Serum and Salivary IgG and IgA Response After COVID-19 Messenger RNA Vaccination

Author:

Gorochov Guy1,Ropers Jacques2,Launay Odile3,Dorgham Karim1,da Mata-Jardin Omaira1,Lebbah Said2,Durier Christine4,Bauer Rebecca4,Radenne Anne5,Desaint Corinne3,Vieillard Louis-Victorien3,Rekacewicz Claire3,Lachatre Marie3,Parfait Béatrice6,Batteux Frédéric7,Hupé Philippe89,Ninove Läétitia10,Lefebvre Maeva11,Conrad Anne12,Dussol Bertrand13,Maakaroun-Vermesse Zoha14,Melica Giovanna15,Nicolas Jean-François16,Verdon Renaud17,Kiladjian Jean-Jacques18,Loubet Paul19,Schmidt-Mutter Catherine20,Dualé Christian21,Ansart Séverine22,Botelho-Nevers Elisabeth23,Lelièvre Jean-Daniel24,de Lamballerie Xavier10,Kieny Marie-Paule25,Tartour Eric26,Paul Stéphane27

Affiliation:

1. Sorbonne Université, Institut National de la Santé et de la Recherche Médicale (INSERM), Centre d’Immunologie et des Maladies Infectieuses (CIMI), Département d’Immunologie, Assistance Publique–Hôpitaux de Paris (AP-HP), Hôpital Pitié-Salpêtrière, Paris, France

2. INSERM, Institut Pierre Louis d’Epidémiologie et de Santé Publique, AP-HP, Hôpital Pitié-Salpêtrière, Département de Santé Publique, Unité de Recherche Clinique Paris Sciences et Lettres (PSL)–CFX, Sorbonne Université, Paris, France

3. Université Paris Cité, INSERM, Centre d’Investigation Clinique (CIC) 1417 Cochin Pasteur, French Clinical Research Infrastructure Network, Innovative Clinical Research Network in Vaccinology, APHP, Hôpital Cochin, Paris, France

4. INSERM SC10-US019, Villejuif, France

5. AP-HP, Hôpitaux Universitaires Pitié-Salpêtrière–Charles Foix, Unité de Recherche Clinique des Hôpitaux Universitaires Pitié-Salpêtrière, Paris, France

6. AP-HP, Hôpital Cochin, Fédération des Centres de Ressources Biologiques–Plateforme de Ressources Biologiques Centre de Ressources Biologique Cochin, Paris, France

7. AP-HP, Hôpital Cochin, Service d’Immunologie Biologique et Plateforme d’Immunomonitoring Vaccinal, Paris, France

8. Institut Curie, PSL Research University, INSERM U900, MINES ParisTech, PSL, Paris, France

9. Centre National de la Recherche Scientifique (CNRS), Unité Mixte de Recherche (UMR) 144, Paris, France

10. Research Institute for Sustainable Development 190, INSERM 1207, Institut Hospitalier Universitaire Méditerranée Infection, Unité des Virus Émergents, Aix Marseille Université, Marseille, France

11. Centre Hospitalier Universitaire (CHU) de Nantes, INSERM CIC 1413, Maladies Infectieuses et Tropicales, Centre de Prévention des Maladies Infectieuses et Transmissibles, Nantes, France

12. Département des Maladies Infectieuses et Tropicales, Hôpital de la Croix-Rousse, Hospices Civils de Lyon, Centre International de Recherche en Infectiologie (CIRI), INSERM U1111, Université Claude Bernard Lyon I, CNRS, UMR5308, École Normale Supérieure de Lyon, Université Lyon, Lyon, France

13. CIC 1409, INSERM–Hôpitaux Universitaires de Marseille–Aix Marseille Université, Hôpital de la Conception, Marseille, France

14. Centre de Vaccination CHU de Tours, CIC 1415, INSERM, Centre Hospitalier Régional et Universitaire de Tours, Tours, France

15. Service d’Immunologie Clinique et Maladies Infectieuses, AP-HP, Hôpital Henri Mondor, Créteil, Centre d’Investigation Clinique 1430 INSERM, AP-HP, Hôpital Henri Mondor, Créteil, France

16. CIRI, INSERM U1111, Université Claude Bernard Lyon I, Lyon, CHU Lyon-Sud, Pierre-Bénite, France

17. Service de Maladies Infectieuses, CHU de Caen, Dynamicure INSERM UMR 1311, Normandie Université, University of Caen Normandy, Caen, France

