Skip to main content
Log in

Role for interferon-γ inducible chemokines in endocrine autoimmunity: An expanding field

  • Short Review
  • Published:
Journal of Endocrinological Investigation Aims and scope Submit manuscript

An Erratum to this article was published on 01 March 2003

Abstract

The chemoattractant cytokines (chemokines) have been classified into 4 major subfamilies in relation to the position of the cysteine residues in their NH2 terminal portion. Interferon-γ inducible chemokines (CXCL9/Mig, CXCL10/IP-10, CXCL11/I-TAC), Strongly associated to Th1-me-diated immune responses, belong to the CXC sub-family. They represent an exception among chemokines in that they specifically interact with a single type of receptor, named CXCR3. A statisti-cally significant increase of CXCL10/IP-10 and CX-CL9/Mig expression, in thyroid tissue specimens obtained from subjects affected by Hashimoto’s thyroiditis and recent onset Graves’ disease has been reported. Furthermore, a statistically signif-icant increase in serumCXCL10/IP-10 levels has been found in newly diagnosed Graves’ patients when compared to healthy subjects as well as patients with long standing disease and a strong statistically significant inverse correlation between circulating CXCL10/IP-10 levels and disease dura-tion has been demonstrated. Similar findings have been obtained when Type 1 autoimmune diabetes affected patients have been taken into account. In conclusion, Such experiences have demonstrated an important role played by interferon-γ inducible CXC chemokines in the pathogenesis of glandular autoimmunity. In fact, it is reasonable to assume that glandular epithelial cells may modulate the autoimmune process at least in its initial phase, through the production of chemokines which induce migration of Th1 lymphocytes into the gland. Interferon-γ secretion by lymphocytes would, in turn, stimulate chemokines production by follicular cells, thus perpetuating the autoimmune cascade.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Zlotnik A., Yoshle O. Chemokines: a new classification system and their role in immunity. Immunity 2000, 12: 121–127.

    Article  PubMed  CAS  Google Scholar 

  2. Arenberg D.A., Polverini P.J., Kunkel S.L. et al. The role of CXC chemokines in the regulation of angiogenesis in non-small cell lung cancer. J. Leukoc. Biol. 1997, 62: 554–562.

    PubMed  CAS  Google Scholar 

  3. Muller A., Homey B., Soto H. et al. Involvement of chemokine receptors in breast cancer metastasis. Nature 2001, 410: 50–56.

    Article  PubMed  CAS  Google Scholar 

  4. Rossi D, Zlotnik A. The biology of chemokines and their receptors. Annu. Rev. Immunol. 2000, 18: 217–242.

    Article  PubMed  CAS  Google Scholar 

  5. Cascieri M.A., Springer M.S. The chemokine/chemokine-receptor family: potential and progress for therapeutic intervention. Curr. Opin. Chem. Biol. 2000, 4: 420–427.

    Article  PubMed  CAS  Google Scholar 

  6. Romagnani P., Annunziato F., Lasagni L. et al. Cell cycle dependent expression of CXC chemokine receptor 3 by endothelial cells mediates angiostatic activity. J. Clin. Invest. 2001, 107: 53–63.

    Article  PubMed Central  PubMed  CAS  Google Scholar 

  7. Serio M. Interferon-γ induced chemochines:impact on metabolic and endocrine diseases. Endocrinol. Invest. 2001, 24: 2 (abstract).

    Google Scholar 

  8. Garciá-López M.A., Sancho D., Sánchez-Madrid F, Marazuela M. Thyrocytes from autoimmune thyroid disorders produce the chemokines IP-10 and Mig and attract CXCR3+ lymphocytes. J. Clin. Endocrinol. Metab. 2001, 86: 5008–5016.

    Article  PubMed  Google Scholar 

  9. Romagnani P., Lazzeri E., Lasagni L. et al. IP-10 and Mig production by glomerular cells in human proliferative glomerulonephritis and regulation by nitric oxide. J. Am. Soc. Nephrol. 2002, 13: 53–64.

    PubMed  CAS  Google Scholar 

  10. Romagnani P, Rotondi M., Lazzeri E. et al. Expression of P-10/CXCL10 and Mig/CXCL9 in the thyroid and increased serum levels of IP-10/CXCL10 in the serum of subjects with recent onset Graves’ disease. Am. J. Pathol. 2002, 161: 195–206.

    Article  PubMed Central  PubMed  CAS  Google Scholar 

  11. Romagnani S. The Th1/Th2 paradigm in disease. R.G. Sandes Company, Austin, Texas, 1996.

    Google Scholar 

  12. Aniszewski J.P., Valyasevi R.W., Bahn R.S. Relationship be-tween disease duration and predominant orbital T cell subset in Graves’ ophtalmopathy. J. Clin. Endocrinol. Metab. 2000, 85: 776–780.

    PubMed  CAS  Google Scholar 

  13. Shimada A, Morimoto J., Kodama K. et al. Elevated serum P-10 levels observed in Type 1 diabetes. Diabetes Care 2001, 24: 510–515.

    Article  PubMed  CAS  Google Scholar 

  14. Nicoletti F., Conget I., Di Mauro M. et al. Serum concen trations of the interferon-gamma-inducible chemokine IP-10/CXCL10 are augmented in both newly diagnosed Type diabetes mellitus patients and subjects at risk of developing the disease. Diabetologia 2002, 45: 1107–1110.

    Article  PubMed  CAS  Google Scholar 

  15. Raz I., Elias D., Avron A, Tamir M, Metzger M., Cohen I.R. β-cell function in new onset type 1 diabetes and im-munomodulation with a heat shock protein peptide (DiaPep277): a randomized, double-blind, phase II trial. Lancet 2001, 358: 1749–1753.

    Article  PubMed  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Mario Serio.

Additional information

An erratum to this article is available at http://dx.doi.org/10.1007/BF03345152.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Rotondi, M., Lazzeri, E., Romagnani, P. et al. Role for interferon-γ inducible chemokines in endocrine autoimmunity: An expanding field. J Endocrinol Invest 26, 177–180 (2003). https://doi.org/10.1007/BF03345149

Download citation

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF03345149

Key-words

Navigation