSERM, Normandie Univ, DYNAMICURE UMR 1311, CHU Rouen, Department of Virology, F-76000 Rouen, France
  17. Sorbonne Université; APHP Virologie Pitié-Salpêtrière, Paris Ile de France, France
  18. Sorbonne Université, APHP Virologie St Antoine - Tenon - Trousseau, Paris Ile de France, France
  19. Virology department, Hôpital Necker - Enfants Malades, Paris, France
  20. Pathogenesis and Control of Chronic and Emerging Infections, Univ Montpellier, INSERM, Établissement Français du Sang, CHU Montpellier, Montpellier, France
  21. Virology Unit, Department of Bacteriology, Virology and Hospital Hygiene, University Hospital of Tours, Tours, France
  22. Laboratoire de Biologie Médicale, microbiologie, CH Victor Dupouy, Argenteuil, France
  23. Virology department, CHRU de Brest, Brest, France
  24. Service de Microbiologie Clinique, CHU Avicenne, AP-HP, Bobigny, Bobigny, France
  25. CHU Orléans, Virologie, Orléans, France ; Université d’Orléans, LI2RSO, Orléans, France
  26. CHU de Bordeaux, Service de Virologie, Bordeaux, France
  27. Laboratoire de virologie, CHU Angers, F-49000, Angers, France
  28. Virology department, CHU de Rennes, Rennes, France
  29. Virology department, CHU de Poitiers, Poitiers, France
  30. CNR associé des Virus Respiratoires, laboratoire Microbiologie, Hôpital Félix Guyon CHU Réunion, La Réunion, France
  31. Virology Department, Hôpital Paul Brousse, INSERM U1193, AP-HP, Université Paris Saclay, France, Paris, France
  32. AGIR, UR4294, Université Picardie Jules Verne, Amiens, France; Laboratoire de Virologie, Centre de Biologie Humaine-CHU Amiens, 80054, Amiens, France
  33. Univ Lille, CHU de Lille, Laboratoire de Virologie ULR3610, Lille, France
  34. Laboratoire de Virologie, CHRU de Nancy Brabois, Vandoeuvre-lès-Nancy, France ; Université de Lorraine, CNRS, LCPME, F-54000 Nancy, France
  35. Virology department, CHU de Limoges, Limoges, France
  36. Virology department, CHU de Strasbourg, Strasbourg, France
  37. IHU Méditerranée Infection, Assistance Publique-Hôpitaux de Marseille (AP-HM), Aix-Marseille Université, Microbes Evolution Phylogeny and Infections (MEPHI), Marseille, France
  38. Microbiology department CHU de Martinique, La Martinique, France
  39. Evolutionary genomics of RNA viruses, Institut Pasteur, Université Paris Cité, Paris, France
  40. Virus and Immunity Unit, Institut Pasteur, Université Paris Cité, CNRS UMR3569, Paris, France
  41. Institut Pasteur, Université Paris Cité, Bioinformatics and Biostatistics Hub, Paris, France 75
  42. IMRB INSERM U955, Team CEpiA, Créteil, France

 

 
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