Medizinische Universität Graz - Research portal

Logo MUG Resarch Portal

Selected Publication:

Aringer, M; Wintersberger, W; Steiner, CW; Kiener, H; Presterl, E; Jaeger, U; Smolen, JS; Graninger, WB.
High levels of bcl-2 protein in circulating T lymphocytes, but not B lymphocytes, of patients with systemic lupus erythematosus.
Arthritis Rheum. 1994; 37(10):1423-1430 Doi: 10.1002/art.1780371004
Web of Science PubMed FullText FullText_MUG

 

Leading authors Med Uni Graz
Graninger Winfried
Altmetrics:

Dimensions Citations:

Plum Analytics:

Scite (citation analytics):

Abstract:
OBJECTIVE. Defective regulation of programmed cell death (apoptosis) may play a role in the development of autoimmune diseases, and the proto-oncogene bcl-2 is involved in the control of apoptosis in immunocompetent cells. We therefore wished to investigate the expression of bcl-2 in the peripheral lymphocytes of patients with systemic lupus erythematosus (SLE), a prototypical autoimmune disease. METHODS. Levels of bcl-2 expression in the lymphocytes of patients with SLE and, for comparison, in the lymphocytes of healthy controls and patients with rheumatoid arthritis (RA), systemic bacterial infections, and chronic B cell lymphocytic leukemia were studied by 2-color cytofluorography and RNA analysis. RESULTS. In SLE patients, a significant proportion of T cells expressed increased amounts of bcl-2 protein. By fluorescence-activated cell sorter analysis, bcl-2--enriched lymphocytes were found in the CD45RO+ as well as in the CD45RO-, and also in the CD4+ and CD8+, lymphocyte subpopulations. Mononuclear cells of patients with SLE showed increased amounts of bcl-2 messenger RNA. An increased percentage of strongly bcl-2 positive peripheral T lymphocytes was found in patients with bacterial infections, but not in those with RA. CONCLUSION. Although the occurrence of circulating T lymphocytes with abnormally high bcl-2 expression is not specific for SLE, it is evidence for a dysregulation of lymphocytic programmed cell death in this autoimmune disease.
Find related publications in this database (using NLM MeSH Indexing)
Adolescent -
Adult -
Aged -
B-Lymphocytes - chemistry
Base Sequence -
Female -
Fluorescent Antibody Technique -
Humans -
Lupus Erythematosus, Systemic - blood
Male -
Middle Aged -
Molecular Sequence Data -
Polymerase Chain Reaction -
Proto-Oncogene Proteins - analysis Proto-Oncogene Proteins - genetics
Proto-Oncogene Proteins c-bcl-2 -
RNA, Messenger - analysis
Severity of Illness Index -
T-Lymphocytes - chemistry

© Med Uni GrazImprint