Human cytomegalovirus in the pancreas of patients with type 2 diabetes: is there a relation to clinical features, mRNA and protein expression of insulin, somatostatin, and MHC class II?

Virchows Arch A Pathol Anat Histopathol. 1992;421(5):371-8. doi: 10.1007/BF01606908.

Abstract

Human cytomegalovirus (HCMV) was recently demonstrated in the pancreas of about half the patients with type 2 diabetes mellitus in the absence of mumps, rubella or Coxsackie B virus. The present study addresses the question as to whether type 2 diabetes with an HCMV-positive pancreas differs from those with HCMV-negative pancreases with respect to age, sex, treatment, duration of disease, volume densities of B-cells and D-cells, mRNA levels of insulin and somatostatin, islet amyloid peptide deposits and major histocompatibility complex (MHC) class I and class II gene transcription, and protein expression. HCMV-positive type 2 diabetic patients showed a tendency towards a shorter duration of disease and significantly increased levels of MHC class II on RNA. In addition, expression of MHC class II product (HLA-DR) was identified in duct epithelial cells and/or islet cells in 9 diabetic pancreases and in 2 non-diabetic glands. No MHC class I expression could be detected. No other clinical differences between HCMV-positive and HCMV-negative glands were found. All 10 HCMV-positive diabetics showed a strong expression of MHC class II mRNA in the pancreas. By immunocytochemistry, 4 of 10 demonstrated expression on the islets; three of ten also expressed MHC DR beta on ductal cells. This finding might be related to the viral infection, as only 2 of the 9 HCMV-negative patients were HLA-DR beta positive and none of the non-diabetic controls showed increased levels of MHC class II mRNA. These data suggest that HCMV infection in the pancreas is associated with type 2 diabetes. However, no conclusions as to a role of this virus in the aetiopathology of type 2 diabetes can be drawn at present.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Aged
  • Aged, 80 and over
  • Amyloid / analysis
  • Amyloid / metabolism
  • Amyloidosis / complications
  • Amyloidosis / metabolism
  • Cytomegalovirus / genetics*
  • Cytomegalovirus / isolation & purification*
  • Cytomegalovirus / physiology
  • Cytomegalovirus Infections / complications*
  • Cytomegalovirus Infections / genetics*
  • Cytomegalovirus Infections / pathology
  • DNA, Viral / analysis
  • DNA, Viral / genetics
  • Diabetes Mellitus, Type 2 / complications*
  • Diabetes Mellitus, Type 2 / genetics*
  • Diabetes Mellitus, Type 2 / microbiology
  • Female
  • Gene Expression / genetics*
  • Histocompatibility Antigens Class II / analysis
  • Histocompatibility Antigens Class II / genetics*
  • Humans
  • Immunohistochemistry
  • In Situ Hybridization
  • Insulin / analysis
  • Insulin / genetics*
  • Islets of Langerhans / pathology
  • Male
  • Middle Aged
  • Pancreas / chemistry
  • Pancreas / microbiology*
  • Pancreas / pathology
  • Pancreatic Diseases / complications
  • Pancreatic Diseases / metabolism
  • RNA, Messenger / analysis*
  • RNA, Messenger / genetics
  • Somatostatin / analysis
  • Somatostatin / genetics*

Substances

  • Amyloid
  • DNA, Viral
  • Histocompatibility Antigens Class II
  • Insulin
  • RNA, Messenger
  • Somatostatin