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Functional CVIDs phenotype clusters identified by the integration of immune parameters after BNT162b2 boosters

Authors :
Eva Piano Mortari
Federica Pulvirenti
Valentina Marcellini
Sara Terreri
Ane Fernandez Salinas
Simona Ferrari
Giulia Di Napoli
Daniele Guadagnolo
Eleonora Sculco
Christian Albano
Marika Guercio
Stefano Di Cecca
Cinzia Milito
Giulia Garzi
Anna Maria Pesce
Livia Bonanni
Matilde Sinibaldi
Veronica Bordoni
Serena Di Cecilia
Silvia Accordini
Concetta Castilletti
Chiara Agrati
Concetta Quintarelli
Salvatore Zaffina
Franco Locatelli
Rita Carsetti
Isabella Quinti
Source :
Frontiers in Immunology, Vol 14 (2023)
Publication Year :
2023
Publisher :
Frontiers Media S.A., 2023.

Abstract

IntroductionAssessing the response to vaccinations is one of the diagnostic criteria for Common Variable Immune Deficiencies (CVIDs). Vaccination against SARS-CoV-2 offered the unique opportunity to analyze the immune response to a novel antigen. We identify four CVIDs phenotype clusters by the integration of immune parameters after BTN162b2 boosters.MethodsWe performed a longitudinal study on 47 CVIDs patients who received the 3rd and 4th vaccine dose of the BNT162b2 vaccine measuring the generation of immunological memory. We analyzed specific and neutralizing antibodies, spike-specific memory B cells, and functional T cells.ResultsWe found that, depending on the readout of vaccine efficacy, the frequency of responders changes. Although 63.8% of the patients have specific antibodies in the serum, only 30% have high-affinity specific memory B cells and generate recall responses.DiscussionThanks to the integration of our data, we identified four functional groups of CVIDs patients with different B cell phenotypes, T cell functions, and clinical diseases. The presence of antibodies alone is not sufficient to demonstrate the establishment of immune memory and the measurement of the in-vivo response to vaccination distinguishes patients with different immunological defects and clinical diseases.

Details

Language :
English
ISSN :
16643224
Volume :
14
Database :
Directory of Open Access Journals
Journal :
Frontiers in Immunology
Publication Type :
Academic Journal
Accession number :
edsdoj.0fcf59fc30ee47eeaefe302b9296e6ea
Document Type :
article
Full Text :
https://doi.org/10.3389/fimmu.2023.1194225