Falk Moritz

EULAR Scleroderma Trials and Research group statement and recommendations on endothelial precursor cells

Systemic sclerosis (SSc) is characterised by a progressive microangiopathy that contributes significantly to the morbidity of patients with SSc. Besides insufficient angiogenesis, defective vasculogenesis with altered numbers of endothelial precursor cells (EPCs) might also contribute to the vascular pathogenesis of SSc. However, different protocols for isolation, enrichment, culture and quantification of EPCs are currently used, which complicate comparison and interpretation of the results from different studies. The aim of the European League Against Rheumatism Scleroderma Trials and Research (EUSTAR) group expert panel was to provide recommendations for standardisation of future research on EPCs. Consensus statements and recommendations were developed in a face to face meeting by an expert panel of the basic science working group of EUSTAR. The findings were: cardiovascular risk factors and medications such as statins should be described in detail. A detailed description of methods considering isolation, culture, enrichment and detection of EPCs should be given. For in vitro culture of EPCs, no protocol has been shown to be superior to another, but coating with laminin and type IV collagen would resemble most closely the situation in vivo. The endothelial phenotype should be confirmed in all in vitro cultures at the end of the culture period. We recommend using CD133, vascular endothelial growth factor type 2 receptor (VEGFR2) and CD34 in combination with a viability marker for quantification of EPCs in the blood. Finally, exact standard operating procedures for fluorescence-activated cell sorting (FACS) analysis are given that should be strictly followed. In summary, the EUSTAR recommendations will help to unify EPC research and allow better comparison between the results of different studies.

The role of membrane lipids in the induction of macrophage apoptosis by microparticles

Microparticles are membrane-derived vesicles that are released from cells during activation or cell death. These particles can serve as mediators of intercellular cross-talk and induce a variety of cellular responses. Previous studies have shown that macrophages undergo apoptosis after phagocytosing microparticles. Here, we have addressed the hypothesis that microparticles trigger this process via lipid pathways. In these experiments, microparticles induced apoptosis in primary macrophage cells or cell lines (RAW 264.7 or U937) with up to a 5-fold increase. Preincubation of macrophages with phosphatidylinositol-3,5-bisphosphate (PtdIns(3,5)BP) reduced the microparticle-induced apoptosis in a dose-dependent manner. PtdIns(3,5)BP is a specific inhibitor of the acid sphingomyelinase and thus can block the generation of pro-apoptotic ceramides. Similarly, the pre-incubation of macrophages with PtdIns(3,5)BP prevented microparticle-induced upregulation of caspase 8, which is a major target molecule of ceramide action in the apoptosis pathway. PtdIns(3,5)BP, however, had no effect on the spontaneous rate of apoptosis. To evaluate further signaling pathways induced by microparticles, the extracellular signal regulated kinase (ERK-) 1 was investigated. This kinase plays a role in activating phospholipases A2 which cleaves membrane phospholipids into arachidonic acid; microparticles have been suggested to be a preferred substrate for phospholipases A2. As shown in our experiments, microparticles strongly increased the amount of phosphorylated ERK1/2 in RAW 264.7 macrophages in a time-dependent manner, peaking 15 min after co-incubation. Addition of PD98059, a specific inhibitor of ERK1, prevented the increase in apoptosis of RAW 264.7 macrophages. Together, these data suggest that microparticles perturb lipid homeostasis of macrophages and thereby induce apoptosis. These results emphasize the importance of biolipids in the cellular cross-talk of immune cells. Based on the fact that in clinical situations with excessive cell death such as malignancies, autoimmune diseases and following chemotherapies high levels of circulating microparticles might modulate phagocytosing cells, a suppression of the immune response might occur due to loss of macrophages.

Technology Insight: gene transfer and the design of novel treatments for rheumatoid arthritis

Rheumatoid arthritis (RA) is a chronic inflammatory disease characterized by systemic inflammation and joint destruction. Novel therapies have emerged during the past decade, marking a new era in the treatment of RA. Meanwhile, in vivo and in vitro gene-transfer studies have provided valuable insights into mechanisms of disease pathogenesis. Advanced gene-delivery techniques and animal models promise further progress in RA research and the development of novel therapeutic strategies for this disease. In this article we provide an overview of the wide spectrum of potential targets that have been identified so far, discuss currently available gene-transfer methods, and outline the barriers that need to be overcome for these approaches to be successfully applied in daily practice.

