Primary biliary cholangitis: a comprehensive overview

Primary biliary cholangitis (PBC) is an autoimmune liver disease characterized by biliary destruction, progressive cholestasis, and potentially liver cirrhosis. Patients develop a well-orchestrated immune reaction, both innate and adaptive, against mitochondrial antigens that specifically targets in...

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Autores:

Tipo de recurso:

Fecha de publicación:

2017

Institución:

Universidad del Rosario

Repositorio:

Repositorio EdocUR - U. Rosario

Idioma:

eng

OAI Identifier:

oai:repository.urosario.edu.co:10336/24193

Acceso en línea:

https://doi.org/10.1007/s12072-017-9830-1
https://repository.urosario.edu.co/handle/10336/24193

Palabra clave:

Alkaline phosphatase
Budesonide
Fibric acid derivative
Immunosuppressive agent
Mitochondrion antibody
Obeticholic acid
Ursodeoxycholic acid
Antiinflammatory agent
Budesonide
Chenodeoxycholic acid
Cholagogue
Immunosuppressive agent
Obeticholic acid
Adaptive immunity
Autoimmune disease
Clinical feature
Disease course
End stage liver disease
Histopathology
Human
Immunofluorescence
Innate immunity
Liver biopsy
Liver transplantation
Nonhuman
Pathogenesis
Pathophysiology
Patient care
Primary biliary cirrhosis
Priority journal
Prognosis
Review
Risk factor
Treatment response
Analogs and derivatives
Autoimmune disease
Biopsy
Cholangitis
Immunology
Liver
Pathology
Anti-inflammatory agents
Autoimmune diseases
Biopsy
Budesonide
Chenodeoxycholic acid
Cholagogues and choleretics
Cholangitis
Fibric acids
Humans
Immunosuppressive agents
Liver
Prognosis
Ursodeoxycholic acid
Antimitochondrial antibodies
Biliary epithelial cells
Epigenetics
Genetics
Obeticholic acid
Primary biliary cholangitis
Prognostic factors
Udca

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