Abstract
Epidemiological studies have associated coxsackie B virus (CBV) with the development of insulin-dependent diabetes mellitus (IDDM) in humans. Infections of genetically susceptible mice with CBV strain 4 (CB4) induce autoimmune diabetes. Herein, we demonstrate that in mice, CB4 infection of insulin-producing pancreatic β cells does not directly cause β cell death. Instead, we observed the phagocytosis of β cells by macrophages following infection. Further, antigen-presenting cells isolated from CB4-infected mice induced diabetes upon adoptive transfer. Therefore, the specificity of CB4 for infection of β cells leads indirectly to the development of IDDM. This generalized mechanism suggests that macrophages are the initiating pathogenic cell type during virus-mediated autoimmune diabetes and that multiple environmental agents specific for β cells could cause IDDM.
Original language | English (US) |
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Pages (from-to) | 134-144 |
Number of pages | 11 |
Journal | Clinical Immunology |
Volume | 110 |
Issue number | 2 |
DOIs | |
State | Published - Feb 2004 |
Externally published | Yes |
Keywords
- Antigen-presenting cells
- Coxsackievirus
- Insulin-dependent diabetes mellitus
- T lymphocytes
ASJC Scopus subject areas
- Immunology and Allergy
- Immunology