Strategies to optimize the outcome of children given T-cell depleted HLA-haploidentical hematopoietic stem cell transplantation

Franco Locatelli*, Luciana Vinti, Giuseppe Palumbo, Francesca Rossi, Alice Bertaina, Angela Mastronuzzi, Maria Ester Bernardo, Sergio Rutella, Paolo Dellabona, Giovanna Giorgiani, Alessandro Moretta, Lorenzo Moretta

*Autore corrispondente per questo lavoro

Risultato della ricerca: Contributo in rivistaArticolo

Abstract

The most advanced frontier of allogeneic hematopoietic stem cell transplantation (allo-HSCT) is represented by the use of an HLA-partially matched relative as donor. In this type of transplantation, donor-derived natural killer (NK) cells, which are alloreactive towardtoward recipient cells, significantly contribute to the eradication of leukemia blasts. Alloreactive NK cells may also kill host dendritic cells and T lymphocytes, thus preventing graft-versus-host disease and graft rejection, respectively. Sophisticated strategies of adoptive infusion of T-cell lines/clones specific for the most life-threatening pathogens (namely cytomegalovirus, Epstein-Barr virus, Aspergillus and Adenovirus) have been envisaged, and successfully tested in a few pilot trials, to protect the recipient in the early post-transplantation period. In these patients, also ex-vivo expanded mesenchymal stromal cells have been shown to be beneficial for preventing graft failure. Novel and effective strategies aimed at further augmenting the graft-versus-leukemia effect and at optimizing prevention/treatment of opportunistic/viral infections are warranted. (C) 2011 Elsevier Ltd. All rights reserved.
Lingua originaleInglese
pagine (da-a)339-349
Numero di pagine11
RivistaBAILLIERE'S BEST PRACTICE IN CLINICAL HAEMATOLOGY
Volume24
Numero di pubblicazione3
DOI
Stato di pubblicazionePubblicato - 2011

All Science Journal Classification (ASJC) codes

  • Oncologia
  • Biochimica Clinica

Keywords

  • NK alloreactivity
  • cellular therapy
  • graft-versus-leukemia effect
  • invariant NKT cells
  • mesenchymal stromal cells
  • pathogen-specific T cells

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