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      Formalin-fixed paraffin-embedded renal biopsy tissues: an underexploited biospecimen resource for gene expression profiling in IgA nephropathy

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          Abstract

          Primary IgA nephropathy (IgAN) diagnosis is based on IgA-dominant glomerular deposits and histological scoring is done on formalin-fixed paraffin embedded tissue (FFPE) sections using the Oxford classification. Our aim was to use this underexploited resource to extract RNA and identify genes that characterize active (endocapillary–extracapillary proliferations) and chronic (tubulo-interstitial) renal lesions in total renal cortex. RNA was extracted from archival FFPE renal biopsies of 52 IgAN patients, 22 non-IgAN and normal renal tissue of 7 kidney living donors (KLD) as controls. Genome-wide gene expression profiles were obtained and biomarker identification was carried out comparing gene expression signatures a subset of IgAN patients with active (N = 8), and chronic (N = 12) renal lesions versus non-IgAN and KLD. Bioinformatic analysis identified transcripts for active ( DEFA4, TNFAIP6, FAR2) and chronic ( LTB, CXCL6, ITGAX) renal lesions that were validated by RT-PCR and IHC. Finally, two of them (TNFAIP6 for active and CXCL6 for chronic) were confirmed in the urine of an independent cohort of IgAN patients compared with non-IgAN patients and controls. We have integrated transcriptomics with histomorphological scores, identified specific gene expression changes using the invaluable repository of archival renal biopsies and discovered two urinary biomarkers that may be used for specific clinical decision making.

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          IgA Nephropathy.

          IgA nephropathy (IgAN) is a leading cause of CKD and renal failure. Recent international collaborative efforts have led to important discoveries that have improved our understanding of some of the key steps involved in the immunopathogenesis of IgAN. Furthermore, establishment of multicenter networks has contributed to rigorous design and execution of clinical trials that have provided important insights regarding immunotherapy in IgAN. In this article, we review emerging developments in clinical and translational IgAN research and describe how these novel findings will influence future strategies to improve the outcome of patients with IgAN.
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            Defensins in innate antiviral immunity.

            Defensins are small antimicrobial peptides that are produced by leukocytes and epithelial cells, and that have an important role in innate immunity. Recent advances in understanding the mechanisms of the antiviral action(s) of defensins indicate that they have a dual role in antiviral defence, acting directly on the virion and on the host cell. This Review focuses on the antiviral activities and mechanisms of action of mammalian defensins, and on the clinical relevance of these activities. Understanding the complex function of defensins in innate immunity against viral infection has implications for the prevention and treatment of viral disease.
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              A Multicenter Study of the Predictive Value of Crescents in IgA Nephropathy

              The Oxford Classification of IgA nephropathy does not account for glomerular crescents. However, studies that reported no independent predictive role of crescents on renal outcomes excluded individuals with severe renal insufficiency. In a large IgA nephropathy cohort pooled from four retrospective studies, we addressed crescents as a predictor of renal outcomes and determined whether the fraction of crescent-containing glomeruli associates with survival from either a ≥50% decline in eGFR or ESRD (combined event) adjusting for covariates used in the original Oxford study. The 3096 subjects studied had an initial mean±SD eGFR of 78±29 ml/min per 1.73 m2 and median (interquartile range) proteinuria of 1.2 (0.7-2.3) g/d, and 36% of subjects had cellular or fibrocellular crescents. Overall, crescents predicted a higher risk of a combined event, although this remained significant only in patients not receiving immunosuppression. Having crescents in at least one sixth or one fourth of glomeruli associated with a hazard ratio (95% confidence interval) for a combined event of 1.63 (1.10 to 2.43) or 2.29 (1.35 to 3.91), respectively, in all individuals. Furthermore, having crescents in at least one fourth of glomeruli independently associated with a combined event in patients receiving and not receiving immunosuppression. We propose adding the following crescent scores to the Oxford Classification: C0 (no crescents); C1 (crescents in less than one fourth of glomeruli), identifying patients at increased risk of poor outcome without immunosuppression; and C2 (crescents in one fourth or more of glomeruli), identifying patients at even greater risk of progression, even with immunosuppression.
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                Author and article information

                Contributors
                sharonnatasha.cox@gmail.com
                paolo.schena@uniba.it
                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group UK (London )
                2045-2322
                16 September 2020
                16 September 2020
                2020
                : 10
                : 15164
                Affiliations
                [1 ]Schena Foundation, Research Center of Kidney Diseases, Strada Provinciale Valenzano-Casamassima Km. 3.00, 70100 Valenzano, Bari, Italy
                [2 ]GRID grid.7644.1, ISNI 0000 0001 0120 3326, Division of Nephrology, Dialysis, and Transplantation, Department of Emergency and Organ Transplantation, , University of Bari, ; Bari, Italy
                [3 ]National Institute of Gastroenterology “S. de Bellis”, Research Hospital, 70013 Castellana Grotte, Bari, Italy
                [4 ]GRID grid.412451.7, ISNI 0000 0001 2181 4941, Department of Medicine and Aging Sciences, , University “G. D’Annunzio” of Chieti-Pescara, ; Chieti, Italy
                [5 ]GRID grid.411475.2, ISNI 0000 0004 1756 948X, Renal Unit, Department of Medicine, , University-Hospital of Verona, ; Verona, Italy
                [6 ]GRID grid.4793.9, ISNI 0000000109457005, Department of Nephrology, Hippokration General Hospital, , Aristotle University of Thessaloniki, ; Thessaloniki, Greece
                [7 ]GRID grid.50956.3f, ISNI 0000 0001 2152 9905, Department of Pathology and Laboratory Medicine, , Cedars-Sinai Medical Center, ; Los Angeles, CA USA
                Article
                72026
                10.1038/s41598-020-72026-2
                7494931
                32938960
                58dee994-1969-482e-b703-a0f365fb09a6
                © The Author(s) 2020

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 24 January 2020
                : 29 June 2020
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/501100003407, Ministero dell’Istruzione, dell’Università e della Ricerca;
                Award ID: COFIN-PRIN 2006069815
                Funded by: FundRef http://dx.doi.org/10.13039/501100009886, Regione Puglia;
                Award ID: BISIMANE project 44/2008
                Categories
                Article
                Custom metadata
                © The Author(s) 2020

                Uncategorized
                transcription,acute kidney injury,chronic kidney disease,gene expression analysis

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