4.7 Article

Laminin-521 is a Novel Target of Autoantibodies Associated with Lung Hemorrhage in Anti-GBM Disease

Journal

JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY
Volume 32, Issue 8, Pages 1887-1897

Publisher

AMER SOC NEPHROLOGY
DOI: 10.1681/ASN.2020101431

Keywords

anti-GBM disease; extracellular matrix; glomerulonephritis; Goodpasture?s syndrome; laminin; autoantibodies; pulmonary hemorrhage; glomerular basement membrane

Funding

  1. National Institute of Minority Health and Health Disparities [U54 MD0007586]
  2. National Key Research and Development Program [2016YFC1305400]
  3. National Natural Science Foundation of China [81870482, 81870486]
  4. Chinese Academy of Medical Sciences Innovation Fund for Medical Sciences [2019-I2M-5-046]
  5. US Department of Defense Congressionally Directed Medical Research Programs [LR190150]
  6. Dialysis Clinic Inc.
  7. Paul Teschan Research Fund grant [2018-04]

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In patients with anti-GBM antibody GN, circulating IgG autoantibodies binding to laminin-521 were found in about one third of patients, but not in healthy controls or patients with other glomerular diseases. Autoreactivity towards laminin-521 was significantly more common in patients with anti-GBM GN and lung hemorrhage than in patients with kidney-limited disease.
Background Antiglomerular basement membrane (anti-GBM) disease is characterized byGNand often pulmonary hemorrhage, mediated by autoantibodies that typically recognize cryptic epitopes within alpha 345( IV) collagen-amajor component of the glomerular and alveolar basementmembranes. Laminin-521 is another major GBM component and a proven target of pathogenic antibodies mediating GN in animal models. Whether laminin-521 is a target of autoimmunity in human anti-GBM disease is not yet known. Methods A retrospective study of circulating autoantibodies from 101 patients with anti-GBM/Goodpasture's disease and 85 controls used a solid-phase immunoassay to measure IgG binding to human recombinant laminin-521 with native-like structure and activity. Results Circulating IgGautoantibodies binding to laminin-521were found in about one third of patientswith anti-GBM antibody GN, but were not detected in healthy controls or in patients with other glomerular diseases. Autoreactivity toward laminin-521 was significantly more common in patients with anti-GBM GN and lung hemorrhage, compared with those with kidney-limited disease (51.5% versus 23.5%, P=0.005). Antilaminin-521autoantibodieswerepredominantly of IgG1 and IgG4 subclasses andsignificantly associated with lung hemorrhage (P=0.005), hemoptysis (P=0.008), and smoking (P=0.01), although not with proteinuria or serum creatinine at diagnosis. Conclusions Besides alpha 345( IV) collagen, laminin-521 is anothermajor autoantigen targeted in anti-GBM disease. Autoantibodies to laminin-521 may have the potential to promote lung injury in anti-GBM disease by increasing the total amount of IgG bound to the alveolar basement membranes.

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