Very late activation antigen on synovial fluid T cells from patients with rheumatoid arthritis and other rheumatic diseases
✍ Scribed by A. Laffon; F. Sánchez-madrid; M. Ort Íz de Landázuri; A. Jim Énez Cuesta; A. Ariza; C. Ossorio; P. Sabando
- Publisher
- John Wiley and Sons
- Year
- 1989
- Tongue
- English
- Weight
- 591 KB
- Volume
- 32
- Category
- Article
- ISSN
- 0004-3591
No coin nor oath required. For personal study only.
✦ Synopsis
We used flow cytometry and immunoprecipitation techniques to study the expression of the activation molecules transferrin receptor, interleukin-2 receptor, HLA-DR, and very late activation antigen 1 (VLA-1) on purified T lymphocytes from peripheral blood and synovial fluid of 9 patients with rheumatoid arthritis and 7 patients with other rheumatic diseases. We found a T cell subset bearing VLA-1 in synovial fluid from 8 rheumatoid arthritis patients and 4 patients with other rheumatic diseases. VLA-1 was not found in peripheral blood T lymphocytes from either group.
Antigen or mitogen stimulation of resting T lymphocytes results in T cell proliferation accompanied by the acquisition of various effector functions. In the course of T cell activation, a number of cell surface glycoproteins are newly expressed and follow a distinct kinetic pattern of appearance. Some molecules, such as interleukin-2 receptors (IL-2R), transferrin receptors (TrR), insulin receptors, 4F2, and early activation antigen 1, appear early, even before DNA synthesis (1-5). Others, such as HLA-DR, CB.1, Ta,, T lineage-specific activation antigen 1 (TLiSA-l), and
📜 SIMILAR VOLUMES
and Kennedy Institute of Rheumat ology a, London Detection of interleukin 8 biological activity in synovial fluids from patients with rheumatoid arthritis and production of interleukin 8 mRNA by isolated synovial cells\* The presence of neutrophils in the synovial joint of patients with rheumatoid
## Abstract ## Objective To determine the signal transduction pathways in CD14+ synovial cells from patients with rheumatoid arthritis (RA) after CD40 ligation, and to examine their role in amplifying synovial inflammation in affected joints. ## Methods Expression of messenger RNA was analyzed u