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 in | The journal of clinical endocrinology and metabolism Vol. 102; no. 7; pp. 2394 - 2400 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Washington, DC
Endocrine Society
01.07.2017
Copyright Oxford University Press Oxford University Press |
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Online Access | Get full text |
ISSN | 0021-972X 1945-7197 1945-7197 |
DOI | 10.1210/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. |
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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 |
Author_xml | – sequence: 1 givenname: Sho surname: Yoneda fullname: Yoneda, Sho organization: 1Department of Metabolic Medicine, Graduate School of Medicine, Osaka University, Suita “565-0871”, Japan – sequence: 2 givenname: Akihisa surname: Imagawa fullname: Imagawa, Akihisa email: imagawa@osaka-med.ac.jp organization: 1Department of Metabolic Medicine, Graduate School of Medicine, Osaka University, Suita “565-0871”, Japan – sequence: 3 givenname: Kenji surname: Fukui fullname: Fukui, Kenji organization: 1Department of Metabolic Medicine, Graduate School of Medicine, Osaka University, Suita “565-0871”, Japan – sequence: 4 givenname: Sae surname: Uno fullname: Uno, Sae organization: 1Department of Metabolic Medicine, Graduate School of Medicine, Osaka University, Suita “565-0871”, Japan – sequence: 5 givenname: Junji surname: Kozawa fullname: Kozawa, Junji organization: 1Department of Metabolic Medicine, Graduate School of Medicine, Osaka University, Suita “565-0871”, Japan – sequence: 6 givenname: Makoto surname: Sakai fullname: Sakai, Makoto organization: 3Internal Medicine, Konan Hospital, Kobe “658-0064”, Japan – sequence: 7 givenname: Toshiki surname: Yumioka fullname: Yumioka, Toshiki organization: 3Internal Medicine, Konan Hospital, Kobe “658-0064”, Japan – sequence: 8 givenname: Hiromi surname: Iwahashi fullname: Iwahashi, Hiromi organization: 1Department of Metabolic Medicine, Graduate School of Medicine, Osaka University, Suita “565-0871”, Japan – sequence: 9 givenname: Iichiro surname: Shimomura fullname: Shimomura, Iichiro organization: 1Department of Metabolic Medicine, Graduate School of Medicine, Osaka University, Suita “565-0871”, Japan |
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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 |
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