Literature DB >> 12393439

Transplantation of highly purified CD34+ progenitor cells from unrelated donors in pediatric leukemia.

Peter Lang1, Rupert Handgretinger, Dietrich Niethammer, Paul G Schlegel, Michael Schumm, Johann Greil, Peter Bader, Corinna Engel, Hans Scheel-Walter, Matthias Eyrich, Thomas Klingebiel.   

Abstract

Unrelated donors are commonly used for hematopoietic stem cell transplants, but graft-versus-host disease (GVHD) is a major problem. We investigated whether transplantation of purified mobilized peripheral-blood CD34(+) stem cells from unrelated donors would prevent acute and chronic GVHD in pediatric patients with leukemia and avert the need for pharmacologic immunosuppression. Thirty-one pediatric patients with acute lymphoblastic leukemia (ALL, n = 16), acute myeloid (n = 7), chronic myeloid (n = 6), or juvenile myelomonocytic leukemia (n = 2) underwent transplantation. The median purity of CD34(+) cells after positive magnet-activated cell sorting was 98.5%. Patients received a median of 8.0 x 10(6) CD34(+) cells and 6 x 10(3) CD3(+) T lymphocytes per kilogram, with no posttransplantation pharmacologic immunosuppression. Primary acute GVHD > or = grade II was seen in only 10% of patients (n = 3) and occurred only after human herpesvirus 6 (HHV 6) infection. Two patients had limited chronic GVHD. Engraftment occurred in all patients (primary engraftment, n = 26; engraftment after reconditioning, n = 5). The 2-year survival estimate was 38% for all patients and 63% for patients with ALL in complete remission. Patients with myeloid malignancies had a poor outcome. In comparison to a historical control group who received unmanipulated bone marrow, our patients had a lower incidence of GVHD (P <.001). No difference was observed in the probability of relapse or survival. Study patients with ALL in remission showed a trend toward better survival (P =.07). Transplantation of purified peripheral-blood CD34(+) cells from unrelated donors effectively minimizes GVHD and may be a good therapeutic option for patients with relapsed ALL.

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Year:  2002        PMID: 12393439     DOI: 10.1182/blood-2002-04-1203

Source DB:  PubMed          Journal:  Blood        ISSN: 0006-4971            Impact factor:   22.113


  11 in total

1.  Poor graft function can be durably and safely improved by CD34+-selected stem cell boosts after allogeneic unrelated matched or mismatched hematopoietic cell transplantation.

Authors:  Sebastian P Haen; Michael Schumm; Christoph Faul; Lothar Kanz; Wolfgang A Bethge; Wichard Vogel
Journal:  J Cancer Res Clin Oncol       Date:  2015-08-14       Impact factor: 4.553

Review 2.  How do I perform hematopoietic progenitor cell selection?

Authors:  Scott T Avecilla; Cheryl Goss; Sharon Bleau; Jo-Ann Tonon; Richard C Meagher
Journal:  Transfusion       Date:  2016-02-25       Impact factor: 3.157

3.  Long-term results after transplantation of CD34+ selected (CellPro) versus unselected peripheral blood progenitor cells (PBPC) from related allogeneic donors.

Authors:  Hans-Georg Kopp; Stefan Wirths; Christoph Faul; Wolfgang Bethge; Stefan Scheding; Wolfram Brugger; Lothar Kanz; Wichard Vogel
Journal:  J Cancer Res Clin Oncol       Date:  2010-03-09       Impact factor: 4.553

4.  Risk factors in patients undergoing haploidentical hematopoietic stem cell transplantation for high-risk childhood acute leukemia.

Authors:  Dong-Mei Han; Xiao-Li Zheng; Li Ding; Hong-Min Yan; Zhi-Dong Wang; Mei Xue; Ling Zhu; Jing Liu; Heng-Xiang Wang
Journal:  Int J Hematol       Date:  2017-08-20       Impact factor: 2.490

5.  Reconstitution of natural killer cell receptors influences natural killer activity and relapse rate after haploidentical transplantation of T- and B-cell depleted grafts in children.

Authors:  Matthias M Pfeiffer; Tobias Feuchtinger; Heiko-Manuel Teltschik; Michael Schumm; Ingo Müller; Rupert Handgretinger; Peter Lang
Journal:  Haematologica       Date:  2010-02-09       Impact factor: 9.941

Review 6.  Perspective on the role of haploidentical transplantation in the management of hematologic malignancies: why do it?

Authors:  Gregory A Hale
Journal:  Curr Hematol Malig Rep       Date:  2007-07       Impact factor: 3.952

Review 7.  T cell depletion in paediatric stem cell transplantation.

Authors:  C Booth; P Veys
Journal:  Clin Exp Immunol       Date:  2013-05       Impact factor: 4.330

8.  Influence of Histone Deacetylase Inhibitors and DNA-Methyltransferase Inhibitors on the NK Cell-Mediated Lysis of Pediatric B-Lineage Leukemia.

Authors:  Matthias Manuel Pfeiffer; Helen Burow; Sabine Schleicher; Rupert Handgretinger; Peter Lang
Journal:  Front Oncol       Date:  2013-04-29       Impact factor: 6.244

9.  Clinical grade purification and expansion of NK cell products for an optimized manufacturing protocol.

Authors:  Ulrike Koehl; Claudia Brehm; Sabine Huenecke; Stefanie-Yvonne Zimmermann; Stephan Kloess; Melanie Bremm; Evelyn Ullrich; Jan Soerensen; Andrea Quaiser; Stephanie Erben; Claudia Wunram; Tanja Gardlowski; Eileen Auth; Torsten Tonn; Christian Seidl; Sandrine Meyer-Monard; Martin Stern; Jakob Passweg; Thomas Klingebiel; Peter Bader; Dirk Schwabe; Ruth Esser
Journal:  Front Oncol       Date:  2013-05-17       Impact factor: 6.244

10.  Capture and enrichment of CD34-positive haematopoietic stem and progenitor cells from blood circulation using P-selectin in an implantable device.

Authors:  Joel C Wojciechowski; Srinivas D Narasipura; Nichola Charles; Deanne Mickelsen; Kuldeeepsinh Rana; Martha L Blair; Michael R King
Journal:  Br J Haematol       Date:  2008-01-22       Impact factor: 6.998

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