Association between humoral serological markers levels and risk of SARS-CoV-2 infection after the primary COVID-19 vaccine course among ANRS0001S COV-POPART cohort participants.


Journal

BMC infectious diseases
ISSN: 1471-2334
Titre abrégé: BMC Infect Dis
Pays: England
ID NLM: 100968551

Informations de publication

Date de publication:
27 Sep 2024
Historique:
received: 31 05 2024
accepted: 02 09 2024
medline: 28 9 2024
pubmed: 28 9 2024
entrez: 28 9 2024
Statut: epublish

Résumé

We assessed the prognostic value of serological humoral markers measured one month after the last dose of the primary COVID-19 vaccine course for predicting the risk of severe acute respiratory syndrome coronavirus 2 SARS-CoV-2 infection over the following six months in specific populations. ANRS0001SCOV-POPART is a French nationwide multicenter prospective observational cohort study assessing the immune response to Covid-19 vaccines routinely administered to 11 subgroups of patients with chronic disease and a control group. Participants from the ANRS0001S COV-POPART were included if they received at least two doses of Covid-19 vaccine for the primary vaccine course, had measurements of anti-Spike, anti-receptor binding domain (RBD) IgG-specific or neutralizing antibodies one month after the end of the primary vaccine course, without being infected by SARS-CoV-2 before the measurement. SARS-CoV-2 infections defined by a positive PCR/antigenic test or seroconversion to detectable anti nucleocapsid antibodies were evaluated until the first COVID-19 booster injection. Cox proportional hazards models taking into account interval-censored data were implemented to estimate the association between each antibody level and the risk of SARS-CoV-2 infection. Predictive performances were evaluated by the area under the receiving operating characteristic curve (AUROC). Two thousand five hundred seventy adults from a specific population and 1,123 from the control group were included. The cumulative probabilities of SARS-CoV-2 infections at five months after serological measurement were 6.0% 95% confidence interval: [5.0; 7.9] and 10.1% 95% confidence interval: [8.3; 11.9], respectively. Higher levels of anti-Spike IgG antibody were associated with a lower risk of SARS-CoV-2 infections in the control group, but not in the specific populations. Among the specific populations, AUROC were 74.5%, 74.9%, and 72.4% for anti-Spike IgG, anti-RBD IgG, and neutralizing antibodies, respectively. AUROC were superior in the specific populations, 82.0%, 81.2%, and 81.4% for anti-Spike IgG, anti-RBD IgG, and neutralizing antibodies, respectively. Vaccine-induced antibody response after the primary course of Covid-19 infection only moderately discriminated between participants developing a SARS-CoV-2 infection during the Omicron wave. NCT04824651 (first posted: 2021-04-01).

Sections du résumé

BACKGROUND BACKGROUND
We assessed the prognostic value of serological humoral markers measured one month after the last dose of the primary COVID-19 vaccine course for predicting the risk of severe acute respiratory syndrome coronavirus 2 SARS-CoV-2 infection over the following six months in specific populations.
METHODS METHODS
ANRS0001SCOV-POPART is a French nationwide multicenter prospective observational cohort study assessing the immune response to Covid-19 vaccines routinely administered to 11 subgroups of patients with chronic disease and a control group. Participants from the ANRS0001S COV-POPART were included if they received at least two doses of Covid-19 vaccine for the primary vaccine course, had measurements of anti-Spike, anti-receptor binding domain (RBD) IgG-specific or neutralizing antibodies one month after the end of the primary vaccine course, without being infected by SARS-CoV-2 before the measurement. SARS-CoV-2 infections defined by a positive PCR/antigenic test or seroconversion to detectable anti nucleocapsid antibodies were evaluated until the first COVID-19 booster injection. Cox proportional hazards models taking into account interval-censored data were implemented to estimate the association between each antibody level and the risk of SARS-CoV-2 infection. Predictive performances were evaluated by the area under the receiving operating characteristic curve (AUROC).
RESULTS RESULTS
Two thousand five hundred seventy adults from a specific population and 1,123 from the control group were included. The cumulative probabilities of SARS-CoV-2 infections at five months after serological measurement were 6.0% 95% confidence interval: [5.0; 7.9] and 10.1% 95% confidence interval: [8.3; 11.9], respectively. Higher levels of anti-Spike IgG antibody were associated with a lower risk of SARS-CoV-2 infections in the control group, but not in the specific populations. Among the specific populations, AUROC were 74.5%, 74.9%, and 72.4% for anti-Spike IgG, anti-RBD IgG, and neutralizing antibodies, respectively. AUROC were superior in the specific populations, 82.0%, 81.2%, and 81.4% for anti-Spike IgG, anti-RBD IgG, and neutralizing antibodies, respectively.
CONCLUSIONS CONCLUSIONS
Vaccine-induced antibody response after the primary course of Covid-19 infection only moderately discriminated between participants developing a SARS-CoV-2 infection during the Omicron wave.
TRIAL REGISTRATION BACKGROUND
NCT04824651 (first posted: 2021-04-01).

Identifiants

pubmed: 39333909
doi: 10.1186/s12879-024-09861-5
pii: 10.1186/s12879-024-09861-5
doi:

Substances chimiques

Antibodies, Viral 0
COVID-19 Vaccines 0
Antibodies, Neutralizing 0
Immunoglobulin G 0
Biomarkers 0
Spike Glycoprotein, Coronavirus 0
spike protein, SARS-CoV-2 0

Banques de données

ClinicalTrials.gov
['NCT04824651']

Types de publication

Journal Article Observational Study Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

1049

Informations de copyright

© 2024. The Author(s).

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Auteurs

Mathieu Chalouni (M)

Université de Bordeaux, ISPED, INSERM, Bordeaux Population Health Research Center, U1219, Bordeaux, F-33000, France.

