Kidney transplanted recipients (KTR) are at high risk of severe SARS-CoV-2 infection dueto immunosuppressive therapy. Although several studies reported antibody production in KTRafter vaccination, data related to immunity to the Omicron (B.1.1.529) variant are sparse. Herein, weanalyzed anti-SARS-CoV-2 immune response in seven KTR and eight healthy controls after thesecond and third dose of the mRNA vaccine (BNT162b2). A significant increase in neutralizingantibody (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. nAbsagainst pseudoviruses expressing the Omicron S protein were low in both groups, with no increaseafter the 3rd dose in KTR. Reactivity of CD4+ T cells after boosting was observed when cells werechallenged with Wuhan-Hu-1 S peptides, while Omicron S peptides were less effective in bothgroups. IFN-? production was detected in KTR in response to ancestral S peptides, confirmingantigen-specific T cell activation. Our study demonstrates that the 3rd mRNA dose induces T cellresponse 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 inboth KTR and healthy vaccinated subjects.
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
Picascia S;D'Apice L;Trovato M;De Berardinis P;Del Pozzo G;Gianfrani C
2023
Abstract
Kidney transplanted recipients (KTR) are at high risk of severe SARS-CoV-2 infection dueto immunosuppressive therapy. Although several studies reported antibody production in KTRafter vaccination, data related to immunity to the Omicron (B.1.1.529) variant are sparse. Herein, weanalyzed anti-SARS-CoV-2 immune response in seven KTR and eight healthy controls after thesecond and third dose of the mRNA vaccine (BNT162b2). A significant increase in neutralizingantibody (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. nAbsagainst pseudoviruses expressing the Omicron S protein were low in both groups, with no increaseafter the 3rd dose in KTR. Reactivity of CD4+ T cells after boosting was observed when cells werechallenged with Wuhan-Hu-1 S peptides, while Omicron S peptides were less effective in bothgroups. IFN-? production was detected in KTR in response to ancestral S peptides, confirmingantigen-specific T cell activation. Our study demonstrates that the 3rd mRNA dose induces T cellresponse 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 inboth KTR and healthy vaccinated subjects.File | Dimensione | Formato | |
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