Your browser doesn't support javascript.
loading
Circulating immune signatures in chronic pancreatitis with and without preceding acute pancreatitis: A pilot study.
Hagn-Meincke, Rasmus; Yadav, Dhiraj; Andersen, Dana K; Vege, Santhi Swaroop; Fogel, Evan L; Serrano, Jose; Bellin, Melena D; Topazian, Mark D; Conwell, Darwin L; Li, Liang; Van Den Eeden, Stephen K; Drewes, Asbjørn M; Pandol, Stephen J; Forsmark, Chris E; Fisher, William E; Hart, Phil A; Olesen, Søren S; Park, Walter G.
Afiliación
  • Hagn-Meincke R; Centre for Pancreatic Diseases and Mech-Sense, Department of Gastroenterology & Hepatology, Aalborg University Hospital, Aalborg, Denmark; Division of Gastroenterology and Hepatology, Department of Medicine, Stanford University School of Medicine, Stanford, CA, USA.
  • Yadav D; Division of Gastroenterology, Hepatology and Nutrition, University of Pittsburgh, Pittsburgh, PA, USA.
  • Andersen DK; Division of Digestive Diseases and Nutrition, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD, USA.
  • Vege SS; Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN, USA.
  • Fogel EL; Division of Gastroenterology and Hepatology, Department of Medicine, Indiana University School of Medicine, Indianapolis, IN, USA.
  • Serrano J; Division of Digestive Diseases and Nutrition, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD, USA.
  • Bellin MD; Division of Pediatric Endocrinology, University of Minnesota, Minnesota, MN, USA.
  • Topazian MD; Division of Digestive Diseases and Nutrition, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD, USA.
  • Conwell DL; Department of Medicine, University of Kentucky, Lexington, KY, USA.
  • Li L; Department of Biostatistics, MD Anderson Cancer Center, Houston, TX, USA.
  • Van Den Eeden SK; Division of Research, Kaiser Permanente Northern California, Oakland, CA, USA.
  • Drewes AM; Centre for Pancreatic Diseases and Mech-Sense, Department of Gastroenterology & Hepatology, Aalborg University Hospital, Aalborg, Denmark.
  • Pandol SJ; Division of Digestive and Liver Diseases, Cedars-Sinai Medical Center, Los Angeles, CA, USA.
  • Forsmark CE; Division of Gastroenterology, Hepatology, and Nutrition. University of Florida, Gainesville, FL, USA.
  • Fisher WE; Division of General Surgery, Baylor College of Medicine, Houston, TX, USA.
  • Hart PA; Division of Gastroenterology, Hepatology, and Nutrition, The Ohio State University Wexner Medical Center, Columbus, OH, USA.
  • Olesen SS; Centre for Pancreatic Diseases and Mech-Sense, Department of Gastroenterology & Hepatology, Aalborg University Hospital, Aalborg, Denmark.
  • Park WG; Division of Gastroenterology and Hepatology, Department of Medicine, Stanford University School of Medicine, Stanford, CA, USA. Electronic address: wgpark@stanford.edu.
Pancreatology ; 24(3): 384-393, 2024 May.
Article en En | MEDLINE | ID: mdl-38461145
ABSTRACT

OBJECTIVE:

To investigate profiles of circulating immune signatures in healthy controls and chronic pancreatitis patients (CP) with and without a preceding history of acute pancreatitis (AP).

METHODS:

We performed a phase 1, cross-sectional analysis of prospectively collected serum samples from the PROspective Evaluation of Chronic Pancreatitis for EpidEmiologic and Translation StuDies (PROCEED) study. All samples were collected during a clinically quiescent phase. CP subjects were categorized into two subgroups based on preceding episode(s) of AP. Healthy controls were included for comparison. Blinded samples were analyzed using an 80-plex Luminex assay of cytokines, chemokines, and adhesion molecules. Group and pairwise comparisons of analytes were performed between the subgroups.

RESULTS:

In total, 133 patients with CP (111 with AP and 22 without AP) and 50 healthy controls were included. Among the 80 analytes studied, CP patients with a history of AP had significantly higher serum levels of pro-inflammatory cytokines (interleukin (IL)-6, IL-8, IL-1 receptor antagonist, IL-15) and chemokines (Cutaneous T-Cell Attracting Chemokine (CTACK), Monokine induced Gamma Interferon (MIG), Macrophage-derived Chemokine (MDC), Monocyte Chemoattractant Protein-1 (MCP-1)) compared to CP without preceding AP and controls. In contrast, CP patients without AP had immune profiles characterized by low systemic inflammation and downregulation of anti-inflammatory mediators, including IL-10.

CONCLUSION:

CP patients with a preceding history of AP have signs of systemic inflammatory activity even during a clinically quiescent phase. In contrast, CP patients without a history of AP have low systemic inflammatory activity. These findings suggest the presence of two immunologically diverse subtypes of CP.
Asunto(s)
Palabras clave

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Citocinas / Pancreatitis Crónica Idioma: En Revista: Pancreatology Asunto de la revista: ENDOCRINOLOGIA / GASTROENTEROLOGIA Año: 2024 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Citocinas / Pancreatitis Crónica Idioma: En Revista: Pancreatology Asunto de la revista: ENDOCRINOLOGIA / GASTROENTEROLOGIA Año: 2024 Tipo del documento: Article