Is the generation of neo-antigenic determinants by free radicals central to the development of autoimmune rheumatoid disease?

Helen R. Griffiths

Research output: Contribution to journalArticle

Abstract

Biomolecules are susceptible to many different post-translational modifications that have important effects on their function and stability, including glycosylation, glycation, phosphorylation and oxidation chemistries. Specific conversion of aspartic acid to its isoaspartyl derivative or arginine to citrulline leads to autoantibody production in models of rheumatoid disease, and ensuing autoantibodies cross-react with native antigens. Autoimmune conditions associate with increased activation of immune effector cells and production of free radical species via NADPH oxidases and nitric oxide synthases. Generation of neo-antigenic determinants by reactive oxygen and nitrogen species ROS and RNS) may contribute to epitope spreading in autoimmunity. The oxidation of amino acids by peroxynitrite, hypochlorous acid and other reactive oxygen species (ROS) increases the antigenicity of DNA, LDL and IgG, generating ligands for which autoantibodies show higher avidity. This review focuses on the evidence for ROS and RNS in promoting the autoimmune responses observed in diseases rheumatoid arthritis (RA) and systemic lupus erythematosus (SLE). It considers the evidence for ROS/RNS-induced antigenicity arising as a consequence of failure to remove or repair ROS/RNS damaged biomolecules and suggests that an associated defect, probably in T cell signal processing or/or antigen presentation, is required for the development of disease.
Original languageEnglish
Pages (from-to)544-549
Number of pages6
JournalAutoimmunity Reviews
Volume7
Issue number7
DOIs
Publication statusPublished - Jul 2008

Fingerprint

Autoimmune Diseases
Free Radicals
Epitopes
Reactive Oxygen Species
Autoantibodies
Autoimmunity
Hypochlorous Acid
Reactive Nitrogen Species
Citrulline
Peroxynitrous Acid
NADPH Oxidase
Antigen Presentation
Post Translational Protein Processing
Glycosylation
Aspartic Acid
Nitric Oxide Synthase
Systemic Lupus Erythematosus
Arginine
Rheumatoid Arthritis
Immunoglobulin G

Bibliographical note

NOTICE: this is the author’s version of a work that was accepted for publication in Autoimmunity reviews. Changes resulting from the publishing process, such as peer review, editing, corrections, structural formatting, and other quality control mechanisms may not be reflected in this document. Changes may have been made to this work since it was submitted for publication. A definitive version was subsequently published in Griffiths, Helen R. (2008). Is the generation of neo-antigenic determinants by free radicals central to the development of autoimmune rheumatoid disease? Autoimmunity reviews, 7 (7), pp. 544-549. DOI 10.1016/j.autrev.2008.04.013

Keywords

  • reactive oxygen species
  • reactive nitrogen species
  • protein oxidation
  • autoantigen
  • neo-antigenic determinant
  • DNA oxidation

Cite this

@article{6b6037b5c89c4dc7b78cfe7d42045df0,
title = "Is the generation of neo-antigenic determinants by free radicals central to the development of autoimmune rheumatoid disease?",
abstract = "Biomolecules are susceptible to many different post-translational modifications that have important effects on their function and stability, including glycosylation, glycation, phosphorylation and oxidation chemistries. Specific conversion of aspartic acid to its isoaspartyl derivative or arginine to citrulline leads to autoantibody production in models of rheumatoid disease, and ensuing autoantibodies cross-react with native antigens. Autoimmune conditions associate with increased activation of immune effector cells and production of free radical species via NADPH oxidases and nitric oxide synthases. Generation of neo-antigenic determinants by reactive oxygen and nitrogen species ROS and RNS) may contribute to epitope spreading in autoimmunity. The oxidation of amino acids by peroxynitrite, hypochlorous acid and other reactive oxygen species (ROS) increases the antigenicity of DNA, LDL and IgG, generating ligands for which autoantibodies show higher avidity. This review focuses on the evidence for ROS and RNS in promoting the autoimmune responses observed in diseases rheumatoid arthritis (RA) and systemic lupus erythematosus (SLE). It considers the evidence for ROS/RNS-induced antigenicity arising as a consequence of failure to remove or repair ROS/RNS damaged biomolecules and suggests that an associated defect, probably in T cell signal processing or/or antigen presentation, is required for the development of disease.",
keywords = "reactive oxygen species, reactive nitrogen species, protein oxidation, autoantigen, neo-antigenic determinant, DNA oxidation",
author = "Griffiths, {Helen R.}",
note = "NOTICE: this is the author’s version of a work that was accepted for publication in Autoimmunity reviews. Changes resulting from the publishing process, such as peer review, editing, corrections, structural formatting, and other quality control mechanisms may not be reflected in this document. Changes may have been made to this work since it was submitted for publication. A definitive version was subsequently published in Griffiths, Helen R. (2008). Is the generation of neo-antigenic determinants by free radicals central to the development of autoimmune rheumatoid disease? Autoimmunity reviews, 7 (7), pp. 544-549. DOI 10.1016/j.autrev.2008.04.013",
year = "2008",
month = "7",
doi = "10.1016/j.autrev.2008.04.013",
language = "English",
volume = "7",
pages = "544--549",
journal = "Autoimmunity Reviews",
issn = "1568-9972",
publisher = "Elsevier",
number = "7",

