Fiche publication


Date publication

mai 2017

Journal

Journal of hematology & oncology

Auteurs

Membres identifiés du Cancéropôle Est :
Pr BENSOUSSAN Danièle , Pr DE CARVALHO BITTENCOURT Marcelo , Dr JEULIN Hélène , Pr DECOT Véronique , Dr D'AVENI-PINEY Maud , Dr POCHON Cécile , Dr REPPEL Loïc


Tous les auteurs :
Qian C, Campidelli A, Wang Y, Cai H, Venard V, Jeulin H, Dalle JH, Pochon C, D'aveni M, Bruno B, Paillard C, Vigouroux S, Jubert C, Ceballos P, Marie-Cardine A, Galambrun C, Cholle C, Clerc Urmes I, Petitpain N, De Carvalho Bittencourt M, Decot V, Reppel L, Salmon A, Clement L, Bensoussan D

Résumé

Allogeneic hematopoietic stem cell transplantation (HSCT), the most widely used potentially curable cellular immunotherapeutic approach in the treatment of hematological malignancies, is limited by life-threatening complications: graft versus host disease (GVHD) and infections especially viral infections refractory to antiviral drugs. Adoptive transfer of virus-specific T cells is becoming an alternative treatment for infections following HSCT. We report here the results of a phase I/II multicenter study which includes a series of adenovirus-specific T cell (ADV-VST) infusion either from the HSCT donor or from a third party haploidentical donor for patients transplanted with umbilical cord blood (UCB).

Mots clés

Adenovirus-specific T cells, Allogeneic stem cell transplantation, Interferon-γ-based immunomagnetic isolation, Third party haploidentical donor, Umbilical cord blood transplantation

Référence

J Hematol Oncol. 2017 May;10(1):102