Academic Journal

Proceedings From the Fourth Haploidentical Stem Cell Transplantation Symposium (HAPLO2016), San Diego, California, December 1, 2016

التفاصيل البيبلوغرافية
العنوان: Proceedings From the Fourth Haploidentical Stem Cell Transplantation Symposium (HAPLO2016), San Diego, California, December 1, 2016
المؤلفون: M. M. Al Malki, R. Jones, Q. Ma, D. Lee, Y. Reisner, J. S. Miller, P. Lang, S. Hongeng, P. Hari, S. Strober, J. Yu, R. Maziarz, D. Mavilio, D. -C. Roy, C. a Bonini, R. E. Champlin, E. J. Fuchs, S. O. Ciurea
المساهمون: M.M. Al Malki, R. Jone, Q. Ma, D. Lee, Y. Reisner, J.S. Miller, P. Lang, S. Hongeng, P. Hari, S. Strober, J. Yu, R. Maziarz, D. Mavilio, D.-. Roy, C.A. Bonini, R.E. Champlin, E.J. Fuch, S.O. Ciurea
بيانات النشر: Elsevier
سنة النشر: 2018
المجموعة: The University of Milan: Archivio Istituzionale della Ricerca (AIR)
مصطلحات موضوعية: cellular therapy, Haploidentical transplantation, immunologic reconstitution, post-transplantation cyclophosphamide, T cell depletion, hematology, transplantation, Settore MED/46 - Scienze Tecniche di Medicina di Laboratorio, Settore MED/04 - Patologia Generale, Settore MED/15 - Malattie del Sangue, Settore MED/06 - Oncologia Medica
الوصف: The resurgence of haploidentical stem cell transplantation (HaploSCT) over the last decade is one of the most important advances in the field of hematopoietic stem cell transplantation (HSCT). The modified platforms of T cell depletion either ex vivo (CD34+cell selection, "megadoses" of purified CD34+cells, or selective depletion of T cells) or newer platforms of in vivo depletion of T cells, with either post-transplantation high-dose cyclophosphamide or intensified immune suppression, have contributed to better outcomes, with survival similar to that in HLA-matched donor transplantation. Further efforts are underway to control viral reactivation using modified T cells, improve immunologic reconstitution, and decrease the relapse rate post-transplantation using donor-derived cellular therapy products, such as genetically modified donor lymphocytes and natural killer cells. Improvements in treatment-related mortality have allowed the extension of haploidentical donor transplants to patients with hemoglobinopathies, such as thalassemia and sickle cell disease, and the possible development of platforms for immunotherapy in solid tumors. Moreover, combining HSCT from a related donor with solid organ transplantation could allow early tapering of immunosuppression in recipients of solid organ transplants and hopefully prevent organ rejection in this setting. This symposium summarizes some of the most important recent advances in HaploSCT and provides a glimpse in the future of fast growing field.
نوع الوثيقة: article in journal/newspaper
اللغة: English
Relation: info:eu-repo/semantics/altIdentifier/pmid/29339270; info:eu-repo/semantics/altIdentifier/wos/WOS:000433400000004; volume:24; issue:5; firstpage:895; lastpage:908; numberofpages:14; journal:BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION; http://hdl.handle.net/2434/551680; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85041640816
DOI: 10.1016/j.bbmt.2018.01.008
الاتاحة: http://hdl.handle.net/2434/551680
https://doi.org/10.1016/j.bbmt.2018.01.008
Rights: info:eu-repo/semantics/closedAccess
رقم الانضمام: edsbas.F9772A60
قاعدة البيانات: BASE
الوصف
DOI:10.1016/j.bbmt.2018.01.008