Peritransplant palifermin use and lymphocyte recovery after T‐cell replete, matched related allogeneic hematopoietic cell transplantation
dc.contributor.author | Rizwan, Romee | en_US |
dc.contributor.author | Levine, John E. | en_US |
dc.contributor.author | DeFor, Todd | en_US |
dc.contributor.author | Ferarra, James L.M. | en_US |
dc.contributor.author | Weisdorf, Daniel J. | en_US |
dc.contributor.author | Blazar, Bruce R. | en_US |
dc.contributor.author | Verneris, Michael R. | en_US |
dc.date.accessioned | 2011-11-10T15:35:40Z | |
dc.date.available | 2012-12-03T21:17:30Z | en_US |
dc.date.issued | 2011-10 | en_US |
dc.identifier.citation | Rizwan, Romee; Levine, John E.; DeFor, Todd; Ferarra, James L.M.; Weisdorf, Daniel J.; Blazar, Bruce R.; Verneris, Michael R. (2011). "Peritransplant palifermin use and lymphocyte recovery after T‐cell replete, matched related allogeneic hematopoietic cell transplantation ." American Journal of Hematology 86(10): 879-882. <http://hdl.handle.net/2027.42/86994> | en_US |
dc.identifier.issn | 0361-8609 | en_US |
dc.identifier.issn | 1096-8652 | en_US |
dc.identifier.uri | https://hdl.handle.net/2027.42/86994 | |
dc.publisher | Wiley Subscription Services, Inc., A Wiley Company | en_US |
dc.title | Peritransplant palifermin use and lymphocyte recovery after T‐cell replete, matched related allogeneic hematopoietic cell transplantation | en_US |
dc.type | Article | en_US |
dc.rights.robots | IndexNoFollow | en_US |
dc.subject.hlbsecondlevel | Molecular, Cellular and Developmental Biology | en_US |
dc.subject.hlbsecondlevel | Oncology and Hematology | en_US |
dc.subject.hlbtoplevel | Health Sciences | en_US |
dc.subject.hlbtoplevel | Science | en_US |
dc.description.peerreviewed | Peer Reviewed | en_US |
dc.contributor.affiliationum | The Blood and Marrow Transplantation Program, University of Michigan, Ann Arbor, Michigan | en_US |
dc.contributor.affiliationother | The Blood and Marrow Transplantation Program, University of Minnesota, Minneapolis | en_US |
dc.contributor.affiliationother | Department of Pediatrics, Division of Hematology/Oncology and Blood and Marrow Transplantation, University of Minnesota, 660 CCRB, 425 East River Road, Minneapolis, MN 55455E‐mail: verneris@umn.edu | en_US |
dc.identifier.pmid | 21922528 | en_US |
dc.description.bitstreamurl | http://deepblue.lib.umich.edu/bitstream/2027.42/86994/1/22136_ftp.pdf | |
dc.identifier.doi | 10.1002/ajh.22136 | en_US |
dc.identifier.source | American Journal of Hematology | en_US |
dc.identifier.citedreference | Ballen KK, King RJ, Chitphakdithai P, et al. The national marrow donor program 20 years of unrelated donor hematopoietic cell transplantation. Biol Blood Marrow Transplant 2008; 14: 2 – 7. | en_US |
dc.identifier.citedreference | Shilling HG, McQueen KL, Cheng NW, et al. Reconstitution of NK cell receptor repertoire following HLA‐matched hematopoietic cell transplantation. Blood 2003; 101: 3730 – 3740. | en_US |
dc.identifier.citedreference | Triplett BM, Horwitz EM, Iyengar R, et al. Effects of activating NK cell receptor expression and NK cell reconstitution on the outcomes of unrelated donor hematopoietic cell transplantation for hematologic malignancies. Leukemia 2009; 23: 1278 – 1287. | en_US |
dc.identifier.citedreference | Douek DC, Vescio RA, Betts MR, et al. Assessment of thymic output in adults after haematopoietic stem‐cell transplantation and prediction of T‐cell reconstitution. Lancet 2000; 355: 1875 – 1881. | en_US |
dc.identifier.citedreference | Heitger A, Neu N, Kern H, et al. Essential role of the thymus to reconstitute naive (CD45RA+) T‐helper cells after human allogeneic bone marrow transplantation. Blood 1997; 90: 850 – 857. | en_US |
dc.identifier.citedreference | Marie‐Cardine A, Divay F, Dutot I, et al. Transitional B cells in humans: Characterization and insight from B lymphocyte reconstitution after hematopoietic stem cell transplantation. Clin Immunol 2008; 127: 14 – 25. | en_US |
dc.identifier.citedreference | Cooley S, McCullar V, Wangen R, et al. KIR reconstitution is altered by T cells in the graft and correlates with clinical outcomes after unrelated donor transplantation. Blood 2005; 106: 4370 – 4376. | en_US |
dc.identifier.citedreference | Szabolcs P, Niedzwiecki D. Immune reconstitution after unrelated cord blood transplantation. Cytotherapy 2007; 9: 111 – 122. | en_US |
dc.identifier.citedreference | Burke MJ, Vogel RI, Janardan SK, et al. Early lymphocyte recovery and outcomes after umbilical cord blood transplantation (UCBT) for hematologic malignancies. Biol Blood Marrow Transplant 2011; 17: 831 – 840. | en_US |
dc.identifier.citedreference | Pavletic ZS, Joshi SS, Pirruccello SJ, et al. Lymphocyte reconstitution after allogeneic blood stem cell transplantation for hematologic malignancies. Bone Marrow Transplant 1998; 21: 33 – 41. | en_US |
