A Histological Study of Fulminant Type 1 Diabetes Mellitus Related to Human Cytomegalovirus Reactivation

Context:Fulminant type 1 diabetes mellitus (T1DM) is thought to be partly caused by virus infection.Objective:This study investigated the mechanism of β cell destruction in fulminant T1DM after drug-induced hypersensitivity syndrome (DIHS).Methods:We determined the localization of human cytomegalovi...

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Published inThe journal of clinical endocrinology and metabolism Vol. 102; no. 7; pp. 2394 - 2400
Main Authors Yoneda, Sho, Imagawa, Akihisa, Fukui, Kenji, Uno, Sae, Kozawa, Junji, Sakai, Makoto, Yumioka, Toshiki, Iwahashi, Hiromi, Shimomura, Iichiro
Format Journal Article
LanguageEnglish
Published Washington, DC Endocrine Society 01.07.2017
Copyright Oxford University Press
Oxford University Press
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ISSN0021-972X
1945-7197
1945-7197
DOI10.1210/jc.2016-4029

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Abstract Context:Fulminant type 1 diabetes mellitus (T1DM) is thought to be partly caused by virus infection.Objective:This study investigated the mechanism of β cell destruction in fulminant T1DM after drug-induced hypersensitivity syndrome (DIHS).Methods:We determined the localization of human cytomegalovirus (HCMV), human herpesvirus 6 (HHV-6), and Epstein-Barr virus (EBV) and the expression of interferon regulatory factor 3 (IRF3) and viral receptors of Z-DNA binding protein 1 (ZBP1) and retinoic acid-inducible gene I (RIG-I), together with inflammatory cells, by immunohistochemistry of the autopsy pancreas of a patient with fulminant T1DM with DIHS and in seven subjects with normal glucose tolerance who underwent pancreatectomy.Results:HCMV-positive cells were detected in islets and exocrine areas in the patient with fulminant T1DM. Greater numbers of macrophages and CD4+ and CD8+ T lymphocytes had infiltrated into HCMV-positive islets than into HCMV-negative islets, and 52.6% of HCMV-positive cells were also positive for IRF3. α Cells expressed IRF3, ZBP1, or RIG-I. No HCMV-positive cells were detected in the control subjects. HHV-6−positive, but not EBV-positive, cells were present in the patient and the control subjects.Conclusions:These findings indicate that the immunoresponse caused by HCMV infection was associated with β cell injury.In a patient who developed fulminant T1DM after DIHS, HCMV-positive cells were detected in islets, into which increased numbers of macrophages and CD4+ and CD8+ T lymphocytes had infiltrated.
AbstractList Context:Fulminant type 1 diabetes mellitus (T1DM) is thought to be partly caused by virus infection.Objective:This study investigated the mechanism of β cell destruction in fulminant T1DM after drug-induced hypersensitivity syndrome (DIHS).Methods:We determined the localization of human cytomegalovirus (HCMV), human herpesvirus 6 (HHV-6), and Epstein-Barr virus (EBV) and the expression of interferon regulatory factor 3 (IRF3) and viral receptors of Z-DNA binding protein 1 (ZBP1) and retinoic acid-inducible gene I (RIG-I), together with inflammatory cells, by immunohistochemistry of the autopsy pancreas of a patient with fulminant T1DM with DIHS and in seven subjects with normal glucose tolerance who underwent pancreatectomy.Results:HCMV-positive cells were detected in islets and exocrine areas in the patient with fulminant T1DM. Greater numbers of macrophages and CD4+ and CD8+ T lymphocytes had infiltrated into HCMV-positive islets than into HCMV-negative islets, and 52.6% of HCMV-positive cells were also positive for IRF3. α Cells expressed IRF3, ZBP1, or RIG-I. No HCMV-positive cells were detected in the control subjects. HHV-6−positive, but not EBV-positive, cells were present in the patient and the control subjects.Conclusions:These findings indicate that the immunoresponse caused by HCMV infection was associated with β cell injury.In a patient who developed fulminant T1DM after DIHS, HCMV-positive cells were detected in islets, into which increased numbers of macrophages and CD4+ and CD8+ T lymphocytes had infiltrated.
