SARS-CoV-2 Neutralizing Responses in Various Populations, at the Time of SARS-CoV-2 Variant Virus Emergence: Evaluation of Two Surrogate Neutralization Assays in Front of Whole Virus Neutralization Test.

COVID-19 SARS-CoV-2 SARS-CoV-2 variants neutralization surrogate assays neutralizing antibodies

Journal

Life (Basel, Switzerland)
ISSN: 2075-1729
Titre abrégé: Life (Basel)
Pays: Switzerland
ID NLM: 101580444

Informations de publication

Date de publication:
09 Dec 2022
Historique:
received: 05 11 2022
revised: 02 12 2022
accepted: 05 12 2022
entrez: 23 12 2022
pubmed: 24 12 2022
medline: 24 12 2022
Statut: epublish

Résumé

The SARS-CoV-2 neutralizing antibodies response is the best indicator of effective protection after infection and/or vaccination, but its evaluation requires tedious cell-based experiments using an infectious virus. We analyzed, in 105 patients with various histories of SARS-CoV-2 infection and/or vaccination, the neutralizing response using a virus neutralization test (VNT) against B.1, Alpha, Beta and Omicron variants, and compared the results with two surrogate assays based on antibody-mediated blockage of the ACE2-RBD interaction (Lateral Flow Boditech and ELISA Genscript). The strongest response was observed for recovered COVID-19 patients receiving one vaccine dose. Naïve patients receiving 2 doses of mRNA vaccine also demonstrate high neutralization titers against B.1, Alpha and Beta variants, but only 34.3% displayed a neutralization activity against the Omicron variant. On the other hand, non-infected patients with half vaccination schedules displayed a weak and inconstant activity against all isolates. Non-vaccinated COVID-19 patients kept a neutralizing activity against B.1 and Alpha up to 12 months after recovery but a decreased activity against Beta and Omicron. Both surrogate assays displayed a good correlation with the VNT. However, an adaptation of the cut-off positivity was necessary, especially for the most resistant Beta and Omicron variants. We validated two simple and reliable surrogate neutralization assays, which may favorably replace cell-based methods, allowing functional analysis on a larger scale.

Identifiants

pubmed: 36556429
pii: life12122064
doi: 10.3390/life12122064
pmc: PMC9782962
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : FIC NIH HHS
ID : K43 TW011957
Pays : United States

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Auteurs

Stephane Marot (S)

Sorbonne Université, INSERM, Institut Pierre Louis d'Epidémiologie et de Santé Publique (iPLESP), F-75012 Paris, France.
Department of Virology, Assistance Publique-Hôpitaux de Paris (AP-HP), Pitié Salpêtrière Hospital, F-75013 Paris, France.

Djeneba Bocar Fofana (D)

Sorbonne Université, INSERM, Institut Pierre Louis d'Epidémiologie et de Santé Publique (iPLESP), F-75012 Paris, France.
Department of Virology, Assistance Publique-Hôpitaux de Paris (AP-HP), Saint-Antoine Hospital, F-75012 Paris, France.

Philippe Flandre (P)

Sorbonne Université, INSERM, Institut Pierre Louis d'Epidémiologie et de Santé Publique (iPLESP), F-75012 Paris, France.

Isabelle Malet (I)

Sorbonne Université, INSERM, Institut Pierre Louis d'Epidémiologie et de Santé Publique (iPLESP), F-75012 Paris, France.
Department of Virology, Assistance Publique-Hôpitaux de Paris (AP-HP), Pitié Salpêtrière Hospital, F-75013 Paris, France.

Karen Zafilaza (K)

Sorbonne Université, INSERM, Institut Pierre Louis d'Epidémiologie et de Santé Publique (iPLESP), F-75012 Paris, France.
Department of Virology, Assistance Publique-Hôpitaux de Paris (AP-HP), Pitié Salpêtrière Hospital, F-75013 Paris, France.

Valentin Leducq (V)

Sorbonne Université, INSERM, Institut Pierre Louis d'Epidémiologie et de Santé Publique (iPLESP), F-75012 Paris, France.
Department of Virology, Assistance Publique-Hôpitaux de Paris (AP-HP), Pitié Salpêtrière Hospital, F-75013 Paris, France.

Diane Vivien (D)

Department of Virology, Assistance Publique-Hôpitaux de Paris (AP-HP), Pitié Salpêtrière Hospital, F-75013 Paris, France.

Sarah Mrabet (S)

Department of Virology, Assistance Publique-Hôpitaux de Paris (AP-HP), Saint-Antoine Hospital, F-75012 Paris, France.

Corentin Poignon (C)

Department of Virology, Assistance Publique-Hôpitaux de Paris (AP-HP), Saint-Antoine Hospital, F-75012 Paris, France.

Vincent Calvez (V)

Sorbonne Université, INSERM, Institut Pierre Louis d'Epidémiologie et de Santé Publique (iPLESP), F-75012 Paris, France.
Department of Virology, Assistance Publique-Hôpitaux de Paris (AP-HP), Pitié Salpêtrière Hospital, F-75013 Paris, France.

Laurence Morand-Joubert (L)

Sorbonne Université, INSERM, Institut Pierre Louis d'Epidémiologie et de Santé Publique (iPLESP), F-75012 Paris, France.
Department of Virology, Assistance Publique-Hôpitaux de Paris (AP-HP), Saint-Antoine Hospital, F-75012 Paris, France.

Anne-Geneviève Marcelin (AG)

Sorbonne Université, INSERM, Institut Pierre Louis d'Epidémiologie et de Santé Publique (iPLESP), F-75012 Paris, France.
Department of Virology, Assistance Publique-Hôpitaux de Paris (AP-HP), Pitié Salpêtrière Hospital, F-75013 Paris, France.

Joel Gozlan (J)

Department of Virology, Assistance Publique-Hôpitaux de Paris (AP-HP), Saint-Antoine Hospital, F-75012 Paris, France.
Centre de Recherche Saint-Antoine, "Cancer Biology and Therapeutics", Sorbonne Université & INSERM UMR_S 938, F-75012 Paris, France.

Classifications MeSH