Roles of the protein tyrosine phosphatase PTPN22 in immunity and autoimmunity

被引:53
作者
Fousteri, Georgia [1 ]
Liossis, Stamatis-Nick C. [2 ]
Battaglia, Manuela [1 ]
机构
[1] Ist Sci San Raffaele, Diabet Res Inst, I-20132 Milan, Italy
[2] Univ Patras, Sch Med, Dept Rheumatol, Patras 26500, Greece
关键词
PTPN22; Autoimmunity; Genetic predisposition; Immune tolerance; T regulatory cells (Treg); Autoreactive cells; SYSTEMIC-LUPUS-ERYTHEMATOSUS; REGULATORY T-CELLS; RHEUMATOID-ARTHRITIS; SUSCEPTIBILITY GENE; R620W POLYMORPHISM; NK CELLS; VARIANT; ASSOCIATION; ALLELE; INTERFERON;
D O I
10.1016/j.clim.2013.10.006
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
PTPN22 is a protein tyrosine phosphatase expressed by the majority of cells belonging to the innate and adaptive immune systems. Polymorphisms in PTPN22 are associated with several autoimmune diseases, such as systemic lupus erythematosus, rheumatoid arthritis and type 1 diabetes. This review discusses the role of PTPN22 in T and B cells, and its function in innate immune cells, such as monocytes, dendritic cells and NK cells. We focus particularly on the complexity that underlies the function of PTPN22 in the biological processes of the immune system; such complexity has led various research groups to produce rather conflicting data. (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:556 / 565
页数:10
相关论文
共 68 条
[1]   Is there a common genetic basis for autoimmune diseases? [J].
Anaya, Juan-Manuel ;
Gomez, Luismiguel ;
Castiblanco, John .
CLINICAL & DEVELOPMENTAL IMMUNOLOGY, 2006, 13 (2-4) :185-195
[2]   Cutting Edge: The PTPN22 Allelic Variant Associated with Autoimmunity Impairs B Cell Signaling [J].
Arechiga, Adrian F. ;
Habib, Tania ;
He, Yantao ;
Zhang, Xian ;
Zhang, Zhong-Yin ;
Funk, Andrew ;
Buckner, Jane H. .
JOURNAL OF IMMUNOLOGY, 2009, 182 (06) :3343-3347
[3]   Type I interferon in systemic lupus erythematosus and other autoimmune diseases [J].
Banchereau, Jacques ;
Pascual, Virginia .
IMMUNITY, 2006, 25 (03) :383-392
[4]   Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes [J].
Barrett, Jeffrey C. ;
Clayton, David G. ;
Concannon, Patrick ;
Akolkar, Beena ;
Cooper, Jason D. ;
Erlich, Henry A. ;
Julier, Cecile ;
Morahan, Grant ;
Nerup, Jorn ;
Nierras, Concepcion ;
Plagnol, Vincent ;
Pociot, Flemming ;
Schuilenburg, Helen ;
Smyth, Deborah J. ;
Stevens, Helen ;
Todd, John A. ;
Walker, Neil M. ;
Rich, Stephen S. .
NATURE GENETICS, 2009, 41 (06) :703-707
[5]   The R620W polymorphism of the protein tyrosine phosphatase PTPN22 is not associated with multiple sclerosis [J].
Begovich, AB ;
Caillier, SJ ;
Alexander, HC ;
Penko, JM ;
Hauser, SL ;
Barcellos, LF ;
Oksenberg, JR .
AMERICAN JOURNAL OF HUMAN GENETICS, 2005, 76 (01) :184-187
[6]   A functional variant of lymphoid tyrosine phosphatase is associated with type I diabetes [J].
Bottini, N ;
Musumeci, L ;
Alonso, A ;
Rahmouni, S ;
Nika, K ;
Rostamkhani, M ;
MacMurray, J ;
Meloni, GF ;
Lucarelli, P ;
Pellecchia, M ;
Eisenbarth, GS ;
Comings, D ;
Mustelin, T .
NATURE GENETICS, 2004, 36 (04) :337-338
[7]   Lack of the Phosphatase PTPN22 Increases Adhesion of Murine Regulatory T Cells to Improve Their Immunosuppressive Function [J].
Brownlie, Rebecca J. ;
Miosge, Lisa A. ;
Vassilakos, Demetrios ;
Svensson, Lena M. ;
Cope, Andrew ;
Zamoyska, Rose .
SCIENCE SIGNALING, 2012, 5 (252)
[8]   Why is PTPN22 a good candidate susceptibility gene for autoimmune disease? [J].
Burn, Garth L. ;
Svensson, Lena ;
Sanchez-Blanco, Cristina ;
Saini, Manoj ;
Cope, Andrew P. .
FEBS LETTERS, 2011, 585 (23) :3689-3698
[9]   A single-nucleotide polymorphism in the gene encoding lymphoid protein tyrosine phosphatase (PTPN22) confers susceptibility to generalised vitiligo [J].
Cantón, I ;
Akhtar, S ;
Gavalas, NG ;
Gawkrodger, DJ ;
Blomhoff, A ;
Watson, PF ;
Weetman, AP ;
Kemp, EH .
GENES AND IMMUNITY, 2005, 6 (07) :584-587
[10]   PTPN22 Modulates Macrophage Polarization and Susceptibility to Dextran Sulfate Sodium-Induced Colitis [J].
Chang, Hui-Hsin ;
Miaw, Shi-Chuen ;
Tseng, William ;
Sun, Yi-Wei ;
Liu, Chih-Chun ;
Tsao, Hsiao-Wei ;
Ho, I-Cheng .
JOURNAL OF IMMUNOLOGY, 2013, 191 (05) :2134-2143