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|dc.contributor.author||Vazquez-del Mercado, M.|
|dc.description.abstract||Objective: To determine IL-1?, TNF?, IL-6, IL-4, IL-10, MMP-1, MMP-3 and MMP-13 expression by freshly isolated peripheral blood (PBMC) and synovial fluid mononuclear cells (SFMC) in early, never-treated (ENT-RA) and non-acute, treated rheumatoid arthritis (NAT-RA) patients. To elucidate whether excessive or inadequate interleukin (IL) and metalloprotease (MMP) expression is influenced by the disease duration. Methods: Fourteen RA patients, 7 with early RA (< 1 year of evolution) never treated with corticosteroids or disease-modifying antirheumatic drugs, and 7 patients with non-acute RA (> 2 years of evolution) treated with disease-modifying antirheumatic drugs, were studied by ELISA and quantitative and semiquantitative RT-PCR. A group of 14 healthy subjects matched for sex and age was included. Results: No statistically significant difference in the protein or transcript levels for the cytokines of interest was found between the ENT-RA and NAT-RA groups. The cytokine mRNA expression by freshly isolated PBMC and SFMC in both groups was as follows: IL-1? > TNF? > IL-10 > IL-6, with no mRNA IL-4 expression. In contrast, cytokine serum levels in ENT-RA and NAT-RA patients were detected in inverse order as follows: IL-6 > IL-10, while IL-1?, TNF? and IL-4 were undetectable. MMP-3 mRNA expression by the PBMC of NAT-RA patients was statistically different to that in ENT-RA patients. Similar levels of mRNA expression of MMP-1, MMP-3 and MMP-13 by the PBMC and SFMC in both RA groups were observed. Conclusions A close equilibrium between MMP and pro/anti-inflammatory cytokine production is observed in ENT-RA and NAT-RA patients. This balance is apparently not influenced by the length of the disease. Highly sensitive methods such as quantitative RT-PCR and ELISA, and even studying freshly isolated MC, showed sustained cytokine secretion at the local level (synovial fluid/SFMC) and scarce translation at the peripheral level (serum/PBMC). Expression of MMP mRNA needs to be further evaluated in order to know whether their peripheral expression reflects their local activity in RA patients.|
|dc.title||Expression of interleukin-1?, tumor necrosis factor ?, interleukins-6, -10 and -4, and metalloproteases by freshly isolated mononuclear cells from early never-treated and non-acute treated rheumatoid arthritis patients|
|dc.relation.ispartofjournal||Clinical and Experimental Rheumatology|
|dc.subject.keyword||Cytokines; Mononuclear cells; Quantitative RT-PCR; Rheumatoid arthritis; Synovial fluid|
|dc.contributor.affiliation||V�zquez-del Mercado, M., Inst. de Biol. Molecular en Medicina, CUCS, Universidad de Guadalajara, Mexico; Delgado-Rizo, V., Inst. de Biol. Molecular en Medicina, CUCS, Universidad de Guadalajara, Mexico; Mu�oz-Valle, J.F., Inst. de Biol. Molecular en Medicina, CUCS, Universidad de Guadalajara, Mexico; Orozco-Alcal�, J., Hospital Civil de Bel�n, Mexico; Volk, H.-D., Institute for Medical Immunology, University of Berlin, Germany; Armend�riz-Borunda, J., Inst. de Biol. Molecular en Medicina, CUCS, Universidad de Guadalajara, Mexico|
|dc.subject.heading||Index Medicus;Acute Disease;Adult;Antirheumatic Agents/ad [Administration & Dosage];Antisense Elements (Genetics);Arthritis, Rheumatoid/dt [Drug Therapy];Arthritis, Rheumatoid/ge [Genetics];Arthritis, Rheumatoid/im [Immunology];Chronic Disease;Collagenases/ge [Genetics];Female;Gene Expression Regulation, Enzymologic/im [Immunology];Humans;Interleukin-1/ge [Genetics];Interleukin-10/ge [Genetics];Interleukin-4/ge [Genetics];Interleukin-6/ge [Genetics];Interleukins/ge [Genetics];Leukocytes, Mononuclear/en [Enzymology];Leukocytes, Mononuclear/im [Immunology];Male;Matrix Metalloproteinase 1/ge [Genetics];Matrix Metalloproteinase 13;Matrix Metalloproteinase 3/ge [Genetics];Matrix Metalloproteinases/ge [Genetics];Middle Aged;RNA, Messenger/an [Analysis];Reverse Transcriptase Polymerase Chain Reaction;Synovial Fluid/ch [Chemistry];Synovial Fluid/en [Enzymology];Synovial Fluid/im [Immunology];Tumor Necrosis Factor-alpha/ge [Genetics]|
|Appears in Collections:||Producción científica UdeG|
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