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dc.contributor.authorHesselton, RuthAnn M.
dc.contributor.authorKoup, Richard A.
dc.contributor.authorCromwell, Mary A.
dc.contributor.authorGraham, Barney S.
dc.contributor.authorJohns, Michael
dc.contributor.authorSullivan, John L.
dc.date2022-08-11T08:08:58.000
dc.date.accessioned2022-08-23T16:14:20Z
dc.date.available2022-08-23T16:14:20Z
dc.date.issued1993-09-01
dc.date.submitted2008-09-25
dc.identifier.citation<p>J Infect Dis. 1993 Sep;168(3):630-40.</p>
dc.identifier.issn0022-1899 (Print)
dc.identifier.doi10.1093/infdis/168.3.630
dc.identifier.pmid8354904
dc.identifier.urihttp://hdl.handle.net/20.500.14038/33835
dc.description.abstractImmune reconstitutions (hu-PBL-SCID mice) resulting from adoptive transfer of human peripheral blood mononuclear cells into 1800 C.B-17 scid-/scid-mice were characterized. Over 90% of reconstitutions were successful as evidenced by human immunoglobulin production. Variability was noted with donor, cell number, and cell type. Human cells (T lymphocytes, few B cells) could be recovered by 5 days after engraftment. High levels of soluble CD8 and interleukin-2 receptors were detected in sera of hu-PBL-SCID mice. Cells recovered from 17 mice proliferated in response to antigens to which the donor had been primed; responses to nonboosted antigen also increased in some animals. After reconstitution, lymphocytes were found in the spleen and lymph nodes without full restoration of normal architecture. The hu-PBL-SCID mouse shows promise as a model system for a variety of immunologic studies. The inherent variation in the system must be minimized for appropriate use of the model.
dc.language.isoen_US
dc.relation<p><a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=8354904&dopt=Abstract">Link to article in PubMed</a></p>
dc.relation.urlhttps://doi.org/10.1093/infdis/168.3.630
dc.subjectAge Factors; Animals; Antigens, CD3; Antigens, CD4; Antigens, CD8; Blood Cells; Humans; Immune System; Immunoglobulins; Leukocytes, Mononuclear; Mice; Mice, SCID; Models, Biological; Peritoneal Cavity; Phenotype; Receptors, Interleukin-2; Species Specificity; Specific Pathogen-Free Organisms; Spleen; Time Factors; Transplantation, Heterologous
dc.subjectLife Sciences
dc.subjectMedicine and Health Sciences
dc.titleHuman peripheral blood xenografts in the SCID mouse: characterization of immunologic reconstitution
dc.typeJournal Article
dc.source.journaltitleThe Journal of infectious diseases
dc.source.volume168
dc.source.issue3
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/gsbs_sp/493
dc.identifier.contextkey638261
html.description.abstract<p>Immune reconstitutions (hu-PBL-SCID mice) resulting from adoptive transfer of human peripheral blood mononuclear cells into 1800 C.B-17 scid-/scid-mice were characterized. Over 90% of reconstitutions were successful as evidenced by human immunoglobulin production. Variability was noted with donor, cell number, and cell type. Human cells (T lymphocytes, few B cells) could be recovered by 5 days after engraftment. High levels of soluble CD8 and interleukin-2 receptors were detected in sera of hu-PBL-SCID mice. Cells recovered from 17 mice proliferated in response to antigens to which the donor had been primed; responses to nonboosted antigen also increased in some animals. After reconstitution, lymphocytes were found in the spleen and lymph nodes without full restoration of normal architecture. The hu-PBL-SCID mouse shows promise as a model system for a variety of immunologic studies. The inherent variation in the system must be minimized for appropriate use of the model.</p>
dc.identifier.submissionpathgsbs_sp/493
dc.contributor.departmentPediatrics
dc.source.pages630-40


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