Abstract Fulminant type 1 diabetes mellitus (T1DM) is thought to be partly caused by virus infection. This study investigated the mechanism of β cell destruction in fulminant T1DM after drug-induced hypersensitivity syndrome (DIHS). We determined the localization of human cytomegalovirus (HCMV), human herpesvirus 6 (HHV-6), and Epstein-Barr virus (EBV) and the expression of interferon regulatory factor 3 (IRF3) and viral receptors of Z-DNA binding protein 1 (ZBP1) and retinoic acid-inducible gene I (RIG-I), together with inflammatory cells, by immunohistochemistry of the autopsy pancreas of a patient with fulminant T1DM with DIHS and in seven subjects with normal glucose tolerance who underwent pancreatectomy. HCMV-positive cells were detected in islets and exocrine areas in the patient with fulminant T1DM. Greater numbers of macrophages and CD4+ and CD8+ T lymphocytes had infiltrated into HCMV-positive islets than into HCMV-negative islets, and 52.6% of HCMV-positive cells were also positive for IRF3. α Cells expressed IRF3, ZBP1, or RIG-I. No HCMV-positive cells were detected in the control subjects. HHV-6-positive, but not EBV-positive, cells were present in the patient and the control subjects. These findings indicate that the immunoresponse caused by HCMV infection was associated with β cell injury. In a patient who developed fulminant T1DM after DIHS, HCMV-positive cells were detected in islets, into which increased numbers of macrophages and CD4+ and CD8+ T lymphocytes had infiltrated.
Fulminant type 1 diabetes mellitus (T1DM) is thought to be partly caused by virus infection. This study investigated the mechanism of β cell destruction in fulminant T1DM after drug-induced hypersensitivity syndrome (DIHS). We determined the localization of human cytomegalovirus (HCMV), human herpesvirus 6 (HHV-6), and Epstein-Barr virus (EBV) and the expression of interferon regulatory factor 3 (IRF3) and viral receptors of Z-DNA binding protein 1 (ZBP1) and retinoic acid-inducible gene I (RIG-I), together with inflammatory cells, by immunohistochemistry of the autopsy pancreas of a patient with fulminant T1DM with DIHS and in seven subjects with normal glucose tolerance who underwent pancreatectomy. HCMV-positive cells were detected in islets and exocrine areas in the patient with fulminant T1DM. Greater numbers of macrophages and CD4+ and CD8+ T lymphocytes had infiltrated into HCMV-positive islets than into HCMV-negative islets, and 52.6% of HCMV-positive cells were also positive for IRF3. α Cells expressed IRF3, ZBP1, or RIG-I. No HCMV-positive cells were detected in the control subjects. HHV-6-positive, but not EBV-positive, cells were present in the patient and the control subjects. These findings indicate that the immunoresponse caused by HCMV infection was associated with β cell injury.
Fulminant type 1 diabetes mellitus (T1DM) is thought to be partly caused by virus infection.ContextFulminant type 1 diabetes mellitus (T1DM) is thought to be partly caused by virus infection.This study investigated the mechanism of β cell destruction in fulminant T1DM after drug-induced hypersensitivity syndrome (DIHS).ObjectiveThis study investigated the mechanism of β cell destruction in fulminant T1DM after drug-induced hypersensitivity syndrome (DIHS).We determined the localization of human cytomegalovirus (HCMV), human herpesvirus 6 (HHV-6), and Epstein-Barr virus (EBV) and the expression of interferon regulatory factor 3 (IRF3) and viral receptors of Z-DNA binding protein 1 (ZBP1) and retinoic acid-inducible gene I (RIG-I), together with inflammatory cells, by immunohistochemistry of the autopsy pancreas of a patient with fulminant T1DM with DIHS and in seven subjects with normal glucose tolerance who underwent pancreatectomy.MethodsWe determined the localization of human cytomegalovirus (HCMV), human herpesvirus 6 (HHV-6), and Epstein-Barr virus (EBV) and the expression of interferon regulatory factor 3 (IRF3) and viral receptors of Z-DNA binding protein 1 (ZBP1) and retinoic acid-inducible gene I (RIG-I), together with inflammatory cells, by immunohistochemistry of the autopsy pancreas of a patient with fulminant T1DM with DIHS and in seven subjects with normal glucose tolerance who underwent pancreatectomy.HCMV-positive cells were detected in islets and exocrine areas in the patient with fulminant T1DM. Greater numbers of macrophages and CD4+ and CD8+ T lymphocytes had infiltrated into HCMV-positive islets than into HCMV-negative islets, and 52.6% of HCMV-positive cells were also positive for IRF3. α Cells expressed IRF3, ZBP1, or RIG-I. No HCMV-positive cells were detected in the control subjects. HHV-6-positive, but not EBV-positive, cells were present in the patient and the control subjects.ResultsHCMV-positive cells were detected in islets and exocrine areas in the patient with fulminant T1DM. Greater numbers of macrophages and CD4+ and CD8+ T lymphocytes had infiltrated into HCMV-positive islets than into HCMV-negative islets, and 52.6% of HCMV-positive cells were also positive for IRF3. α Cells expressed IRF3, ZBP1, or RIG-I. No HCMV-positive cells were detected in the control subjects. HHV-6-positive, but not EBV-positive, cells were present in the patient and the control subjects.These findings indicate that the immunoresponse caused by HCMV infection was associated with β cell injury.ConclusionsThese findings indicate that the immunoresponse caused by HCMV infection was associated with β cell injury.
