Toll-like receptors pathway in common variable immune deficiency (CVID) and X-linked agammaglobulinemia (XLA)

被引:0
|
作者
Parsova Tavasolian
Laleh Sharifi
Asghar Aghamohammadi
Farshid Noorbakhsh
Rouzbeh Sanaei
Mahsima Shabani
Nima Rezaei
机构
[1] Tehran University of Medical Sciences,Department of Immunology, School of Medicine
[2] Tehran University of Medical Sciences,Research Center for Immunodeficiencies, Pediatrics Center of Excellence, Children’s Medical Center
[3] Universal Scientific Education and Research Network (USERN),Primary Immunodeficiency Diseases Network (PIDNet)
[4] Iran University of Medical Sciences,Department of Immunology, School of Medicine
[5] Universal Scientific Education and Research Network (USERN),International Hematology/Oncology of Pediatrics Experts (IHOPE)
[6] Universal Scientific Education and Research Network (USERN),Network of Immunity in Infection, Malignancy and Autoimmunity (NIIMA)
[7] Children’s Medical Center Hospital,undefined
来源
European Cytokine Network | 2018年 / 29卷
关键词
CVID; XLA; TLR; TNF-α; IFN-α;
D O I
暂无
中图分类号
学科分类号
摘要
Common variable immunodeficiency (CVID) and X-linked agammaglobulinemia (XLA) are two major humoral immunodeficiencies, causing a high rate of early age mortality in children. In order to identifiy the possible factors involved in the pathogenesis of CVID and XLA, recent studies have focused on Toll-like receptors (TLRs) and demonstrate the defects in different TLR pathways in immune cells of CVID and XLA patients. Herein, we measured TLR-4 and TLR-9 RNA levels and consequently TNF-α and IFN-α production in peripheral blood mononuclear cells (PBMCs) of patients with CVID and XLA. Contrary to healthy individuals, TLR-9 expression was not significantly increased after ligand stimulation, whereas ligand-induced TLR-4 expression was not significantly different from that in healthy control PBMCs. Lipopolysaccharide (LPS)-stimulated TNF-α production was significantly reduced in patients compared to controls, whereas IFN-α production was increased in all groups after CpG stimulation without any significant inter-group difference. Our data suggest that defects in TLR-9 activated pathways may be a result of the decreased TLR-9 expression, although TLR-9 is not the only modulator of IFN-α production in these patients. On the other hand, impaired signaling in TLR-4 activated pathways which results in significant reduction in TNF-α production are not related to a defect in TLR-4 expression.
引用
收藏
页码:153 / 158
页数:5
相关论文
共 50 条
  • [41] Killer cell immunoglobulin-like receptors are associated with common variable immune deficiency pathogenesis
    Wang, Yuge
    Hwangpo, Tracy
    Martin, Maureen P.
    Vince, Nicolas
    Qi, Ying
    Reynolds, Richard J.
    Absher, Devin
    Gao, Xiaojiang
    Ballinger, Carol A.
    Burrows, Peter D.
    Atkinson, T. Prescott
    Brown, Elizabeth E.
    Elgavish, Ada
    Liu, Cunren
    Carrington, Mary
    Schroeder, Harry W.
    JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2016, 138 (05) : 1495 - 1498
  • [42] KILLER CELL IMMUNOGLOBULIN-LIKE RECEPTORS ARE ASSOCIATED WITH COMMON VARIABLE IMMUNE DEFICIENCY PATHOGENESIS
    Wang, Y.
    Schroeder, H.
    JOURNAL OF INVESTIGATIVE MEDICINE, 2016, 64 (02) : 642 - 642
  • [43] Chronic Diarrhea with Villous Blunting of the Small Intestine Under Capsule Endoscopy in Common Variable Immunodeficiency and X-Linked Agammaglobulinemia: A Case Series
    Deng, Feihong
    Wang, Hanyu
    Wang, Xuehong
    JOURNAL OF ASTHMA AND ALLERGY, 2023, 16 : 997 - 1006
  • [44] SCID like picture with B cell deficiency and CD4 lymphopenia in a family with CVID and an X-linked inheritance pattern.
    Tachdjian, R.
    Land, M. H.
    Lin, E.
    Riedl, M. A.
    Roberts, R. L.
    ANNALS OF ALLERGY ASTHMA & IMMUNOLOGY, 2007, 98 (01) : A100 - A100
  • [45] A common pathway mediated through Toll-like receptors leads to T- and natural killer-cell immunosuppression
    Vaknin, Ilan
    Blinder, Liora
    Wang, Lynn
    Gazit, Roi
    Shapira, Elena
    Genina, Olga
    Pines, Mark
    Pikarsky, Eli
    Baniyash, Michal
    BLOOD, 2008, 111 (03) : 1437 - 1447
  • [46] Toll-like receptors 1 and 2 cooperatively mediate immune responses to curli, a common amyloid from enterobacterial biofilms
    Tukel, Cagla
    Nishimori, Jessalyn H.
    Wilson, R. Paul
    Winter, Maria G.
    Keestra, A. Marijke
    van Putten, Jos P. M.
    Baumler, Andreas J.
    CELLULAR MICROBIOLOGY, 2010, 12 (10) : 1495 - 1505
  • [47] Molecular immune mechanisms of HPV-infected HaCaT cells in vitro based on toll-like receptors signaling pathway
    Ying, Zuolin
    Li, Xiaojie
    Dang, Hong
    Yin, Na
    Gao, Chuang
    JOURNAL OF CLINICAL LABORATORY ANALYSIS, 2020, 34 (03)
  • [48] Sex-specific association between X-linked Toll-like receptor 7 with the outcomes of hepatitis C virus infection
    Yue, Ming
    Feng, Le
    Tang, Shai-di
    Wang, Jia-jia
    Xue, Xing-xin
    Ding, Wei-liang
    Zhang, Yun
    Deng, Xiao-zhao
    GENE, 2014, 548 (02) : 244 - 250
  • [49] Common variable immunodeficiency revisited: normal generation of naturally occurring dendritic cells that respond to Toll-like receptors 7 and 9
    Taraldsrud, E.
    Fevang, B.
    Aukrust, P.
    Beiske, K. H.
    Floisand, Y.
    Froland, S.
    Rollag, H.
    Olweus, J.
    CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 2014, 175 (03): : 439 - 448
  • [50] Sex-specific association of X-linked Toll-like receptor 7 (TLR7) with male systemic lupus erythematosus
    Shen, Nan
    Fu, Qiong
    Deng, Yun
    Qian, Xiaoxia
    Zhao, Jian
    Kaufman, Kenneth M.
    Wu, Yee Ling
    Yu, C. Yung
    Tang, Yuanjia
    Chen, Ji-Yih
    Yang, Wanling
    Wong, Maida
    Kawasaki, Aya
    Tsuchiya, Naoyuki
    Sumida, Takayuki
    Kawaguchi, Yasushi
    Howe, Hwee Siew
    Mok, Mo Yin
    Bang, So-Young
    Liu, Fei-Lan
    Chang, Deh-Ming
    Takasaki, Yoshinari
    Hashimoto, Hiroshi
    Harley, John B.
    Guthridge, Joel M.
    Grossman, Jennifer M.
    Cantor, Rita M.
    Song, Yeong Wook
    Bae, Sang-Cheol
    Chen, Shunle
    Hahn, Bevra H.
    Lau, Yu Lung
    Tsao, Betty P.
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2010, 107 (36) : 15838 - 15843