Expression and function of toll-like receptors in peripheral blood mononuclear cells of patients with polymyalgia rheumatica and giant cell arteritis

被引:34
作者
Alvarez Rodriguez, Lorena
Lopez-Hoyos, Marcos [2 ]
Mata, Cristina [3 ]
Fontalba, Ana [4 ]
Calvo Alen, Jaime [3 ]
Jose Marin, Maria
Luis Fernandez-Luna, Jose [4 ]
Aguero Balbin, Jesus [5 ]
Aranzamendi Zaldunbide, Maitane [5 ]
Blanco, Ricardo
Martinez-Taboada, Victor M. [1 ]
机构
[1] Univ Cantabria, Fac Med, Div Rheumatol,Serv Reumatol, Hosp Univ Marques de Valdecilla,IFIMAV, Santander 39008, Spain
[2] Hosp Univ Marques de Valdecilla, Serv Inmunol, IFIMAV, Santander, Spain
[3] Hosp Sierrallana, Secc Reumatol, Torrelavega, Cantabria, Spain
[4] Hosp Univ Marques de Valdecilla, Unidad Genet Mol, IFIMAV, Santander, Spain
[5] Hosp Univ Marques de Valdecilla, Microbiol Serv, IFIMAV, Santander, Spain
关键词
CHRONIC HCV-INFECTION; INNATE IMMUNITY; TEMPORAL ARTERITIS; CHLAMYDIA-PNEUMONIAE; PATHOGEN RECOGNITION; ASSOCIATION; DISEASE; TLR7; POLYMORPHISM; INFLUENZA;
D O I
10.1136/ard.2010.140194
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective To investigate the expression and function of the Toll-like receptor (TLR) family in peripheral blood mononuclear cells (PBMCs) of patients with polymyalgia rheumatica (PMR) and giant cell arteritis (GCA). Methods The authors analysed 70 patients with PMR, 20 with GCA, and 24 healthy controls (HC). TLR expression was assessed by flow cytometry. TLR function was assessed by stimulating PBMCs with specific ligands. Results A significantly increased expression of TLR7 in PBMCs of patients with active disease compared with HC was found. Despite increased expression of TLR7, circulating monocytes from patients showed a significantly lower in vitro response to TLR7 agonists. No amino acid substitutions predicted to be functionally damaging were found in TLR7. A normal response to specific TLR7 agonists in patients in complete remission eliminated a genetic defect. TLR expression and function were also affected to some degree in other diseases characterised by a strong acute phase response. Conclusion These data suggest activation of TLR7 during the active phase of PMR and GCA which resolves with complete disease remission. Whether this finding is the consequence of the marked inflammatory process in these disorders or activation by natural ligands remains to be explored.
引用
收藏
页码:1677 / 1683
页数:7
相关论文
共 51 条
[1]   Pathogen recognition and innate immunity [J].
Akira, S ;
Uematsu, S ;
Takeuchi, O .
CELL, 2006, 124 (04) :783-801
[2]   Toll-like receptors: critical proteins linking innate and acquired immunity [J].
Akira, S ;
Takeda, K ;
Kaisho, T .
NATURE IMMUNOLOGY, 2001, 2 (08) :675-680
[3]   Pathogen recognition by innate immunity and its signaling [J].
Akira, Shizuo .
PROCEEDINGS OF THE JAPAN ACADEMY SERIES B-PHYSICAL AND BIOLOGICAL SCIENCES, 2009, 85 (04) :143-156
[4]   Circulating cytokines in active polymyalgia rheumatica [J].
Alvarez-Rodriguez, L. ;
Lopez-Hoyos, M. ;
Mata, C. ;
Jose Marin, M. ;
Calvo-Alen, J. ;
Blanco, R. ;
Aurrecoechea, E. ;
Ruiz-Soto, M. ;
Martinez-Taboada, V. M. .
ANNALS OF THE RHEUMATIC DISEASES, 2010, 69 (01) :263-269
[5]  
ALVAREZRODRIGUE.L, 2011, RHEUMATOLOG IN PRESS
[6]   Up-regulation of TLR9 gene expression by LPS in mouse macrophages via activation of NF-κB, ERK and p38 MAPK signal pathways [J].
An, HZ ;
Xu, HM ;
Yu, YZ ;
Zhang, MH ;
Qi, RZ ;
Yan, XY ;
Liu, SX ;
Wang, WY ;
Guo, ZH ;
Qin, ZH ;
Cao, XT .
IMMUNOLOGY LETTERS, 2002, 81 (03) :165-169
[7]   Innate immunity at the mucosal surface: Role of toll-like receptor 3 and toll-like receptor 9 in cervical epithelial cell responses to microbial pathogens [J].
Andersen, JM ;
Al-Khairy, D ;
Ingalls, RR .
BIOLOGY OF REPRODUCTION, 2006, 74 (05) :824-831
[8]  
[Anonymous], REV ESP REUMATOL
[9]   THE AMERICAN-RHEUMATISM-ASSOCIATION 1987 REVISED CRITERIA FOR THE CLASSIFICATION OF RHEUMATOID-ARTHRITIS [J].
ARNETT, FC ;
EDWORTHY, SM ;
BLOCH, DA ;
MCSHANE, DJ ;
FRIES, JF ;
COOPER, NS ;
HEALEY, LA ;
KAPLAN, SR ;
LIANG, MH ;
LUTHRA, HS ;
MEDSGER, TA ;
MITCHELL, DM ;
NEUSTADT, DH ;
PINALS, RS ;
SCHALLER, JG ;
SHARP, JT ;
WILDER, RL ;
HUNDER, GG .
ARTHRITIS AND RHEUMATISM, 1988, 31 (03) :315-324
[10]   TLR-dependent and TLR-independent pathways of type I interferon induction in systemic autoimmunity [J].
Baccala, Roberto ;
Hoebe, Kasper ;
Kono, Dwight H. ;
Beutler, Bruce ;
Theofilopoulos, Argyrios N. .
NATURE MEDICINE, 2007, 13 (05) :543-551