18. Université Paris Cité, AP-HP, Hôpital Saint-Louis, Centre d’Investigations Cliniques, INSERM, CIC 1427, Paris, France

19. Virulence Bactérienne et Maladies Infectieuses, INSERM U1047, Department of Infectious and Tropical Diseases, CHU 37 Nîmes, Université de Montpellier, Nîmes, France

20. INSERM CIC 1434, CHU Strasbourg, Strasbourg, France

21. CIC, INSERM CIC1405, CHU Clermont-Ferrand, Clermont-Ferrand, France

22. CIC 1412, INSERM, CHU Brest, Brest, France

23. INSERM CIC 1408, Axe Vaccinologie, CHU de Saint-Étienne, Service d’Infectiologie, Saint-Étienne, France

24. INSERM U955, Vaccine Research Institute, Créteil, France

25. INSERM 101, Paris, France

26. AP-HP, Hôpital Européen Georges Pompidou, INSERM U970, Paris Cardiovascular Research Center, Université Paris Cité, Paris, France

27. INSERM, U1111, CNRS, UMR 5308, CIRI-GIMAP, Université Claude Bernard Lyon 1, Université Jean Monnet, Immunology and Immunomonitoring Laboratory, iBiothera, CIC 1408, Saint-Étienne, France

Abstract

ImportanceThere is still considerable controversy in the literature regarding the capacity of intramuscular messenger RNA (mRNA) vaccination to induce a mucosal immune response.ObjectiveTo compare serum and salivary IgG and IgA levels among mRNA-vaccinated individuals with or without previous SARS-CoV-2 infection.Design, Setting, and ParticipantsIn this cohort study, SARS-CoV-2–naive participants and those with previous infection were consecutively included in the CoviCompare P and CoviCompare M mRNA vaccination trials and followed up to day 180 after vaccination with either the BNT162b2 (Pfizer-BioNTech) vaccine or the mRNA-1273 (Moderna) vaccine at the beginning of the COVID-19 vaccination campaign (from February 19 to June 8, 2021) in France. Data were analyzed from October 25, 2022, to July 13, 2023.Main Outcomes and MeasuresAn ultrasensitive digital enzyme-linked immunosorbent assay was used for the comparison of SARS-CoV-2 spike-specific serum and salivary IgG and IgA levels. Spike-specific secretory IgA level was also quantified at selected times.ResultsA total of 427 individuals were included in 3 groups: participants with SARS-CoV-2 prior to vaccination who received 1 single dose of BNT162b2 (Pfizer-BioNTech) (n = 120) and SARS-CoV-2–naive individuals who received 2 doses of mRNA-1273 (Moderna) (n = 172) or 2 doses of BNT162b2 (Pfizer-BioNTech) (n = 135). The median age was 68 (IQR, 39-75) years, and 228 (53.4%) were men. SARS-CoV-2 spike-specific IgG saliva levels increased after 1 or 2 vaccine injections in individuals with previous infection and SARS-CoV-2–naive individuals. After vaccination, SARS-CoV-2–specific saliva IgA levels, normalized with respect to total IgA levels, were significantly higher in participants with previous infection, as compared with the most responsive mRNA-1273 (Moderna) recipients (median normalized levels, 155 × 10−5 vs 37 × 10−5 at day 29; 107 × 10−5 vs 54 × 10−5 at day 57; and 104 × 10−5 vs 70 × 10−5 at day 180 [P < .001]). In contrast, compared with day 1, spike-specific IgA levels in the BNT162b2-vaccinated SARS-CoV-2–naive group increased only at day 57 (36 × 10−5 vs 49 × 10−5 [P = .01]). Bona fide multimeric secretory IgA levels were significantly higher in individuals with previous infection compared with SARS-CoV-2–naive individuals after 2 antigenic stimulations (median optical density, 0.36 [IQR, 0.16-0.63] vs 0.16 [IQR, 0.10-0.22]; P < .001).Conclusions and RelevanceThe findings of this cohort study suggest that mRNA vaccination was associated with mucosal immunity in individuals without prior SARS-CoV-2 infection, but at much lower levels than in previously infected individuals. Further studies are needed to determine the association between specific saliva IgA levels and prevention of infection or transmission.

Publisher

American Medical Association (AMA)

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