Natural antibody and complement activation characterize patients with idiopathic nephrotic syndrome

Author:

Trachtman Howard1,Laskowski Jennifer2,Lee Cameron2,Renner Brandon2,Feemster Andrew1,Parikh Samir3,Panzer Sarah E.4,Zhong Weixiong4,Cravedi Paolo5,Cantarelli Chiara6,Kulik Liudmila2,You Zhiying2,Satchell Simon7,Rovin Brad3,Liu Fei8,Kalled Susan L.8,Holers V. Michael2,Jalal Diana9,Thurman Joshua M.2ORCID

Affiliation:

1. Department of Pediatrics, Langone Medical Center, New York University School of Medicine, New York, New York

2. Department of Medicine, Anschutz Medical Campus, University of Colorado School of Medicine, Aurora, Colorado

3. Department of Internal Medicine, Ohio State University Wexner Medical Center, Columbus, Ohio

4. Department of Medicine, University of Wisconsin-Madison Hospital and Clinics, Madison, Wisconsin

5. Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, New York

6. Dipartimento di Medicina e Chirurgia, Università di Parma, UO Nefrologia, Azienda Ospedaliero-Universitaria di Parma, Parma, Italy

7. Bristol Renal, Faculty of Health Sciences, University of Bristol, Bristol, United Kingdom

8. Q32 Bio, Incorporated, Cambridge, Massachusetts

9. Department of Medicine, University of Iowa Hospitals and Clinics, Iowa City, Iowa

Abstract

IgM is detected in biopsies from some patients with nephrotic syndrome, although this has been attributed to passive trapping of the protein. We found, however, that IgM colocalizes with complement activation fragments in some glomeruli. We also found that affected patients had higher levels of IgM reactive to glomerular endothelial cell epitopes. Thus, IgM activates the complement system in the glomeruli of some patients with nephrotic syndrome and may contribute to injury.

Funder

HHS | NIH | National Institute of Diabetes and Digestive and Kidney Diseases

Nephcure Foundation

U.S. Department of Defense

Publisher

American Physiological Society

Subject

Physiology

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