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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
来源:
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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