Critical role for CD8 in binding of MHC tetramers to TCR: CD8 antibodies block specific binding of human tumor-specific MHC-peptide tetramers to TCR
- PMID: 11418659
- DOI: 10.4049/jimmunol.167.1.270
Critical role for CD8 in binding of MHC tetramers to TCR: CD8 antibodies block specific binding of human tumor-specific MHC-peptide tetramers to TCR
Abstract
There are conflicting opinions about the role that the T cell coreceptors CD4 and CD8 play in TCR binding and activation. Recent evidence from transgenic mouse models suggests that CD8 plays a critical role in TCR binding and activation by peptide-MHC complex multimers (tetramers). Here we show with a human CTL clone specific for a tumor-associated MHC-peptide complex that the binding of tetramers to the TCR on these cells is completely blocked by anti-human CD8 Abs. Moreover, the staining of CTLs with specific MHC-peptide tetramers simultaneously with anti-CD8 Abs was completely blocked with three different anti-CD8 Abs. This blockage was mediated by anti-CD8 Abs but not anti-CD3 Abs and was dose dependent. The blocking effect of the anti-CD8 Abs was attributable to directly inhibiting tetramer binding and was not attributable to Ab-mediated TCR-CD8 internalization and down-regulation. Our results have important implications in TCR binding to MHC-peptide tetramers. MHC-peptide tetramers are widely used today in combination with anti-CD8 Abs for the phenotypic analysis of T cell populations and in the study of T cell responses under various pathological conditions such as infectious diseases and cancer. Our results indicate that also in the human system CD8 plays a critical role in the interaction of MHC-peptide multimers with TCR.
Similar articles
-
Anti-CD8 antibodies can inhibit or enhance peptide-MHC class I (pMHCI) multimer binding: this is paralleled by their effects on CTL activation and occurs in the absence of an interaction between pMHCI and CD8 on the cell surface.J Immunol. 2003 Dec 15;171(12):6650-60. doi: 10.4049/jimmunol.171.12.6650. J Immunol. 2003. PMID: 14662868
-
High affinity xenoreactive TCR:MHC interaction recruits CD8 in absence of binding to MHC.J Immunol. 2003 Jan 1;170(1):373-83. doi: 10.4049/jimmunol.170.1.373. J Immunol. 2003. PMID: 12496422
-
Specificity of CTL interactions with peptide-MHC class I tetrameric complexes is temperature dependent.J Immunol. 1999 Oct 15;163(8):4342-8. J Immunol. 1999. PMID: 10510374
-
[MHC tetramers: tracking specific immunity].Acta Med Croatica. 2003;57(4):255-9. Acta Med Croatica. 2003. PMID: 14639858 Review. Croatian.
-
Recognition surfaces of MHC class I.Immunol Rev. 1998 Jun;163:121-8. doi: 10.1111/j.1600-065x.1998.tb01191.x. Immunol Rev. 1998. PMID: 9700505 Review.
Cited by
-
IL-15/IL-15Ralpha-mediated avidity maturation of memory CD8+ T cells.Proc Natl Acad Sci U S A. 2004 Oct 19;101(42):15154-9. doi: 10.1073/pnas.0406649101. Epub 2004 Oct 11. Proc Natl Acad Sci U S A. 2004. PMID: 15477598 Free PMC article.
-
Therapeutic Antibodies against Intracellular Tumor Antigens.Front Immunol. 2017 Aug 18;8:1001. doi: 10.3389/fimmu.2017.01001. eCollection 2017. Front Immunol. 2017. PMID: 28868054 Free PMC article. Review.
-
Persistent viral infection in humans can drive high frequency low-affinity T-cell expansions.Immunology. 2010 Dec;131(4):537-48. doi: 10.1111/j.1365-2567.2010.03326.x. Epub 2010 Aug 16. Immunology. 2010. PMID: 20722762 Free PMC article.
-
Interplay between TCR affinity and necessity of coreceptor ligation: high-affinity peptide-MHC/TCR interaction overcomes lack of CD8 engagement.J Immunol. 2003 Nov 1;171(9):4493-503. doi: 10.4049/jimmunol.171.9.4493. J Immunol. 2003. PMID: 14568922 Free PMC article.
-
In situ detection of antigen-specific T cells in cryo-sections using MHC class I tetramers after dendritic cell vaccination of melanoma patients.Cancer Immunol Immunother. 2007 Oct;56(10):1667-76. doi: 10.1007/s00262-007-0304-5. Epub 2007 Apr 18. Cancer Immunol Immunother. 2007. PMID: 17440724 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Research Materials