Context:Fulminant type 1 diabetes mellitus (T1DM) is thought to be partly caused by virus infection.Objective:This study investigated the mechanism of β cell destruction in fulminant T1DM after drug-induced hypersensitivity syndrome (DIHS).Methods:We determined the localization of human cytomegalovirus (HCMV), human herpesvirus 6 (HHV-6), and Epstein-Barr virus (EBV) and the expression of interferon regulatory factor 3 (IRF3) and viral receptors of Z-DNA binding protein 1 (ZBP1) and retinoic acid-inducible gene I (RIG-I), together with inflammatory cells, by immunohistochemistry of the autopsy pancreas of a patient with fulminant T1DM with DIHS and in seven subjects with normal glucose tolerance who underwent pancreatectomy.Results:HCMV-positive cells were detected in islets and exocrine areas in the patient with fulminant T1DM. Greater numbers of macrophages and CD4+ and CD8+ T lymphocytes had infiltrated into HCMV-positive islets than into HCMV-negative islets, and 52.6% of HCMV-positive cells were also positive for IRF3. α Cells expressed IRF3, ZBP1, or RIG-I. No HCMV-positive cells were detected in the control subjects. HHV-6−positive, but not EBV-positive, cells were present in the patient and the control subjects.Conclusions:These findings indicate that the immunoresponse caused by HCMV infection was associated with β cell injury.
Author Fukui, Kenji
Yoneda, Sho
Iwahashi, Hiromi
Yumioka, Toshiki
Uno, Sae
Kozawa, Junji
Sakai, Makoto
Imagawa, Akihisa
Shimomura, Iichiro
AuthorAffiliation 1)Department of Metabolic Medicine, Graduate School of Medicine, Osaka University, Suita, Japan. 2)Department of Internal Medicine (I), Osaka Medical College, Takatsuki, Japan 3)Internal Medicine, Konan Hospital, Kobe, Japan
AuthorAffiliation_xml – name: 1)Department of Metabolic Medicine, Graduate School of Medicine, Osaka University, Suita, Japan. 2)Department of Internal Medicine (I), Osaka Medical College, Takatsuki, Japan 3)Internal Medicine, Konan Hospital, Kobe, Japan
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  fullname: Imagawa, Akihisa
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  organization: 3Internal Medicine, Konan Hospital, Kobe “658-0064”, Japan
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Snippet Context:Fulminant type 1 diabetes mellitus (T1DM) is thought to be partly caused by virus infection.Objective:This study investigated the mechanism of β cell...
Fulminant type 1 diabetes mellitus (T1DM) is thought to be partly caused by virus infection. This study investigated the mechanism of β cell destruction in...
Abstract Fulminant type 1 diabetes mellitus (T1DM) is thought to be partly caused by virus infection. This study investigated the mechanism of β cell...
Fulminant type 1 diabetes mellitus (T1DM) is thought to be partly caused by virus infection.ContextFulminant type 1 diabetes mellitus (T1DM) is thought to be...
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SubjectTerms Aged
Autopsy
Beta cells
Biopsy, Needle
Case-Control Studies
CD4 antigen
CD8 antigen
Cell injury
Cells, Cultured
Cytomegalovirus
Cytomegalovirus - pathogenicity
Cytomegalovirus Infections - physiopathology
Diabetes
Diabetes mellitus
Diabetes mellitus (insulin dependent)
Diabetes Mellitus, Type 1 - pathology
Diabetes Mellitus, Type 1 - physiopathology
DNA structure
DNA-Binding Proteins - metabolism
Epstein-Barr virus
Glucose tolerance
Herpes viruses
Humans
Hypersensitivity
Immunohistochemistry
Immunological tolerance
Inflammation
Insulin-Secreting Cells - metabolism
Insulin-Secreting Cells - virology
Interferon regulatory factor
Interferon regulatory factor 3
Interferon Regulatory Factor-3 - metabolism
Localization
Lymphocytes T
Macrophages
Male
Pancreas
Reference Values
Retinoic acid
Severity of Illness Index
Statistics, Nonparametric
Virus Activation
Z-form
Title A Histological Study of Fulminant Type 1 Diabetes Mellitus Related to Human Cytomegalovirus Reactivation
URI https://www.ncbi.nlm.nih.gov/pubmed/28398495
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