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Multiorgan dysfunction syndrome in sepsis: Is macrophage activation syndrome secondary to infection?
Arnab Nandy1, Tanushree Mondal2, Mihir Sarkar3
1Department of Pediatrics, NB Medical College, Darjeeling, India.
Insights
Macrophage activation syndrome (MAS) significantly increases in children with septic shock progressing to multiorgan dysfunction syndrome (MODS). MAS is a key factor in sepsis-induced MODS, warranting further research for therapeutic strategies.
Area of Science:
- Pediatric critical care medicine
- Rheumatology
- Immunology
Background:
- Sepsis is a life-threatening organ dysfunction caused by dysregulated host response to infection.
- Macrophage activation syndrome (MAS) is a severe, hyperinflammatory condition.
- The relationship between MAS and multiorgan dysfunction syndrome (MODS) in pediatric septic shock requires further elucidation.
Purpose of the Study:
- To investigate the prevalence and progression of macrophage activation syndrome (MAS) in children experiencing septic shock.
- To determine if MAS is a contributing factor to the development of multiorgan dysfunction syndrome (MODS) in pediatric septic shock.
Main Methods:
- A prospective observational study involving 127 children (6 months to 12 years) with septic shock.
- Application of the Paediatric Rheumatology International Trials Organisation Collaborative Initiative (PRINTO) criteria for MAS at different stages of sepsis.
- Comparison of MAS criteria fulfillment between patients who progressed to MODS and those who recovered without MODS.
Main Results:
- At initial septic shock assessment, MAS criteria were met by comparable proportions of subjects in both eventual MODS and non-MODS groups (approx. 20-25%).
- By the time of MODS progression, 81.13% of the MODS cohort met MAS criteria, compared to 16.18% in the non-MODS cohort (p<0.001).
- A significant increase in MAS prevalence was observed as sepsis progressed to MODS, while it declined in recovered patients.
Conclusions:
- The study supports the hypothesis that MODS in pediatric sepsis is a manifestation of MAS secondary to the infection.
- Findings suggest a strong link between MAS and the development of MODS in pediatric septic shock.
- Larger cohort studies are recommended to validate these findings and explore potential therapeutic interventions targeting MAS in sepsis.
Objective:
To assess macrophage activation syndrome (MAS) in septic shock leading to multiorgan dysfunction syndrome (MODS).
Methods:
A prospective observational study was conducted at a tertiary care hospital to evaluate the MAS criteria in different stages of sepsis. Children aged 6 months to 12 years in different stages of septic shock were recruited. The Paediatric Rheumatology International Trials Organisation Collaborative Initiative (PRINTO) criteria of MAS were applied initially at the stage of septic shock and subsequently at the stage of MODS (MODS cohort) or following recovery from septic shock without going through MODS (non-MODS cohort).
Results:
A total of 127 subjects were studied, with 53 comprising the MODS cohort and the rest 74 the non-MODS cohort. At the initial assessment, a comparable proportion of subjects in the MODS and non-MODS groups satisfied the MAS criteria (20.75% and 25.68%, respectively; p=0.529). However, by the time of progression to MODS, 81.13% of the subjects satisfied the MAS criteria in the MODS group, whereas only 16.18% subjects in the non-MODS group continued to satisfy the MAS criteria (p<0.001). Thus, there was a definite increase in the proportion of subjects showing MAS by the time they progressed to multiorgan dysfunction (p<0.001). In contrast, the proportion declined significantly (25.68% to 16.18%; p=0.008) in the subjects who had recovered.
Conclusion:
The findings bear out the hypothesis that MODS in sepsis is a reflection of MAS secondary to sepsis. However, studies in larger cohorts are needed to validate these findings and explore the therapeutic implications.
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