Literature DB >> 9683555

Soluble CD16 in the treatment of murine lupus nephritis.

H Watanabe1, D Sherris, G S Gilkeson.   

Abstract

To determine if soluble CD16 (sCD16) could alter the expression of lupus-like disease, groups of 10 female NZB/NZW mice (age 16-20 weeks) were given sCD16 three times a week for 5 weeks (control; 100 microg; 200 microg/dose) after onset of proteinuria. Results of this study indicate that the administration of sCD16 after onset of disease lowered anti-DNA levels, delayed the development of proteinuria, and significantly prolonged survival while the mice were on treatment. These results indicate that sCD16 alters the expression of autoantibodies and the progression of renal disease in NZB/NZW mice, suggesting that therapies directed at Fc receptors may be useful in the treatment of SLE. Copyright 1998 Academic Press.

Entities:  

Mesh:

Substances:

Year:  1998        PMID: 9683555     DOI: 10.1006/clin.1998.4553

Source DB:  PubMed          Journal:  Clin Immunol Immunopathol        ISSN: 0090-1229


  3 in total

Review 1.  The FcγR/IgG Interaction as Target for the Treatment of Autoimmune Diseases.

Authors:  Peter Sondermann
Journal:  J Clin Immunol       Date:  2016-04-02       Impact factor: 8.317

Review 2.  Therapy of systemic lupus erythematosus: a look into the future.

Authors:  Josef S Smolen
Journal:  Arthritis Res       Date:  2002-05-09

3.  The spliceosomal phosphopeptide P140 controls the lupus disease by interacting with the HSC70 protein and via a mechanism mediated by gammadelta T cells.

Authors:  Nicolas Page; Nicolas Schall; Jean-Marc Strub; Marc Quinternet; Olivier Chaloin; Marion Décossas; Manh Thong Cung; Alain Van Dorsselaer; Jean-Paul Briand; Sylviane Muller
Journal:  PLoS One       Date:  2009-04-23       Impact factor: 3.240

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.