Author
Listed:
- Eva Maria Stork
(Leiden University Medical Center, Albinusdreef 2)
- Danique M. H. Rijswijck
(Padualaan 8
Padualaan 8)
- Karin A. Schie
(Leiden University Medical Center, Albinusdreef 2)
- Max Hoek
(Padualaan 8
Padualaan 8)
- Theresa Kissel
(Leiden University Medical Center, Albinusdreef 2)
- Hans Ulrich Scherer
(Leiden University Medical Center, Albinusdreef 2)
- Tom W. J. Huizinga
(Leiden University Medical Center, Albinusdreef 2)
- Albert J. R. Heck
(Padualaan 8
Padualaan 8)
- Rene E. M. Toes
(Leiden University Medical Center, Albinusdreef 2)
- Albert Bondt
(Padualaan 8
Padualaan 8)
Abstract
The presence of autoantibodies is a defining feature of many autoimmune diseases. The number of unique autoantibody clones is conceivably limited by immune tolerance mechanisms, but unknown due to limitations of the currently applied technologies. Here, we introduce an autoantigen-specific liquid chromatography-mass spectrometry-based IgG1 Fab profiling approach using the anti-citrullinated protein antibody (ACPA) repertoire in rheumatoid arthritis (RA) as an example. We show that each patient harbors a unique and diverse ACPA IgG1 repertoire dominated by only a few antibody clones. In contrast to the total plasma IgG1 antibody repertoire, the ACPA IgG1 sub-repertoire is characterised by an expansion of antibodies that harbor one, two or even more Fab glycans, and different glycovariants of the same clone can be detected. Together, our data indicate that the autoantibody response in a prominent human autoimmune disease is complex, unique to each patient and dominated by a relatively low number of clones.
Suggested Citation
Eva Maria Stork & Danique M. H. Rijswijck & Karin A. Schie & Max Hoek & Theresa Kissel & Hans Ulrich Scherer & Tom W. J. Huizinga & Albert J. R. Heck & Rene E. M. Toes & Albert Bondt, 2024.
"Antigen-specific Fab profiling achieves molecular-resolution analysis of human autoantibody repertoires in rheumatoid arthritis,"
Nature Communications, Nature, vol. 15(1), pages 1-12, December.
Handle:
RePEc:nat:natcom:v:15:y:2024:i:1:d:10.1038_s41467-024-47337-x
DOI: 10.1038/s41467-024-47337-x
Download full text from publisher
Corrections
All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:nat:natcom:v:15:y:2024:i:1:d:10.1038_s41467-024-47337-x. See general information about how to correct material in RePEc.
If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.
We have no bibliographic references for this item. You can help adding them by using this form .
If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.
For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Sonal Shukla or Springer Nature Abstracting and Indexing (email available below). General contact details of provider: http://www.nature.com .
Please note that corrections may take a couple of weeks to filter through
the various RePEc services.