1. Volume 61, Issue 2, Pages 439-445 (August 2014)
Modulation of monocyte/macrophage function: A therapeutic strategy in the treatment of acute liver failure 
Lucia A. Possamai, Mark R. Thursz, Julia A. Wendon, Charalambos Gustav Antoniades 
Journal of Hepatology 
Volume 61, Issue 2, Pages (August 2014)
DOI: /j.jhep
Copyright © 2014 European Association for the Study of the Liver Terms and Conditions

2. Fig. 1
A simplified model of monocyte and macrophage function in acute liver failure. KCs detect hepatocyte death through DAMP/TLR signalling and initiate a pro-inflammatory response. Bone-marrow derived monocytes traffic to the liver to contribute to an expanded macrophage population which are initially pro-inflammatory. During the propagation phase, immune activation is self-perpetuating with recruitment of effectors driving further cytokine and chemokine production. The release of cytokines and vasoactive mediators into the systemic circulation provokes SIRS. Macrophage-derived mediators contribute to vascular endothelial dysfunction and microcirculatory disturbances that result in extra-hepatic organ dysfunction. Later, the presence of pro-resolution macrophages aids tissue recovery. The spill over of anti-inflammatory mediators from the liver into the circulation contributes to functional monocyte deactivation and an increased susceptibility to sepsis.
Journal of Hepatology  , DOI: ( /j.jhep )
Copyright © 2014 European Association for the Study of the Liver Terms and Conditions

3. Fig. 2
Microenvironmental mediators are key determinants of macrophage functional polarization. This simplified schematic shows how the dominant microenvironmental mediators can reversibly influence macrophage function. In the presence of TLR ligands and IFNγ, macrophages adopt a ‘M1-like’ profile with high expression levels of pro-inflammatory cytokines, including IL-12 and IL-23. If the local microenvironment contains anti-inflammatory signals such as glucocorticoids, SPMs (e.g., resolvins, maresins), and IL-10 an ‘M2-like’ activation state is induced. These phenotypes are simplified, with numerous potential macrophage phenotypes possible, which are likely to be tissue-specific and depend on the precise tissue milieu at different stages of disease.
Journal of Hepatology  , DOI: ( /j.jhep )
Copyright © 2014 European Association for the Study of the Liver Terms and Conditions

4. Fig. 3
A schematic representation of mechanistic biomarkers in acute liver failure. Biomarkers may help to define the stage of hepatic injury in acute liver failure and guide the timing of potential immune therapies. The initiation stage is characterised by the presence of biomarkers of hepatocyte death, which peak early and decline. Markers of macrophage activation are also elevated early in the course of ALF, but tend to persist. Late markers of regeneration and immunosuppression characterise the regenerative phase. This model is simplified and the dynamic changes of these biomarkers are likely to be most instructive (i.e., falling cell death markers, with rising macrophage activation markers).
Journal of Hepatology  , DOI: ( /j.jhep )
Copyright © 2014 European Association for the Study of the Liver Terms and Conditions

5. Journal of Hepatology 2014 61, 439-445DOI: (10. 1016/j. jhep. 2014. 03
Copyright © 2014 European Association for the Study of the Liver Terms and Conditions