Literature DB >> 26170177

Immunosuppressive Medications.

Alexander C Wiseman1.   

Abstract

Immunosuppressive agents are commonly used in the nephrologist's practice in the treatment of autoimmune and immune-mediated diseases and transplantation, and they are investigational in the treatment of AKI and ESRD. Drug development has been rapid over the past decades as mechanisms of the immune response have been better defined both by serendipity (the discovery of agents with immunosuppressive activity that led to greater understanding of the immune response) and through mechanistic study (the study of immune deficiencies and autoimmune diseases and the critical pathways or mutations that contribute to disease). Toxicities of early immunosuppressive agents, such as corticosteroids, azathioprine, and cyclophosphamide, stimulated intense investigation for agents with more specificity and less harmful effects. Because the mechanisms of the immune response were better delineated over the past 30 years, this specialty is now bestowed with a multitude of therapeutic options that have reduced rejection rates and improved graft survival in kidney transplantation, provided alternatives to cytotoxic therapy in immune-mediated diseases, and opened new opportunities for intervention in diseases both common (AKI) and rare (atypical hemolytic syndrome). Rather than summarizing clinical indications and clinical trials for all currently available immunosuppressive medications, the purpose of this review is to place these agents into mechanistic context together with a brief discussion of unique features of development and use that are of interest to the nephrologist.
Copyright © 2016 by the American Society of Nephrology.

Entities:  

Keywords:  GN; activation; cell; cytokines; immunology; kidney transplantation

Mesh:

Substances:

Year:  2015        PMID: 26170177      PMCID: PMC4741049          DOI: 10.2215/CJN.08570814

Source DB:  PubMed          Journal:  Clin J Am Soc Nephrol        ISSN: 1555-9041            Impact factor:   8.237


  106 in total

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Journal:  Am J Transplant       Date:  2008-09-18       Impact factor: 8.086

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Review 6.  Once-daily extended-release versus twice-daily standard-release tacrolimus in kidney transplant recipients: a systematic review.

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  64 in total

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7.  Tacrolimus variability is associated with de novo donor-specific antibody development in pediatric renal transplant recipients.

Authors:  Sonia Solomon; Adriana Colovai; Marcela Del Rio; Nicole Hayde
Journal:  Pediatr Nephrol       Date:  2019-11-15       Impact factor: 3.714

8.  Human Immunodeficiency Virus (HIV)- and Non-HIV-Associated Immunosuppression and Risk of Cervical Neoplasia.

Authors:  Michael J Silverberg; Wendy A Leyden; Aileen Chi; Steven Gregorich; Megan J Huchko; Shalini Kulasingam; Miriam Kuppermann; Anna Seto; Karen K Smith-McCune; George F Sawaya
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Authors:  Binjie Xu; Qiuhua Wei; M Ryan Mettetal; Jie Han; Lindsey Rau; Jinfeng Tie; Rhea M May; Eric T Pathe; Shravanthi T Reddy; Lauren Sullivan; Albert E Parker; Donald H Maul; Anthony B Brennan; Ethan E Mann
Journal:  J Med Microbiol       Date:  2017-10-06       Impact factor: 2.472

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