scholarly journals Single-cell analysis reveals sexually dimorphic repertoires of Interferon-γ and IL-17A producing T cells in salivary glands of Sjögren’s syndrome mice

2017 ◽  
Vol 7 (1) ◽  
Author(s):  
Arun Wanchoo ◽  
Alexandria Voigt ◽  
Sukesh Sukumaran ◽  
Carol M. Stewart ◽  
Indraneel Bhattacharya ◽  
...  
JCI Insight ◽  
2016 ◽  
Vol 1 (8) ◽  
Author(s):  
Michelle L. Joachims ◽  
Kerry M. Leehan ◽  
Christina Lawrence ◽  
Richard C. Pelikan ◽  
Jacen S. Moore ◽  
...  

PLoS ONE ◽  
2013 ◽  
Vol 8 (3) ◽  
pp. e58127 ◽  
Author(s):  
Cuong Q. Nguyen ◽  
Adebola O. Ogunniyi ◽  
Afife Karabiyik ◽  
J. Christopher Love

2018 ◽  
Vol 192 ◽  
pp. 58-67 ◽  
Author(s):  
Alexandria Voigt ◽  
Katherine Bohn ◽  
Sukesh Sukumaran ◽  
Carol M. Stewart ◽  
Indraneel Bhattacharya ◽  
...  

Rheumatology ◽  
2020 ◽  
Author(s):  
Xiaomin Chen ◽  
Shan Jiang ◽  
Zihao Zhou ◽  
Xin Xu ◽  
Senhong Ying ◽  
...  

Abstract Objective To determine the upregulation of IL-21-inducible genes in minor salivary glands (MSGs) in 28 primary SS (pSS) patients and 12 non-pSS subjects and correlate it with disease characteristics. Methods RNA sequencing was utilized to compare IL-21-inducible genes expression in the MSGs between pSS and non-pSS subjects. The subgroups were characterized according to the IL-21 score calculated by seven IL-21-inducible genes. Furthermore, the disease characteristics and transcripts implicated in hypoxia and interferon signalling were assessed in two pSS subgroups. Results We observed that the expression of the IL-21-inducible genes (IL-21, IL-21R, JAK3, STAT1, HLA-B, CCR7 and CXCL10), the so-called IL-21 signature genes, was significantly increased in pSS patients. The upregulation of JAK3 expression may be induced by hypomethylation of the JAK3 promoter in pSS patients and putatively associated with POU2F2. The patients with increased IL-21 signature gene expression showed an increased EULAR Sjögren’s Syndrome Disease Activity Index score and increased enrichment of B cells, memory B cells, CD4+ T cells and CD8+ T cells. Furthermore, the IL-21 scores in the anti-SSA+, SSB+, ANA+ and high IgG samples were higher than those in the respective antibody-negative samples and normal IgG. In addition, we found both hypoxia and IFN-relevant genes showed strong correlation with IL-21 signature gene expression, indicating their interaction in pSS. Conclusion IL-21 signature gene was associated with typical disease characteristics in pSS, which provides insight into the contribution of the IL-21 signalling pathway to the pathogenesis of the disease and might provide a novel treatment strategy for this subtype of pSS.


1997 ◽  
Vol 40 (12) ◽  
pp. 2271-2274 ◽  
Author(s):  
Takayuki Sumida ◽  
Tomohiro Kato ◽  
Tomoko Hasunuma ◽  
Toshiro Maeda ◽  
Kusuki Nishioka ◽  
...  

2004 ◽  
Vol 202 (4) ◽  
pp. 496-502 ◽  
Author(s):  
Frédéric Lavie ◽  
Corinne Miceli-Richard ◽  
Jeanine Quillard ◽  
Sophie Roux ◽  
Philippe Leclerc ◽  
...  

2021 ◽  
Vol 22 (5) ◽  
pp. 2302
Author(s):  
Mie Kurosawa ◽  
Yosuke Shikama ◽  
Masae Furukawa ◽  
Rieko Arakaki ◽  
Naozumi Ishimaru ◽  
...  

Immunosenescence is characterized by age-associated changes in immunological functions. Although age- and autoimmune-related sialadenitis cause dry mouth (xerostomia), the roles of immunosenescence and cellular senescence in the pathogenesis of sialadenitis remain unknown. We demonstrated that acquired immune cells rather than innate immune cells infiltrated the salivary glands (SG) of aged mice. An analysis of isolated epithelial cells from SG revealed that the expression levels of the chemokine CXCL13 were elevated in aged mice. Senescence-associated T cells (SA-Ts), which secrete large amounts of atypical pro-inflammatory cytokines, are involved in the pathogenesis of metabolic disorders and autoimmune diseases. The present results showed that SA-Ts and B cells, which express the CXCL13 receptor CXCR5, accumulated in the SG of aged mice, particularly females. CD4+ T cells derived from aged mice exhibited stronger in vitro migratory activity toward CXCL13 than those from young mice. In a mouse model of Sjögren’s syndrome (SS), SA-Ts also accumulated in SG, presumably via CXCL12-CXCR4 signaling. Collectively, the present results indicate that SA-Ts accumulate in SG, contribute to the pathogenesis of age- and SS-related sialadenitis by up-regulating chemokines in epithelial cells, and have potential as therapeutic targets for the treatment of xerostomia caused by these types of sialadenitis.


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