Healthy-like CD4 + Regulatory and CD4 + Conventional T-Cell Receptor Repertoires Predict Protection from GVHD Following Donor Lymphocyte Infusion.
Jessica SchneiderLeonie KuhlmannYankai XiaoSolaiman RahaGünter BernhardtMichael StadlerFelicitas TholMichael HeuserMatthias EderArnold GanserSarina RavensReinhold FörsterImmo PrinzChristian KoeneckeChristian R Schultze-FloreyPublished in: International journal of molecular sciences (2022)
Donor lymphocyte infusion (DLI) can (re-)induce durable remission in relapsing patients after allogeneic hematopoietic stem-cell transplantation (alloHSCT). However, DLI harbors the risk of increased non-relapse mortality due to the co-occurrence of graft-versus-host disease (GVHD). GVHD onset may be caused or accompanied by changes in the clonal T-cell receptor (TCR) repertoire. To investigate this, we analyzed T cells in a cohort of 21 patients receiving DLI after alloHSCT. We performed deep T-cell receptor β ( TRB ) sequencing of sorted CD4 + CD25 + CD127 low regulatory T cells (T reg cells) and CD4 + conventional T cells (T con cells) in order to track longitudinal changes in the TCR repertoire. GVHD following DLI was associated with less diverse but clonally expanded CD4 + CD25 + CD127 low T reg and CD4 + T con TCR repertoires, while patients without GVHD exhibited healthy-like repertoire properties. Moreover, the diversification of the repertoires upon GVHD treatment was linked to steroid-sensitive GVHD, whereas decreased diversity was observed in steroid-refractory GVHD. Finally, the unbiased sample analysis revealed that the healthy-like attributes of the CD4 + CD25 + CD127 low T reg TCR repertoire were associated with reduced GVHD incidence. In conclusion, CD4 + CD25 + CD127 low T reg and CD4 + T con   TRB repertoire dynamics may provide a helpful real-time tool to improve the diagnosis and monitoring of treatment in GVHD following DLI.
Keyphrases
- allogeneic hematopoietic stem cell transplantation
- regulatory t cells
- acute lymphoblastic leukemia
- end stage renal disease
- nk cells
- induced apoptosis
- multiple sclerosis
- chronic kidney disease
- oxidative stress
- ejection fraction
- type diabetes
- cardiovascular disease
- peritoneal dialysis
- coronary artery disease
- single cell
- systemic lupus erythematosus
- endoplasmic reticulum stress
- cell proliferation