rdf:type |
|
lifeskim:mentions |
umls-concept:C0017262,
umls-concept:C0034790,
umls-concept:C0037791,
umls-concept:C0086418,
umls-concept:C0185117,
umls-concept:C0205460,
umls-concept:C0330390,
umls-concept:C0441513,
umls-concept:C0441655,
umls-concept:C0591833,
umls-concept:C0598622,
umls-concept:C1527177,
umls-concept:C2003941,
umls-concept:C2911684
|
pubmed:issue |
3
|
pubmed:dateCreated |
1991-2-25
|
pubmed:abstractText |
Murine/human chimeric antibodies with specificity for the human TCR-alpha/beta have been produced by genetic engineering. The L and H chain V region exons encoding the murine mAb BMA 031 were isolated and inserted into mammalian expression vectors containing the human kappa and gamma 1 or gamma 4 C region exons. The chimeric genes were transfected into murine Sp2/O hybridoma cells by electroporation and transfectomas secreting chimeric antibody were isolated. Secretion levels ranged from 1 to 7 pg/cell/24 h. The chimeric antibodies bound specifically to T cells and competed effectively with the parental murine mAb for binding to these sites. The ability to promote antibody-dependent cell-mediated cytolysis was significantly enhanced in the chimeric antibodies as compared with murine BMA 031. C-dependent cytolysis, however, was not detectable with any of the antibodies. Chimeric BMA 031 is a clinically relevant, genetically engineered antibody with potential uses in transplantation, graft-vs-host disease, autoimmune diseases and other T cell-related disorders.
|
pubmed:language |
eng
|
pubmed:journal |
|
pubmed:citationSubset |
AIM
|
pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Antibodies, Monoclonal,
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, CD3,
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, Differentiation...,
http://linkedlifedata.com/resource/pubmed/chemical/DNA,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Antigen, T-Cell
|
pubmed:status |
MEDLINE
|
pubmed:month |
Feb
|
pubmed:issn |
0022-1767
|
pubmed:author |
|
pubmed:issnType |
Print
|
pubmed:day |
1
|
pubmed:volume |
146
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
928-35
|
pubmed:dateRevised |
2004-11-17
|
pubmed:meshHeading |
pubmed-meshheading:1824850-Animals,
pubmed-meshheading:1824850-Antibodies, Monoclonal,
pubmed-meshheading:1824850-Antigens, CD3,
pubmed-meshheading:1824850-Antigens, Differentiation, T-Lymphocyte,
pubmed-meshheading:1824850-Base Sequence,
pubmed-meshheading:1824850-Cytotoxicity, Immunologic,
pubmed-meshheading:1824850-DNA,
pubmed-meshheading:1824850-Humans,
pubmed-meshheading:1824850-Hybridomas,
pubmed-meshheading:1824850-Lymphocyte Activation,
pubmed-meshheading:1824850-Mice,
pubmed-meshheading:1824850-Molecular Sequence Data,
pubmed-meshheading:1824850-RNA, Messenger,
pubmed-meshheading:1824850-Receptors, Antigen, T-Cell,
pubmed-meshheading:1824850-T-Lymphocytes,
pubmed-meshheading:1824850-Transfection
|
pubmed:year |
1991
|
pubmed:articleTitle |
Construction, expression, and biologic activity of murine/human chimeric antibodies with specificity for the human alpha/beta T cell receptor.
|
pubmed:affiliation |
Genzyme Corporation, Framingham, MA 01701.
|
pubmed:publicationType |
Journal Article
|