rdf:type |
|
lifeskim:mentions |
umls-concept:C0003241,
umls-concept:C0023693,
umls-concept:C0024348,
umls-concept:C0027651,
umls-concept:C0030956,
umls-concept:C0039194,
umls-concept:C0039617,
umls-concept:C0079731,
umls-concept:C0086418,
umls-concept:C0087111,
umls-concept:C0205263,
umls-concept:C0205369,
umls-concept:C0301869,
umls-concept:C0337112,
umls-concept:C1332714,
umls-concept:C1511636,
umls-concept:C1524075,
umls-concept:C1948027
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pubmed:issue |
2
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pubmed:dateCreated |
1994-3-22
|
pubmed:abstractText |
Anti-idiotype antibody therapy of B-cell lymphomas, despite numerous promising experimental and clinical studies, has so far met with limited success. Tailor-made monoclonal anti-idiotype antibodies have been injected into a large series of lymphoma patients, with a few impressive complete tumour remissions but a large majority of negative responses. The results presented here suggest that, by coupling to antilymphoma idiotype antibodies a few molecules of the tetanus toxin universal epitope peptide P2 (830-843), one could markedly increase the efficiency of this therapy. We show that after 2-hr incubation with conjugates consisting of the tetanus toxin peptide P2 coupled by an S-S bridge to monoclonal antibodies directed to the lambda light chain of human immunoglobulin, human B-lymphoma cells can be specifically lysed by a CD4 T-lymphocyte clone specific for the P2 peptide. Antibody without peptide did not induce B-cell killing by the CD4 T-lymphocyte clone. The free cysteine-peptide was also able to induce lysis of the B-lymphoma target by the T-lymphocyte clone, but at a molar concentration 500 to 1000 times higher than that of the coupled peptide. Proliferation assays confirmed that the antibody-peptide conjugate was antigenically active at a much lower concentration than the free peptide. They also showed that antibody-peptide conjugates required an intact processing function of the B cell for peptide presentation, which could be selectively inhibited by leupeptin and chloroquine.(ABSTRACT TRUNCATED AT 250 WORDS)
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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, Anti-Idiotypic,
http://linkedlifedata.com/resource/pubmed/chemical/Antibodies, Monoclonal,
http://linkedlifedata.com/resource/pubmed/chemical/Chloroquine,
http://linkedlifedata.com/resource/pubmed/chemical/Histocompatibility Antigens Class II,
http://linkedlifedata.com/resource/pubmed/chemical/Immunoglobulin Light Chains,
http://linkedlifedata.com/resource/pubmed/chemical/Immunotoxins,
http://linkedlifedata.com/resource/pubmed/chemical/Leupeptins,
http://linkedlifedata.com/resource/pubmed/chemical/Peptides,
http://linkedlifedata.com/resource/pubmed/chemical/Tetanus Toxin,
http://linkedlifedata.com/resource/pubmed/chemical/leupeptin
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pubmed:status |
MEDLINE
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pubmed:month |
Jan
|
pubmed:issn |
0020-7136
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pubmed:author |
|
pubmed:issnType |
Print
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pubmed:day |
15
|
pubmed:volume |
56
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
244-8
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pubmed:dateRevised |
2007-7-24
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pubmed:meshHeading |
pubmed-meshheading:7906251-Amino Acid Sequence,
pubmed-meshheading:7906251-Animals,
pubmed-meshheading:7906251-Antibodies, Anti-Idiotypic,
pubmed-meshheading:7906251-Antibodies, Monoclonal,
pubmed-meshheading:7906251-CD4-Positive T-Lymphocytes,
pubmed-meshheading:7906251-Chloroquine,
pubmed-meshheading:7906251-Histocompatibility Antigens Class II,
pubmed-meshheading:7906251-Humans,
pubmed-meshheading:7906251-Immunoglobulin Light Chains,
pubmed-meshheading:7906251-Immunotoxins,
pubmed-meshheading:7906251-Leupeptins,
pubmed-meshheading:7906251-Lymphoma, B-Cell,
pubmed-meshheading:7906251-Mice,
pubmed-meshheading:7906251-Mice, Inbred BALB C,
pubmed-meshheading:7906251-Molecular Sequence Data,
pubmed-meshheading:7906251-Peptides,
pubmed-meshheading:7906251-Tetanus Toxin
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pubmed:year |
1994
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pubmed:articleTitle |
Peptide-antibody conjugates for tumour therapy: a MHC-class-II-restricted tetanus toxin peptide coupled to an anti-Ig light chain antibody can induce cytotoxic lysis of a human B-cell lymphoma by specific CD4 T cells.
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pubmed:affiliation |
Institute of Biochemistry, University of Lausanne, Switzerland.
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pubmed:publicationType |
Journal Article,
Comparative Study
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