| Literature DB >> 30031939 |
Luisa Sisinni1, Mercedes Gasior2, Raquel de Paz2, Sergio Querol3, David Bueno4, Lucia Fernández5, Julia Marsal6, Ana Sastre4, Ramon Gimeno7, Laura Alonso8, Isabel Badell9, Eduardo López-Granados10, Juan Torres10, Laura Medina3, Montserrat Torrent9, Cristina Diaz de Heredia8, Adela Escudero11, Antonio Pérez-Martínez4.
Abstract
The CD45RA T cell depletion (TCD) method has been used to deplete naive T cells, preventing graft-versus-host disease (GVHD) but preserving memory cells, providing immediate functional T cells with anti-infection, antileukemia, and antirejection effects. We describe a series of 25 consecutive high-risk patients with leukemia who received haploidentical hematopoietic stem cell transplantation (haplo-HSCT) with CD45RA TCD. Each patient received 2 cell products: 1 created by CD34 positive selection and the other through CD45RA depletion from the CD34 negative fraction by a CliniMACS device. CD45RA-depleted haplo-HSCT was well tolerated, with rapid engraftment and low risk of severe acute GVHD and chronic GVHD. Although this treatment achieved a good control of viral reactivations, such as cytomegalovirus and adenovirus, we observed an unexpectedly high rate of limbic encephalitis due to human herpesvirus-6 (HHV-6; 8 cases). Characteristically, the infection appeared early in almost all patients, just after the engraftment. Although no patient died from encephalitis, 1 patient showed neuropsychological sequelae, and another experienced secondary graft failure just after the HHV-6 reactivation.Entities:
Keywords: Encephalitis; Haploidentical transplantation; Human herpesvirus-6
Mesh:
Year: 2018 PMID: 30031939 DOI: 10.1016/j.bbmt.2018.07.016
Source DB: PubMed Journal: Biol Blood Marrow Transplant ISSN: 1083-8791 Impact factor: 5.742