Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1
pubmed:dateCreated
2006-12-27
pubmed:abstractText
Allogeneic hematopoietic stem cell transplantation (SCT) regimens incorporating the lymphocytotoxic CD52 antibody alemtuzumab demonstrate efficient engraftment and reduced graft-versus-host disease (GVHD). However, these protocols substantially impair posttransplantation antiviral and antitumor immunity. To accelerate immune reconstitution after alemtuzumab-based reduced-intensity SCT, we administered prophylactic CD8-depleted donor lymphocyte infusions (DLIs) starting on days 60 and 120 after transplantation. DLIs were processed in an immunomagnetic good manufacturing practice depletion procedure resulting in a 2.5- to 6-log reduction in CD8 T cells. Of 23 high-risk patients with hematologic malignancies, 11 received a total of 21 CD8-depleted DLIs. Five patients developed transient grade I acute GVHD following transfer. Only 2 patients with HLA-C-mismatched donors showed grade II and III acute GVHD and subsequently progressed to limited chronic GVHD. Following DLIs, 4 patients with declining hematopoietic donor chimerism converted to full chimeras. A 2.1-fold median increase of circulating CD4 T cells was observed within 2 weeks after infusion. Non-DLI patients did not show a comparable rise in CD4 counts. Four patients demonstrated enhanced frequencies of cytomegalovirus-specific CD4 and CD8 T cells following transfer. Our results suggest that prophylactic CD8-depleted DLIs accelerate immune reconstitution after lymphodepleted HLA-matched SCT and carry a low risk of inducing severe GVHD.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jan
pubmed:issn
0006-4971
pubmed:author
pubmed:issnType
Print
pubmed:day
1
pubmed:volume
109
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
374-82
pubmed:dateRevised
2011-11-17
pubmed:meshHeading
pubmed-meshheading:16940425-Adult, pubmed-meshheading:16940425-Antibodies, Monoclonal, pubmed-meshheading:16940425-Antibodies, Monoclonal, Humanized, pubmed-meshheading:16940425-Antibodies, Neoplasm, pubmed-meshheading:16940425-CD8-Positive T-Lymphocytes, pubmed-meshheading:16940425-Female, pubmed-meshheading:16940425-Follow-Up Studies, pubmed-meshheading:16940425-Graft Survival, pubmed-meshheading:16940425-Graft vs Host Disease, pubmed-meshheading:16940425-HLA Antigens, pubmed-meshheading:16940425-Hematologic Neoplasms, pubmed-meshheading:16940425-Humans, pubmed-meshheading:16940425-Immunomagnetic Separation, pubmed-meshheading:16940425-Immunotherapy, Adoptive, pubmed-meshheading:16940425-K562 Cells, pubmed-meshheading:16940425-Langerhans Cells, pubmed-meshheading:16940425-Lymphocyte Depletion, pubmed-meshheading:16940425-Male, pubmed-meshheading:16940425-Middle Aged, pubmed-meshheading:16940425-Peripheral Blood Stem Cell Transplantation, pubmed-meshheading:16940425-Transplantation Conditioning, pubmed-meshheading:16940425-Treatment Outcome
pubmed:year
2007
pubmed:articleTitle
Prophylactic transfer of CD8-depleted donor lymphocytes after T-cell-depleted reduced-intensity transplantation.
pubmed:affiliation
Department of Medicine III, Hematology and Oncology, Johannes Gutenberg-University, Mainz, Germany.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't, Multicenter Study, Clinical Trial, Phase I