Antibody Response after 3-Dose Booster against SARS-CoV-2 mRNA Vaccine in Kidney Transplant Recipients.
Domenico TripodiRoberto DominiciDavide SaccoGennaro SantorelliRodolfo RiveraSandro AcquavivaMarino MarchisioPaolo BrambillaGraziana BattiniValerio LeoniPublished in: Vaccines (2024)
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is associated with a high rate of mortality in kidney transplant recipients (KTRs). Current vaccine strategies for KTRs seem to be unable to provide effective protection against coronavirus disease 2019 (COVID-19), and the occurrence of severe disease in some vaccinated KTRs suggested a lack of immunity. We initially analyzed the antibody response in a group of 32 kidney transplant recipients (KTRs) followed at the nephrology and dialysis unit of the Hospital Pio XI of Desio, ASST-Brianza, Italy. Thus, we studied the differences in antibody levels between subjects who contracted SARS-CoV-2 after the booster (8 individuals) and those who did not contract it (24 individuals). Furthermore, we verified if the antibody response was in any way associated with creatinine and eGFR levels. We observed a significant increase in the antibody response pre-booster compared to post-booster using both a Roche assay and DIAPRO assay. In the latter, through immunotyping, we highlight that the major contribution to this increase is specifically due to IgG S1 IgM S2. We observed a significant increase in IgA S1 and IgA NCP ( p = 0.045, 0.02) in the subjects who contracted SARS-CoV-2. We did not find significant associations for the p -value corrected for false discovery rate (FDR) between the antibody response to all assays and creatinine levels. This observation allows us to confirm that patients require additional vaccine boosters due to their immunocompromised status and therapy in order to protect them from infections related to viral variants. This is in line with the data reported in the literature, and it could be worthwhile to deeply explore these phenomena to better understand the role of IgA S1 and IgA NCP antibodies in SARS-CoV-2 infection.
Keyphrases
- sars cov
- respiratory syndrome coronavirus
- coronavirus disease
- high throughput
- end stage renal disease
- chronic kidney disease
- small cell lung cancer
- systematic review
- healthcare
- peritoneal dialysis
- risk assessment
- small molecule
- dna methylation
- newly diagnosed
- risk factors
- ejection fraction
- intensive care unit
- epidermal growth factor receptor
- bone marrow
- mesenchymal stem cells
- uric acid
- big data
- stem cells
- coronary artery disease
- metabolic syndrome
- tyrosine kinase
- gene expression
- cell therapy