Pathophysiology and Clinical Perception of Immune Dysregulation in Chronic Liver Disease Accelerated by Acute Kidney Injury

Abstraction Immune dysfunction, in particular cirrhosis-associated immune dysfunction (CAID), has been associated to chronic liver disease (CLD), a global health concern the fact that places patients vulnerable for infections and systemic inflammation. Because of variables like hepatorenal syndrome, sepsis, and hypovolemia, acute kidney injury (AKI) commonly exacerbates immune-mediated dysregulation and complicates chronic renal failure (CLD). This review examines the complicated relationship between immune system dysfunction and AKI in CLD. T-cell exhaustion and impaired B-cell activity influence adaptive immunity in CLD, while faulty neutrophils, monocytes, and natural killer cells describe poor innate immunity. By generating damage-associated molecular patterns (DAMPs) and advancing cytokine storms, AKI aggravates these processes, leading to immune-mediated paralysis and systemic inflammation. This review highlights the critical need for mechanistic studies, early diagnostic tools, and customised therapeutic approaches to mitigate the profound impact of AKI on immune dysfunction in CLD and improve patient outcomes. The combined consequences of CLD and AKI enhance the likelihood of serious illnesses, like spontaneous bacterial peritonitis and sepsis, and contribute to adverse clinical outcomes, including greater mortality and prolonged being hospitalised. Rising biomarkers and therapies, such as probiotics and anti-inflammatory agents, offer promising avenues for managing immune dysfunction in AKI-CLD interplay. Key words: DAMP, Immune dysfunction, adaptive immunity, Innate immunity

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Publication Details

Journal
International Journal of Health Sciences and Research
Published
2025-02-20
DOI
https://doi.org/10.52403/ijhsr.20250232
Primary Topic
Drug-Induced Hepatotoxicity and Protection
Type
article
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article

Pathophysiology and Clinical Perception of Immune Dysregulation in Chronic Liver Disease Accelerated by Acute Kidney Injury

T. Rama Rao, S. M. Quadri, K. Mallikarjun Rao, P. Kishore Kumar et al.
International Journal of Health Sciences and Research
Drug-Induced Hepatotoxicity and Protection
article

Pathophysiology and Clinical Perception of Immune Dysregulation in Chronic Liver Disease Accelerated by Acute Kidney Injury

T. Rama Rao, S. M. Quadri, K. Mallikarjun Rao, P. Kishore Kumar, Bagadam Aparna
article en

Abstract

Abstraction Immune dysfunction, in particular cirrhosis-associated immune dysfunction (CAID), has been associated to chronic liver disease (CLD), a global health concern the fact that places patients vulnerable for infections and systemic inflammation. Because of variables like hepatorenal syndrome, sepsis, and hypovolemia, acute kidney injury (AKI) commonly exacerbates immune-mediated dysregulation and complicates chronic renal failure (CLD). This review examines the complicated relationship between immune system dysfunction and AKI in CLD. T-cell exhaustion and impaired B-cell activity influence adaptive immunity in CLD, while faulty neutrophils, monocytes, and natural killer cells describe poor innate immunity. By generating damage-associated molecular patterns (DAMPs) and advancing cytokine storms, AKI aggravates these processes, leading to immune-mediated paralysis and systemic inflammation. This review highlights the critical need for mechanistic studies, early diagnostic tools, and customised therapeutic approaches to mitigate the profound impact of AKI on immune dysfunction in CLD and improve patient outcomes. The combined consequences of CLD and AKI enhance the likelihood of serious illnesses, like spontaneous bacterial peritonitis and sepsis, and contribute to adverse clinical outcomes, including greater mortality and prolonged being hospitalised. Rising biomarkers and therapies, such as probiotics and anti-inflammatory agents, offer promising avenues for managing immune dysfunction in AKI-CLD interplay. Key words: DAMP, Immune dysfunction, adaptive immunity, Innate immunity

International Journal of Health Sciences and ResearchVol. 15(2)
Indian Institute of Technology Hyderabad (IN)
Openalex Percentile: Top 96%
Drug-Induced Hepatotoxicity and Protection
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