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Human TH17 lymphocytes promote blood-brain barrier disruption and central nervous system inflammation


TH17 lymphocytes appear to be essential in the pathogenesis of numerous inflammatory diseases. We demonstrate here the expression of IL-17 and IL-22 receptors on blood-brain barrier endothelial cells (BBB-ECs) in multiple sclerosis lesions, and show that IL-17 and IL-22 disrupt BBB tight junctions in vitro and in vivo. Furthermore, TH17 lymphocytes transmigrate efficiently across BBB-ECs, highly express granzyme B, kill human neurons and promote central nervous system inflammation through CD4+ lymphocyte recruitment.

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Figure 1: TH17 lymphocytes migrate efficiently across the BBB in vitro and in vivo and kill human neurons.
Figure 2: IL-17 and IL-22 receptors are expressed on human brain endothelium, and their activation permeabilizes the BBB.

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  1. Renno, T. et al. Int. Immunol. 6, 347–354 (1994).

    Article  CAS  Google Scholar 

  2. Bettelli, E. et al. J. Exp. Med. 200, 79–87 (2004).

    Article  CAS  Google Scholar 

  3. Steinman, L. Nat. Med. 13, 139–145 (2007).

    Article  CAS  Google Scholar 

  4. Cua, D.J. et al. Nature 421, 744–748 (2003).

    Article  CAS  Google Scholar 

  5. Langrish, C.L. et al. J. Exp. Med. 201, 233–240 (2005).

    Article  CAS  Google Scholar 

  6. Sospedra, M. & Martin, R. Annu. Rev. Immunol. 23, 683–747 (2005).

    Article  CAS  Google Scholar 

  7. Biernacki, K., Prat, A., Blain, M. & Antel, J.P. J. Neuropathol. Exp. Neurol. 60, 1127–1136 (2001).

    Article  CAS  Google Scholar 

  8. Prat, A., Biernacki, K. & Antel, J.P. J. Autoimmun. 24, 119–124 (2005).

    Article  CAS  Google Scholar 

  9. Liang, S.C. et al. J. Exp. Med. 203, 2271–2279 (2006).

    Article  CAS  Google Scholar 

  10. Chung, Y. et al. Cell Res. 16, 902–907 (2006).

    Article  CAS  Google Scholar 

  11. Zheng, Y. et al. Nature 445, 648–651 (2007).

    Article  CAS  Google Scholar 

  12. Komiyama, Y. et al. J. Immunol. 177, 566–573 (2006).

    Article  CAS  Google Scholar 

  13. Uyttenhove, C. & Van, S.J. Eur. J. Immunol. 36, 2868–2874 (2006).

    Article  CAS  Google Scholar 

  14. Wosik, K. et al. J. Neurosci. 27, 9032–9042 (2007).

    Article  CAS  Google Scholar 

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This study was supported by funding from the Multiple Sclerosis Society of Canada (MSSC) and from the Canadian Fund for Innovation to A.P. The animal studies were supported through grants from the US National MS Society and the Swiss National Science Foundation (B.B.). H.K., I.I., A.D.-D. and R.C. hold studentships from the MSSC and the Canadian Institutes of Health Research (CIHR)/Strategic Training Initiative in Health Research Neuroinflammation Training Program. K.K. has a fellowship from the Center for Neurosciences in Zurich. N.A. holds a CIHR Senior Research Fellowship Phase 2. B.B. is a Neuroscience Scholar of the US National MS Society. A.P. is a Research Scholar from the Fonds de la Recherche en Santé du Québec, and holds the Donald Paty Career Award of the MSSC. We thank I. Gutcher, S. Haak, D. Pasichnyk and J. Laganière for their excellent technical assistance. We are grateful to V.K. Kuchroo (Harvard Medical School), who kindly provided the 2D2 mice, and to J.P. Antel (McGill University) for providing assistance and human tissue.

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H.K. conducted most of the experiments; K.K. performed and analyzed animal studies; I.I. and A.D.-D. contributed to immunostaining and in vitro protocols; R.C. assisted with confocal microscopy and performed some EAE experiments; M.B. assisted with BBB-EC isolation and culture; F.G. performed the killing assay; N.A. provided critical input on data analysis; B.B. designed and supervised the animal studies; H.K. and A.P. designed the study, analyzed the data and wrote the manuscript; A.P. secured the funding.

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Correspondence to Alexandre Prat.

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Kebir, H., Kreymborg, K., Ifergan, I. et al. Human TH17 lymphocytes promote blood-brain barrier disruption and central nervous system inflammation. Nat Med 13, 1173–1175 (2007).

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