ESTABLISHMENT AND CHARACTERIZATION OF A MURINE CD4(-CELL LINE AND CLONE THAT INDUCE EXPERIMENTAL AUTOIMMUNE UVEORETINITIS IN B10.A MICE() T)

Citation
Lv. Rizzo et al., ESTABLISHMENT AND CHARACTERIZATION OF A MURINE CD4(-CELL LINE AND CLONE THAT INDUCE EXPERIMENTAL AUTOIMMUNE UVEORETINITIS IN B10.A MICE() T), The Journal of immunology, 156(4), 1996, pp. 1654-1660
Citations number
52
Categorie Soggetti
Immunology
Journal title
The Journal of immunology
ISSN journal
00221767 → ACNP
Volume
156
Issue
4
Year of publication
1996
Pages
1654 - 1660
Database
ISI
SICI code
0022-1767(1996)156:4<1654:EACOAM>2.0.ZU;2-Q
Abstract
B10.A mice develop experimental autoimmune uveoretinitis after active immunization with the interphotoreceptor retinoid-binding protein (IRB P), CD4(+) T cells play an important role in the development of the di sease, In this study we have isolated and characterized a CD4(+) T cel l line and a T cell clone that induce experimental autoimmune uveoreti nitis when transferred into naive B10.A mice, The cell line was isolat ed from draining lymph nodes of IRBP-immunized animals by repeated cyc les of IRBP stimulation, The line was shown to be pathogenic after 4 r ounds of in vitro stimulation with IRBP at 5 x 10(6) cells/mouse, A T cell clone derived from this line by limiting dilution was shown to be pathogenic when the same number of cells was injected; incidence and severity of disease, however, were much lower, After 16 rounds of IRBP -specific stimulation the cell line was pathogenic at 10(5) cells/mous e. Analysis of the VP repertoire revealed that at this point the line was mostly composed of V beta 8.2- and V beta 6-positive cells (>80% o f the population), The uveitogenic clone expressed V beta 8.2. Both th e T cell line and the clone elaborated an unrestricted lymphokine prof ile in vitro, However, when these cells were adoptively transferred in to naive recipients, mRNA isolated from the uveitic retina showed only Th1 type cytokines, These data help to characterize the nature of pat hogenic cells involved in ocular autoimmunity.