Back to Search
Start Over
BLyS and APRIL form biologically active heterotrimers that are expressed in patients with systemic immune-based rheumatic diseases.
- Source :
-
Journal of immunology (Baltimore, Md. : 1950) [J Immunol] 2002 Oct 15; Vol. 169 (8), pp. 4314-21. - Publication Year :
- 2002
-
Abstract
- BLyS and APRIL are two members of the TNF superfamily that are secreted by activated myeloid cells and have costimulatory activity on B cells. BLyS and APRIL share two receptors, TACI and BCMA, whereas a third receptor, BAFF-R, specifically binds BLyS. Both BLyS and APRIL have been described as homotrimeric molecules, a feature common to members of the TNF superfamily. In this study, we show that APRIL and BLyS can form active heterotrimeric molecules when coexpressed and that circulating heterotrimers are present in serum samples from patients with systemic immune-based rheumatic diseases. These findings raise the possibility that active BLyS/APRIL heterotrimers may play a role in rheumatic and other autoimmune diseases and that other members of the TNF ligand superfamily may also form active soluble heterotrimers.
- Subjects :
- Animals
Arthritis, Psoriatic blood
Arthritis, Psoriatic immunology
Arthritis, Reactive blood
Arthritis, Reactive immunology
Arthritis, Rheumatoid blood
Arthritis, Rheumatoid immunology
B-Cell Activation Factor Receptor
B-Lymphocytes metabolism
Cell Line
Cells, Cultured
Female
Humans
Lupus Erythematosus, Systemic blood
Lupus Erythematosus, Systemic immunology
Lymphocyte Activation genetics
Membrane Proteins blood
Membrane Proteins isolation & purification
Mice
Mice, Inbred BALB C
Polymyositis blood
Polymyositis immunology
Receptors, Tumor Necrosis Factor blood
Receptors, Tumor Necrosis Factor isolation & purification
Rheumatic Diseases blood
Spondylitis, Ankylosing blood
Spondylitis, Ankylosing immunology
Transfection
Tumor Cells, Cultured
Tumor Necrosis Factor Ligand Superfamily Member 13
Tumor Necrosis Factor-alpha isolation & purification
B-Lymphocytes immunology
Membrane Proteins biosynthesis
Membrane Proteins physiology
Receptors, Tumor Necrosis Factor biosynthesis
Receptors, Tumor Necrosis Factor physiology
Rheumatic Diseases immunology
Tumor Necrosis Factor-alpha biosynthesis
Tumor Necrosis Factor-alpha physiology
Subjects
Details
- Language :
- English
- ISSN :
- 0022-1767
- Volume :
- 169
- Issue :
- 8
- Database :
- MEDLINE
- Journal :
- Journal of immunology (Baltimore, Md. : 1950)
- Publication Type :
- Academic Journal
- Accession number :
- 12370363
- Full Text :
- https://doi.org/10.4049/jimmunol.169.8.4314