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      Call for Papers: Epidemiology of CKD and its Complications

      Submit here by August 31, 2024

      About Kidney and Blood Pressure Research: 2.1 Impact Factor I 3.8 CiteScore I 0.728 Scimago Journal & Country Rank (SJR)

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      suPAR: An Inflammatory Mediator for Kidneys

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          Abstract

          Background

          Inflammation is a common feature of many kidney diseases. The implicated inflammatory mediators and their underlying molecular mechanisms however are often not clear.

          Summary

          suPAR is the soluble form of urokinase-type plasminogen activator receptor (uPAR), associated with inflammation and immune activation. It has evolved into a unique circulating kidney disease factor over the last 10 years. In particular, suPAR has multiple looks due to enzymatic cleavage and alternative transcriptional splicing of the uPAR gene. Most recently, suPAR has emerged as a systemic mediator for COVID-19 infection, associated with lung as well as kidney dysfunction. Like membrane-bound uPAR, suPAR could interact with integrins (e.g., αvβ3 integrin) on podocytes, providing the molecular basis for some glomerular kidney diseases. In addition, there have been numerous studies suggesting that suPAR connects acute kidney injury to chronic kidney disease as a special kidney risk factor. Moreover, the implication of circulating suPAR levels in kidney transplantation and plasmapheresis not only indicates its relevance in monitoring for recurrence but also implies suPAR as a possible therapeutic target. In fact, the therapeutic concept of manipulating suPAR function has been evidenced in several kidney disease experimental models.

          Key Messages

          The last 10 years of research has established suPAR as a unique inflammatory mediator for kidneys. While open questions remain and deserve additional studies, modulating suPAR function may represent a promising novel therapeutic strategy for kidney disease.

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          Most cited references120

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          Integrin ligands at a glance.

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            Immune response in COVID-19: addressing a pharmacological challenge by targeting pathways triggered by SARS-CoV-2

            To date, no vaccines or effective drugs have been approved to prevent or treat COVID-19 and the current standard care relies on supportive treatments. Therefore, based on the fast and global spread of the virus, urgent investigations are warranted in order to develop preventive and therapeutic drugs. In this regard, treatments addressing the immunopathology of SARS-CoV-2 infection have become a major focus. Notably, while a rapid and well-coordinated immune response represents the first line of defense against viral infection, excessive inflammatory innate response and impaired adaptive host immune defense may lead to tissue damage both at the site of virus entry and at systemic level. Several studies highlight relevant changes occurring both in innate and adaptive immune system in COVID-19 patients. In particular, the massive cytokine and chemokine release, the so-called “cytokine storm”, clearly reflects a widespread uncontrolled dysregulation of the host immune defense. Although the prospective of counteracting cytokine storm is compelling, a major limitation relies on the limited understanding of the immune signaling pathways triggered by SARS-CoV-2 infection. The identification of signaling pathways altered during viral infections may help to unravel the most relevant molecular cascades implicated in biological processes mediating viral infections and to unveil key molecular players that may be targeted. Thus, given the key role of the immune system in COVID-19, a deeper understanding of the mechanism behind the immune dysregulation might give us clues for the clinical management of the severe cases and for preventing the transition from mild to severe stages.
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              Neutrophil‐to‐lymphocyte ratio and lymphocyte‐to‐C‐reactive protein ratio in patients with severe coronavirus disease 2019 (COVID‐19): A meta‐analysis

