Antibody to CMRF35-Like Molecule 2, CD300e A Novel Biomarker Detected in Patients with Fulminant Type 1 Diabetes

被引:11
作者
Haseda, Fumitaka [1 ]
Imagawa, Akihisa [1 ,2 ]
Nishikawa, Hiroyoshi [3 ,4 ]
Mitsui, Shinobu [1 ]
Tsutsumi, Chiharu [1 ]
Fujisawa, Reiko [1 ]
Sano, Hiroyuki [1 ]
Murase-Mishiba, Yuko [1 ]
Terasaki, Jungo [1 ]
Sakaguchi, Shimon [3 ]
Hanafusa, Toshiaki [1 ]
机构
[1] Osaka Med Coll, Dept Internal Med 1, Takatsuki, Osaka, Japan
[2] Osaka Univ, Grad Sch Med, Dept Metab Med, Suita, Osaka, Japan
[3] Osaka Univ, Immunol Frontier Res Ctr, Expt Immunol, Suita, Osaka, Japan
[4] Natl Canc Ctr, Exploratory Oncol Res & Clin Trial Ctr, Div Canc Immunol, Kashiwa, Chiba, Japan
关键词
GALECTIN-3; PROTEIN; ONSET; MELLITUS; AUTOANTIBODIES; AUTOANTIGEN; MONOCYTES; RESPONSES; RECEPTOR; SUBTYPE;
D O I
10.1371/journal.pone.0160576
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Aims/Hypothesis Fulminant type 1 diabetes (FT1D) is a distinct subtype of type 1 diabetes and is fatal without immediate diagnosis and treatment. At present, there are no biomarkers for early and predictive detection of FT1D. Methods First, we analyzed a total of 6 serum samples from 3 patients with FT1D (1 sample in the acute and 1 in the sub-acute phases from each patient) by seromic analysis. Second, titres of the antibody were measured by ELISA in sera from 30 patients with FT1D (both in the acute and sub-acute phases), 13 patients with FT1D in the chronic phase, 32 patients with autoimmune type 1 (type 1A) diabetes (T1AD), 30 patients with type 2 diabetes (T2D), 23 patients with autoimmune thyroid disease (AITD) and 31 healthy control subjects (HC). Results Seromic analysis revealed 9 antibodies which showed high signals from all 3 patients with FT1D in the acute phase. Among them, the titre of anti-CD300e antibody was significantly higher in FT1D patients in the acute phase than that in T1AD, T2D, AITD patients and HC, as determined by ELISA (P<0.01, respectively). The titre of anti-CD300e antibody was also higher in FT1D in the acute phase than that in the sub-acute phase (P = 0.0018, Wilcoxon signed-rank test). The titre of anti-LGALS3 antibody in FT1D patients in the acute phase did not differ from that in patients with FT1D in the sub-acute phase, T1AD, T2D, AITD and HC. Conclusion/Interpretation The titre of a novel antibody, anti-CD300e, was high in sera from patients with FT1D. This antibody might be a diagnostic marker and provide new insight into the pathogenesis of FT1D.
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页数:13
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