Source:http://linkedlifedata.com/resource/pubmed/id/18452562
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
7
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pubmed:dateCreated |
2008-5-30
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pubmed:abstractText |
Cancer immunotherapy using heat shock protein (HSP) derived from autologous tumor requires cluster of differentiation (CD)4(+) as well as CD8(+) T-cells for the prolongation of patient survival, suggesting that a humoral immune response through CD4(+) T-cells is important in addition to cellular immunity. However, the role of humoral responses in HSP-based autologous tumor immunotherapy remains unclear. In the present study, we investigated whether leukemia-specific antibodies and antibody-mediated cytotoxicity against autologous leukemia cells have a crucial role in a mouse A20 leukemia model by immunizing A20-derived HSP70. Immunization with A20-derived HSP70 induced the production of anti-A20-antibodies and the antibodies recognized HSP70-binding peptides derived from A20. One of those was a major histocompatibility complex (MHC) class-I binding peptide, which has been clarified as the target peptide of CD8+ cytotoxic T-cells (CTL) against A20. The anti-A20-antibodies produced by immunization with A20-derived HSP70 induced complement-dependent cytotoxicity (CDC) against A20 in vitro. In addition, immunization with A20-derived HSP70 increased intracellular interleukin-4 (IL4)-production of CD4(+) T-cells, confirming the activation of type-2 helper T-cells. Taken together, immunization with leukemia-cell-derived HSP70 induces antibodies against leukemia-cell-specific peptides and might play a crucial role in the eradication of leukemia cells by CDC in mice. These findings will enable future establishment of a novel therapeutic strategy using antileukemia antibodies in HSP-based autologous tumor immunotherapy.
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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, Neoplasm,
http://linkedlifedata.com/resource/pubmed/chemical/Cancer Vaccines,
http://linkedlifedata.com/resource/pubmed/chemical/HSP70 Heat-Shock Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Immunoglobulin G,
http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-4
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pubmed:status |
MEDLINE
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pubmed:month |
Jul
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pubmed:issn |
1349-7006
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
99
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1427-34
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pubmed:meshHeading |
pubmed-meshheading:18452562-Animals,
pubmed-meshheading:18452562-Antibodies, Neoplasm,
pubmed-meshheading:18452562-CD4-Positive T-Lymphocytes,
pubmed-meshheading:18452562-Cancer Vaccines,
pubmed-meshheading:18452562-Cytotoxicity, Immunologic,
pubmed-meshheading:18452562-Enzyme-Linked Immunosorbent Assay,
pubmed-meshheading:18452562-Female,
pubmed-meshheading:18452562-HSP70 Heat-Shock Proteins,
pubmed-meshheading:18452562-Immunization,
pubmed-meshheading:18452562-Immunoglobulin G,
pubmed-meshheading:18452562-Interleukin-4,
pubmed-meshheading:18452562-Leukemia,
pubmed-meshheading:18452562-Mice,
pubmed-meshheading:18452562-Mice, Inbred BALB C
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pubmed:year |
2008
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pubmed:articleTitle |
Induction of leukemia-specific antibodies by immunotherapy with leukemia-cell-derived heat shock protein 70.
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pubmed:affiliation |
Division of Gastroenterology and Hematology/Oncology, Department of Medicine, Asahikawa Medical College, Asahikawa, Japan.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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