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      T Cells and Acute Kidney Injury: A Two-Way Relationship

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          Abstract

          Acute Kidney Injury (AKI) complicates up to 10% of hospital admissions substantially increasing patient morbidity and mortality. Experimental evidence supports that AKI initiation and maintenance results from immune-mediated damage. Exogenous injury sources directly damage renal cells which produce pro-inflammatory mediators recruiting immune cells and furthering kidney injury. Many AKI studies focus on activation of innate immunity; major components include complement pathways, neutrophils, and monocytes. Recently, growing evidence emphasizes T lymphocytes role in affecting AKI pathogenesis and magnitude. In particular, T helper 17 lymphocytes enhance tissue injury by recruiting neutrophils and other inflammatory cells, while regulatory T cells conversely reduce renal injury and facilitate repair. Intriguingly, evidence supports local parenchymal-T cell interactions as essential to producing T cell phenotypic changes affecting long-term kidney and patient survival. Herein, we review T cells effects on AKI and patient outcomes and discuss related new therapeutic approaches to improve outcomes of affected individuals.

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          Most cited references68

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          KDIGO Clinical Practice Guidelines for Acute Kidney Injury

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            Cardiac surgery-associated acute kidney injury: risk factors, pathophysiology and treatment

            Cardiac surgery-associated acute kidney injury (CSA-AKI) is the most common complication in adult patients undergoing open heart surgery. In this Review, the authors discuss the definition, epidemiology, pathophysiology and risk factors of CSA-AKI. The authors also explore the use of novel biomarkers of AKI and their potential utility in preventing or treating CSA-AKI.
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              Adverse Renal Effects of Immune Checkpoint Inhibitors: A Narrative Review

              Background: Cancer immunotherapy, such as anti-cytotoxic T-lymphocyte-associated protein 4 (CTLA-4) and anti-programmed death 1 (PD-1), has revolutionized the treatment of malignancies by engaging the patient's own immune system against the tumor rather than targeting the cancer directly. These therapies have demonstrated a significant benefit in the treatment of melanomas and other cancers. Summary: In order to provide an extensive overview of the renal toxicities induced by these agents, a Medline search was conducted of published literature related to ipilimumab-, pembrolizumab-, and nivolumab-induced kidney toxicity. In addition, primary data from the initial clinical trials of these agents and the FDA adverse reporting system database were also reviewed to determine renal adverse events. Acute interstitial nephritis (AIN), podocytopathy, and hyponatremia were toxicities caused by ipilimumab. The main adverse effect associated with both the PD-1 inhibitors was AIN. The onset of kidney injury seen with PD-1 inhibitors is usually late (3-10 months) compared to CTLA-4 antagonists related renal injury, which happens earlier (2-3 months). PD-1 as opposed to CTLA-4 inhibitors has been associated with kidney rejection in transplantation. Steroids appear to be effective in treating the immune-related adverse effects noted with these agents. Key Message: Although initially thought to be rare, the incidence rates of renal toxicities might be higher (9.9-29%) as identified by recent studies. As a result, obtaining knowledge about renal toxicities of immune checkpoint inhibitors is extremely important.
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                Author and article information

                Contributors
                Journal
                Front Immunol
                Front Immunol
                Front. Immunol.
                Frontiers in Immunology
                Frontiers Media S.A.
                1664-3224
                17 July 2020
                2020
                : 11
                : 1546
                Affiliations
                [1] 1Icahn School of Medicine at Mount Sinai , New York, NY, United States
                [2] 2Division of Nephrology, White Plains Hospital , White Plains, NY, United States
                Author notes

                Edited by: Giuseppe Castellano, University of Bari Aldo Moro, Italy

                Reviewed by: Ankit Saxena, National Institutes of Health (NIH), United States; Rui Li, Perelman School of Medicine at the University of Pennsylvania, United States

                *Correspondence: Paolo Cravedi paolo.cravedi@ 123456mssm.edu

                This article was submitted to Inflammation, a section of the journal Frontiers in Immunology

                Article
                10.3389/fimmu.2020.01546
                7379378
                32765535
                48cd7465-d501-4efe-98dc-a320d7d357af
                Copyright © 2020 Dellepiane, Leventhal and Cravedi.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 06 May 2020
                : 11 June 2020
                Page count
                Figures: 1, Tables: 0, Equations: 0, References: 76, Pages: 8, Words: 6399
                Categories
                Immunology
                Mini Review

                Immunology
                aki,iri,regulatory t cell,treg,th1,th2,th17
                Immunology
                aki, iri, regulatory t cell, treg, th1, th2, th17

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