A novel pathway of antigen presentation by dendritic and endothelial cells: Implications for allorecognition and infectious diseases
- PMID: 16829787
- DOI: 10.1097/01.tp.0000231347.06149.ca
A novel pathway of antigen presentation by dendritic and endothelial cells: Implications for allorecognition and infectious diseases
Abstract
Dendritic cells (DCs) are the major antigen presenting cells capable of stimulating T cell responses following either organ transplantation or a viral infection. In the context of allorecognition, T cells can be activated following presentation of alloantigens by donor DCs (direct), as well as by recipient DCs presenting processed donor major histocompatibility complex (MHC) as peptides (indirect). We have recently described another mechanism by which alloreactive T cells are activated. Recipient DCs can acquire donor MHC through cell-to-cell contact and this acquired MHC can stimulate a T cell response (the semidirect pathway). Similarly, during a viral infection, DCs are capable of stimulating T cells directly, as occurs when infected DCs present processed viral antigens, or indirectly by a process known as cross-presentation. Although cross-presentation of exogenous antigen is an important mechanism for controlling infectious diseases, it is possible that peptide:MHC acquisition (the semidirect pathway) may also play a part in immunity against pathogens. In this review, we discuss the possible contributions of the semidirect pathway/MHC transfer in infectious disease.
Similar articles
-
Efficiency of peptide presentation by dendritic cells compared with other cell types: implications for cross-priming.Int Immunol. 2006 Dec;18(12):1647-54. doi: 10.1093/intimm/dxl098. Epub 2006 Oct 11. Int Immunol. 2006. PMID: 17035346
-
Regulation of antigen presentation and cross-presentation in the dendritic cell network: facts, hypothesis, and immunological implications.Adv Immunol. 2005;86:241-305. doi: 10.1016/S0065-2776(04)86007-3. Adv Immunol. 2005. PMID: 15705424 Review.
-
Follicular and marginal zone B cells fail to cross-present MHC class I-restricted epitopes derived from viral particles.J Immunol. 2009 May 15;182(10):6261-6. doi: 10.4049/jimmunol.0804035. J Immunol. 2009. PMID: 19414779
-
Antigen-presentation properties of plasmacytoid dendritic cells.Immunity. 2008 Sep 19;29(3):352-61. doi: 10.1016/j.immuni.2008.09.002. Immunity. 2008. PMID: 18799143 Review.
-
Control of dendritic cell cross-presentation by the major histocompatibility complex class I cytoplasmic domain.Nat Immunol. 2003 Nov;4(11):1065-73. doi: 10.1038/ni989. Epub 2003 Oct 19. Nat Immunol. 2003. PMID: 14566337
Cited by
-
Direct presentation is sufficient for an efficient anti-viral CD8+ T cell response.PLoS Pathog. 2010 Feb 12;6(2):e1000768. doi: 10.1371/journal.ppat.1000768. PLoS Pathog. 2010. PMID: 20169189 Free PMC article.
-
Induction Therapy and Therapeutic Antibodies.Handb Exp Pharmacol. 2022;272:85-116. doi: 10.1007/164_2021_570. Handb Exp Pharmacol. 2022. PMID: 35474024
-
Innate immunity and resistance to tolerogenesis in allotransplantation.Front Immunol. 2012 Apr 19;3:73. doi: 10.3389/fimmu.2012.00073. eCollection 2012. Front Immunol. 2012. PMID: 22566954 Free PMC article.
-
Extracellular Vesicles in Liver Transplantation: Current Evidence and Future Challenges.Int J Mol Sci. 2023 Aug 31;24(17):13547. doi: 10.3390/ijms241713547. Int J Mol Sci. 2023. PMID: 37686354 Free PMC article. Review.
-
Alloreactive CD8 T cell tolerance requires recipient B cells, dendritic cells, and MHC class II.J Immunol. 2008 Jul 1;181(1):165-73. doi: 10.4049/jimmunol.181.1.165. J Immunol. 2008. PMID: 18566381 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical
Research Materials