Pathophysiological roles of cytokine-chemokine immune network

doi:10.1155/2014/615130

Editorial

. 2014:2014:615130.

doi: 10.1155/2014/615130. Epub 2014 Sep 11.

Pathophysiological roles of cytokine-chemokine immune network

Jong-Young Kwak¹, Mizuko Mamura², Jana Barlic-Dicen³, Evelin Grage-Griebenow⁴

Affiliations

¹ Department of Biochemistry, School of Medicine and Immune-Network Pioneer Research Center, Dong-A University, 32 Daesin-gongwon-ro, Seo-gu, Busan 602-714, Republic of Korea.
² Department of Molecular Pathology, Tokyo Medical University, 6-1-1 Shinjuku, Shinjuku-ku, Tokyo 160-8402, Japan ; Department of Internal Medicine, Kyungpook National University, 50 Samduk-2ga, Jun-gu, Daegu 700-721, Republic of Korea.
³ Cardiovascular Biology, Oklahoma Medical Research Foundation and Department of Cell Biology, University of Oklahoma Health Sciences Center, 825 N.E. 13th Street, Oklahoma City, OK 73104, USA.
⁴ Institute for Experimental Medicine, Inflammatory Carcinogenesis, UK S-H, Kiel Campus, Arnold-Heller-Straße 3, Building 17, 24105 Kiel, Germany.

PMID: 25295287
PMCID: PMC4180646
DOI: 10.1155/2014/615130

Editorial

Pathophysiological roles of cytokine-chemokine immune network

Jong-Young Kwak et al. J Immunol Res. 2014.

. 2014:2014:615130.

doi: 10.1155/2014/615130. Epub 2014 Sep 11.

Authors

Jong-Young Kwak¹, Mizuko Mamura², Jana Barlic-Dicen³, Evelin Grage-Griebenow⁴

Affiliations

¹ Department of Biochemistry, School of Medicine and Immune-Network Pioneer Research Center, Dong-A University, 32 Daesin-gongwon-ro, Seo-gu, Busan 602-714, Republic of Korea.
² Department of Molecular Pathology, Tokyo Medical University, 6-1-1 Shinjuku, Shinjuku-ku, Tokyo 160-8402, Japan ; Department of Internal Medicine, Kyungpook National University, 50 Samduk-2ga, Jun-gu, Daegu 700-721, Republic of Korea.
³ Cardiovascular Biology, Oklahoma Medical Research Foundation and Department of Cell Biology, University of Oklahoma Health Sciences Center, 825 N.E. 13th Street, Oklahoma City, OK 73104, USA.
⁴ Institute for Experimental Medicine, Inflammatory Carcinogenesis, UK S-H, Kiel Campus, Arnold-Heller-Straße 3, Building 17, 24105 Kiel, Germany.

PMID: 25295287
PMCID: PMC4180646
DOI: 10.1155/2014/615130

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References

1. Szabo SJ, Kim ST, Costa GL, Zhang X, Fathman CG, Glimcher LH. A novel transcription factor, T-bet, directs Th1 lineage commitment. Cell. 2000;100(6):655–669. - PubMed
1. Do JS, Asosingh K, Baldwin WM, III, Min B. Cutting edge: IFN-γR signaling in non-T cell targets regulates T cell-mediated intestinal inflammation through multiple mechanisms. Journal of Immunololy. 2014;192(6):2537–2541. - PMC - PubMed
1. Takahashi R, Nishimoto S, Muto G, et al. SOCS1 is essential for regulatory T cell functions by preventing loss of Foxp3 expression as well as IFN-γ and IL-17A production. The Journal of Experimental Medicine. 2011;208(10):2055–2067. - PMC - PubMed
1. Hanahan D, Weinberg RA. Hallmarks of cancer: the next generation. Cell. 2011;144(5):646–674. - PubMed
1. Scheiermann C, Kunisaki Y, Frenette PS. Circadian control of the immune system. Nature Reviews Immunology. 2013;13(3):190–198. - PMC - PubMed

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[1] Szabo SJ, Kim ST, Costa GL, Zhang X, Fathman CG, Glimcher LH. A novel transcription factor, T-bet, directs Th1 lineage commitment. Cell. 2000;100(6):655–669. - PubMed

[2] Szabo SJ, Kim ST, Costa GL, Zhang X, Fathman CG, Glimcher LH. A novel transcription factor, T-bet, directs Th1 lineage commitment. Cell. 2000;100(6):655–669. - PubMed

[3] Do JS, Asosingh K, Baldwin WM, III, Min B. Cutting edge: IFN-γR signaling in non-T cell targets regulates T cell-mediated intestinal inflammation through multiple mechanisms. Journal of Immunololy. 2014;192(6):2537–2541. - PMC - PubMed

[4] Do JS, Asosingh K, Baldwin WM, III, Min B. Cutting edge: IFN-γR signaling in non-T cell targets regulates T cell-mediated intestinal inflammation through multiple mechanisms. Journal of Immunololy. 2014;192(6):2537–2541. - PMC - PubMed

[5] Takahashi R, Nishimoto S, Muto G, et al. SOCS1 is essential for regulatory T cell functions by preventing loss of Foxp3 expression as well as IFN-γ and IL-17A production. The Journal of Experimental Medicine. 2011;208(10):2055–2067. - PMC - PubMed

[6] Takahashi R, Nishimoto S, Muto G, et al. SOCS1 is essential for regulatory T cell functions by preventing loss of Foxp3 expression as well as IFN-γ and IL-17A production. The Journal of Experimental Medicine. 2011;208(10):2055–2067. - PMC - PubMed

[7] Hanahan D, Weinberg RA. Hallmarks of cancer: the next generation. Cell. 2011;144(5):646–674. - PubMed

[8] Hanahan D, Weinberg RA. Hallmarks of cancer: the next generation. Cell. 2011;144(5):646–674. - PubMed

[9] Scheiermann C, Kunisaki Y, Frenette PS. Circadian control of the immune system. Nature Reviews Immunology. 2013;13(3):190–198. - PMC - PubMed

[10] Scheiermann C, Kunisaki Y, Frenette PS. Circadian control of the immune system. Nature Reviews Immunology. 2013;13(3):190–198. - PMC - PubMed

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Pathophysiological roles of cytokine-chemokine immune network

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Pathophysiological roles of cytokine-chemokine immune network

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