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      Targeted Transcriptional Analysis of IgA Vasculitis, IgA Nephropathy, and IgA-Dominant Infection-Related Glomerulonephritis Reveals Both Distinct and Overlapping Immune Signatures

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          Abstract

          Key Points

          • Skin IL-9, calprotectin, and KIR gene expression may be predictive of subsequent kidney involvement in patients with IgAV.

          • Histologically similar patients with IgAN, IgAV, and IgA-IRGN can be distinguished by their immune transcriptomes.

          • Kidney biopsies from patients with IgA-IRGN are enriched for transcripts involved in granulocyte chemotaxis.

          Background

          IgA vasculitis (IgAV), IgA nephropathy (IgAN), and IgA-dominant infection-related glomerulonephritis (IgA-IRGN) have shared histopathologic features, but differences in clinical management and prognosis. The most serious IgAV organ involvement is in the kidneys (IgAV nephritis). In this study, we hypothesized that targeted immune transcript profiling could aid in ( 1) predicting the development of IgAV nephritis in patients with cutaneous IgAV and ( 2) differentiating IgAN, IgAV, and IgA-IRGN.

          Methods

          RNA was extracted from 24 formalin-fixed paraffin-embedded tissue specimens (16 kidney, 8 skin) from 21 patients with IgAV nephritis (n=7), IgAN (n=5), and IgA-IRGN (n=4), and IgAV skin biopsies from patients with (n=3) and without (n=5) IgAV nephritis. Differential gene expression and gene set enrichment analysis were performed on a total of 594 transcripts (Nanostring immunology panel) profiled using the nCounter system.

          Results

          Skin biopsies in patients with IgAV who develop kidney involvement exhibit reduced S100A8/S100A9, IL9, and killer cell immunoglobulin-like receptor expression. The kidney tissue immune transcriptomes of IgAN, IgAV, and IgA-IRGN are largely overlapping. IgA-IRGN kidney biopsies are, however, uniquely enriched for transcripts involved in granulocyte chemotaxis.

          Conclusion

          This study identifies immune transcript signatures that may predict IgAV nephritis in skin biopsies and distinguish IgA-IRGN from IgAN and IgAV in kidney biopsies.

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          Most cited references32

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          IgA nephropathy.

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            The incidence of primary glomerulonephritis worldwide: a systematic review of the literature.

            Little is known about the worldwide variation in incidence of primary glomerulonephritis (GN). The objective of this review was to critically appraise studies of incidence published in 1980-2010 so that an overall view of trends of these diseases can be found. This would provide important information for determining changes in rates and understanding variations between countries. All relevant papers found through searches of Medline, Embase and ScienceDirect were critically appraised and an assessment was made of the reliability of the reported incidence data. This review includes 40 studies of incidence of primary GN from Europe, North and South America, Canada, Australasia and the Middle East. Rates for the individual types of disease were found to be in adults, 0.2/100,000/year for membrano-proliferative GN, 0.2/100,000/year for mesangio-proliferative GN, 0.6/100,000/year for minimal change disease, 0.8/100,000/year for focal segmental glomerulosclerosis, 1.2/100,000/year for membranous nephropathy and 2.5/100,000/year for IgA nephropathy. Rates were lower in children at around 0.1/100,000/year with the exception of minimal change disease where incidence was reported to be 2.0/100,000/year in Caucasian children with higher rates in Arabian children (9.2/100,000/year) and Asian children (6.2-15.6/100,000/year). This study found that incidence rates of primary GN vary between 0.2/100,000/year and 2.5/100,000/year. The incidence of IgA nephropathy is at least 2.5/100,000/year in adults; this disease can exist subclinically and is therefore only detected by chance in some patients. In addition, referral policies for diagnostic biopsy vary between countries. This will affect the incidence rates found.
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              IL-9 induces differentiation of TH17 cells and enhances function of FoxP3+ natural regulatory T cells.

              The development of T helper (T(H))17 and regulatory T (T(reg)) cells is reciprocally regulated by cytokines. Transforming growth factor (TGF)-beta alone induces FoxP3(+) T(reg) cells, but together with IL-6 or IL-21 induces T(H)17 cells. Here we demonstrate that IL-9 is a key molecule that affects differentiation of T(H)17 cells and T(reg) function. IL-9 predominantly produced by T(H)17 cells, synergizes with TGF-beta1 to differentiate naïve CD4(+) T cells into T(H)17 cells, while IL-9 secretion by T(H)17 cells is regulated by IL-23. Interestingly, IL-9 enhances the suppressive functions of FoxP3(+) CD4(+) T(reg) cells in vitro, and absence of IL-9 signaling weakens the suppressive activity of nT(regs) in vivo, leading to an increase in effector cells and worsening of experimental autoimmune encephalomyelitis. The mechanism of IL-9 effects on T(H)17 and T(regs) is through activation of STAT3 and STAT5 signaling. Our findings highlight a role of IL-9 as a regulator of pathogenic versus protective mechanisms of immune responses.
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                Author and article information

                Journal
                Kidney360
                Kidney360
                KIDNEY
                Kidney360
                Kidney360
                American Society of Nephrology
                2641-7650
                June 2023
                8 April 2023
                : 4
                : 6
                : e759-e768
                Affiliations
                [1 ]Department of Pathology and Laboratory Medicine, Oregon Health & Science University, Oregon Health & Science University, Portland, Oregon
                [2 ]Department of Medicine, Division of Nephrology and Hypertension, Oregon Health & Science University, Portland, Oregon
                [3 ]Department of Medicine, Division of Rheumatology, Oregon Health & Science University, Portland, Oregon
                [4 ]Department of Dermatology, Oregon Health & Science University, Portland, Oregon
                [5 ]Knight Diagnostic Laboratories, Knight Cancer Institute, Oregon Health & Science University, Portland, Oregon
                Author notes
                Correspondence: Vanderlene L. Kung, Department of Pathology and Laboratory Medicine, Oregon Health & Science University, 3181 SW Sam Jackson Park Road, L113, Portland, OR 97239. Email: kungv@ 123456ohsu.edu
                Author information
                https://orcid.org/0000-0001-6560-7266
                https://orcid.org/0000-0001-8432-2186
                https://orcid.org/0000-0001-6722-2159
                https://orcid.org/0000-0002-8358-9062
                Article
                K360-2023-000279 00011
                10.34067/KID.0000000000000123
                10371378
                37036681
                2c8dbfaa-0336-4fb6-9554-eb8b972a4b81
                Copyright © 2023 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American Society of Nephrology

                This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 24 August 2022
                : 27 February 2023
                Page count
                Figures: 3, Tables: 2, References: 32, Pages: 0
                Categories
                Original Investigation
                Glomerular and Tubulointerstitial Diseases
                Custom metadata
                YES

                glomerular and tubulointerstitial diseases,calprotectin,iga dominant infection related glomerulonephritis,iga nephropathy,iga vasculitis,il9,kir,mrsa,nanostring,staphylococcus aureus,transcriptome

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