Functional redundancy of CXCR3/CXCL10 signaling in the recruitment of diabetogenic cytotoxic T lymphocytes to pancreatic islets in a virally induced autoimmune diabetes model

Diabetes

Volumn 62, Issue 7, 2013, Pages 2492-2499

  Coppieters, Ken T ^a,b   Amirian, Natalie ^a   Pagni, Philippe P ^a   Jones, Carmen B ^a   Wiberg, Anna ^a   Lasch, Stanley ^c   Hintermann, Edith ^c   Christen, Urs ^c   Von Herrath, Matthias G ^a,b  

^a LA JOLLA INSTITUTE FOR ALLERGY AND IMMUNOLOGY   (United States)

^b NOVO NORDISK INC   (United States)

^c UNIVERSITY HOSPITAL FRANKFURT   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

CHEMOKINE RECEPTOR CXCR3; GAMMA INTERFERON INDUCIBLE PROTEIN 10; CXCL10 PROTEIN, MOUSE; CXCR3 PROTEIN, MOUSE; NEUTRALIZING ANTIBODY;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CELL DEATH; CELL MIGRATION; CONTROLLED STUDY; CYTOTOXIC T LYMPHOCYTE; DISEASE COURSE; INSULIN DEPENDENT DIABETES MELLITUS; MOUSE; NONHUMAN; PANCREAS; PANCREAS ISLET; PANCREAS ISLET BETA CELL; PRIORITY JOURNAL; PROTEIN PROTEIN INTERACTION; SIGNAL TRANSDUCTION; UPREGULATION; VIRAL CLEARANCE; ANIMAL; DRUG ANTAGONISM; EXPERIMENTAL DIABETES MELLITUS; IMMUNOLOGY; VIROLOGY;

ANIMALS; ANTIBODIES, NEUTRALIZING; CHEMOKINE CXCL10; DIABETES MELLITUS, EXPERIMENTAL; DIABETES MELLITUS, TYPE 1; ISLETS OF LANGERHANS; MICE; RECEPTORS, CXCR3; SIGNAL TRANSDUCTION; T-LYMPHOCYTES, CYTOTOXIC;

EID: 84883667327     PISSN: 00121797     EISSN: 1939327X     Source Type: Journal    
DOI: 10.2337/db12-1370     Document Type: Article

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