}

Is the generation of neo-antigenic determinants by free radicals central to the development of autoimmune rheumatoid disease? / Griffiths, Helen R.

In: Autoimmunity Reviews, Vol. 7, No. 7, 07.2008, p. 544-549.

Research output: Contribution to journalArticle

TY - JOUR

T1 - Is the generation of neo-antigenic determinants by free radicals central to the development of autoimmune rheumatoid disease?

AU - Griffiths, Helen R.

N1 - NOTICE: this is the author’s version of a work that was accepted for publication in Autoimmunity reviews. Changes resulting from the publishing process, such as peer review, editing, corrections, structural formatting, and other quality control mechanisms may not be reflected in this document. Changes may have been made to this work since it was submitted for publication. A definitive version was subsequently published in Griffiths, Helen R. (2008). Is the generation of neo-antigenic determinants by free radicals central to the development of autoimmune rheumatoid disease? Autoimmunity reviews, 7 (7), pp. 544-549. DOI 10.1016/j.autrev.2008.04.013

PY - 2008/7

Y1 - 2008/7

N2 - Biomolecules are susceptible to many different post-translational modifications that have important effects on their function and stability, including glycosylation, glycation, phosphorylation and oxidation chemistries. Specific conversion of aspartic acid to its isoaspartyl derivative or arginine to citrulline leads to autoantibody production in models of rheumatoid disease, and ensuing autoantibodies cross-react with native antigens. Autoimmune conditions associate with increased activation of immune effector cells and production of free radical species via NADPH oxidases and nitric oxide synthases. Generation of neo-antigenic determinants by reactive oxygen and nitrogen species ROS and RNS) may contribute to epitope spreading in autoimmunity. The oxidation of amino acids by peroxynitrite, hypochlorous acid and other reactive oxygen species (ROS) increases the antigenicity of DNA, LDL and IgG, generating ligands for which autoantibodies show higher avidity. This review focuses on the evidence for ROS and RNS in promoting the autoimmune responses observed in diseases rheumatoid arthritis (RA) and systemic lupus erythematosus (SLE). It considers the evidence for ROS/RNS-induced antigenicity arising as a consequence of failure to remove or repair ROS/RNS damaged biomolecules and suggests that an associated defect, probably in T cell signal processing or/or antigen presentation, is required for the development of disease.

AB - Biomolecules are susceptible to many different post-translational modifications that have important effects on their function and stability, including glycosylation, glycation, phosphorylation and oxidation chemistries. Specific conversion of aspartic acid to its isoaspartyl derivative or arginine to citrulline leads to autoantibody production in models of rheumatoid disease, and ensuing autoantibodies cross-react with native antigens. Autoimmune conditions associate with increased activation of immune effector cells and production of free radical species via NADPH oxidases and nitric oxide synthases. Generation of neo-antigenic determinants by reactive oxygen and nitrogen species ROS and RNS) may contribute to epitope spreading in autoimmunity. The oxidation of amino acids by peroxynitrite, hypochlorous acid and other reactive oxygen species (ROS) increases the antigenicity of DNA, LDL and IgG, generating ligands for which autoantibodies show higher avidity. This review focuses on the evidence for ROS and RNS in promoting the autoimmune responses observed in diseases rheumatoid arthritis (RA) and systemic lupus erythematosus (SLE). It considers the evidence for ROS/RNS-induced antigenicity arising as a consequence of failure to remove or repair ROS/RNS damaged biomolecules and suggests that an associated defect, probably in T cell signal processing or/or antigen presentation, is required for the development of disease.

KW - reactive oxygen species

KW - reactive nitrogen species

KW - protein oxidation

KW - autoantigen

KW - neo-antigenic determinant

KW - DNA oxidation

UR - http://www.scopus.com/inward/record.url?scp=50949105388&partnerID=8YFLogxK

U2 - 10.1016/j.autrev.2008.04.013

DO - 10.1016/j.autrev.2008.04.013

M3 - Article

VL - 7

SP - 544

EP - 549

JO - Autoimmunity Reviews

JF - Autoimmunity Reviews

SN - 1568-9972

IS - 7

ER -