| Literature DB >> 15302847 |
Elma Z Tchilian1, Ritu Dawes, Lisa Hyland, Maria Montoya, Agnes Le Bon, Persephone Borrow, Sam Hou, David Tough, Peter C L Beverley.
Abstract
Transgenic mice have been constructed expressing high (CD45RABC) and low (CD45R0) molecular weight CD45 isoforms on a CD45-/- background. Phenotypic analysis and in vivo challenge of these mice with influenza and lymphocytic choriomeningitis viruses shows that T cell differentiation and peripheral T cell function are related to the level of CD45 expression but not to which CD45 isoform is expressed. In contrast, B cell differentiation is not restored, irrespective of the level of expression of a single isoform. All CD45 trangenic mice have T cells with an activated phenotype and increased T cell turnover. These effects are more prominent in CD8 than CD4 cells. The transgenic mice share several properties with humans expressing variant CD45 alleles and provide a model to understand immune function in variant individuals.Entities:
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Year: 2004 PMID: 15302847 DOI: 10.1093/intimm/dxh135
Source DB: PubMed Journal: Int Immunol ISSN: 0953-8178 Impact factor: 4.823