dc.identifier.citedreference | Le Blanc K, Barrett AJ, Schaffer M, et al. Lymphocyte recovery is a major determinant of outcome after matched unrelated myeloablative transplantation for myelogenous malignancies. Biol Blood Marrow Transplant 2009; 15: 1108 – 1115. | en_US |
dc.identifier.citedreference | Kumar S, Chen MG, Gastineau DA, et al. Lymphocyte recovery after allogeneic bone marrow transplantation predicts risk of relapse in acute lymphoblastic leukemia. Leukemia 2003; 17: 1865 – 1870. | en_US |
dc.identifier.citedreference | Kumar S, Chen MG, Gastineau DA, et al. Effect of slow lymphocyte recovery and type of graft‐versus‐host disease prophylaxis on relapse after allogeneic bone marrow transplantation for acute myelogenous leukemia. Bone Marrow Transplant 2001; 28: 951 – 956. | en_US |
dc.identifier.citedreference | Ishaqi MK, Afzal S, Dupuis A, et al. Early lymphocyte recovery post‐allogeneic hematopoietic stem cell transplantation is associated with significant graft‐versus‐leukemia effect without increase in graft‐versus‐host disease in pediatric acute lymphoblastic leukemia. Bone Marrow Transplant 2008; 41: 245 – 252. | en_US |
dc.identifier.citedreference | Kim DH, Kim JG, Sohn SK, et al. Clinical impact of early absolute lymphocyte count after allogeneic stem cell transplantation. Br J Haematol 2004; 125: 217 – 224. | en_US |
dc.identifier.citedreference | Kelly RM, Goren EM, Taylor PA, et al. Short‐term inhibition of p53 combined with keratinocyte growth factor improves thymic epithelial cell recovery and enhances T‐cell reconstitution after murine bone marrow transplantation. Blood 2010; 115: 1088 – 1097. | en_US |
dc.identifier.citedreference | Rossi SW, Jeker LT, Ueno T, et al. Keratinocyte growth factor (KGF) enhances postnatal T‐cell development via enhancements in proliferation and function of thymic epithelial cells. Blood 2007; 109: 3803 – 3811. | en_US |
dc.identifier.citedreference | Min D, Taylor PA, Panoskaltsis‐Mortari A, et al. Protection from thymic epithelial cell injury by keratinocyte growth factor: A new approach to improve thymic and peripheral T‐cell reconstitution after bone marrow transplantation. Blood 2002; 99: 4592 – 4600. | en_US |
dc.identifier.citedreference | Min D, Panoskaltsis‐Mortari A, Kuro OM, et al. Sustained thymopoiesis and improvement in functional immunity induced by exogenous KGF administration in murine models of aging. Blood 2007; 109: 2529 – 2537. | en_US |
dc.identifier.citedreference | Napolitano LA, Schmidt D, Gotway MB, et al. Growth hormone enhances thymic function in HIV‐1‐infected adults. J Clin Invest 2008; 118: 1085 – 1098. | en_US |
dc.identifier.citedreference | Erickson M, Morkowski S, Lehar S, et al. Regulation of thymic epithelium by keratinocyte growth factor. Blood 2002; 100: 3269 – 3278. | en_US |
dc.identifier.citedreference | Alpdogan O, Hubbard VM, Smith OM, et al. Keratinocyte growth factor (KGF) is required for postnatal thymic regeneration. Blood 2006; 107: 2453 – 2460. | en_US |
dc.identifier.citedreference | Rossi S, Blazar BR, Farrell CL, et al. Keratinocyte growth factor preserves normal thymopoiesis and thymic microenvironment during experimental graft‐versus‐host disease. Blood 2002; 100: 682 – 691. | en_US |
dc.identifier.citedreference | Seggewiss R, Lore K, Guenaga FJ, et al. Keratinocyte growth factor augments immune reconstitution after autologous hematopoietic progenitor cell transplantation in rhesus macaques. Blood 2007; 110: 441 – 449. | en_US |
dc.identifier.citedreference | Kelly RM, Highfill SL, Panoskaltsis‐Mortari A, et al. Keratinocyte growth factor and androgen blockade work in concert to protect against conditioning regimen‐induced thymic epithelial damage and enhance T‐cell reconstitution after murine bone marrow transplantation. Blood 2008; 111: 5734 – 5744. | en_US |
dc.identifier.citedreference | Blazar BR, Weisdorf DJ, Defor T, et al. Phase 1/2 randomized, placebo‐control trial of palifermin to prevent graft‐versus‐host disease (GVHD) after allogeneic hematopoietic stem cell transplantation (HSCT). Blood 2006; 108: 3216 – 3222. | en_US |
dc.identifier.citedreference | Levine JE, Blazar BR, DeFor T, et al. Long‐term follow‐up of a phase I/II randomized, placebo‐controlled trial of palifermin to prevent graft‐versus‐host disease (GVHD) after related donor allogeneic hematopoietic cell transplantation (HCT). Biol Blood Marrow Transplant 2008; 14: 1017 – 1021. | en_US |
dc.identifier.citedreference | Savani BN, Mielke S, Rezvani K, et al. Absolute lymphocyte count on day 30 is a surrogate for robust hematopoietic recovery and strongly predicts outcome after T cell‐depleted allogeneic stem cell transplantation. Biol Blood Marrow Transplant 2007; 13: 1216 – 1223. | en_US |
dc.identifier.citedreference | Seggewiss R, Einsele H. Immune reconstitution after allogeneic transplantation and expanding options for immunomodulation: An update. Blood 2010; 115: 3861 – 3868. | en_US |
dc.owningcollname | Interdisciplinary and Peer-Reviewed |
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