Booster Dose of SARS-CoV-2 mRNA Vaccine in Kidney Transplanted Patients Induces Wuhan-Hu-1 Specific Neutralizing Antibodies and T Cell Activation but Lower Response against Omicron Variant

Author:

Del Mastro Andrea1,Picascia Stefania2ORCID,D’Apice Luciana2ORCID,Trovato Maria2ORCID,Barba Pasquale2,Di Biase Immacolata3,Di Biase Sebastiano3,Laccetti Marco1,Belli Antonello4,Amato Gerardino4,Di Muro Potito5,Credendino Olga5,Picardi Alessandra6ORCID,De Berardinis Piergiuseppe2,Del Pozzo Giovanna7ORCID,Gianfrani Carmen2

Affiliation:

1. AORN A. Cardarelli–Internal Medicine Division 1–Immunology Unit, 80131 Naples, Italy

2. Institute of Biochemistry and Cell Biology, Italian National Council of Research, 80131 Naples, Italy

3. MeriGen Diagnostic&C, SAS, 80131 Naples, Italy

4. AORN A. Cardarelli–Clinical Pathology Division, 80131 Naples, Italy

5. AORN A. Cardarelli–Nephrology and Dialysis Unit, 80131 Naples, Italy

6. AORN A. Cardarelli–Molecular Biology Laboratory–Hematology and HSC Transplantation Unit, 80131 Naples, Italy

7. Institute of Genetics and Biophysics, Italian National Council of Research, 80131 Naples, Italy

Abstract

Kidney transplanted recipients (KTR) are at high risk of severe SARS-CoV-2 infection due to immunosuppressive therapy. Although several studies reported antibody production in KTR after vaccination, data related to immunity to the Omicron (B.1.1.529) variant are sparse. Herein, we analyzed anti-SARS-CoV-2 immune response in seven KTR and eight healthy controls after the second and third dose of the mRNA vaccine (BNT162b2). A significant increase in neutralizing antibody (nAb) titers were detected against pseudoviruses expressing the Wuhan-Hu-1 spike (S) protein after the third dose in both groups, although nAbs in KTR were lower than controls. nAbs against pseudoviruses expressing the Omicron S protein were low in both groups, with no increase after the 3rd dose in KTR. Reactivity of CD4+ T cells after boosting was observed when cells were challenged with Wuhan-Hu-1 S peptides, while Omicron S peptides were less effective in both groups. IFN-γ production was detected in KTR in response to ancestral S peptides, confirming antigen-specific T cell activation. Our study demonstrates that the 3rd mRNA dose induces T cell response against Wuhan-Hu-1 spike peptides in KTR, and an increment in the humoral immunity. Instead, humoral and cellular immunity to Omicron variant immunogenic peptides were low in both KTR and healthy vaccinated subjects.

Funder

Ministry of Education, Universities and Research

Regione Campania

European Union

Publisher

MDPI AG

Subject

Virology,Infectious Diseases

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