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The autoimmune regulator (Aire) controls iNKT cell development and maturation

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A Retraction to this article was published on 01 September 2006

Abstract

The mechanism underlying the autoimmune polyglandular syndrome type-1 (APS1) has been attributed to defective T-cell negative selection resulting from reduced expression and presentation of autoantigens in thymic medullary epithelial cells (MECs). It has also been postulated that Aire is involved in development of regulatory T cells, although supporting evidence is lacking. Here we show that expression of Aire in MECs is required for development of iNKT cells, suggesting a role for iNKT cells in APS1. NOTE: We are retracting this report as it contains several errors, including duplications and manipulations of some flow cytometry plots in Figure 1a and in Supplementary Figure 2 online, incorrect juxtaposition of data in Figure 1g (spleen) that in fact derive from different experiments, and inaccurate reporting of the absolute number of iNKT cells and s.d. values, even though the statistical significance remains unchanged. Although original data exist for each figure that largely support the conclusions drawn, we believe that the number of figures affected means that the appropriate response is to retract this paper.

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Figure 1: The number of iNKT cells is reduced in Aire-deficient mice.
Figure 2: iNKT cell development and maturation are impaired in Aire-deficient mice.

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References

  1. Ruan, Q.G. & She, J.X. Clin. Lab. Med. 24, 305–317 (2004).

    Article  Google Scholar 

  2. Anderson, M.S. et al. Science 298, 1395–1401 (2002).

    Article  CAS  Google Scholar 

  3. Kuroda, N. et al. J. Immunol. 174, 1862–1870 (2005).

    Article  CAS  Google Scholar 

  4. Ramsey, C. et al. Hum. Mol. Genet. 11, 397–409 (2002).

    Article  CAS  Google Scholar 

  5. Liston, A. et al. Nat. Immunol. 4, 350–354 (2003).

    Article  CAS  Google Scholar 

  6. Anderson, M.S. et al. Immunity 23, 227–239 (2005).

    Article  CAS  Google Scholar 

  7. Mathis, D. & Benoist, C. Immunity 20, 509–516 (2004).

    Article  CAS  Google Scholar 

  8. Matsuda, J.L. & Gapin, L. Curr. Opin. Immunol. 17, 122–130 (2005).

    Article  CAS  Google Scholar 

  9. Mi, Q.S. et al. Diabetes 53, 1303–1310 (2004).

    Article  CAS  Google Scholar 

  10. Sivakumar, V. et al. J. Exp. Med. 197, 1613–1621 (2003).

    Article  CAS  Google Scholar 

  11. Wagner, M.J. et al. J. Immunol. 174, 6764–6771 (2005).

    Article  CAS  Google Scholar 

  12. Heino, M. et al. Eur. J. Immunol. 30, 1884–1893 (2000).

    Article  CAS  Google Scholar 

  13. Zhou, D. et al. Science 306, 1786–1789 (2004).

    Article  CAS  Google Scholar 

  14. Wei, D.G. et al. J. Exp. Med. 202, 239–248 (2005).

    Article  CAS  Google Scholar 

  15. Chin, R.K. et al. Nat. Immunol. 4, 1121–1127 (2003).

    Article  CAS  Google Scholar 

Download references

Acknowledgements

We thank R. Brutkiewicz and K. Hayakawa for the gifts of NKT cell lines, L. Peltonen for providing the initial Aire−/− mice and Kirin Brewery Pharmaceutical Co. for α-GalCer. We acknowledge H. He for his assistance with artwork. This work was supported in part by grants from the American Diabetes Association (to Q.-S.M.), the Juvenile Diabetes Research Foundation International (to Q.-S.M.), the US National Institutes of Health (to J.-X.S.) and the Canadian Institutes of Health Research (to T.L.D.).

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Correspondence to Qing-Sheng Mi or Jin-Xiong She.

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The authors declare no competing financial interests.

Supplementary information

Supplementary Fig. 1

The number of iNKT cells is reduced in NOD. Aire-deficient mice. (PDF 134 kb)

Supplementary Fig. 2

Percentages of CD4, CD8, iNKT and NK cells in Aire-deficient mice. (PDF 1100 kb)

Supplementary Fig. 3

Autoantibodies in bone marrow recipient mice. (PDF 627 kb)

Supplementary Fig. 4

Gene expression analyzed by quantitative RT-PCR. (PDF 539 kb)

Supplementary Methods (PDF 141 kb)

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Mi, QS., Deng, ZB., Joshi, S. et al. The autoimmune regulator (Aire) controls iNKT cell development and maturation. Nat Med 12, 624–626 (2006). https://doi.org/10.1038/nm1424

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