Decreased peripheral blood T cell cytokine gene expression in rheumatoid arthritis

Citation
P. Louhet-lescoulie et al., Decreased peripheral blood T cell cytokine gene expression in rheumatoid arthritis, SC J RHEUM, 28(4), 1999, pp. 244-251
Citations number
44
Categorie Soggetti
Rheumatology,"da verificare
Journal title
SCANDINAVIAN JOURNAL OF RHEUMATOLOGY
ISSN journal
03009742 → ACNP
Volume
28
Issue
4
Year of publication
1999
Pages
244 - 251
Database
ISI
SICI code
0300-9742(1999)28:4<244:DPBTCC>2.0.ZU;2-7
Abstract
Currently, few informations are available about spontaneous production of T cell cytokines in rheumatoid arthritis (RA) peripheral blood (PB), because these cytokines are generally under the detection threshold of ELISAs. Bec ause the Th1/Th2 balance could help to determine the outcome of RA, we used a sensitive and quantitative reverse transcriptase-polymerase chain reacti on (RT-PCR) method to mesure spontaneous T cell production of IL-2, IL-4, I L-10, and IFN-gamma mRNAs using unstimulated PBMC from 25 active RA patient s, not taking any DMARDs for at least 6 weeks, and 19 healthy controls. Spo ntaneous IL-2 and IL-4 mRNA expressions are significantly lower in RA patie nts compared to healthy controls. Levels of IL-10 and IFN-gamma are similar in the two groups. No correlation was found between cytokine mRNA levels a nd clinical parameters. Spontaneous IL-4 and IL-10 mRNA levels are respecti vely correlated to the number of CD4+ T cells and to the number of monocyte s in PB. After in vitro stimulation, IFN-gamma mRNA production by RA PBMC i s significantly decreased. Most of the patients cannot be classified as hav ing a T cell cytokine type 1 or type 2 secretion pattern in PB. IL-2 and IL -4 mRNAs in PB of active RA are produced at a low spontaneous level and the response to in vitro activation by mitogen is weak.