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Beneficial Effects of Human Anti-Interleukin-15 Antibody in Gluten-Sensitive Rhesus Macaques with Celiac Disease.
Sestak, Karol; Dufour, Jason P; Liu, David X; Rout, Namita; Alvarez, Xavier; Blanchard, James; Faldas, Anne; Laine, David J; Clarke, Adam W; Doyle, Anthony G.
Afiliação
  • Sestak K; Division of Microbiology, Tulane National Primate Research Center, Covington, LA, United States.
  • Dufour JP; PreCliniTria LLC, Mandeville, LA, United States.
  • Liu DX; Division of Veterinary Medicine, Tulane National Primate Research Center, Covington, LA, United States.
  • Rout N; Division of Clinical Research, Integrated Research Facility, National Institute of Allergy and Infectious Disease, Frederick, MD, United States.
  • Alvarez X; Division of Immunology, Tulane National Primate Research Center, Covington, LA, United States.
  • Blanchard J; Division of Comparative Pathology, Tulane National Primate Research Center, Covington, LA, United States.
  • Faldas A; Division of Veterinary Medicine, Tulane National Primate Research Center, Covington, LA, United States.
  • Laine DJ; Teva Pharmaceuticals, R&D, Biologics, Lead Antibody Discovery, Sydney, NSW, Australia.
  • Clarke AW; Teva Pharmaceuticals, R&D, Biologics, Lead Antibody Discovery, Sydney, NSW, Australia.
  • Doyle AG; Teva Pharmaceuticals, R&D, Biologics, Lead Antibody Discovery, Sydney, NSW, Australia.
Front Immunol ; 9: 1603, 2018.
Article em En | MEDLINE | ID: mdl-30050538
ABSTRACT
Overexpression of interleukin-15 (IL-15) is linked with immunopathology of several autoimmune disorders including celiac disease. Here, we utilized an anti-human IL-15 antibody 04H04 (anti-IL-15) to reverse immunopathogenesis of celiac disease. Anti-IL-15 was administered to six gluten-sensitive rhesus macaques with celiac disease characteristics including gluten-sensitive enteropathy (GSE), and the following celiac-related metrics were evaluated morphology (villous height/crypt depth ratio) of small intestine, counts of intestinal intraepithelial lymphocytes, IFN-γ-producing CD8+ and CD4+ T cells, plasma levels of anti-gliadin and anti-intestinal tissue transglutaminase IgG antibodies, as well as peripheral effector memory (CD3+CD28-CD95+) T cells. Anti-IL-15 treatment reversed the clinically relevant disease endpoints, intraepithelial lymphocyte counts, and villous height/crypt depth ratios within jejunal biopsies to normal levels (P < 0.001). Additionally, intestinal CD8+ and CD4+ T cell IFN-γ production was reduced (P < 0.05). Extra-intestinally, anti-IL-15 treatment reduced peripheral NK cell counts (P < 0.001), but otherwise, non-NK peripheral lymphocytes including effector memory T cells and serum blood chemistry were unaffected. Overall, providing the beneficial disease-modulatory and immunomodulatory effects observed, anti-IL-15 treatment might be considered as a novel therapy to normalize intestinal lymphocyte function in celiac disease patients with GSE.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies Idioma: En Revista: Front Immunol Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies Idioma: En Revista: Front Immunol Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Estados Unidos