Common T-Cell-Receptor Motifs and Features in Patients with Cytomegalovirus (CMV)-Seronegative End-Stage Renal Disease Receiving a Peptide Vaccination against CMV.
Lukas BunseClaudia SommererChin Leng TanFelix KorellAnita SchmittAngela Hückelhoven-KraussBrigitte NeuberThomas MertensMichael PlattenEdward W GreenMartin ZeierMichael SchmittPublished in: International journal of molecular sciences (2022)
After solid-organ transplantation, reactivation of the cytomegalovirus (CMV) is often observed in seronegative patients and associated with a high risk of disease and mortality. CMV-specific T cells can prevent CMV reactivation. In a phase 1 trial, CMV-seronegative patients with end-stage renal disease listed for kidney transplantation were subjected to CMV phosphoprotein 65 (CMVpp65) peptide vaccination and further investigated for T-cell responses. To this end, CMV-specific CD8 + T cells were characterized by bulk T-cell-receptor (TCR) repertoire sequencing and combined single-cell RNA and TCR sequencing. In patients mounting an immune response to the vaccine, a common SYE(N)E TCR motif known to bind CMVpp65 was detected. CMV-peptide-vaccination-responder patients had TCR features distinct from those of non-responders. In a non-responder patient, a monoclonal inflammatory T-cell response was detected upon CMV reactivation. The identification of vaccine-induced CMV-reactive TCRs motifs might facilitate the development of cellular therapies for patients wait-listed for kidney transplantation.
Keyphrases
- end stage renal disease
- chronic kidney disease
- peritoneal dialysis
- ejection fraction
- kidney transplantation
- newly diagnosed
- single cell
- prognostic factors
- regulatory t cells
- stem cells
- cardiovascular disease
- oxidative stress
- patient reported outcomes
- endothelial cells
- high glucose
- patient reported
- atomic force microscopy