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Cellular and Humoral Immune responses in Type 1 Diabetic patients participating in a Phase III GAD-alum Intervention Trial

Axelsson, Stina (author)
Linköpings universitet,Avdelningen för kliniska vetenskaper,Hälsouniversitetet
Cheramy, Mikael (author)
Linköpings universitet,Avdelningen för kliniska vetenskaper,Hälsouniversitetet
Åkerman, Linda (author)
Linköpings universitet,Avdelningen för kliniska vetenskaper,Hälsouniversitetet
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Pihl, Mikael (author)
Linköpings universitet,Avdelningen för kliniska vetenskaper,Hälsouniversitetet
Ludvigsson, Johnny (author)
Östergötlands Läns Landsting,Linköpings universitet,Avdelningen för kliniska vetenskaper,Hälsouniversitetet,Barn- och ungdomskliniken i Linköping
Casas, Rosaura (author)
Linköpings universitet,Avdelningen för kliniska vetenskaper,Hälsouniversitetet
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 (creator_code:org_t)
2013-10-15
2013
English.
In: Diabetes Care. - : American Diabetes Association. - 0149-5992 .- 1935-5548. ; 36:11, s. 3418-3424
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • OBJECTIVEGAD formulated in aluminum hydroxide (GAD-alum) has previously been shown to induce preservation of residual insulin secretion in recent-onset type 1 diabetes, but recent phase II and III GAD-alum trials failed to reach primary outcomes. The European phase III study was therefore closed after 15 months, and only a minority of patients completed the 30 months of follow-up.RESEARCH DESIGN AND METHODSThis study aimed to characterize cellular and humoral responses in the Swedish patients (n = 148) participating in the phase III trial, receiving four (4D) or two (2D) GAD-alum doses or placebo. Serum GAD(65) antibody (GADA) levels, GADA IgG1-4 subclass distribution, cytokine secretion, and proliferative responses in peripheral blood mononuclear cells (PBMCs) were analyzed.RESULTSThe GAD(65)-induced cytokine profile tended to switch toward a predominant Th2-associated profile over time both in the 2D and 4D group. The groups also displayed increased GADA levels and PBMC proliferation compared with placebo, whereas GADA IgG subclass distribution changed in 4D patients.CONCLUSIONSBoth 2D and 4D patients displayed GAD(65)-specifc cellular and humoral effects after GAD-alum treatment, but at different time points and magnitudes. No specific immune markers could be associated with treatment efficacy.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine (hsv//eng)

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By the author/editor
Axelsson, Stina
Cheramy, Mikael
Åkerman, Linda
Pihl, Mikael
Ludvigsson, John ...
Casas, Rosaura
About the subject
MEDICAL AND HEALTH SCIENCES
MEDICAL AND HEAL ...
and Clinical Medicin ...
Articles in the publication
Diabetes Care
By the university
Linköping University

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