Background and Objectives : Immune functions are impaired after allogeneic
stem cell transplantation for several months depending on the age of the re
cipient, initial pathology, degree of HLA and minor histocompatibility anti
gens mismatches, origin and manipulation of the graft (unmanipulated or T-c
ell depleted bone marrow transplantation cord blood) and post-transplantati
on events (acute or chronic graft-versus-host disease, relapse and infectio
us complications).
Material and Methods, Results and Conclusion : In addition to lpmphocyte ph
enotyping and functional assays, new tools are now available to monitor spe
cific aspects of the immune response in the follow-up of hematopoietic stem
eel transplantation reconstitution of T cell diversity (spectratyping or I
mmunoscope), thymic function (TREC or "T-cell receptor rearrangement excisi
on DNA circles") and antigen-specific T cell responses (HLA tetramers).