Source:http://linkedlifedata.com/resource/pubmed/id/11128812
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
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pubmed:dateCreated |
2000-12-20
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pubmed:abstractText |
The idiotype (Id) determinants on the multiple myeloma immunoglobulin can serve as tumor-specific antigens. An anti-Id immune response may stem the growth of the malignant clone. We report on 26 patients treated at our institution with high-dose chemotherapy and peripheral blood progenitor cell transplantation (PBPCT) and vaccinated with the Id protein. The patients received chemotherapy and PBPCT to establish a minimal residual disease state. After high-dose therapy, the patients received a series of monthly immunizations consisting of 2 intravenous infusions of dendritic cells (DCs) pulsed with either Id protein or Id coupled with keyhole limpet hemocyanin (KLH) as an immunogenic carrier protein, followed by subcutaneous boosts of Id-KLH conjugates. DCs were obtained in all patients from a leukapheresis product 3 to 9 months after PBPCT. Patients were observed for toxicity, immune responses, and tumor status. The DC infusions and the administration of Id-KLH boosts were well tolerated, with patients experiencing only minor and transient side effects. Of the patients, 24 of 26 generated a KLH-specific cellular proliferative immune response. Only 4 patients developed an Id-specific proliferative immune response. Three of these immune responders were in complete remission at the time of vaccination. A total of 17 patients are alive at a median follow-up of 30 months after transplantation. Id vaccination with autologous DCs is feasible for myeloma patients after transplantation. Id-specific cellular responses can be induced in patients who are in complete remission. Further studies are needed to increase the rate of anti-Id immune responses in patients who do not achieve complete remission.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:issn |
1083-8791
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
6
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
621-7
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:11128812-Adult,
pubmed-meshheading:11128812-Antineoplastic Combined Chemotherapy Protocols,
pubmed-meshheading:11128812-Combined Modality Therapy,
pubmed-meshheading:11128812-Dendritic Cells,
pubmed-meshheading:11128812-Female,
pubmed-meshheading:11128812-Hematopoietic Stem Cell Transplantation,
pubmed-meshheading:11128812-Humans,
pubmed-meshheading:11128812-Immunoglobulin Idiotypes,
pubmed-meshheading:11128812-Immunotherapy,
pubmed-meshheading:11128812-Male,
pubmed-meshheading:11128812-Middle Aged,
pubmed-meshheading:11128812-Multiple Myeloma,
pubmed-meshheading:11128812-Transplantation, Autologous,
pubmed-meshheading:11128812-Vaccination
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pubmed:year |
2000
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pubmed:articleTitle |
Idiotype vaccination using dendritic cells after autologous peripheral blood progenitor cell transplantation for multiple myeloma.
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pubmed:affiliation |
Division of Oncology, Stanford University Medical Center, California 94305-5151, USA.
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pubmed:publicationType |
Journal Article,
Clinical Trial,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
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