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Rationale for enteroviral vaccination and antiviral therapies in human type 1 diabetes

Dunne, Jessica L. (author)
Juvenile Diabetes Research Foundation
Richardson, Sarah J. (author)
University of Exeter
Atkinson, Mark A. (author)
University of Florida
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Craig, Maria E. (author)
University of New South Wales
Dahl-Jørgensen, Knut (author)
University of Oslo,Oslo university hospital
Flodström-Tullberg, Malin (author)
Karolinska Institutet,Karolinska Institute,Karolinska University Hospital
Hyöty, Heikki (author)
University of Tampere,Pirkanmaa Hospital District
Insel, Richard A. (author)
Insel Consulting, LLC
Lernmark, Åke (author)
Lund University,Lunds universitet,Celiaki och diabetes,Forskargrupper vid Lunds universitet,Celiac Disease and Diabetes Unit,Lund University Research Groups,Skåne University Hospital
Lloyd, Richard E. (author)
Baylor College of Medicine
Morgan, Noel G. (author)
University of Exeter
Pugliese, Alberto (author)
University of Miami
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 (creator_code:org_t)
2019-01-23
2019
English.
In: Diabetologia. - : Springer Science and Business Media LLC. - 0012-186X .- 1432-0428. ; 62:5, s. 744-753
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • In type 1 diabetes, pancreatic beta cells are destroyed by chronic autoimmune responses. The disease develops in genetically susceptible individuals, but a role for environmental factors has been postulated. Viral infections have long been considered as candidates for environmental triggers but, given the lack of evidence for an acute, widespread, cytopathic effect in the pancreas in type 1 diabetes or for a closely related temporal association of diabetes onset with such infections, a role for viruses in type 1 diabetes remains unproven. Moreover, viruses have rarely been isolated from the pancreas of individuals with type 1 diabetes, mainly (but not solely) due to the inaccessibility of the organ. Here, we review past and recent literature to evaluate the proposals that chronic, recurrent and, possibly, persistent enteroviral infections occur in pancreatic beta cells in type 1 diabetes. We also explore whether these infections may be sustained by different virus strains over time and whether multiple viral hits can occur during the natural history of type 1 diabetes. We emphasise that only a minority of beta cells appear to be infected at any given time and that enteroviruses may become replication defective, which could explain why they have been isolated from the pancreas only rarely. We argue that enteroviral infection of beta cells largely depends on the host innate and adaptive immune responses, including innate responses mounted by beta cells. Thus, we propose that viruses could play a role in type 1 diabetes on multiple levels, including in the triggering and chronic stimulation of autoimmunity and in the generation of inflammation and the promotion of beta cell dysfunction and stress, each of which might then contribute to autoimmunity, as part of a vicious circle. We conclude that studies into the effects of vaccinations and/or antiviral drugs (some of which are currently on-going) is the only means by which the role of viruses in type 1 diabetes can be finally proven or disproven.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Endokrinologi och diabetes (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Endocrinology and Diabetes (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Infektionsmedicin (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Infectious Medicine (hsv//eng)

Keyword

Antiviral therapy
Autoimmunity
Beta cells
Enterovirus
Pancreas
Prevention
Type 1 diabetes
Vaccine
Virus

Publication and Content Type

art (subject category)
ref (subject category)

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