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Presence in Peripheral Blood of Healthy Individuals of Autoreactive T Cells to a Membrane Antigen Present on Bone Marrow-Derived Cells

Authors :
Filion, Mario C.
Proulx, Chantal
Bradley, Amanda J.
Devine, Dana V.
Sekaly, Rafick-Pierre
Decary, Francine
Chartrand, Pierre
Source :
Blood; September 1996, Vol. 88 Issue: 6 p2144-2150, 7p
Publication Year :
1996

Abstract

Intrathymic clonal deletion is thought to be the major mechanism responsible for tolerance to nonsequestered antigens such as the ones expressed by bone marrow-derived cells. In the case of sequestered antigens that potentially do not come in contact with T cells in the thymus, it is thought that autoreactive T cells are present in periphery but are tightly regulated to prevent autoimmune diseases. Indeed, autoreactive T cells to sequestered antigens can be isolated in healthy individuals. However, the presence of autoreactive T cells to nonsequestered circulating antigens had not been observed. In this report, we present evidence for the presence, in the periphery of all healthy individuals tested (n = 25), of autoreactive T cells to Gpllb-llla, a membrane antigen present on bone marrow-derived cells that is expressed on circulating platelets and on the cell surface of the epithelial cells of the thymic stroma early in intrauterine life. Using an in vitro T-cell proliferation assay, we have demonstrated that activation of these specific Gpllb-llla autoreactive αβTCR+CD4+CD8-T cells requires internalization and processing of the Gpllb-llla by antigen-presenting cells and its presentation by HLA-DR class II molecules in the presence of exogenous interleukin 2 (IL-2). This indicates that some autoreactive T cells directed against membrane antigens present on bone marrow-derived cells and also expressed in the thymus are not necessarily eliminated by intrathymic deletion.

Details

Language :
English
ISSN :
00064971 and 15280020
Volume :
88
Issue :
6
Database :
Supplemental Index
Journal :
Blood
Publication Type :
Periodical
Accession number :
ejs56980395
Full Text :
https://doi.org/10.1182/blood.V88.6.2144.bloodjournal8862144