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Selection of a low antigenic variant subline from the TA3St ascites carcinoma by repeated passage of antibody-coated cells through anti-immunoglobulin columns.

Abstract
TA3St mouse ascites carcinoma cells of strain A origin (H-2a) were coated with anti-H-2a serum and passaged through mouse immunoglobulin-anti-immunoglobulin columns repeatedly prior to each in vivo passage. After six passages in vivo, a variant cell line emerged with significantly decreased H-2a expression and an increased ability to grow progressively across H-2 allograft barriers. Chromosome analysis of the variant cell line revealed no major changes in karyotype. The application of the method for studies on the generation of immunoresistant tumor cell variants and on the relationship between antibody-binding sites and rejection target sites is discussed.
AuthorsT Dallanis, G Klein, B Andersson
JournalJournal of the National Cancer Institute (J Natl Cancer Inst) Vol. 63 Issue 2 Pg. 383-8 (Aug 1979) ISSN: 0027-8874 [Print] United States
PMID379399 (Publication Type: Journal Article, Research Support, U.S. Gov't, P.H.S.)
Chemical References
  • Antibodies, Anti-Idiotypic
  • H-2 Antigens
  • Immunoglobulins
  • Isoantibodies
Topics
  • Animals
  • Antibodies, Anti-Idiotypic
  • Cell Line
  • Cell Separation (methods)
  • Chromosome Aberrations
  • H-2 Antigens (immunology)
  • Immunoglobulins (immunology)
  • Immunosorbent Techniques
  • Isoantibodies (administration & dosage)
  • Mice
  • Mice, Inbred Strains
  • Neoplasm Transplantation
  • Neoplasms, Experimental (genetics, immunology)
  • Transplantation, Homologous

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