2017
DOI: 10.1007/s10238-017-0475-0
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Expression of MIF and TNFA in psoriatic arthritis: relationship with Th1/Th2/Th17 cytokine profiles and clinical variables

Abstract: Psoriatic arthritis (PsA) is an autoimmune inflammatory disease associated with psoriasis. The cause of this pathology is still unknown, but research suggests the diseases are caused by a deregulated cytokine production. MIF is a cytokine associated with immunomodulation of Th1, Th2, and Th17 cytokine profiles in inflammatory diseases. Based on this knowledge, the aim of this study was to determine the association of MIF and TNFA expression with Th1, Th2, and Th17 cytokine profiles in serum levels of PsA patie… Show more

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Cited by 14 publications
(6 citation statements)
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“…3. TNF-α is an inflammatory cytokine in the serum and may also be the indicator of severity of inflammation (Bautista-Herrera et al, 2018). In our experiments, TNF-α level was dramatically increased by RA induction, and these elevations were recovered by either FK506 medication or each treatment (Fig.…”
Section: Inflammatory Cytokine Measurement In Serumsupporting
confidence: 52%
“…3. TNF-α is an inflammatory cytokine in the serum and may also be the indicator of severity of inflammation (Bautista-Herrera et al, 2018). In our experiments, TNF-α level was dramatically increased by RA induction, and these elevations were recovered by either FK506 medication or each treatment (Fig.…”
Section: Inflammatory Cytokine Measurement In Serumsupporting
confidence: 52%
“…This finding differs from prior studies of patients with psoriasis, which found that levels of serum Th2 cytokines, including IL-4 and IL-10, were unaffected. [14][15][16][17] This discrepancy may arise because GPP is associated with an immune regulation network that is overlapping but distinct from that of psoriasis vulgaris, as revealed by a recent gene profiling study. 7 Moreover, a serum cytokine analysis in six patients with GPP indicated that levels of IL-4 and IL-10 were considerably associated with disease severity.…”
Section: Discussionmentioning
confidence: 99%
“…2,5 It is well established that PsA is an IL-17/IL-23 axismediated disease with a strong deregulation of proinflammatory cytokine production. 1,16 IL-17 is a cytokine family of six members named IL-17A to IL-17F, synthesized mainly by Th17 cells, which are differentiated from naïve T cells through several cytokine combinations such as IL-1β and IL-23 in the presence of IL-6, tumor necrosis factor α (TNFα), IL-21, and transforming growth factor β (TGFβ). [17][18][19] The expression of the Th17 cell effector molecules depends on their master regulator, the transcription factor RORγt, encoded by the RORC gene, which is activated by the signal transducer and activator of transcription 3 (STAT3), under the stimulation of polarizing cytokines.…”
Section: Discussionmentioning
confidence: 99%
“…27 This positive correlation between IL-17A and TNFα has previously been observed at the systemic level in PsA patients in our population. 16 In inflammatory arthritis, IL-17A can induce MMP production driving the degradation of the extracellular matrix in the joint. 28 In addition, IL-17A can upregulate the RANK (receptor activator of nuclear factor kappa-Β) ligand on osteoblasts and T cells, promoting osteoclast activation and consequently bone destruction.…”
Section: Discussionmentioning
confidence: 99%