Maintenance of immune tolerance to a neo-self acetylcholine receptor antigen with aging: Implications for late-onset autoimmunity

Sue Stacy, Earlanda L. Williams, Nathan E. Standifer, Amanda Pasquali, Keith A Krolick, Anthony J Infante, Ellen B Kraig

Research output: Contribution to journalArticle

4 Citations (Scopus)

Abstract

Age-related changes in immune regulation are likely to account for the age-associated increase in serum autoantibody levels and in certain autoimmune disorders, such as myasthenia gravis (MG). To demonstrate directly a loss of immune tolerance in older individuals, responses to the acetylcholine receptor, the autoantigen in MG, were assessed in transgenic mice expressing the Torpedo californica acetylcholine receptor (TAChR) α-chain as a neo-self Ag. T cells from young transgenic mice had been shown to be tolerant to p146-162, the TAChR α-chain peptide that dominated young nontransgenic T cell responses in vitro. The immunodominance of p146-162 was not lost with age; fine specificity was preserved. Moreover, T cell tolerance to p146-162, as well as to other epitopes of the TAChR α-chain extracellular domain, was maintained in old transgenic mice. Even multiple TAChR immunizations coupled with the MG-enhancing cytokine, IL-12, did not break tolerance. In addition, T cells exhibiting CD4 upregulation, an early activation marker, were reduced in frequency equivalently in old and young transgenic animals, suggesting that immune regulation in this model was not impacted by aging. Moreover, B cell tolerance was also maintained with age. The persistence of immune tolerance was accompanied by an increase in the proportion of T regulatory cells; it is speculated that this may compensate for deficiencies in central tolerance that occur owing to thymic involution. In summary, our study reveals, for the first time, that some immune tolerance mechanisms do survive aging; this suggests that certain late-onset autoimmune disorders may be induced by a specific insult that disrupts immune homeostasis.

Original languageEnglish (US)
Pages (from-to)6067-6075
Number of pages9
JournalJournal of Immunology
Volume184
Issue number11
DOIs
StatePublished - Jun 1 2010

Fingerprint

Immune Tolerance
Cholinergic Receptors
Torpedo
Autoimmunity
Maintenance
Myasthenia Gravis
Antigens
Transgenic Mice
T-Lymphocytes
Central Tolerance
Genetically Modified Animals
Autoantigens
Regulatory T-Lymphocytes
Interleukin-12
Autoantibodies
Epitopes
Immunization
Homeostasis
B-Lymphocytes
Up-Regulation

ASJC Scopus subject areas

  • Immunology
  • Medicine(all)

Cite this

Maintenance of immune tolerance to a neo-self acetylcholine receptor antigen with aging : Implications for late-onset autoimmunity. / Stacy, Sue; Williams, Earlanda L.; Standifer, Nathan E.; Pasquali, Amanda; Krolick, Keith A; Infante, Anthony J; Kraig, Ellen B.

In: Journal of Immunology, Vol. 184, No. 11, 01.06.2010, p. 6067-6075.

Research output: Contribution to journalArticle

Stacy, Sue ; Williams, Earlanda L. ; Standifer, Nathan E. ; Pasquali, Amanda ; Krolick, Keith A ; Infante, Anthony J ; Kraig, Ellen B. / Maintenance of immune tolerance to a neo-self acetylcholine receptor antigen with aging : Implications for late-onset autoimmunity. In: Journal of Immunology. 2010 ; Vol. 184, No. 11. pp. 6067-6075.
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