ACR Meeting Abstracts

ACR Meeting Abstracts

  • Meetings
    • ACR Convergence 2024
    • ACR Convergence 2023
    • 2023 ACR/ARP PRSYM
    • ACR Convergence 2022
    • ACR Convergence 2021
    • ACR Convergence 2020
    • 2020 ACR/ARP PRSYM
    • 2019 ACR/ARP Annual Meeting
    • 2018-2009 Meetings
    • Download Abstracts
  • Keyword Index
  • Advanced Search
  • Your Favorites
    • Favorites
    • Login
    • View and print all favorites
    • Clear all your favorites
  • ACR Meetings

Abstract Number: 295

Ex Vivo Induced Neutrophil Extracellular Traps Are Intrinsically Different in Anca-Associated Vasculitis and Systemic Lupus Erythematosus

Laura van Dam1, Tineke Kraaij1, Sylvia Kamerling1, Hans U. Scherer2, Charles Pusey3, Ton Rabelink1, Cees van Kooten1 and Onno Teng1, 1Nephrology, Leiden University Medical Center, Leiden, Netherlands, 2Rheumatology, Leiden University Medical Center, Leiden, Netherlands, 3Imperial College, London, United Kingdom

Meeting: 2017 ACR/ARHP Annual Meeting

Date of first publication: September 18, 2017

Keywords: Auto-immunity, autoantigens and vasculitis, NETosis, SLE

  • Tweet
  • Click to email a link to a friend (Opens in new window) Email
  • Click to print (Opens in new window) Print
Session Information

Date: Sunday, November 5, 2017

Title: Innate Immunity and Rheumatic Disease Poster I

Session Type: ACR Poster Session A

Session Time: 9:00AM-11:00AM

–          Background/Purpose: Neutrophil extracellular traps (NETs) are immunogenic, extracellular DNA structures that harness important autoantigens to be recognized by the adaptive immune system. NETs are thought to play a pivotal role in the pathogenesis of ANCA-associated vasculitis (AAV) and SLE. However it is still unclear how and if NETs can act as a common pathway in the pathophysiology of these clinically divergent autoimmune diseases. The aim of the present study is to characterize AAV- and SLE-induced NETs.

–          Methods: The present study involved 88 AAV patients according to the Chapel Hill consensus definitions of 2012, 59 SLE patients  according to the ACR criteria 1997 and 10 healthy controls. Healthy neutrophils were stimulated with 10% serum of AAV or SLE patients to induce NETs. Ex vivo NET induction by serum and IgG-depleted serum was measured by a novel, highly-sensitive NET quantification assay using 3D-confocal microscopy1. Qualitative characteristics of NETs were studied by immunofluorescence to detect NET-related auto-antigens. Additionally, the morphology and kinetics of AAV- and SLE-induced NETosis were visualized by live cell imaging and electron microscopy.

 

–          Results: Ex vivo NET induction by AAV sera was 19.36 [9.161 – 73.08], (median [Q1 –  Q3]) fold higher than sera of healthy controls (n=10) and also significantly higher than NET induction by SLE sera 5.56 [2.34 – 14.33] (Figure 1). Depletion of IgG from serum did not reduce NET induction in AAV, but it decreased NET induction significantly in SLE, indicating that different triggers mediate the induction of neutrophil extracellular traps in these autoimmune diseases. Additionally, the colocalisation of NET-related auto-antigens was different: citrullinated histon-3 (CitH3) was predominantly found on AAV-induced NETs, whereas high mobility group box protein-1 (HMGB-1) was exclusively found on SLE-induced NETs. Moreover, live cell imaging demonstrated that the kinetics of SLE-induced NETs peaked at 60 minutes, while AAV-induced NETs peaked at 4 hours (Figure 2). Intriguingly, SLE sera induced immediate clustering of neutrophils surrounding NETs whereas AAV sera induced NETs composed of long, thin DNA-fibres through lytic expulsion.

 

–          Conclusion: We demonstrate intrinsically distinct features of AAV- and SLE-induced NETs, indicating that NET formation in AAV and SLE is based on different mechanisms. Future studies should be directed at unravelling how different NETs are involved in causing SLE- or AAV-associated glomerulonephritis.

1.       T. Kraaij et al. – Autoimmunity Reviews 15 (2016) 577–584


Disclosure: L. van Dam, None; T. Kraaij, None; S. Kamerling, None; H. U. Scherer, None; C. Pusey, None; T. Rabelink, None; C. van Kooten, None; O. Teng, None.

To cite this abstract in AMA style:

van Dam L, Kraaij T, Kamerling S, Scherer HU, Pusey C, Rabelink T, van Kooten C, Teng O. Ex Vivo Induced Neutrophil Extracellular Traps Are Intrinsically Different in Anca-Associated Vasculitis and Systemic Lupus Erythematosus [abstract]. Arthritis Rheumatol. 2017; 69 (suppl 10). https://acrabstracts.org/abstract/ex-vivo-induced-neutrophil-extracellular-traps-are-intrinsically-different-in-anca-associated-vasculitis-and-systemic-lupus-erythematosus/. Accessed .
  • Tweet
  • Click to email a link to a friend (Opens in new window) Email
  • Click to print (Opens in new window) Print

« Back to 2017 ACR/ARHP Annual Meeting

ACR Meeting Abstracts - https://acrabstracts.org/abstract/ex-vivo-induced-neutrophil-extracellular-traps-are-intrinsically-different-in-anca-associated-vasculitis-and-systemic-lupus-erythematosus/

Advanced Search

Your Favorites

You can save and print a list of your favorite abstracts during your browser session by clicking the “Favorite” button at the bottom of any abstract. View your favorites »

All abstracts accepted to ACR Convergence are under media embargo once the ACR has notified presenters of their abstract’s acceptance. They may be presented at other meetings or published as manuscripts after this time but should not be discussed in non-scholarly venues or outlets. The following embargo policies are strictly enforced by the ACR.

Accepted abstracts are made available to the public online in advance of the meeting and are published in a special online supplement of our scientific journal, Arthritis & Rheumatology. Information contained in those abstracts may not be released until the abstracts appear online. In an exception to the media embargo, academic institutions, private organizations, and companies with products whose value may be influenced by information contained in an abstract may issue a press release to coincide with the availability of an ACR abstract on the ACR website. However, the ACR continues to require that information that goes beyond that contained in the abstract (e.g., discussion of the abstract done as part of editorial news coverage) is under media embargo until 10:00 AM ET on November 14, 2024. Journalists with access to embargoed information cannot release articles or editorial news coverage before this time. Editorial news coverage is considered original articles/videos developed by employed journalists to report facts, commentary, and subject matter expert quotes in a narrative form using a variety of sources (e.g., research, announcements, press releases, events, etc.).

Violation of this policy may result in the abstract being withdrawn from the meeting and other measures deemed appropriate. Authors are responsible for notifying colleagues, institutions, communications firms, and all other stakeholders related to the development or promotion of the abstract about this policy. If you have questions about the ACR abstract embargo policy, please contact ACR abstracts staff at [email protected].

Wiley

  • Online Journal
  • Privacy Policy
  • Permissions Policies
  • Cookie Preferences

© Copyright 2025 American College of Rheumatology