Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1-2
pubmed:dateCreated
1998-10-2
pubmed:abstractText
Gene targeting in mouse embryonic stem (ES) cells was used to replace (i) the mouse immunoglobulin heavy chain (IgH) Cgamma2a gene segment (mCgamma2a) with the human Cgamma1 gene segment (hCgamma1), and (ii) the mouse immunoglobulin light chain (IgL) Ckappa gene segment (mC kappa) with its human counterpart (hC kappa). ES cells carrying these gene conversions were used to generate chimeric mice that transmitted the human alleles through the germ line. Mice homozygous for both gene alterations were generated by breeding. Serum from homozygous mutant mice contained comparable amounts of antibodies with chimeric kappa or mouse lambda light chains but only small fractions of basal serum IgG or antibodies elicited against immunizing agents contained chimeric heavy chains. A relative increase in immunogen-specific hCgamma1 antibodies was seen following immunization in combination with the saponin adjuvant QS-21. The effect of this was to shift the IgG1-dominated response to an IgG subclass profile that included significant amounts of IgG2a, IgG2b and IgG3 and chimeric IgG. The amounts of antibody secreted by hybridomas derived from mutant and wild-type mice were similar. Sequencing confirmed correct splicing of hCgamma1 and hCkappa gene segments to mouse J gene segments in hybridoma Ig gene transcripts. In conclusion, IgHhCgamma1/IgLhCkappa double mutant mice provide a useful animal model for deriving humanized antibodies with potential applications in immunotherapy and diagnostics in vivo as well as for investigating hCgamma1 associated functions.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jun
pubmed:issn
0022-1759
pubmed:author
pubmed:issnType
Print
pubmed:day
1
pubmed:volume
215
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
27-37
pubmed:dateRevised
2007-11-15
pubmed:meshHeading
pubmed-meshheading:9744745-Animals, pubmed-meshheading:9744745-Antibodies, Monoclonal, pubmed-meshheading:9744745-Antibody Specificity, pubmed-meshheading:9744745-Base Sequence, pubmed-meshheading:9744745-Cloning, Molecular, pubmed-meshheading:9744745-Embryo, Mammalian, pubmed-meshheading:9744745-Female, pubmed-meshheading:9744745-Flow Cytometry, pubmed-meshheading:9744745-Gene Targeting, pubmed-meshheading:9744745-Humans, pubmed-meshheading:9744745-Immunoglobulin G, pubmed-meshheading:9744745-Immunoglobulin gamma-Chains, pubmed-meshheading:9744745-Immunoglobulin kappa-Chains, pubmed-meshheading:9744745-Male, pubmed-meshheading:9744745-Mice, pubmed-meshheading:9744745-Mice, Inbred Strains, pubmed-meshheading:9744745-Molecular Sequence Data, pubmed-meshheading:9744745-Recombinant Fusion Proteins, pubmed-meshheading:9744745-Spleen, pubmed-meshheading:9744745-Stem Cells
pubmed:year
1998
pubmed:articleTitle
Generation of chimeric monoclonal antibodies from mice that carry human immunoglobulin Cgamma1 heavy of Ckappa light chain gene segments.
pubmed:affiliation
Swiss Tropical Institute, Basel, Switzerland. pluschke@ubaclu.unibas.ch
pubmed:publicationType
Journal Article