Use of severe combined immunodeficient (SCID) mice to produce human hybridoma ascites
Use of severe combined immunodeficient (SCID) mice to produce human hybridoma ascites
McKnight, Michael E. ; Prather, Karen ; Koda, Keiji ; DeBoer, Kenneth F. ; Glassy, Mark C.
1991-01-01 00:00:00
The use of the severe combined immunodeficient mouse (SCID), CB-17/Icr//Imd-SCID, was investigated for the production of human hybridoma ascites containing human antibody. Human-human hybridomas, generated from the fusion of lymphocytes isolated from regional draining lymph nodes of cancer patients with the SHFP-1 fusion partner, were injected i.p. at various cell concentrations into pristane-primed SCID mice. Ascites growth was typically observed at 7–14 days postinoculation. No significant differences in ascites yield or production were observed between IgG- and IgM-secreting hybridomas. Yields of immunoreactive human immunoglobulin ranged from approximately 0.5 to 3 mg/ml of harvested ascites. The ease and relatively low cost suggest that the use of SCID mice is preferred over conventional and costly large-scale industrial procedures.
http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.pngHuman AntibodiesIOS Presshttp://www.deepdyve.com/lp/ios-press/use-of-severe-combined-immunodeficient-scid-mice-to-produce-human-8fYgBURIIh
Use of severe combined immunodeficient (SCID) mice to produce human hybridoma ascites
The use of the severe combined immunodeficient mouse (SCID), CB-17/Icr//Imd-SCID, was investigated for the production of human hybridoma ascites containing human antibody. Human-human hybridomas, generated from the fusion of lymphocytes isolated from regional draining lymph nodes of cancer patients with the SHFP-1 fusion partner, were injected i.p. at various cell concentrations into pristane-primed SCID mice. Ascites growth was typically observed at 7–14 days postinoculation. No significant differences in ascites yield or production were observed between IgG- and IgM-secreting hybridomas. Yields of immunoreactive human immunoglobulin ranged from approximately 0.5 to 3 mg/ml of harvested ascites. The ease and relatively low cost suggest that the use of SCID mice is preferred over conventional and costly large-scale industrial procedures.
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