Paul Loubet (P)

INSERM, F-CRIN, Reseau Innovative Clinical Research in Vaccinology (IREIVAC), Paris, France; Service des Maladies infectieuses et Tropicales, CHU de Nîmes, Nîmes, France; INSERM U1047 - Université de Montpellier, Nîmes, France.

Edouard Lhomme (E)

Université de Bordeaux, ISPED, INSERM, Bordeaux Population Health Research Center, U1219, Bordeaux, F-33000, France.
INRIA SISTM team, Talence, France.
Service d'Information médicale, CHU de Bordeaux, Bordeaux, F-33000, France.

Laetitia Ninove (L)

Unite des Virus Emergents, Aix-Marseille Université, Institut de Recherche pour le Développement 190, Inserm 1207, Institut Hospitalo-Universitaire Méditerranée Infection, Marseille, France.

Benoit Barrou (B)

Service de Transplantation Rénale, Pitié Salpêtrière, APHP, Sorbonne Université, Paris, France.

Jean-Yves Blay (JY)

Centre Léon-Bérard, Département de cancérologie médicale, Lyon, France; Université Claude Bernard Lyon, Unicancer, Lyon, France.

Maryvonne Hourmant (M)

Service de Néphrologie-Immunologie clinique, CHU Nantes, Nantes, France.

Jérome de Seze (J)

CIC INSERM 1434, Strasbourg university hospital, Strasbourg, France.

Martine Laville (M)

INSERM U1191/UMR 5203, Université de Montpellier, Montpellier, France.
CHU de Lyon, Université de Lyon, Association Française d'Etudes et de Recherche de l'Obésité, INSERM, F-CRIN -French Obesity Research Centre of Excellence (FORCE) Network, Lyon, France.

Bruno Laviolle (B)

Université de Rennes, CHU Rennes, INSERM, CIC 1414, Rennes, France.

Jean-Daniel Lelièvre (JD)

Vaccine Research Institute, INSERM et APHP, Hôpital H. Mondor, Créteil, France.

Jacques Morel (J)

Département de Rhumatologie, CHU et Université de Montpellier, Montpellier, France.

Stéphanie Nguyen Quoc (SN)

Centre d'Immunologie et des Maladies Infectieuses-Paris, APHP-Sorbonne Université, INSERM U1135, CNRS ERL 8255, Paris, France.

Jean-Philippe Spano (JP)

INSERM, institut Pierre-Louis d'épidémiologie et de santé publique (IPLESP), équipe TheraVir, AP-HP, Sorbonne université, hôpital universitaire Pitié-Salpêtrière, Oncologie médicale, CLIP2 Galilée, Sorbonne université, Paris, France.

Benjamin Terrier (B)

Service de Médecine Interne, Hôpital Cochin, APHP, Paris, France.

Anne Thiebaut (A)

Département d'Hématologie, CHU Grenoble Alpes, Grenoble, France.

Jean-Francois Viallard (JF)

Université de Bordeaux, Hôpital Haut-Lévêque, Bordeaux, France.

François Vrtovsnik (F)

Département Hospitalo-Universitaire Fire, Service de Néphrologie, Hôpital Bichat-Claude Bernard, APHP, Université de Paris, Paris, France.

Sophie Circosta (S)

INSERM, SC10-US019 Essais thérapeutiques et Maladies Infectieuses, Paris, France.

Aude Barquin (A)

Université de Bordeaux, ISPED, INSERM, Bordeaux Population Health Research Center, U1219, Bordeaux, F-33000, France.

Mariam Gharib (M)

ANRS Maladies infectieuses émergentes (ANRS MIE), Paris, France.

Eric Tartour (E)

Service d'Immunologie biologique, Hôpital européen Georges Pompidou/APHP, Paris, France.

Béatrice Parfait (B)

Centre de ressources Biologiques, Hôpital Cochin, Assistance Publique-Hôpitaux de Paris, Paris, France.

Rodolphe Thiébaut (R)

Université de Bordeaux, ISPED, INSERM, Bordeaux Population Health Research Center, U1219, Bordeaux, F-33000, France.
INRIA SISTM team, Talence, France.
Service d'Information médicale, CHU de Bordeaux, Bordeaux, F-33000, France.

Laurence Meyer (L)

Université Paris Saclay, CESP Inserm U1018, APHP Service de Santé Publique, le Kremlin- Bicêtre, 94276, France.

Xavier de Lamballerie (X)

Unite des Virus Emergents, Aix-Marseille Université, Institut de Recherche pour le Développement 190, Inserm 1207, Institut Hospitalo-Universitaire Méditerranée Infection, Marseille, France.

Odile Launay (O)

INSERM, F-CRIN, Reseau Innovative Clinical Research in Vaccinology (IREIVAC), Paris, France; Service des Maladies infectieuses et Tropicales, CHU de Nîmes, Nîmes, France; INSERM U1047 - Université de Montpellier, Nîmes, France.
INSERM, F-CRIN, Reseau Innovative Clinical Research in Vaccinology (IREIVAC), Paris, France; Centre d'Investigation Clinique Cochin Pasteur, Hôpital Cochin/APHP, INSERM CIC 1417, Paris, France; Université de Paris, Paris, France.

Linda Wittkop (L)

Université de Bordeaux, ISPED, INSERM, Bordeaux Population Health Research Center, U1219, Bordeaux, F-33000, France. linda.wittkop@u-bordeaux.fr.
INRIA SISTM team, Talence, France. linda.wittkop@u-bordeaux.fr.
Service d'Information médicale, CHU de Bordeaux, Bordeaux, F-33000, France. linda.wittkop@u-bordeaux.fr.

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