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- Circiumaru, Alexandra, et al.
(author)
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Anti-Citrullinated Protein Antibody Reactivity towards Neutrophil-Derived Antigens : Clonal Diversity and Inter-Individual Variation
- 2023
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In: Biomolecules. - : MDPI. - 2218-273X. ; 13:4
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Journal article (peer-reviewed)abstract
- Background: Why the adaptive immune system turns against citrullinated antigens in rheumatoid arthritis (RA) and whether anti-citrullinated protein antibodies (ACPAs) contribute to pathogenesis are questions that have triggered intense research, but still are not fully answered. Neutrophils may be crucial in this context, both as sources of citrullinated antigens and also as targets of ACPAs. To better understand how ACPAs and neutrophils contribute to RA, we studied the reactivity of a broad spectrum of RA patient-derived ACPA clones to activated or resting neutrophils, and we also compared neutrophil binding using polyclonal ACPAs from different patients.Methods: Neutrophils were activated by Ca2+ ionophore, PMA, nigericin, zymosan or IL-8, and ACPA binding was studied using flow cytometry and confocal microscopy. The roles of PAD2 and PAD4 were studied using PAD-deficient mice or the PAD4 inhibitor BMS-P5.Results: ACPAs broadly targeted NET-like structures, but did not bind to intact cells or influence NETosis. We observed high clonal diversity in ACPA binding to neutrophil-derived antigens. PAD2 was dispensable, but most ACPA clones required PAD4 for neutrophil binding. Using ACPA preparations from different patients, we observed high patient-to-patient variability in targeting neutrophil-derived antigens and similarly in another cellular effect of ACPAs, the stimulation of osteoclast differentiation.Conclusions: Neutrophils can be important sources of citrullinated antigens under conditions that lead to PAD4 activation, NETosis and the extrusion of intracellular material. A substantial clonal diversity in targeting neutrophils and a high variability among individuals in neutrophil binding and osteoclast stimulation suggest that ACPAs may influence RA-related symptoms with high patient-to-patient variability.
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| 2. |
- Krishnamurthy, Akilan, et al.
(author)
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Combination of Two Monoclonal Anti–Citrullinated Protein Antibodies Induced Tenosynovitis, Pain, and Bone Loss in Mice in a Peptidyl Arginine Deiminase-4–Dependent Manner
- 2023
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In: Arthritis & Rheumatology. - : Wiley. - 2326-5191 .- 2326-5205. ; 75:2, s. 164-170
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Journal article (peer-reviewed)abstract
- Objective. The appearance of anti–citrullinated protein antibodies (ACPAs) in the circulation represents a major risk factor for developing rheumatoid arthritis (RA). Patient-derived ACPAs have been shown to induce pain and bone erosion in mice, suggesting an active role in the pathogenicity of RA. We undertook this study to investigate whether ACPAs can induce tenosynovitis, an early sign of RA, in addition to pain and bone loss and whether these symptoms are dependent on peptidyl arginine deiminase 4 (PAD4).Methods. Monoclonal ACPAs generated from plasma cells of RA patients were transferred to wild-type and PAD4-deficient mice. Pain-like behavior and macroscopic inflammation were monitored for a period of 4 weeks, followed by the analyses of tenosynovitis in the ankle joints using magnetic resonance imaging (MRI) and bone microarchitecture in the tibia using an X-ray microscope. Microscopic changes in the tendon sheath were analyzed in decalcified ankle joint sections.Results. The combination of 2 monoclonal ACPAs (1325:04C03 and 1325:01B09) induced long-lasting pain-like behavior and trabecular bone loss in mice. Although no synovitis was observed macroscopically, we detected tenosynovitis in the ACPA-injected mice by MRI. Microscopic analyses of the joints revealed a cellular hyperplasia and a consequent enlargement of the tendon sheath in the ACPA-treated group. In PAD4−/− mice, the effects of ACPAs on pain-like behavior, tenosynovitis, and bone loss were significantly reduced.Conclusion. Monoclonal ACPAs can induce tenosynovitis in addition to pain and bone loss via mechanisms dependent on PAD4-mediated citrullination.