              To the Editor, Since March 11, 2020, the World Health Organization defined coronavirus disease 2019 (COVID‐19) as a pandemic, with a series of confirmed cases that currently exceeded 300,000 people worldwide and with approximately 14,500 deaths. 1 Accumulated evidence suggests that a subgroup of patients with severe COVID‐19 could have a dysregulation of the immune response that allows the development of viral hyperinflammation. 2 Thus, all patients with severe COVID‐19 should be screened for hyperinflammation using laboratory parameters to improve mortality. Neutrophil‐to‐lymphocyte ratio (NLR) and lymphocyte‐to‐C‐reactive protein ratio (LCR) are established inflammation markers that reflect systemic inflammatory response, 3 , 4 and both are available in almost all laboratories. In this study, a meta‐analysis was performed to investigate whether NLR and LCR values can help predict clinical severity in patients with COVID‐19. First, we conducted an electronic search in different search engines that included Medline (PubMed interface), Scopus, Web of Science via Raven and Google Scholar, using the keywords “Severe 2019‐nCoV” OR "Severe COVID‐19" without date (i.e. until March 23, 2020) or language restrictions. The title, abstract, and full text of all the articles identified according to these search criteria were analyzed, considering for our meta‐analysis only those that reported data in COVID‐19 patients with or without severe disease (defined as severe or with the need to enter the intensive care unit or the use of mechanical ventilation). Six studies were included in our meta‐analysis, four of them allowed us to calculate both NLR and LCR. The other two articles, one was considered only for NLR calculations and the other only for LCR calculations. Mean and standard deviation were extrapolated from the median, range, and sample size according to Hozo et al. 5 For NLR, the number of neutrophils and lymphocytes was taken per 109/L, while LCR was calculated as follows: lymphocyte count (number/μL)/C‐reactive protein (mg/dL). Meta‐analysis was performed using Comprehensive Meta‐Analysis Software version 3 (2013, Biostat, Englewood, NJ) calculating the standardized mean difference (SMD) and the 95% confidence interval (95% CI) of the NLR and LCR values in patients with COVID‐19 with or without severe disease. All the studies were carried out in China and included a total number of 828 patients, where 407 patients had severe disease (49.15%) and the sample size varied between 41 and 452 patients. The SMD of the five studies used for each parameter is summarized in Figure 1. Since heterogeneity (I2 statistics) exceeded 50% in both meta‐analyses, a random effects model was used. The NLR values were found to increase significantly in patients with COVID‐19 with severe disease (SMD = 2.404, 95% CI = 0.98‐3.82), while LCR values were decreased significantly (SMD = −0.912, 95% CI = −1.275 to −0.550). Figure 1 Standardized mean difference (SMD) and 95% confidence interval (95% CI) of neutrophil‐to‐lymphocyte ratio and lymphocyte‐to‐C‐reactive protein ratio in coronavirus disease 2019 (COVID‐19) patients with or without severe disease Despite several reports describing increased levels of neutrophils and C‐reactive protein along with a decrease in lymphocyte numbers in patients with COVID‐19, 2 , 6 , 7 , 8 , 9 , 10 until now, very few reports have considered the cost‐effective markers NLR and LCR to aid complication predictions. Acute respiratory distress syndrome, which is a type of respiratory failure characterized by a rapid onset of generalized inflammation in the lungs, is the leading cause of mortality of patients with COVID‐19. Thus, increased NLR levels and low LCR levels reflecting an enhanced inflammatory process may suggest a poor prognosis. CONFLICT OF INTERESTS The author declares that there is no conflict of interests.

                Author and article information

                Journal
                Kidney Dis (Basel)
                Kidney Dis (Basel)
                KDD
                Kidney Diseases
                S. Karger AG (Allschwilerstrasse 10, P.O. Box · Postfach · Case postale, CH–4009, Basel, Switzerland · Schweiz · Suisse, Phone: +41 61 306 11 11, Fax: +41 61 306 12 34, karger@karger.com )
                2296-9381
                2296-9357
                July 2022
                8 June 2022
                8 June 2022
                : 8
                : 4
                : 265-274
                Affiliations
                Department of Internal Medicine, Rush University, Chicago, Illinois, USA
                Author notes
                Article
                kdd-0008-0265
                10.1159/000524965
                9251480
                35949208
                f4981f8d-f334-4273-8746-cacaea885ca4
                Copyright © 2022 by S. Karger AG, Basel

                This article is licensed under the Creative Commons Attribution-NonCommercial 4.0 International License (CC BY-NC). Usage and distribution for commercial purposes requires written permission. Drug Dosage: The authors and the publisher have exerted every effort to ensure that drug selection and dosage set forth in this text are in accord with current recommendations and practice at the time of publication. However, in view of ongoing research, changes in government regulations, and the constant flow of information relating to drug therapy and drug reactions, the reader is urged to check the package insert for each drug for any changes in indications and dosage and for added warnings and precautions. This is particularly important when the recommended agent is a new and/or infrequently employed drug. Disclaimer: The statements, opinions and data contained in this publication are solely those of the individual authors and contributors and not of the publishers and the editor(s). The appearance of advertisements or/and product references in the publication is not a warranty, endorsement, or approval of the products or services advertised or of their effectiveness, quality or safety. The publisher and the editor(s) disclaim responsibility for any injury to persons or property resulting from any ideas, methods, instructions or products referred to in the content or advertisements.

                History
                : 8 February 2022
                : 8 May 2022
                : 2022
                Page count
                Figures: 1, References: 120, Pages: 10
                Categories
                Review Article

                soluble urokinase-type plasminogen activator receptor,kidney,integrin,covid-19,biomarker,therapeutics

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