[an error occurred while processing this directive] ����Ƥ���Բ�ѧ��־ 2011, 37(2) 84-87 DOI:     ISSN: 2096-5540 CN: 32-1880/R

����Ŀ¼ | ����Ŀ¼ | ������� | �߼�����                                                            [��ӡ��ҳ]   [�ر�]
����
��չ����
������Ϣ
Supporting info
PDFȫ��
[HTMLȫ��]
�����
�����뷴��
�ѱ����Ƽ�������
�����ҵ����
�������ù�����
����
Email Alert
���·���
���������Ϣ
���Ĺؼ����������
���������Լ���
���������������
�˿���
ʷ����
PubMed
Article by Gu,J.Y
Article by Shi,Y.L

Th22ϸ�������������Լ����е�����

�˿���1,ʷ����2

1. ͬ�ô�ѧ������ʮ����ҽԺ
2. ͬ�ô�ѧ�����Ϻ��е�ʮ����ҽԺ

ժҪ��

Th22ϸ����Ⱥ�ǽ������·��ֵ�һ��CD4+ϸ����Ⱥ����Ҫ���ڰ׽���-22���׽���-13���׽���-26��ϸ�����ӣ���������������-γ�Ͱ׽���-4���书����Ҫͨ���׽���-22��ʵ�֣��ɽ鵼��֢��Ӧ�����������Լ����������ȣ��ڻ������ߵ��ڡ�������������֯�޸��з�����Ҫ���á�����Ҫ���ǣ�Th22ϸ�����ܲ���ϸ���������ֻ��������ĵ��ڹ��̡��о��������������������Լ����İ׽���-22����쳣����ʾTh22ϸ����Tϸ���鵼�����������Լ����йء�

�ؼ����� ���������Լ���  

Roles of Th22 cells in autoimmune diseases

Abstract:

Th22 cells are a new subset of CD4+ T cells identified in recent years. They mainly secrete interleukin ��IL-22, IL-13 and IL-26, but not interferon-γ ��IFN-γ�� or IL-4, and exert their function mainly via IL-22. They can mediate inflammatory reactions, autoimmune diseases, tumors, etc, and play an important role in immune regulation, host defense and tissue repair. Most importantly, Th22 cells can modulate cell proliferation, differentiation and apoptosis. Studies have shown an abnormal expression of IL-22 in a variety of autoimmune diseases, hinting that Th22 cells are involved in T cell-mediated autoimmune diseases.

Keywords: autoimmune diseases  
�ո����� 2010-09-06 �޻����� 2010-10-23 ����淢������ 2011-03-10 
DOI:
������Ŀ:

IL-21����м��Th17��Tregϸ�����ߵ��ڵ��о�

ͨѶ����: �˿���
���߼��:

