EXPRESSION OF THE MULTIDRUG-RESISTANCE GLYCOPROTEIN-170 IN THE PERIPHERAL-BLOOD LYMPHOCYTES OF RHEUMATOID-ARTHRITIS PATIENTS - THE PERCENTAGE OF LYMPHOCYTES EXPRESSING GLYCOPROTEIN-170 IS INCREASED IN PATIENTSTREATED WITH PREDNISOLONE

Citation
Jf. Maillefert et al., EXPRESSION OF THE MULTIDRUG-RESISTANCE GLYCOPROTEIN-170 IN THE PERIPHERAL-BLOOD LYMPHOCYTES OF RHEUMATOID-ARTHRITIS PATIENTS - THE PERCENTAGE OF LYMPHOCYTES EXPRESSING GLYCOPROTEIN-170 IS INCREASED IN PATIENTSTREATED WITH PREDNISOLONE, British journal of rheumatology, 35(5), 1996, pp. 430-435
Citations number
36
Categorie Soggetti
Rheumatology
ISSN journal
02637103
Volume
35
Issue
5
Year of publication
1996
Pages
430 - 435
Database
ISI
SICI code
0263-7103(1996)35:5<430:EOTMGI>2.0.ZU;2-E
Abstract
The objective was to evaluate the expression of the multidrug resistan ce P-glycoprotein (P-gp) in peripheral blood lymphocytes (PBL) of pati ents with rheumatoid arthritis (RA). PBL from 68 RA patients and 44 co ntrols were evaluated. RA patients had a mean disease duration of 10.7 yr, with a mean number of past resistances to DMARDs of 0.82, and wer e treated with NSAIDs (n = 34), DMARDs (n = 25) and prednisolone (n = 40). Fluorescence flow cytometry was used to assess P-gp membrane expr ession on PBL. In the RA group, the percentage of PBL expressing P-gp was higher in patients treated with prednisolone than in other patient s [mean +/- S.D.: 10.7 +/- 15.8% vs 3.3 +/- 7.6%, P < 0.03, Student] a nd was not related to other therapies, age, sex, RA duration, number o f past resistances to DMARDs, activity, ESR, CRP. The percentage of PB L expressing P-gp did not differ in RA and control groups, but was hig her in the prednisolone-treated RA patients than in controls. Predniso lone could induce a rise in the percentage of PBL expressing P-gp. On the contrary, patients with a high percentage of PBL expressing P-gp c ould be more resistant to DMARDs and need prednisolone earlier. Furthe r studies are needed to address this question and to evaluate the pote ntial implication of P-gp in drug resistance in RA.