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pubmed-article:8396561pubmed:abstractTextC.B-17 SCID mice were inoculated with human peripheral blood leukocytes (PBLs) from normal Epstein-Barr virus (EBV)-seropositive and -seronegative donors. Confirmation of a functioning human immune response was demonstrated by the detection of human antibody after inoculation with rotavirus, tetanus toxoid, or EBV. One group of animals inoculated with PBLs from an EBV-seropositive donor developed immunoblastic lymphomas approximately 9 weeks after transplantation. Confirmation of the species and sex of origin of the tumor cells was established using a spontaneous cell line prepared from the tumor. At passage I, the tumor-cell line (AGTI) showed 15% of the metaphases with a translocation involving chromosomes 5 and 14. A lymphoblastoid cell line (AGLCL) established from the same PBLs from the same donor at the time of inoculation of the mice had a normal female karyotype. The AGLCL and a clone of AGTI cells were analyzed for rearrangement of immunoglobulin heavy chain (IgH) genes; both cell lines showed rearrangement of both IgH alleles. The results outlined in this report suggest that a spontaneous chromosomal translocation involving chromosome 14 occurred in normal PBLs in the SCID mouse.lld:pubmed
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pubmed-article:8396561pubmed:articleTitleSpontaneous development of a chromosomal translocation 5;14 in an Epstein-Barr-virus-associated B-cell lymphoma in a SCID mouse.lld:pubmed
pubmed-article:8396561pubmed:affiliationDepartment of Medical Microbiology and Immunology, Ohio State University College of Medicine, Columbus 43210.lld:pubmed
pubmed-article:8396561pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:8396561pubmed:publicationTypeResearch Support, U.S. Gov't, P.H.S.lld:pubmed
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