Disease Tolerance during Viral-Bacterial Co-Infections
Tarani Kanta Barman1, Dennis W Metzger1
1Department of Immunology and Microbial Disease, Albany Medical College, Albany, NY 12208, USA.
Disease tolerance helps hosts survive viral and bacterial co-infections by controlling organ damage, not pathogen load. This review details host cytokines and immune cells crucial for recovery and survival.
Area of Science:
- Immunology
- Pathology
- Virology
Background:
- Viral-bacterial co-infections, like influenza and Streptococcus pneumoniae, pose significant health risks.
- Disease tolerance is a host survival strategy distinct from resistance, focusing on mitigating damage rather than eliminating pathogens.
- Understanding tolerance mechanisms is crucial for managing severe co-infections.
Purpose of the Study:
- To review host cytokines and innate immune cells that mediate disease tolerance during viral-bacterial co-infection.
- To highlight mechanisms that promote tissue integrity and organ protection.
- To identify factors contributing to host homeostasis and survival.
Main Methods:
- Literature review of studies on host responses to viral-bacterial co-infections.
- Analysis of the roles of specific cytokines (e.g., IL-10, TGF-β) in disease tolerance.
- Examination of innate immune cell functions (e.g., macrophages, neutrophils) in mediating tolerance.
Main Results:
- Certain host cytokines and innate immune cells promote tissue protection and limit organ damage.
- Dysregulated immune responses can lead to immunopathology, increasing morbidity and mortality.
- Disease tolerance mechanisms are essential for restoring homeostasis and ensuring host survival.
Conclusions:
- Host cytokines and innate immune cells are key mediators of disease tolerance.
- Targeting these pathways offers a therapeutic strategy for co-infections.
- Promoting disease tolerance is vital for improving outcomes in complex infections.
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