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PMID: 1697609 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Autoreactive T lymphocytes in multiple sclerosis determined by antigen-induced secretion of interferon-gamma.

The Journal of clinical investigation ·Vol. 86 ·No. 3 ·1990-09-00 ·Pages 981-5

Olsson T, Zhi WW, Höjeberg B, Kostulas V, Jiang YP, Anderson G, Ekre HP, Link H

Abstract

Multiple sclerosis (MS) is a disease with unknown cause characterized by inflammation and demyelination in the central nervous system. Although an autoimmune pathogenesis has been suggested, there are no conclusive data on the number of T cells autoreactive with myelin antigens in MS compared to controls. We showed that T lymphocytes secreting interferon-gamma in response to possible target autoantigens are severalfold more common among PBL mononuclear cells in patients with MS than in patients with aseptic meningitis and tension headache. On average T cells reactive with myelin basic protein (MBP), two different MBP peptides, or with proteolipid protein amounted to 2.7-5.2/10(5) PBL from MS patients. MBP-reactive T cells were still more frequent among mononuclear cells isolated from the cerebrospinal fluid (CSF; 185/10(5) CSF cells). We concluded that T cells reactive with myelin autoantigens are strongly increased in MS. This approach to detect them could allow definition of immunodominant T cell epitopes in individual MS patients, and thereby enable further development towards specific immunotherapy.

