Source:http://linkedlifedata.com/resource/pubmed/id/12937844
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
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pubmed:dateCreated |
2003-8-25
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pubmed:abstractText |
Allogeneic hematopoietic stem cell transplantation is the treatment of choice for many hematological malignancies. Its efficacy is limited by graft-versus-host disease (GVHD), the leading cause of post-transplant morbidity and mortality. GVHD is mediated by a subpopulation of T cells in the stem cell graft. Ex vivo T cell depletion of all T cells of the graft can prevent development of GVHD but can lead to a delay in immune reconstitution and an increase of potentially lethal opportunistic infections and leukemic relapses. Hypothetically, an approach that enables a selective depletion of the alloreactive donor T cells that cause GVHD while preserving third party (anti-leukemic and anti-microbial) reactivity would be optimal for recipients of HSCT. Our preliminary data demonstrated that an anti-CD25 immunotoxin, which reacts with a cell surface activation antigen, can selectively deplete alloreactive donor T cells activated by non-leukemic recipient white blood cells while preserving the beneficial third-party reactivity in vitro. In this report we describe a method for clinical-scale ex vivo selective depletion of alloreactive donor T cells using the anti-CD25 immunotoxin, RFT5-SMPT-dgRTA. Two logs of alloreactive T cells could be selectively depleted while preserving third party reactivity. This method was reproducible in 10 pre-clinical experiments with 8 HLA-mismatched healthy volunteer pairs and 2 HLA-matched sibling donor/patient pairs.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Antibodies, Monoclonal,
http://linkedlifedata.com/resource/pubmed/chemical/Immunoconjugates,
http://linkedlifedata.com/resource/pubmed/chemical/RFT5-SMPT-dgA immunotoxin,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Interleukin-2,
http://linkedlifedata.com/resource/pubmed/chemical/Ricin
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pubmed:status |
MEDLINE
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pubmed:issn |
0028-2685
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
50
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
296-9
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pubmed:dateRevised |
2011-11-17
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pubmed:meshHeading |
pubmed-meshheading:12937844-Antibodies, Monoclonal,
pubmed-meshheading:12937844-Feasibility Studies,
pubmed-meshheading:12937844-Graft vs Host Disease,
pubmed-meshheading:12937844-Hematopoietic Stem Cell Transplantation,
pubmed-meshheading:12937844-Humans,
pubmed-meshheading:12937844-Immunoconjugates,
pubmed-meshheading:12937844-Lymphocyte Depletion,
pubmed-meshheading:12937844-Receptors, Interleukin-2,
pubmed-meshheading:12937844-Reproducibility of Results,
pubmed-meshheading:12937844-Ricin,
pubmed-meshheading:12937844-T-Lymphocytes,
pubmed-meshheading:12937844-Transplantation Conditioning
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pubmed:year |
2003
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pubmed:articleTitle |
Clinical-scale selective depletion of alloreactive T cells using an anti-CD25 immunotoxin.
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pubmed:affiliation |
Cancer Immunobiology Center, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX 75390 USA. jmichal@med.muni.cz
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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