Allogeneic hematopoietic stem cell transplantation (allo-HSCT) is a potentially curative treatment for a variety of hematological malignancies. However, patients who have received this treatment have a persistent deficit in humoral immunity up to one year post-transplant. To date, the design of new therapeutic strategies to improve immune recovery in allo-HSCT patients is still hampered by the fact that post-transplant regenerative hematopoiesis has never been studied, and more generally by our currently limited knowledge on the development and function of human B lymphocytes. The main objective of our study is to study early B-cell progenitor reconstitution after allogeneic hematopoietic stem cell transplantation.
Study Type
OBSERVATIONAL
Enrollment
60
B cells reconstitution
B cell clusters as assess by CyTOF technology
Time frame: at day 100 days post-transplant
B cells reconstitution
B cell clusters as assess by CyTOF technology
Time frame: at 6 months post-transplant
Perturbations in growth or differentiation of progenitor/precursor of B cells
Perturbations in growth or differentiation of progenitor/precursor of B cells will be assessed by cytometry technology
Time frame: at 100 days post transplant
Perturbations in growth or differentiation of progenitor/precursor of B cells
Perturbations in growth or differentiation of progenitor/precursor of B cells will be assessed by cytometry technology
Time frame: at 6 months post-transplant
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