Mechanism of NKT cell activation by intranasal coadministration of α-galactosylceramide, which can induce cross-protection against influenza viruses

H. Kamijuku; Y. Nagata; X. Jiang; T. Ichinohe; T. Tashiro; K. Mori; M. Taniguchi; K. Hase; H. Ohno; T. Shimaoka; S. Yonehara; T. Odagiri; M. Tashiro; T. Sata; H. Hasegawa; K. I. Seino

doi:10.1038/mi.2008.2

Mechanism of NKT cell activation by intranasal coadministration of α-galactosylceramide, which can induce cross-protection against influenza viruses

H. Kamijuku, Y. Nagata, X. Jiang, T. Ichinohe, T. Tashiro, K. Mori, M. Taniguchi, K. Hase, H. Ohno, T. Shimaoka, S. Yonehara, T. Odagiri, M. Tashiro, T. Sata, H. Hasegawa, K. I. Seino

Research output: Contribution to journal › Article

79 Citations (Scopus)

Abstract

In a nasal vaccine against influenza, the activation of natural killer T (NKT) cells by intranasal coadministration of α-galactosylceramide (α-GalCer) can potently enhance protective immune responses. The results of this study show that the NKT cell-activated nasal vaccine can induce an effective cross-protection against different strains of influenza virus, including H5 type. To analyze the mechanism of NKT cell activation by this nasal vaccine, we prepared fluorescence-labeled α-GalCer by which we detect a direct interaction between NKT cells and α-GalCer-stored dendritic cells in nasal mucosa-associated tissues. Accordingly, although very few NKT cells exist at mucosa, the nasal vaccination induced a localized increase in NKT cell population, which is partly dependent on CXCL16/CXCR6. Furthermore, we found that NKT cell activation stimulates mucosal IgA production by a mechanism that is dependent on interleukin (IL)-4 production. These results strengthen the basis of nasal vaccination via NKT cell activation, which can induce immune cross-protection.

Original language	English
Pages (from-to)	208-218
Number of pages	11
Journal	Mucosal Immunology
Volume	1
Issue number	3
DOIs	https://doi.org/10.1038/mi.2008.2
Publication status	Published - 2008 May 1
Externally published	Yes

ASJC Scopus subject areas

Immunology and Allergy
Immunology

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Kamijuku, H., Nagata, Y., Jiang, X., Ichinohe, T., Tashiro, T., Mori, K., Taniguchi, M., Hase, K., Ohno, H., Shimaoka, T., Yonehara, S., Odagiri, T., Tashiro, M., Sata, T., Hasegawa, H., & Seino, K. I. (2008). Mechanism of NKT cell activation by intranasal coadministration of α-galactosylceramide, which can induce cross-protection against influenza viruses. Mucosal Immunology, 1(3), 208-218. https://doi.org/10.1038/mi.2008.2

Mechanism of NKT cell activation by intranasal coadministration of α-galactosylceramide, which can induce cross-protection against influenza viruses. / Kamijuku, H.; Nagata, Y.; Jiang, X.; Ichinohe, T.; Tashiro, T.; Mori, K.; Taniguchi, M.; Hase, K.; Ohno, H.; Shimaoka, T.; Yonehara, S.; Odagiri, T.; Tashiro, M.; Sata, T.; Hasegawa, H.; Seino, K. I.

In: Mucosal Immunology, Vol. 1, No. 3, 01.05.2008, p. 208-218.

Research output: Contribution to journal › Article

Kamijuku, H, Nagata, Y, Jiang, X, Ichinohe, T, Tashiro, T, Mori, K, Taniguchi, M, Hase, K, Ohno, H, Shimaoka, T, Yonehara, S, Odagiri, T, Tashiro, M, Sata, T, Hasegawa, H & Seino, KI 2008, 'Mechanism of NKT cell activation by intranasal coadministration of α-galactosylceramide, which can induce cross-protection against influenza viruses', Mucosal Immunology, vol. 1, no. 3, pp. 208-218. https://doi.org/10.1038/mi.2008.2

Kamijuku, H. ; Nagata, Y. ; Jiang, X. ; Ichinohe, T. ; Tashiro, T. ; Mori, K. ; Taniguchi, M. ; Hase, K. ; Ohno, H. ; Shimaoka, T. ; Yonehara, S. ; Odagiri, T. ; Tashiro, M. ; Sata, T. ; Hasegawa, H. ; Seino, K. I. / Mechanism of NKT cell activation by intranasal coadministration of α-galactosylceramide, which can induce cross-protection against influenza viruses. In: Mucosal Immunology. 2008 ; Vol. 1, No. 3. pp. 208-218.

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abstract = "In a nasal vaccine against influenza, the activation of natural killer T (NKT) cells by intranasal coadministration of α-galactosylceramide (α-GalCer) can potently enhance protective immune responses. The results of this study show that the NKT cell-activated nasal vaccine can induce an effective cross-protection against different strains of influenza virus, including H5 type. To analyze the mechanism of NKT cell activation by this nasal vaccine, we prepared fluorescence-labeled α-GalCer by which we detect a direct interaction between NKT cells and α-GalCer-stored dendritic cells in nasal mucosa-associated tissues. Accordingly, although very few NKT cells exist at mucosa, the nasal vaccination induced a localized increase in NKT cell population, which is partly dependent on CXCL16/CXCR6. Furthermore, we found that NKT cell activation stimulates mucosal IgA production by a mechanism that is dependent on interleukin (IL)-4 production. These results strengthen the basis of nasal vaccination via NKT cell activation, which can induce immune cross-protection.",

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AU - Hase, K.

AU - Ohno, H.

AU - Shimaoka, T.

AU - Yonehara, S.

AU - Odagiri, T.

AU - Tashiro, M.

AU - Sata, T.

AU - Hasegawa, H.

AU - Seino, K. I.

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