Immunomodulatory Approaches in Diabetes-Induced Cardiorenal Syndromes
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Frontiers Media S.A.
Abstract
Immunomodulatory approaches are defined as all interventions that modulate and curb the immune response of the host rather than targeting the disease itself with the aim of disease prevention or treatment. A better understanding of the immune system continues to offer innovative drug targets and methods for immunomodulatory interventions. Cardiorenal syndrome is a clinical condition that defines disorders of the heart and kidneys, both of which communicate with one another through multiple pathways in an interdependent relationship. Cardiorenal syndrome denotes the confluence of heart-kidney relationships across numerous interfaces. As such, a dysfunctional heart or kidney has the capacity to initiate disease in the other organ via common hemodynamic, neurohormonal, immunological, and/or biochemical feedback pathways. Understanding how immunomodulatory approaches are implemented in diabetes-induced cardiovascular and renal diseases is important for a promising regenerative medicine, which is the process of replacing cells, tissues or organs to establish normal function. In this article, after a brief introduction on the immunomodulatory approaches in diseases, we will be reviewing the epidemiology and classifications of cardiorenal syndrome. We will be emphasizing on the hemodynamic factors and non-hemodynamic factors linking the heart and the kidneys. In addition, we will be elaborating on the immunomodulatory pathways involved in diabetes-induced cardiorenal syndrome namely, RAS, JAK/STAT, and oxidative stress. Moreover, we will be addressing possible therapeutic approaches that target the former pathways in an attempt to modulate the immune system. Copyright © 2021 Ammar, Nahlawi, Shayya, Ghadieh, Azar, Harb and Eid.
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Keywords
Cardiorenal syndromes, Diabetes mellitus, Immunomodulatory approaches, Jak/stat pathway, Oxidative stress, Ras pathway, Angiotensin converting enzyme 2, Angiotensin ii, Cyclooxygenase 2, Dipeptidyl carboxypeptidase, Endothelin 1, Gelatinase b, Immunoglobulin enhancer binding protein, Intercellular adhesion molecule 1, Interleukin 10, Interleukin 17, Interleukin 1beta, Interleukin 6, Janus kinase, Lipopolysaccharide, Mitogen activated protein kinase 1, Mitogen activated protein kinase 3, Nicotinamide adenine dinucleotide phosphate, Nitric oxide, Nitric oxide synthase, Prostaglandin e2, Protein kinase c, Ras protein, Reactive oxygen metabolite, Reduced nicotinamide adenine dinucleotide phosphate oxidase, Renin, Stat protein, Stat3 protein, Streptozocin, Suppressor of cytokine signaling 3, Toll like receptor 4, Transcription factor nfat3, Transforming growth factor beta, Tumor necrosis factor, Vascular cell adhesion molecule 1, Adrenergic system, Antiinflammatory activity, Antioxidant assay, Cardiogenic shock, Cardiorenal syndrome, Cardiovascular disease, Cytokine production, Dendritic cell, Dialysis, Disease classification, Disease severity, Epithelial mesenchymal transition, Glomerulus basement membrane, Glomerulus filtration rate, Heart failure, Hemodynamics, Human, Hypertension, Immune response, Immune system, Immunomodulation, Immunotherapy, Jak-stat signaling, Kidney blood flow, Kidney dysfunction, Kidney fibrosis, Lung edema, Nonhuman, Pathogenesis, Physiological feedback, Prophylaxis, Renin angiotensin aldosterone system, Review, Signal transduction, Streptozotocin-induced diabetes mellitus, Th17 cell