Enterovirus Infection, CXC Chemokine Ligand 10 (CXCL10), and CXCR3 Circuit A Mechanism of Accelerated β-Cell Failure in Fulminant Type 1 Diabetes

被引:136
作者
Tanaka, Shoichiro [1 ]
Nishida, Yoriko [1 ]
Aida, Kaoru [1 ]
Maruyama, Taro [2 ]
Shimada, Akira [3 ]
Suzuki, Masako [4 ]
Shimura, Hiroki [1 ]
Takizawa, Soichi [1 ]
Takahashi, Masashi [1 ]
Akiyama, Daiichiro [1 ]
Arai-Yamashita, Sayaka [1 ]
Furuya, Fumihiko [1 ]
Kawaguchi, Akio [1 ]
Kaneshige, Masahiro [1 ]
Katoh, Ryohei [5 ]
Endo, Toyoshi [1 ]
Kobayashi, Tetsuro [1 ]
机构
[1] Univ Yamanashi, Interdisciplinary Grad Sch Med & Engn, Dept Internal Med 3, Yamanashi, Japan
[2] Saitama Social Insurance Hosp, Dept Internal Med, Saitama, Japan
[3] Keio Univ, Dept Internal Med, Tokyo, Japan
[4] Sayama Hosp, Dept Pathol, Saitama, Japan
[5] Univ Yamanashi, Interdisciplinary Grad Sch Med & Engn, Dept Pathol, Yamanashi, Japan
关键词
GAMMA-INDUCIBLE PROTEIN; PANCREATIC-ISLETS; MONOCLONAL-ANTIBODY; AUTOIMMUNE-DISEASE; INTERFERON-GAMMA; RAPID-ONSET; MELLITUS; EXPRESSION; IDENTIFICATION; INFILTRATION;
D O I
10.2337/db09-0091
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVE-Fulminant type 1 diabetes is characterized by the rapid onset of severe hyperglycemia and ketoacidosis, with subsequent poor prognosis of diabetes complications. Causative mechanisms for accelerated beta-cell failure are unclear. RESEARCH DESIGN AND METHODS-Subjects comprised three autopsied patients who died from diabetic ketoacidosis within 2-5 days after onset of fulminant type 1 diabetes. We examined islet cell status, including the presence of enterovirus and chemokine/cytokine/major histocompatibility complex (MHC) expressions in the pancreata using immunohistochemical analyses and RT-PCR. RESULTS-Immunohistochemical analysis revealed the presence of enterovirus-capsid protein in all three affected pancreata. Extensive infiltration of CXCR3 receptor-bearing T-cells and macrophages into islets was observed. Dendritic cells were stained in and around the islets. Specifically, interferon-gamma and CXC chemokine ligand 10 (CXCL10) were strongly coexpressed in all subtypes of islet cells, including beta-cells and alpha-cells. No CXCL10 was expressed in exocrine pancreas. Serum levels of CXCL10 were increased. Expression of MHC class II and hyperexpression of MHC class I was observed in some islet cells. CONCLUSIONS-These results strongly suggest the presence of a circuit for the destruction of beta-cells in fulminant type 1 diabetes. Enterovirus infection of the pancreas initiates coexpression of interferon-gamma and CXCL10 in beta-cells. CXCL10 secreted from beta-cells activates and attracts autoreactive T-cells and macrophages to the islets via CXCR3. These infiltrating autoreactive T-cells and macrophages release inflammatory cytokines including interferon-gamma in the islets, not only damaging beta-cells but also accelerating CXCL10 generation in residual beta-cells and thus further activating cell-mediated autoimmunity until all beta-cells have been destroyed. Diabetes 58:2285-2291, 2009
引用
收藏
页码:2285 / 2291
页数:7
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