Direct evidence for functional self-protein/Ia-molecule complexes in vivo
- PMID: 2839836
- PMCID: PMC281720
- DOI: 10.1073/pnas.85.14.5220
Direct evidence for functional self-protein/Ia-molecule complexes in vivo
Abstract
Through the development of a panel of murine hybridomas reactive to murine hemoglobin, we have been able to study the processing and presentation of self antigens by antigen-presenting cells. Our results demonstrate that peritoneal macrophages in vivo can process and potentially present the self-antigen hemoglobin. We have extended this finding to show that, directly after removal from the mouse, antigen-presenting cells from a variety of tissues stimulate our hemoglobin-specific hybridomas without any manipulation or addition of exogenous antigen. This constitutes direct functional proof that in a nondisease state self proteins are processed constitutively and can be presented in a fashion similar to that in which foreign antigens are presented. Our demonstration that antigen-presenting cells can process and potentially present self as well as foreign molecules implies that self-tolerance occurs at the level of the T cell. This constitutive processing and presentation of self antigens has potentially far-reaching implications in self-tolerance, autoimmunity, and alloreactivity.
Similar articles
-
Constitutive presentation of dominant epitopes from endogenous naturally processed self-beta 2-microglobulin to class II-restricted T cells leads to self-tolerance.J Immunol. 1995 Jan 15;154(2):545-54. J Immunol. 1995. PMID: 7814867
-
Dendritic cells are the most efficient in presenting endogenous naturally processed self-epitopes to class II-restricted T cells.J Immunol. 1995 Jan 15;154(2):536-44. J Immunol. 1995. PMID: 7529278
-
Constitutive competition by self proteins for antigen presentation can be overcome by receptor-enhanced uptake.J Immunol. 1990 Mar 1;144(5):1600-6. J Immunol. 1990. PMID: 2307835
-
Bacterial antigen delivery systems: phagocytic processing of bacterial antigens for MHC-I and MHC-II presentation to T cells.Behring Inst Mitt. 1997 Feb;(98):197-211. Behring Inst Mitt. 1997. PMID: 9382741 Review.
-
Dissection of the Hb(64-76) determinant reveals that the T cell receptor may have the capacity to differentially signal.Adv Exp Med Biol. 1992;323:17-21. doi: 10.1007/978-1-4615-3396-2_3. Adv Exp Med Biol. 1992. PMID: 1485563 Review. No abstract available.
Cited by
-
Self-awareness: how self-peptide/MHC complexes are essential in the development of T cells.Mol Immunol. 2013 Sep;55(2):186-9. doi: 10.1016/j.molimm.2012.10.028. Epub 2012 Nov 26. Mol Immunol. 2013. PMID: 23196128 Free PMC article. Review.
-
Endogenous altered peptide ligands can affect peripheral T cell responses.J Exp Med. 1996 Apr 1;183(4):1311-21. doi: 10.1084/jem.183.4.1311. J Exp Med. 1996. PMID: 8666889 Free PMC article.
-
Virus entry and antigen biosynthesis in the processing and presentation of class-II MHC-restricted T-cell determinants of influenza virus.Immunol Res. 1990;9(2):103-14. doi: 10.1007/BF02918201. Immunol Res. 1990. PMID: 2140852 Review.
-
Nuclear myxovirus-resistance protein Mx is a minor histocompatibility antigen.Proc Natl Acad Sci U S A. 1990 Mar;87(5):2021-5. doi: 10.1073/pnas.87.5.2021. Proc Natl Acad Sci U S A. 1990. PMID: 2308961 Free PMC article.
-
Effects of pH and polysaccharides on peptide binding to class II major histocompatibility complex molecules.Proc Natl Acad Sci U S A. 1991 Apr 1;88(7):2740-4. doi: 10.1073/pnas.88.7.2740. Proc Natl Acad Sci U S A. 1991. PMID: 2011583 Free PMC article.
References
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources