نتایج جستجو برای: hla dq8

تعداد نتایج: 40088  

2016
Isabelle Serr Rainer W. Fürst Peter Achenbach Martin G. Scherm Füsun Gökmen Florian Haupt Eva-Maria Sedlmeier Annette Knopff Leonard Shultz Richard A. Willis Anette-Gabriele Ziegler Carolin Daniel

Immune tolerance is executed partly by Foxp3(+)regulatory T (Treg) cells, which suppress autoreactive T cells. In autoimmune type 1 diabetes (T1D) impaired tolerance promotes destruction of insulin-producing β-cells. The development of autoantigen-specific vaccination strategies for Foxp3(+)Treg-induction and prevention of islet autoimmunity in patients is still in its infancy. Here, using huma...

2017
Anna Parkkola Antti-Pekka Laine Markku Karhunen Taina Härkönen Samppa J Ryhänen Jorma Ilonen Mikael Knip

Genetic predisposition could be assumed to be causing clustering of autoimmunity in individuals and families. We tested whether HLA and non-HLA loci associate with such clustering of autoimmunity. We included 1,745 children with type 1 diabetes from the Finnish Pediatric Diabetes Register. Data on personal or family history of autoimmune diseases were collected with a structured questionnaire a...

Journal: :Gut 2003
K E A Lundin L M Sollid

espite its heterogeneous clinical appearance, coeliac disease has a remarkable uniform human leuco-cyte antigen (HLA) association. The majority of coeliac disease patients carry a certain variant of HLA-DQ2, the rest carry HLA-DQ8. 1 2 As the physiological role of the HLA system is to present pep-tide fragments of antigens to T cells, it would seem logical that the HLA-DQ2 and HLA-DQ8 molecules...

Journal: :The Journal of clinical investigation 2010
Kenji Yoshida Adam L Corper Rana Herro Bana Jabri Ian A Wilson Luc Teyton

Genetic susceptibility to autoimmunity is frequently associated with specific MHC alleles. Diabetogenic MHC class II molecules, such as human HLA-DQ8 and mouse I-Ag7, typically have a small, uncharged amino acid residue at position 57 of their beta chain (beta57); this results in the absence of a salt bridge between beta57 and Argalpha76, which is adjacent to the P9 pocket of the peptide-bindin...

Journal: :Blood 1996
J Gaschet M A Treviño M Cherel R Vivien A Garcia-Sahuquillo M M Hallet M Bonneville J L Harrousseau R Bragado N Milpied H Vié

To study the repertoire and specificity of T lymphocytes infiltrating skin lesions during graft-versus-host disease (GVHD), we performed an exhaustive molecular and functional analysis of 146 T-cell clones derived from the skin of three patients undergoing an acute GVHD after allogeneic bone marrow transplantation (BMT) from HLA-mismatched related donors. Analysis of T-cell receptor (TCR) rearr...

Journal: :Revista espanola de enfermedades digestivas : organo oficial de la Sociedad Espanola de Patologia Digestiva 2011
Luis Rodrigo Sáez Dolores Fuentes Álvarez Isabel Pérez Martínez Noemí Alvarez Mieres Pilar Niño García Ruth de Francisco García Sabino Riestra Menéndez Santiago Vivas Alegre José Luis Olcoz Goñi

INTRODUCTION refractory iron-deficiency anemia has a multifactorial origin related to various gastrointestinal conditions, with celiac disease plus malabsorption and IBD together with isolated gluten intolerance being most common. OBJECTIVES to determine the prevalence of serum, genetic, and histological markers for gluten intolerance, and to analyze the response to gluten withdrawal from the...

Journal: :Vestnik Rossiiskoi akademii meditsinskikh nauk 2015
I I Dedov M V Shestakova T L Kuraeva E V Titovich T V Nikonova

Article is devoted to the review of literature data, and also the analysis of results of own researches concerning genetics, molecular genetics and immunological violations at various forms of the autoimmune diabetes (DM) including classical T1DM, LADA type and an autoimmune polyglandular syndrome of 1 type (APS1). In case of T1DM more than 80% of patients are carriers of one or two strongest p...

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