�ο����ף�

[1] Duhen T, Geiger R, Jarrossay D, et al. Production of interleukin 22 but not interleukin 17 by a subset of human skin-homing memory T cells. Nat Immunol, 2009, 10:857-863. [2] Trifari S, Kaplan CD, Tran EH, et al. Identification of a human helper T cell population that has abundant production of interleukin 22 and is distinct from T(H)-17, T(H)1and T(H)2 cells. Nat Immunol, 2009, 10:864-871. [3] Eyerich Stefanie , Eyerich Kilian, Pennino Davide��et al.Th22 cells represent a distinct human T cell subset involved in epidermal immunity and remodeling. Journal of Clinical Investigation, 2009, 19:3573-3585. [4 ] Sa S M��Valdez P A��Wu J et al��The effects of IL-20 subfamily cytokines on reconstituted human epidermis suggest potential roles in cutaneous innate defense and pathogenic adaptive immunity in psoriasis. J Immunol, 2007, 178: 2229-2240. [5] Wolk K��Witte E��Wallace E et al��IL-22 regulates the expression of genes responsible for antimicrobial defense��cellular differentation��and mobility in keratinocytes��a potential role in psoriasis��Eur J Imnmnol, 2006, 36: 1309-1323. [6] ������,����,������.Th22��ϸ������֢�Լ����Ĺ�ϵ.ϸ�����������ѧ��־,2010,26:89-90. [7] ����껣����ֶ�.��ϸ������-22��ϸ���ź�ת��ͨ·��Ӱ��.�������ѧ��־,2009,36:849��852. [8] ׯ԰,ʯ��,��ȫ��. IL-22��Thl7ϸ������ҪЧӦ����.�й�����ѧ��־��2009,25:761-7649. [9] Andoh A, Zhang Z, Inatomi O, et al . Interleukin-22, a member of the IL-10 subfamily, induces inflammatory responses in colonic subepithelial myofibroblasts. Gastroenterology, 2005, 129: 969-984. [10] Ikeuchi H, Kuroiwa T, Hiramatsu N, et al. Expression of interleukin-22 in rheumatoid arthritis-potential role as a proinflammatory cytokine.Arthritis Rheum, 2005, 52: 1037-1046. [11] Boniface K��Bernard FX��Garcia M��el al��IL-22 inhibits epidermal differentiation and induces proinflammatory gene expression and migration of human keratinocytes. J Immunol, 2005, 174: 3695-3702. [12] Zheng Y��Danflenko DM��Valdez P��et al��Interleukin-22��a T(H)17 cytokine��mediates IL-23-induced dermal inflammation and aeanthesia��Nature, 2007, 445: 648-651. [13] Yeh J H��Sidhu S S��Olan A C��et al. Regulation of a lated phase of T cell polarity and effector functions by Crtam��Cell, 2008, 132: 846-859. [14] Kagami S, Rizzo HL, Lee JJ, et al. Circulating Th17, Th22, and Th1 cells are increased in psoriasis. J Invest Dermatol, 2010, 130: 1373-83. [15 ] Wolk K, Witte E, Warszawska K, et al. The Th17 cytokine IL-22 induces IL-20 production in keratinocytes: a novel immunological cascade with potential relevance in psoriasis. Eur J Immunol, 2009, 39: 3570–3581. [16] Shen H, Goodall JC, Hill Gaston JS. Frequency and phenotype of peripheral blood Th17 cells in ankylosing spondylitis and rheumatoid arthritis. Arthritis Rheum, 2009, 60:1647–1656. [17] Geboes L��Dumoutier L��Kelchtermans H��et al.Proinflammatory role of the Th17 cytokine interleukin-22 in collagen-induced arthritis in C57BL/6 mice��Arthritis Rheum,2009, 60: 390-395. [18] Brand S, Beigel F, Olszak T, et al.IL-22 is increased in active Crohn’s disease and promotes proinflammatory gene expression and intestinal epithelial cell migration. Am J Physiol Gastrointest Liver Physiol, 2006, 290: 827–838. [19 ] Wolk K, Witte E, Hoffmann U, et al.IL-22 induces lipopolysaccharide-binding protein in hepatocytes: a potential systemic role of IL-22 in Crohn’s disease. J Immunol, 2007, 178: 5973–5981. [20] Schmechel S, Konrad A, Diegelmann J, et al. Linking genetic susceptibility to Crohn’s disease with Th17 cell function: IL-22 serum levels are increased in Crohn’s disease and correlate with disease activity and IL-23R Genotype status. Infamm Bowel Dis, 2008, 14: 204-212. [21] Sugimoto K, Ogawa A, Mizoguchi E. IL-22 ameliorates intestinal inflammation in a mouse model of ulcerative colitis. J Clin Invest, 2008, 118: 534-544. [22] Kebir H��Kreymbor8 K, Ifergan I, et al��Human THl7 lymphocytes promote blood-brain barrier disruption and central nervous system inflammation��Nat Med, 2007, 13: 1173-1175. [23] Chang H, Hanawa H, Liu H, et al��Hydrodynamic-based delivery of an interleukin-22-Ig fusion gene ameliorates experimental autoimmune myocarditis in rats. J Immunol, 2006, 177: 3635–3643. [24] Pan HF��Zhan XF��Yuan H��et al��Decrease serum IL-22 levels in patients with systemic lupus erythematous��Clin Chim Aeta, 2009��401: 179-180. [25] Ma H L, Liang S, Li J .IL-22 is required for TH17 cell-mediated pathology in a mouse model of psoriasis-like skin inflammation. Clin Invest, 2008, 118: 597-607. [26] Bard JD, Gelebart P, Anand M, et al. Aberrant expression of IL-22 receptor 1 and autocrine IL-22 stimulation contribute to tumorigenicity in ALK+ anaplastic large cell lymphoma. Leukemia, 2008, 22: 1595–1603. [27] Zhang W, Chen Y, Wei H, et al. Antiapoptotic activity of autocrine interleukin-22 and therapeutic effects of interleukin-22-small interfering RNA on human lung cancer xenografts. Clin Cancer Res, 2008, 14: 6432–6439.

�������������
1���ﴴ��,������,��ȫ��,.�׽���17������������Ƥ����[J]. ����Ƥ���Բ�ѧ��־, 2008,34(4): 230-231
2��������, ���������, ��������У.�����������ߺ����������Լ���[J]. ����Ƥ���Բ�ѧ��־, 1999,25(2): 77-80
3������������, ��־ǿ��У, ��������У.�ܰ�ϸ�����������������Լ���[J]. ����Ƥ���Բ�ѧ��־, 2000,26(2): 84-88

�������� (��ע��:��վʵ�������Ը�, �벻Ҫ������ѧ���޹ص�����!�������ݲ�����վ�۵�.)

Copyright 2008 by ����Ƥ���Բ�ѧ��־