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One-month humoral response following two or three doses of messenger RNA coronavirus disease 2019 vaccines as primary vaccination in specific populations in France: first results from the Agence Nationale Recherche contre le Sida (ANRS)0001S COV-POPART cohort.
Loubet, Paul; Wittkop, Linda; Ninove, Laetitia; Chalouni, Mathieu; Barrou, Benoit; Blay, Jean-Yves; Hourmant, Maryvonne; Thouvenot, Eric; Laville, Martine; Laviolle, Bruno; Lelievre, Jean-Daniel; Morel, Jacques; Quoc, Stéphanie Nguyen; Spano, Jean-Philippe; Terrier, Benjamin; Thiebaut, Anne; Viallard, Jean-Francois; Vrtovsnik, François; Circosta, Sophie; Esterle, Laure; Levier, Axel; Vanhems, Philippe; Tartour, Eric; Parfait, Beatrice; de Lamballerie, Xavier; Launay, Odile.
  • 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. Electronic address: paul.loubet@chu-nimes.fr.
  • Wittkop L; Université de Bordeaux, ISPED, INSERM, Bordeaux Population Health Research Center, U1219, CIC-EC 1401, Bordeaux, France; Inria équipe SISTM, Talence, France; CHU de Bordeaux, Service d'information médicale, INSERM, Institut Bergonié, CIC-EC 1401, Bordeaux, France.
  • 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.
  • Chalouni M; Université de Bordeaux, ISPED, INSERM, Bordeaux Population Health Research Center, U1219, CIC-EC 1401, Bordeaux, France.
  • Barrou B; Service de Transplantation Rénale, Pitié Salpêtrière, APHP, Sorbonne Université, Paris, France.
  • Blay JY; Centre Léon-Bérard, Département de cancérologie médicale, Lyon, France; Université Claude Bernard Lyon, Unicancer, Lyon, France.
  • Hourmant M; Service de Néphrologie-Immunologie clinique, CHU Nantes, Nantes, France.
  • Thouvenot E; Service de Neurologie, CHU de Nîmes, Nîmes, France.
  • 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.
  • Laviolle B; Université de Rennes, CHU Rennes, INSERM, CIC 1414, Rennes, France.
  • Lelievre JD; Vaccine Research Institute, INSERM et APHP, Hôpital H. Mondor, Créteil, France.
  • Morel J; Département de Rhumatologie, CHU et Université de Montpellier, Montpellier, France.
  • Quoc SN; APHP-Sorbonne Université, INSERM U1135, CNRS ERL 8255, Centre d'Immunologie et des Maladies Infectieuses-Paris, Paris, France.
  • Spano JP; Sorbonne université, 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, Paris, France.
  • Terrier B; Service de Médecine Interne, Hôpital Cochin, APHP, Paris, France.
  • Thiebaut A; Département d'Hématologie, CHU Grenoble Alpes, Grenoble, France.
  • Viallard JF; Université de Bordeaux, Hôpital Haut-Lévêque, Bordeaux, France.
  • Vrtovsnik F; Service de Néphrologie, Hôpital Bichat-Claude Bernard, APHP, Département Hospitalo-Universitaire Fire, Université de Paris, Paris, France.
  • Circosta S; INSERM, SC10-US019 Essais thérapeutiques et Maladies Infectieuses, Paris, France.
  • Esterle L; Université de Bordeaux, ISPED, INSERM, Bordeaux Population Health Research Center, U1219, CIC-EC 1401, Bordeaux, France.
  • Levier A; ANRS MIE, Paris, France.
  • Vanhems P; Service d'Hygiène, Epidémiologie et Prévention, Hôpital Edouard Herriot, Hospices Civils de Lyon, Equipe Epidémiologie et Santé Publique, Université de Lyon, Université Lyon 1, Lyon, France.
  • Tartour E; Service d'Immunologie biologique, Hôpital européen Georges Pompidou/APHP, Paris, France.
  • Parfait B; Centre de ressources Biologiques, Hôpital Cochin, Assistance Publique-Hôpitaux de Paris, Paris, France.
  • 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.
  • Launay O; 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.
Clin Microbiol Infect ; 2022 Oct 14.
Article in English | MEDLINE | ID: covidwho-2269725
ABSTRACT

OBJECTIVES:

We aimed to investigate the 1-month humoral response to two or three doses of a messenger RNA coronavirus disease 2019 (COVID-19) vaccine as a primary vaccination regimen in specific populations compared with that in healthy adults.

METHODS:

Agence Nationale Recherche contre le Sida (ANRS)0001S-COV-POPART (NCT04824651) is a French nation-wide, multi-centre, prospective, observational cohort study assessing the immune response to COVID-19 vaccines routinely administered to 11 sub-groups of patients with chronic conditions and two control groups. Patients and controls who received at least two vaccine doses and whose results 1 month after the second dose were available were included. The humoral response was assessed 1 month after the first, second and third doses (if applicable) based on the percentage of responders (positive for anti-Spike severe acute respiratory syndrome coronavirus 2 [SARS-CoV-2] IgG antibodies), geometric means of anti-Spike SARS-CoV-2 IgG antibodies (enzyme-linked immunosorbent assay) and proportion of participants with anti-SARS-CoV-2-specific neutralizing antibodies (in vitro neutralization assay for the original SARS-CoV-2 strain). All analyses were centralized.

RESULTS:

We included 4091 participants in this

analysis:

2979 participants from specific sub-populations and 1112 controls. Only 522 (17.5%) participants from the specific populations received three doses as a primary vaccination regimen. Patients living with human immunodeficiency virus, cancer and diabetes had high percentages of responders after two doses, whereas patients with solid organ transplants, allogeneic hematopoietic stem cell transplants and hypogammaglobulinaemia had the lowest percentage of responders (35.9% [95% CI, 29.2-43.0], 57.4% [95% CI, 48.1-66.3] and 77.1% [95% CI, 65.6-86.3], respectively). In those who received the third dose, the percentage of responders reached 54.2% (95% CI, 42.9-65.2) (vs. 32.3% [95% CI, 16.7-51.4] after 2 doses) among those with solid organ transplants and 73.9% (95% CI, 58.9-85.7) (vs. 56.1% [95% CI, 46.2-65.7] after 2 doses) among those with hematopoietic stem cell transplants. Similar results were found with anti-SARS-CoV-2-specific neutralizing antibodies.

CONCLUSIONS:

A lower humoral response to COVID-19 vaccines was observed in the specific populations compared with that in the controls. The third dose of this vaccine in the primary regimen had a positive effect on the percentages of patients who developed anti-Spike IgG antibodies and specific neutralizing antibodies.
Keywords

Full text: Available Collection: International databases Database: MEDLINE Type of study: Cohort study / Experimental Studies / Observational study / Prognostic study / Randomized controlled trials Topics: Vaccines Language: English Journal subject: Communicable Diseases / Microbiology Year: 2022 Document Type: Article

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Full text: Available Collection: International databases Database: MEDLINE Type of study: Cohort study / Experimental Studies / Observational study / Prognostic study / Randomized controlled trials Topics: Vaccines Language: English Journal subject: Communicable Diseases / Microbiology Year: 2022 Document Type: Article