MeSH Terms
Adult Aged Autoantigens/immunology Autoimmune Diseases/immunology Cerebrospinal Fluid/cytology Humans Interferon-gamma/biosynthesis Middle Aged Multiple Sclerosis/immunology Myelin Basic Protein/immunology Myelin Proteins/immunology Myelin Proteolipid Protein T-Lymphocytes/immunology
Chemicals
Autoantigens Myelin Basic Protein Myelin Proteins Myelin Proteolipid Protein Interferon-gamma
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Olsson T
Department of Neurology, Karolinska Institutet, Huddinge University Hospital, Sweden.
Zhi W W
Höjeberg B
Kostulas V
Jiang Y P
Anderson G
Ekre H P
Link H
References (41)
41 references, click to expand
  1. Treatment of multiple sclerosis with gamma interferon: exacerbations associated with activation of the immune system.
    Neurology. 1987 Jul;37(7):1097-102 PMID: 3110648
  2. Interferon-gamma regulates an antigen specific for endothelial cells involved in lymphocyte traffic.
    Proc Natl Acad Sci U S A. 1986 Dec;83(23):9114-8 PMID: 3097642
  3. Peptides of myelin basic protein stimulate T lymphocytes from patients with multiple sclerosis.
    J Neuroimmunol. 1989 Mar;22(1):23-30 PMID: 2465311
  4. Myelin basic protein-specific CD4+ cytolytic T-lymphocyte clones isolated from multiple sclerosis patients.
    Hum Immunol. 1988 Jun;22(2):97-109 PMID: 2458331
  5. Human T-cell response to myelin basic protein in multiple sclerosis patients and healthy subjects.
    J Neurosci Res. 1988;19(1):149-56 PMID: 2449544
  6. Peptide specificities of myelin basic protein-reactive human T-cell clones.
    Neurology. 1988 May;38(5):739-42 PMID: 2452382
  7. Myelin basic protein and proteolipid protein reactivity of brain- and cerebrospinal fluid-derived T cell clones in multiple sclerosis and postinfectious encephalomyelitis.
    J Immunol. 1987 Jul 1;139(1):68-72 PMID: 2438352
  8. Cell-mediated immunity to myelin-associated glycoprotein, proteolipid protein, and myelin basic protein in multiple sclerosis.
    J Neuroimmunol. 1986 Nov;13(1):99-108 PMID: 2428837
  9. The basis for the immunoregulatory role of macrophages and other accessory cells.
    Science. 1987 May 1;236(4801):551-7 PMID: 2437650
  10. The relation between major histocompatibility complex (MHC) restriction and the capacity of Ia to bind immunogenic peptides.
    Science. 1987 Mar 13;235(4794):1353-8 PMID: 2435001
  11. Specificity of T lymphocyte lines for peptides of myelin basic protein.
    J Immunol. 1985 Jul;135(1):229-33 PMID: 2582033
  12. Alternative splicing accounts for the four forms of myelin basic protein.
    Cell. 1985 Dec;43(3 Pt 2):721-7 PMID: 2416470
  13. Phenotypic and functional analysis of T cells cloned directly from the blood and cerebrospinal fluid of patients with multiple sclerosis.
    Ann Neurol. 1985 Oct;18(4):451-8 PMID: 2416267
  14. Predominance of Borrelia burgdorferi specific B cells in cerebrospinal fluid in neuroborreliosis.
    Lancet. 1989 Jul 8;2(8654):71-4 PMID: 2567872
  15. Monoclonal antibody two-site ELISA for human IFN-gamma. Adaptation for determinations in human serum or plasma.
    J Immunol Methods. 1989 Dec 20;125(1-2):89-96 PMID: 2514232
  16. Phenotypic markers and functional characteristics of T lymphocyte clones from cerebrospinal fluid in multiple sclerosis.
    J Neuroimmunol. 1984 Dec;7(2-3):151-62 PMID: 6210303
  17. Widespread and selective induction of major histocompatibility complex-determined antigens in vivo by gamma interferon.
    J Exp Med. 1985 Nov 1;162(5):1645-64 PMID: 3932581
  18. Antimyelin basic protein and antimyelin antibody-producing cells in multiple sclerosis.
    Ann Neurol. 1990 Feb;27(2):132-6 PMID: 1690527
  19. Regulation of macrophage function by interferon-gamma. Somatic cell genetic approaches in murine macrophage cell lines to mechanisms of growth inhibition, the oxidative burst, and expression of the chronic granulomatous disease gene.
    J Clin Invest. 1990 Feb;85(2):563-9 PMID: 2153711
  20. The rapid isolation of clonable antigen-specific T lymphocyte lines capable of mediating autoimmune encephalomyelitis.
    Eur J Immunol. 1981 Mar;11(3):195-9 PMID: 6165588
  21. Isolation of myelin basic protein-reactive T-cell lines from normal human blood.
    Cell Immunol. 1983 Oct 15;81(2):435-40 PMID: 6196128
  22. Expansion of antigen-specific T cells from cerebrospinal fluid of patients with multiple sclerosis.
    J Neuroimmunol. 1983 Dec;5(3):317-24 PMID: 6197427
  23. Genetic control of autoimmune encephalomyelitis and recognition of the critical nonapeptide moiety of myelin basic protein in guinea pigs are exerted through interaction of lymphocytes and macrophages.
    Eur J Immunol. 1981 Apr;11(4):311-6 PMID: 6166480
  24. The relationship between immune interferon production and proliferation in antigen-specific, MHC-restricted T cell lines and clones.
    J Immunol. 1983 Sep;131(3):1049-55 PMID: 6193170
  25. Proteolipids.
    Scand J Immunol Suppl. 1982;9:147-66 PMID: 6763766
  26. Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications.
    Proc Natl Acad Sci U S A. 1979 Sep;76(9):4350-4 PMID: 388439
  27. Large scale preparation of myelin basic protein from central nervous tissue of several mammalian species.
    Prep Biochem. 1972;2(2):139-65 PMID: 4623901
  28. AN ELECTROPHORETIC STUDY OF THE PROTEIN COMPONENTS IN CEREBROSPINAL FLUID AND THEIR RELATIONSHIP TO THE SERUM PROTEINS.
    J Clin Invest. 1942 Sep;21(5):571-7 PMID: 16694947
  29. A study of the chemical nature of components of bovine white matter effective in producing allergic encephalomyelitis in the rabbit.
    J Exp Med. 1954 Nov 1;100(5):451-71 PMID: 13211907
  30. Antigen recognition in autoimmune encephalomyelitis and the potential for peptide-mediated immunotherapy.
    Cell. 1989 Oct 20;59(2):247-55 PMID: 2478291
  31. Vaccination against experimental allergic encephalomyelitis with T cell receptor peptides.
    Science. 1989 Nov 3;246(4930):668-70 PMID: 2814489
  32. Immunization with a synthetic T-cell receptor V-region peptide protects against experimental autoimmune encephalomyelitis.
    Nature. 1989 Oct 12;341(6242):541-4 PMID: 2477708
  33. T cell specificity for class II (I-A) and the encephalitogenic N-terminal epitope of the autoantigen myelin basic protein.
    J Immunol. 1987 Aug 15;139(4):1075-9 PMID: 2440944
  34. Limiting dilution analysis of the frequency of antigen-reactive lymphocytes isolated from the central nervous system of Lewis rats with experimental allergic encephalomyelitis.
    Cell Immunol. 1987 Aug;108(1):203-13 PMID: 2440588
  35. Anti-idiotypic network induced by T cell vaccination against experimental autoimmune encephalomyelitis.
    Science. 1988 Jan 8;239(4836):181-3 PMID: 2447648
  36. Experimental allergic encephalomyelitis mediated by murine encephalitogenic T cell lines specific for myelin proteolipid apoprotein.
    J Immunol. 1987 Jan 1;138(1):179-84 PMID: 3491156
  37. Characterization of a major encephalitogenic T cell epitope in SJL/J mice with synthetic oligopeptides of myelin basic protein.
    J Neuroimmunol. 1988 Aug;19(1-2):21-32 PMID: 2456304
  38. In vitro synthesis of immunoglobulins and autoantibodies by lymphocytes from various body compartments during chronic relapsing experimental allergic encephalomyelitis.
    J Neuroimmunol. 1985 Sep;9(5):293-305 PMID: 2410454
  39. Molecular transductional mechanisms by which IFN gamma and other signals regulate macrophage development.
    Immunol Rev. 1987 Jun;97:5-27 PMID: 2957307
  40. Reverse ELISPOT assay for clonal analysis of cytokine production. I. Enumeration of gamma-interferon-secreting cells.
    J Immunol Methods. 1988 May 25;110(1):29-36 PMID: 3131436
  41. Response of human T lymphocyte lines to myelin basic protein: association of dominant epitopes with HLA class II restriction molecules.
    J Neurosci Res. 1989 Jun;23(2):207-16 PMID: 2474079
Article Info
Journal
The Journal of clinical investigation
Abbr.
J Clin Invest
ISSN
0021-9738
Published
1990-09-00
Pages
981-5
Language
English
Region
United States
NLM ID
7802877
PMCID
PMC296818
Subset
IM
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