rdf:type |
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lifeskim:mentions |
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pubmed:issue |
1
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pubmed:dateCreated |
2004-1-7
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pubmed:abstractText |
Production of monoclonal antibodies requires immortalization of splenocytes by somatic fusion to a myeloma cell line partner (hybridomas). Although hybridomas can be immortal, they may depend on a feeder cell layer and may be genetically unstable. Since the inception of hybridoma technology, efforts to improve efficiency and stability of monoclonal antibody-producing cell lines have not brought about substantial progress. Moreover, suitable human multiple myeloma-derived cell lines for the production of human antibodies have been very difficult to develop. Here we report a strategy that greatly simplifies the generation of antibodies and eliminates the need for hybridomas. We show that splenocytes derived from transgenic mice harboring a mutant temperature-sensitive simian virus 40 large tumor antigen under the control of a mouse major histocompatibility promoter are conditionally immortal at permissive temperatures and produce monoclonal antibodies. This simple approach may become a method of choice for generation and production of both polyclonal and monoclonal antibodies with advantages in high-throughput discovery and antibody-based immunotherapy.
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pubmed:grant |
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pubmed:commentsCorrections |
http://linkedlifedata.com/resource/pubmed/commentcorrection/14688405-11017048,
http://linkedlifedata.com/resource/pubmed/commentcorrection/14688405-11172031,
http://linkedlifedata.com/resource/pubmed/commentcorrection/14688405-1172191,
http://linkedlifedata.com/resource/pubmed/commentcorrection/14688405-12782605,
http://linkedlifedata.com/resource/pubmed/commentcorrection/14688405-1711218,
http://linkedlifedata.com/resource/pubmed/commentcorrection/14688405-1987490,
http://linkedlifedata.com/resource/pubmed/commentcorrection/14688405-6247241,
http://linkedlifedata.com/resource/pubmed/commentcorrection/14688405-7678459,
http://linkedlifedata.com/resource/pubmed/commentcorrection/14688405-8011287,
http://linkedlifedata.com/resource/pubmed/commentcorrection/14688405-8159246,
http://linkedlifedata.com/resource/pubmed/commentcorrection/14688405-8390670,
http://linkedlifedata.com/resource/pubmed/commentcorrection/14688405-9020839,
http://linkedlifedata.com/resource/pubmed/commentcorrection/14688405-9263031
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Jan
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pubmed:issn |
0027-8424
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:day |
6
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pubmed:volume |
101
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
257-9
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pubmed:dateRevised |
2009-11-18
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pubmed:meshHeading |
pubmed-meshheading:14688405-Animals,
pubmed-meshheading:14688405-Antibodies, Monoclonal,
pubmed-meshheading:14688405-Antigens, Polyomavirus Transforming,
pubmed-meshheading:14688405-Clone Cells,
pubmed-meshheading:14688405-H-2 Antigens,
pubmed-meshheading:14688405-Hybridomas,
pubmed-meshheading:14688405-Mice,
pubmed-meshheading:14688405-Mice, Transgenic,
pubmed-meshheading:14688405-Mutation,
pubmed-meshheading:14688405-Spleen,
pubmed-meshheading:14688405-Temperature
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pubmed:year |
2004
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pubmed:articleTitle |
Hybridoma-free generation of monoclonal antibodies.
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pubmed:affiliation |
University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA. rpasqual@mdanderson.org
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
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