Year: 2021
Type: article
Abstract: Activation of self-reactive CD8+T cells induces a peripheral tolerance mechanism that involves loss of CD8 expression. Because genetic deficiency ofFasandFaslcauses the accumulation of double-negative (DN; CD3+TCR-αβ+CD4-CD8-) T cells that have been proposed to derive from CD8+cells, we decided to explore the role of Fas and FasL in self-antigen-induced CD8 downregulation. To this end, we quantified Fas and FasL induction by different stimuli and analyzed the effects of Fas/FasL deficiency during a protective immune response and after exposure to self-antigens. Our data describes how Fas and FasL upregulation differs depending on the setting of CD8 T cell activation and demonstrates that Fas/FasL signaling maintains CD8 expression during repetitive antigen stimulation and following self-antigen encounter. Together, our results reveal an unexpected role of Fas/FasL signaling and offer a new insight into the role of these molecules in the regulation of immune tolerance.
Source: Frontiers in Immunology
Language: English
Topic: T-cell and B-cell Immunology
Subfield: Immunology
Field: Immunology and Microbiology
Domain: Life Sciences
Open Access status: gold
Estimated APC paid: $2,950
Awards: G1204010915, G1288195445, G7148135681
OpenAlex ID: W3136299349
