Sandbox: spontaneous bacterial peritonitis: Difference between revisions

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# '''Epithelial barrier with the gut-associated lymphatic tissue (GALT) and autonomic nervous system''': This is a mechanical barrier with local immunological response elements (e.g., TNF and other pro-inflammatory cytokines) that  rapidly detects and kill the pathogen that manage to penetrate
# '''Epithelial barrier with the gut-associated lymphatic tissue (GALT) and autonomic nervous system''': This is a mechanical barrier with local immunological response elements (e.g., TNF and other pro-inflammatory cytokines) that  rapidly detects and kill the pathogen that manage to penetrate
# '''Systemic immune system:''' This includes hematogenous (portal venous) and lymphatic (ductus thoracicus) route of delivery that acts as a third immune barrier to prevent or minimize the pathogen to disseminate systemically from local immune system such as lymph nodes.
# '''Systemic immune system:''' This includes hematogenous (portal venous) and lymphatic (ductus thoracicus) route of delivery that acts as a third immune barrier to prevent or minimize the pathogen to disseminate systemically from local immune system such as lymph nodes.
'''Mechanism of pathological bacterial translocation'''
Breaking these immune barriers can progress physiological BT into pathological BT.
Breaking these immune barriers can progress physiological BT into pathological BT.



Revision as of 19:18, 26 January 2017

Overview

Spontaneous bacterial peritonitis(SBP) is an advanced clinical expression of a pathological bacterial translocation as it develops from normal inhabitant gut bacteria through breakage of immune barriers.[1]

Pathogenesis

Bacterial Translocation

It is defined as the translocation of either bacteria or bacterial products such as lipopolysacharides (LPS), bacterial DNA, peptidoglycans, muramyl-dipeptides from gut into mesenteric lymph nodes.[2]

Physiological: It is the normal bacterial translocation in healthy individuals due to lack of pro-inflammatory responses against commensal bacteria. Physiological translocation is crucial for the development of host immunity response.

Pathological: It is developed due to abnormal increase in physiological translocation in both rate and degree by breaking the normal immunological barriers.

Barriers that limit pathological transmission:

  1. Interstinal lumen and it's secretory components such as inner and outer mucus layer, antimicrobial peptides: This is the primary barrier that limit direct contact between the intestinal bacteria and the epithelial cell surface
  2. Epithelial barrier with the gut-associated lymphatic tissue (GALT) and autonomic nervous system: This is a mechanical barrier with local immunological response elements (e.g., TNF and other pro-inflammatory cytokines) that rapidly detects and kill the pathogen that manage to penetrate
  3. Systemic immune system: This includes hematogenous (portal venous) and lymphatic (ductus thoracicus) route of delivery that acts as a third immune barrier to prevent or minimize the pathogen to disseminate systemically from local immune system such as lymph nodes.

Mechanism of pathological bacterial translocation

Breaking these immune barriers can progress physiological BT into pathological BT.

References