| Literature DB >> 18817834 |
George Vlad1, Raffaello Cortesini, Nicole Suciu-Foca.
Abstract
Similar to helper and cytotoxic T cells, CD8(+) T suppressor cells (Ts) acquire antigen specificity via direct interaction with antigen-presenting cells (APC). They induce the upregulation of the inhibitory receptor immunoglobulin-like transcript (ILT)3 on professional and nonprofessional APC, rendering these cells tolerogenic and able to induce the differentiation of further waves of regulatory and suppressor T cells. This review sums up evidence that ILT3 is the centerpiece of CD8(+) Ts-driven suppression and acts as a master switch in the regulation of CD8(+) and CD4(+) T-cell responses to antigens in transplantation, autoimmunity, allergy, and cancer.Entities:
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Year: 2008 PMID: 18817834 DOI: 10.1016/j.humimm.2008.08.286
Source DB: PubMed Journal: Hum Immunol ISSN: 0198-8859 Impact factor: 2.850