The elevation of plasma galectin-9 levels in patients with psoriasis and its associations with inflammatory and immune checkpoint molecules in skin tissues

被引:3
|
作者
Chagan-Yasutan, Haorile [1 ,2 ]
He, Nagongbilige [1 ,3 ]
Arlud, Sarnai [1 ]
Fang, Jun [1 ,3 ]
Hattori, Toshio [2 ,4 ]
机构
[1] Int Mongolian Med Hosp Inner Mongolia, Mongolian Psychosomat Med Dept, Hohhot 010065, Peoples R China
[2] Kibi Int Univ, Res Inst Hlth & Welf, 8 Iga machi, Takahashi, Okayama 7168508, Japan
[3] Inner Mongolia Inst Chinese & Mongolian Med, Hohhot 010010, Peoples R China
[4] Shizuoka Grad Univ Publ Hlth, 4-27-2 Kita Ando Aoi Ku, Shizuoka 4200881, Japan
关键词
Psoriasis; Galectin-9; Skin RNA; Immune checkpoint molecules; Inflammatory molecules; CELL-DEATH; T-CELLS; EXPRESSION; TIM-3; PATHOGENESIS; KERATINOCYTES; INVOLVEMENT; ACTIVATION; SEVERITY; PATHWAY;
D O I
10.1016/j.humimm.2023.110741
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Psoriasis is a chronic, immune-mediated disorder that mainly affects the skin, with an estimated global prevalence of 2-3%. Galectin-9 (Gal-9) is a beta-galactoside-binding lectin capable of promoting or suppressing the progression of infectious and immune-mediated diseases. Here, we determined if the expression of Gal-9 is observed in psoriasis. Gal-9 levels were measured in plasma of psoriasis (n = 62) and healthy control (HC) (n = 31) using an enzyme-linked immunosorbent assay. In addition, skin samples from seven patients were screened for RNA transcriptomes and the expression of Gal-9 was compared with inflammatory, immune checkpoint molecules (ICMs) and Foxp3. The plasma Gal-9 levels in patients with psoriasis were significantly higher (841 pg/mL) than in HCs (617 pg/mL) (P < 0.0001) and were associated with white blood cell numbers, eosinophils (%) and alanine transaminase. The levels of inflammatory molecules IL-36B, IL-17RA, IL-6R, IL-10, IRF8, TGFb1, and IL-37, and those of ICMs of Tim-3, CTLA-4, CD86, CD80, PD-1LG2, CLEC4G, and Foxp3 were significantly correlated with Gal-9 (LGALS9) in skin. However, HMGB1, CD44, CEACAM1 and PDL1-known to be associated with a variety of Gal-9 biological functions were not correlated with LGALS9. Thus, it is likely that Gal-9 expression affects the disease state of PS.
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页数:7
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