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      Levamisole in Children with Idiopathic Nephrotic Syndrome: Clinical Efficacy and Pathophysiological Aspects

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          Abstract

          Steroid sensitive nephrotic syndrome is one of the most common pediatric glomerular diseases. Unfortunately, it follows a relapsing and remitting course in the majority of cases, with 50% of all cases relapsing once or even more often. Most children with idiopathic nephrotic syndrome respond initially to steroid therapy, nevertheless repeated courses for patients with relapses induce significant steroid toxicity. Patients with frequent relapses or steroid dependency thus require alternative treatment, such as cyclophosphamide, cyclosporine, tacrolimus, mycophenolate mofetil, levamisole, or rituximab. To reduce the relapse rate, several drugs have been used. Among these, levamisole has been considered the least toxic and least expensive therapy. Several randomized controlled trials (RCT) showed that levamisole is effective in reducing the relapse risk in steroid sensitive forms of nephrotic syndrome with a low frequency of side effects. Levamisole is a synthetic imidazothiazole derivative with immune-modulatory properties. In this article, we review recent data from randomized trials and observational studies to assess the efficacy of levamisole in frequently relapsing nephrotic syndrome and steroid-dependent nephrotic syndrome.

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          Predominant TH2-like bronchoalveolar T-lymphocyte population in atopic asthma.

          In atopic asthma, activated T helper lymphocytes are present in bronchial-biopsy specimens and bronchoalveolar-lavage (BAL) fluid, and their production of cytokines may be important in the pathogenesis of this disorder. Different patterns of cytokine release are characteristic of certain subgroups of T helper cells, termed TH1 and TH2, the former mediating delayed-type hypersensitivity and the latter mediating IgE synthesis and eosinophilia. The pattern of cytokine production in atopic asthma is unknown. We assessed cells obtained by BAL in subjects with mild atopic asthma and in normal control subjects for the expression of messenger RNA (mRNA) for interleukin-2, 3, 4, and 5, granulocyte-macrophage colony-stimulating factor (GM-CSF), and interferon gamma by in situ hybridization with 32P-labeled complementary RNA. Localization of mRNA to BAL T cells was assessed by simultaneous in situ hybridization and immunofluorescence and by in situ hybridization after immunomagnetic enrichment or depletion of T cells. As compared with the control subjects, the subjects with asthma had more BAL cells per 1000 cell that were positive for mRNA for interleukin-2 (P less than 0.05), 3 (P less than 0.01), 4 (P less than 0.001), and 5 (P less than 0.001) and GM-CSF (P less than 0.001). There was no significant difference between the two groups in the number of cells expressing mRNA for interferon gamma. In the subjects with asthma, mRNA for interleukin-4 and 5 was expressed predominantly by T lymphocytes. Atopic asthma is associated with activation in the bronchi of the interleukin-3, 4, and 5 and GM-CSF gene cluster, a pattern compatible with predominant activation of the TH2-like T-cell population.
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            Cell biology and pathology of podocytes.

            As an integral member of the filtration barrier in the kidney glomerulus, the podocyte is in a unique geographical position: It is exposed to chemical signals from the urinary space (Bowman's capsule), it receives and transmits chemical and mechanical signals to/from the glomerular basement membrane upon which it elaborates, and it receives chemical and mechanical signals from the vascular space with which it also communicates. As with every cell, the ability of the podocyte to receive signals from the surrounding environment and to translate them to the intracellular milieu is dependent largely on molecules residing on the cell membrane. These molecules are the first-line soldiers in the ongoing battle to sense the environment, to respond to friendly signals, and to defend against injurious foes. In this review, we take a membrane biologist's view of the podocyte, examining the many membrane receptors, channels, and other signaling molecules that have been implicated in podocyte biology. Although we attempt to be comprehensive, our goal is not to capture every membrane-mediated pathway but rather to emphasize that this approach may be fruitful in understanding the podocyte and its unique properties.
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              Actin up: regulation of podocyte structure and function by components of the actin cytoskeleton.

              Podocytes of the renal glomerulus are unique cells with a complex cellular organization consisting of a cell body, major processes and foot processes. Podocyte foot processes form a characteristic interdigitating pattern with foot processes of neighboring podocytes, leaving in between the filtration slits that are bridged by the glomerular slit diaphragm. The highly dynamic foot processes contain an actin-based contractile apparatus comparable to that of smooth muscle cells or pericytes. Mutations affecting several podocyte proteins lead to rearrangement of the actin cytoskeleton, disruption of the filtration barrier and subsequent renal disease. The fact that the dynamic regulation of the podocyte cytoskeleton is vital to kidney function has led to podocytes emerging as an excellent model system for studying actin cytoskeleton dynamics in a physiological context.
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                Author and article information

                Journal
                J Clin Med
                J Clin Med
                jcm
                Journal of Clinical Medicine
                MDPI
                2077-0383
                16 June 2019
                June 2019
                : 8
                : 6
                : 860
                Affiliations
                [1 ]Department of Pediatrics, University Hamburg-Eppendorf, 20246 Hamburg, Germany; a.dettmar@ 123456uke.de (A.K.M.); j.oh@ 123456uke.de (J.O.)
                [2 ]Department of Nephrology, Yonsei University Wonju College of Medicine, Wonju, Kangwon 26426, Korea; junyoung07@ 123456yonsei.ac.kr (J.Y.L.); kidney74@ 123456yonsei.ac.kr (J.W.Y.)
                [3 ]Department of Pediatrics, Asklepios Klink Nord-Heidberg, 22417 Hamburg, Germany; m.kemper@ 123456asklepios.com
                [4 ]Department of Internal Medicine IV (Nephrology and Hypertension), Medical University Innsbruck, Innsbruck 6020, Austria; andreas.kronbichler@ 123456i-med.ac.at
                [5 ]Department of Pediatric Nephrology, Chungnam National University Hospital, Daejeon 35015, Korea; jwmleemd@ 123456gmail.com
                [6 ]Department of Pediatrics, Yonsei University College of Medicine, Seoul 03722, Korea
                [7 ]Division of Pediatric Nephrology, Severance Children’s Hospital, Seoul 03722, Korea
                [8 ]Institute of Kidney Disease Research, Yonsei University College of Medicine, Seoul 03722, Korea
                Author notes
                [* ]Correspondence: shinji@ 123456yuhs.ac ; Tel.: +82-2-228-2050; Fax: +82-2-393-9118
                [†]

                These authors contributed equally to this work.

                Author information
                https://orcid.org/0000-0001-8047-4190
                https://orcid.org/0000-0002-2945-2946
                https://orcid.org/0000-0003-3689-5865
                https://orcid.org/0000-0003-3932-614X
                https://orcid.org/0000-0003-2326-1820
                https://orcid.org/0000-0003-1846-675X
                Article
                jcm-08-00860
                10.3390/jcm8060860
                6617114
                31208104
                c319300d-39cd-4747-b43f-7637ec77931e
                © 2019 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 30 May 2019
                : 12 June 2019
                Categories
                Review

                levamisole,nephrotic syndrome,podocyte,steroid-dependent nephrotic syndrome

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