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| 4. |
- Krishnamurthy, Akilan
(author)
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Molecular studies on the autoantibody-mediated bone destruction in rheumatoid arthritis
- 2017
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Doctoral thesis (other academic/artistic)abstract
- Autoantibody-positive rheumatoid arthritis (RA), also called seropositive RA, is characterised by the presence of anti citrullinated proteins antibodies (ACPA) that can be detected in blood several years before disease onset. Joint inflammation, pain and bone destruction are major features of the disease. Classically bone destruction and pain have been considered to be late events in the disease development, resulting from long lasting and uncontrolled inflammation. However, both bone loss and pain have been reported in both seropositive individuals not yet having the disease and those seropositive individuals just being diagnosed with seropositive RA. Taken together these findings suggest that other factors than uncontrolled joint inflammation might drive the process of bone loss and pain in RA. We hypothesized that antibodies themselves and specifically ACPA might play a direct role in mediating bone loss and pain and aimed to investigate the role of ACPAs in bone metabolism and pain-like behaviour in mice. To investigate bone metabolism, we focused on studies of osteoclasts (OC), cells responsible for bone loss in vitro (by assessing formation and maturation of OC in cell cultures and estimating their capacity to degrade bone matrix in vitro) and in vivo (by micro-CT analysis of the bone density). We have demonstrated that polyclonal and monoclonal ACPAs isolated from the blood and synovial fluid of RA patients enhance the number of OC and of their bone resorptive capacity in vitro. This effect was accompanied by a significant increase of IL-8 levels in OC supernatants and abolished by neutralizing anti IL-8 antibodies. Further, ACPA injected in mice were shown to bind to CD68-positive OC precursors in bone marrow in the vicinity of the joints and to promote trabecular bone loss, which was also reversed by blocking the mice homologues of IL-8, CXCL1/2 by using reparixin. In parallel to bone destruction ACPA also induced pain-like behaviour in mice, that similar to bone loss was also abolished by CXCL1/2 blocking. Taken together these findings suggest that ACPA promote bone loss by inducing IL-8 that in turn can further amplify the bone loss process and induce pain-behaviour. As ACPA, but no other immunoglobulins (non-ACPA immunoglobulins from RA patients, non-ACPA Ig from healthy individuals) were able to promote bone loss, we investigated the role of citrullination in ACPA-mediated osteoclastogenesis. We demonstrated that citrullination by peptidyl arginine deiminases (PAD) enzymes is essential for the physiological development and maturation of OCs but no other cells (such as synovial fibroblasts). This finding might explain the ACPA preference for OCs. Further we showed that ACPA bind to targets expressed on the surface of OCs. Blocking the citrullination machinery by PAD enzyme inhibitors significantly abrogates ACPA binding to OCs and ACPA-mediated osteoclastogenesis. OCs could develop from different cell precursors and inflammatory conditions, such as joint inflammation in RA, promote the transdifferentitation of immature DC (iDC) into OCs. In order to investigate if ACPA might also play a role in this proces, we analyzed the capacity of polyclonal and monoclonal ACPA to promote the in vitro transdifferentation of iDC to OC. We showed that despite a clearly distinct protein profile as compared to classical macrophage OC precursors, iDC are able to develop into remarkably similar OCs. Plasticity towards OC differentiation correlated with PAD activity and protein citrullination expression levels in iDC cultures. Citrullinated actin and vimentin were present in iDCs and iDC-derived OCs and both proteins were deposited on the cell surface, co-localising with ACPAs binding to the cells. ACPAs enhanced OC differentiation from both monocyte-derived iDCs and from circulating CD1c+ DCs. Blocking either PAD activity or ACPA-induced IL-8 secretion completely abolished the stimulatory effects of citrulline-targeting antibodies on DC-OC transdifferentiation. We further explored the mechanisms involved in the plasticity of iDC and their capacity to develop into OCs showing that cell culture densities and lactate concentrations are essential mediators. DCs originating from dense cultures developed in the presence of high lactic acid doses, have high PAD activity and increased efficiency to convert into OC and erode bone. In contrast, DCs from sparse cultures have low PAD activity with decreased OC potential. In conclusion, the current thesis describes novel mechanisms by which RA-associated antibodies target OC to induce bone loss and pain. Our studies provide insights into the mechanisms by which systemic autoimmunity might target the joints and suggest potential novel ways to prevent this.
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| 6. |
- Steen, Johanna, et al.
(author)
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Recognition of Amino Acid Motifs, Rather Than Specific Proteins, by Human Plasma Cell-Derived Monoclonal Antibodies to Posttranslationally Modified Proteins in Rheumatoid Arthritis
- 2019
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In: Arthritis & Rheumatology. - : WILEY. - 2326-5191 .- 2326-5205. ; 71:2, s. 196-209
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Journal article (peer-reviewed)abstract
- Objective: Antibodies against posttranslationally modified proteins are a hallmark of rheumatoid arthritis (RA), but the emergence and pathogenicity of these autoantibodies are still incompletely understood. The aim of this study was to analyze the antigen specificities and mutation patterns of monoclonal antibodies (mAb) derived from RA synovial plasma cells and address the question of antigen cross-reactivity.Methods: IgG-secreting cells were isolated from RA synovial fluid, and the variable regions of the immunoglobulins were sequenced (n = 182) and expressed in full-length mAb (n = 93) and also as germline-reverted versions. The patterns of reactivity with 53,019 citrullinated peptides and 49,211 carbamylated peptides and the potential of the mAb to promote osteoclastogenesis were investigated.Results: Four unrelated anti-citrullinated protein autoantibodies (ACPAs), of which one was clonally expanded, were identified and found to be highly somatically mutated in the synovial fluid of a patient with RA. The ACPAs recognized >3,000 unique peptides modified by either citrullination or carbamylation. This highly multireactive autoantibody feature was replicated for Ig sequences derived from B cells from the peripheral blood of other RA patients. The plasma cell-derived mAb were found to target distinct amino acid motifs and partially overlapping protein targets. They also conveyed different effector functions as revealed in an osteoclast activation assay.Conclusion: These findings suggest that the high level of cross-reactivity among RA autoreactive B cells is the result of different antigen encounters, possibly at different sites and at different time points. This is consistent with the notion that RA is initiated in one context, such as in the mucosal organs, and thereafter targets other sites, such as the joints.
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