Treg-protected donor lymphocyte infusions: a new tool to address the graft-versus-leukemia effect in the absence of graft-versus-host disease in patients relapsed after HSCT.
Mauro Di IanniPaola OliosoRaffaella GiancolaStella SantaroneAnnalisa NataleGabriele PapalinettiIda VillanovaStefano BaldoniAmbra Di TommasoTiziana BonfiniPatrizia AccorsiPaolo Di BartolomeoPublished in: International journal of hematology (2017)
In high-risk acute leukemia patients undergoing haploidentical hematopoietic stem cell transplantation (HSCT), adoptive immunotherapy with T regulatory cells (Tregs) and T conventional cells (Tcons) prevented acute and chronic graft-versus-host disease (GvHD), favored post-transplant immunological reconstitution and was associated with a powerful graft-versus-leukemia (GvL) effect. With a particularly innovative approach, we developed a treatment with a Treg-protected donor lymphocyte infusion (DLI) for patients with early relapse after HSCT and we report here the results obtained in the first patient with APL (M3v) relapsed after a second matched allogeneic HSCT (15% blasts and 75% of donor cells in bone marrow). The patient received a first infusion of 2.5 × 106/kg Tregs derived from matched donor followed 7 days later by 5 × 106/kg Tcons. GvL effect was strongly evident as the percentage of leukemic cells decreased to 5%. A second infusion of Tregs (2.5 × 106/kg) and Tcons (2 × 106/kg) was performed. No GvHD was observed. Disease evaluation showed the absence of blastic cells at flow-cytometry, a normal caryotype and full donor chimerism. We also observed NOTCH1 down-regulation in peripheral blood. This new immunotherapy approach showed that Treg-protected DLI is effective in preventing GvHD and is associated with a strong GvL effect.
Keyphrases
- induced apoptosis
- bone marrow
- acute myeloid leukemia
- peripheral blood
- cell cycle arrest
- patients undergoing
- low dose
- flow cytometry
- endoplasmic reticulum stress
- allogeneic hematopoietic stem cell transplantation
- mesenchymal stem cells
- end stage renal disease
- oxidative stress
- cell proliferation
- chronic kidney disease
- transcription factor
- signaling pathway
- intensive care unit
- multiple myeloma
- hodgkin lymphoma
- diffuse large b cell lymphoma
- prognostic factors
- patient reported outcomes
- replacement therapy