Abstract
T-regs and Th17 cells are the new generation of CD4+T-cells which play crucial role in autoimmunity. Both of subsets can influence each other and probably have common precursor. A key question for understanding the mechanism of autoimmunity is to recognize how T-regs and Th17 cells turn from self-protection to autoreactivity. Based on literature data and own observations, we have constructed a conception of age-dependent thymic T-cells maturation peripherialisation as cause of errors in Th17-T-reg cells interrelations. The connection of T-regs with thymus is determined currently. Connection of Th17 cells with thymus remains to be determined properly. Main, there may be naturally occurring Tregs of thymic origin that are resistant to cell death and serve as reserve pool for autoimmunity protective suppressors. This mechanism could be affected by external factors producing profound lymphopenia [1]. Previously we found that RA patients with numerous rheumatoid nodules (RN) and lymphopenia had statistically reliable decrease of CD3+T-cells level. We found definite negative correlation between CD3+PBL amount and RN number (p = 0,029). In all RA patients with and without RN we didn't found the decrease of CD4 receptor. Hereby we expected to find unusual CD3-4+ and CD3-8+ cells in RA. Otherwise the percentage of CD3+4+ and CD3+8+ cells was normal in general. But in 4 RA patients after magnetic separation of CD3+T-cells we detected reliable amount of CD3-4+ lymphocytes (25-28%) These cells were not detected before separation. One of possible explanation of this phenomenon is CD3 molecule modulation after the contact with anti-CD3 antibodies conjugated with magnetic particles. So the presence of T-cells with unusual phenotype in peripheral blood of RA patients doesn't give absolute evidence of T-cells maturation disorders. According to our viewpoint recent thymic emigrants (RTE) fraction presence among T-regs and hypothetically among Th17-cells is the sign of normal Th17/T-regs function. Otherwise the absence of RTE among them leads to immunopathology. CD31 receptor and T cell receptor rearrangement excision circles (TREC) are now markers of RTE. We investigated the number of CD4+CD31+T-cells in RA patients. The preliminary results permit us to suggest the diminution of RTE in RA (less then 1%/ml) We also found the diminution of TREC amount in PBL of 22 rheumatoid arthritis patients, (Median 0,035539 units). FOXP3, RORγ, RORα and CD31 expression in RA will permit to establish role of RTE in autoimmunity.
Highlights
Acute isolated neurological syndromes, such as optic neuropathy or transverse myelopathy, may cause diagnostic problems since they can be the first presentations in a number of demyelinating disorders including multiple sclerosis (MS) and collagen diseases
tumor necrosis factor (TNF) therapy and demyelinating event: A report indicates that adverse events such as the demyelinating lesion in the brain, optic neuritis, and neuropathy occurred after treatment with anti-TNF alpha therapy in collagen disease, and TNF antagonizing therapy showed worsening in a clinical trial with MS
Believing on the similarities of normal joints in humans and monkeys, we have employed a model of collagen-induced arthritis in Macaca fascicularis in an attempt to evaluate the histological alterations caused by such condition in the extracellular matrix of the articular cartilage
Summary
Acute isolated neurological syndromes, such as optic neuropathy or transverse myelopathy, may cause diagnostic problems since they can be the first presentations in a number of demyelinating disorders including multiple sclerosis (MS) and collagen diseases. Acute Serum Amyloid A (A-SAA) is an acute phase protein strongly expressed in rheumatoid arthritis (RA) synovial tissue (ST) critically involved in regulating cell migration and angiogenesis These processes are dependent on downstream interactions between extracellular matrix and cytoskeletal components. Conclusions: These results indicate that Egr-1 contributes to IL-1mediated down-regulation of PPARg expression in OA chondrocytes and suggest that this pathway could be a potential target for pharmacologic intervention in the treatment of OA and possibly other arthritic diseases. Immune cell-derived microparticles (MPs) are present at increased amounts in synovial fluid of rheumatoid arthritis (RA) patients [1] and can activate disease-relevant signalling pathways in RA synovial fibroblasts (SF) [2,3].
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