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Cutting edge: B cells promote CD8+ T cell activation in MRL-Fas(lpr) mice independently of MHC class I antigen presentation.

作者信息

Chan O T, Shlomchik M J

机构信息

Section of Immunobiology, Department of Laboratory Medicine, Yale University School of Medicine, New Haven, CT 06520, USA.

出版信息

J Immunol. 2000 Feb 15;164(4):1658-62. doi: 10.4049/jimmunol.164.4.1658.

DOI:10.4049/jimmunol.164.4.1658
PMID:10657607
Abstract

Spontaneous CD8+ T cell activation in MRL-Faslpr mice is B cell dependent. It is unclear whether this B-dependent activation is mediated by direct Ag presentation via MHC class I proteins (i.e., cross-presentation) or whether activation occurs by an indirect mechanism, e.g., via effects on CD4+ cells. To determine how CD8+ T cell activation is promoted by B cells, we created mixed bone marrow chimeras where direct MHC class I Ag presentation by B cells was abrogated while other leukocyte compartments could express MHC class I. Surprisingly, despite the absence of B cell class I-restricted Ag presentation, CD8+ T cell activation was intact in the chimeric mice. Therefore, the spontaneous B cell-dependent CD8+ T cell activation that occurs in systemic autoimmunity is not due to direct presentation by B cells to CD8+ T cells.

摘要

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