Literature DB >> 34907031

Secondary Immunodeficiency Related to Kidney Disease (SIDKD)-Definition, Unmet Need, and Mechanisms.

Stefanie Steiger1, Jan Rossaint2, Alexander Zarbock2, Hans-Joachim Anders3.   

Abstract

Kidney disease is a known risk factor for poor outcomes of COVID-19 and many other serious infections. Conversely, infection is the second most common cause of death in patients with kidney disease. However, little is known about the underlying secondary immunodeficiency related to kidney disease (SIDKD). In contrast to cardiovascular disease related to kidney disease, which has triggered countless epidemiologic, clinical, and experimental research activities or interventional trials, investments in tracing, understanding, and therapeutically targeting SIDKD have been sparse. As a call for more awareness of SIDKD as an imminent unmet medical need that requires rigorous research activities at all levels, we review the epidemiology of SIDKD and the numerous aspects of the abnormal immunophenotype of patients with kidney disease. We propose a definition of SIDKD and discuss the pathogenic mechanisms of SIDKD known thus far, including more recent insights into the unexpected immunoregulatory roles of elevated levels of FGF23 and hyperuricemia and shifts in the secretome of the intestinal microbiota in kidney disease. As an ultimate goal, we should aim to develop therapeutics that can reduce mortality due to infections in patients with kidney disease by normalizing host defense to pathogens and immune responses to vaccines.
Copyright © 2022 by the American Society of Nephrology.

Entities:  

Keywords:  chronic inflammation; immunodeficiency; infection; kidney disease

Mesh:

Substances:

Year:  2021        PMID: 34907031      PMCID: PMC8819985          DOI: 10.1681/ASN.2021091257

Source DB:  PubMed          Journal:  J Am Soc Nephrol        ISSN: 1046-6673            Impact factor:   10.121


  242 in total

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2.  Impaired humoral and cellular immunity after SARS-CoV-2 BNT162b2 (tozinameran) prime-boost vaccination in kidney transplant recipients.

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Journal:  J Clin Invest       Date:  2021-07-15       Impact factor: 14.808

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4.  Infection in advanced chronic kidney disease leads to increased risk of cardiovascular events, end-stage kidney disease and mortality.

Authors:  Hicham I Cheikh Hassan; Mila Tang; Ognjenka Djurdjev; David Langsford; Manish M Sood; Adeera Levin
Journal:  Kidney Int       Date:  2016-08-31       Impact factor: 10.612

Review 5.  Iron and infection.

Authors:  S I Patruta; W H Hörl
Journal:  Kidney Int Suppl       Date:  1999-03       Impact factor: 10.545

Review 6.  Potential risk for infection and atherosclerosis due to iron therapy.

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7.  Effect of dialysis dose and membrane flux in maintenance hemodialysis.

Authors:  Garabed Eknoyan; Gerald J Beck; Alfred K Cheung; John T Daugirdas; Tom Greene; John W Kusek; Michael Allon; James Bailey; James A Delmez; Thomas A Depner; Johanna T Dwyer; Andrew S Levey; Nathan W Levin; Edgar Milford; Daniel B Ornt; Michael V Rocco; Gerald Schulman; Steve J Schwab; Brendan P Teehan; Robert Toto
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Authors:  Kirsten Anding; Peter Gross; Jan M Rost; Dirk Allgaier; Enno Jacobs
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9.  Salt-responsive gut commensal modulates TH17 axis and disease.

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Journal:  Nature       Date:  2017-11-15       Impact factor: 49.962

10.  Risk factors for catheter-related infections in patients receiving permanent dialysis catheter.

Authors:  Fani Delistefani; Manuel Wallbach; Gerhard A Müller; Michael J Koziolek; Clemens Grupp
Journal:  BMC Nephrol       Date:  2019-05-31       Impact factor: 2.388

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Review 2.  The Fatal Circle of NETs and NET-Associated DAMPs Contributing to Organ Dysfunction.

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3.  Seroresponse to Third Doses of SARS-CoV-2 Vaccine Among Patients Receiving Maintenance Dialysis.

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Review 4.  Vaccination in patients with kidney failure: lessons from COVID-19.

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5.  Emerging trends and focus for the link between the gastrointestinal microbiome and kidney disease.

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6.  Major cardiovascular events in patients with severe COPD with and without asthma: a nationwide cohort study.

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7.  Biological drugs for systemic lupus erythematosus or active lupus nephritis and rates of infectious complications. Evidence from large clinical trials.

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  7 in total

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