Angiogenese – therapeutische Interventionsmöglichkeiten bei rheumatischen Erkrankungen

In contrast to vasculogenesis, angiogenesis is defined as the formation of new vessels from preexisting ones. Physiologically, this multistep process occurs in adults during the reproductive cycle and during pregnancy, pathophysiologically it can be found in wound healing, inflammation and carcinogenesis. The underlying mechanisms are vasodilatation and increasing permeability, destabilization of vessel walls and degradation of extracellular matrix, followed by the proliferation and migration of endothelial cells. Migrated endothelial cells form vascular tubes at sites of ischemia and these tubes are finally stabilized by pericytes and smooth muscle cells. This process is controlled by a complex interaction of angiogenic and angiostatic factors. In contrast to carcinogenesis, the role of angiogenesis for the pathogenesis and therapy of rheumatic diseases is less understood. Two examples for pathologically disturbed angiogenesis, rheumatoid arthritis and systemic sclerosis, are discussed in this review with respect to therapeutic options.ZusammenfassungIm Gegensatz zur Vaskulogenese bedeutet Angiogenese die Formation neuer Blutgefäße aus bereits bestehenden Gefäßen. Dieser vielschrittige Prozess tritt beim Erwachsenen physiologisch nur während des Reproduktionszyklus und der Schwangerschaft auf, pathophysiologisch bei Wundheilung und Entzündung, aber auch bei Tumorwachstum und Metastasierung. Zugrunde liegende Mechanismen sind Vasodilatation und Steigerung der Gefäßpermeabilität, gefolgt von einer Destabilisierung der Gefäßwände und der extrazellulären Matrix mit anschließender Endothelzellproliferation und -migration, die zur Bildung eines neuen Gefäßsystems führt, das schließlich durch Perizyten und glatte Muskelzellen stabilisiert wird. Dieser Ablauf wird durch ein komplexes Zusammenspiel proangiogener und angiostatischer Faktoren kontrolliert. Im Gegensatz zur Karzinogenese ist die Bedeutung der Angiogenese für die Pathogenese und Therapie rheumatischer Erkrankungen bisher weniger gut untersucht.In diesem Übersichtsartikel werden verschiedene Aspekte pathologischer Angiogenese im Hinblick auf therapeutische Optionen bei der rheumatoiden Arthritis (RA) und der systemischen Sklerose (SSc) diskutiert.AbstractIn contrast to vasculogenesis, angiogenesis is defined as the formation of new vessels from preexisting ones. Physiologically, this multistep process occurs in adults during the reproductive cycle and during pregnancy, pathophysiologically it can be found in wound healing, inflammation and carcinogenesis. The underlying mechanisms are vasodilatation and increasing permeability, destabilization of vessel walls and degradation of extracellular matrix, followed by the proliferation and migration of endothelial cells. Migrated endothelial cells form vascular tubes at sites of ischemia and these tubes are finally stabilized by pericytes and smooth muscle cells. This process is controlled by a complex interaction of angiogenic and angiostatic factors. In contrast to carcinogenesis, the role of angiogenesis for the pathogenesis and therapy of rheumatic diseases is less understood. Two examples for pathologically disturbed angiogenesis, rheumatoid arthritis and systemic sclerosis, are discussed in this review with respect to therapeutic options.

Cardiovascular manifestations in rheumatoid arthritis

ZusammenfassungDie Rheumatoide Arthritis (RA) ist eine systemische Erkrankung des Bindegewebes, die durch eine polyartikuläre Entzündung mit synovialer Hyperplasie und progredienter Gelenkzerstörung, aber auch durch extraartikuläre Manifestationen und systemische pathologische Immunphänomene charakterisiert ist. Eine erhöhte Mortalität innerhalb der RA-Patientenpopulation ist seit langem bekannt und vor allem auf ein erhöhtes kardiovaskuläres Risiko zurückzuführen. Die Korrelation der kardiovaskulären Morbidität und Mortalität mit der Erkrankungsaktivität sowie dem Ausmaß extraartikulärer Manifestationen war der Ausgangspunkt für die Suche nach entzündungs- und erkrankungsassoziierten Pathomechanismen. Endothelzelldysfunktion und vaskuläre Inflammation konnten als zentrale Mechanismen der Atheroskleroseinduktion und deren Progression charakterisiert werden. Beide Phänomene stellen eine uniforme Reaktionsweise von Gefäßen unter dem Einfluss klassischer Risikofaktoren sowie einer systemischen-Entzündung dar. Für die akzelerierte Atherosklerose von RA-Patienten sind neben den klassischen Risikofaktoren erkrankungsbedingte Faktoren wie Immobilität, medikamentöse Therapie sowie Entzündungsmediatoren zu berücksichtigen. Bei den beschriebenen entzündungsvermittelten Mechanismen der Gefäßschädigung kommt vor allem den bei RA-Patienten als Folge der Synovialitis exzessiv gebildeten pro-inflammatorischen Zytokinen eine Bedeutung zu. Die Frage, ob der Entzündungsmarker CRP gleichzeitig einen kardiovaskulären Risikoindikator und einen Mediator atherosklerotischer Gefäßschädigung darstellt, bedarf noch endgültiger Beantwortung durch weitere Studien. Neben diesen unspezifischen entzündungsassoziierten Mechanismen können bei der Rheumatoiden Arthritis zusätzlich krankheitsspezifische Immunphänomene, wie die klonal expandierten autoreaktiven T-Zellen für die kardiovaskuläre Morbidität und Mortalität von Bedeutung sein. Die neueren TNFα-hemmenden Basistherapeutika interferieren auf unterschiedlichen Ebenen mit pro-atherosklerotischen Prozessen. Die Zukunft wird zeigen, wie sich diese Medikamente auf die kardiovaskuläre Morbidität und Mortalität auswirken.SummaryRheumatoid arthritis (RA) is a chronic inflammatory disease, characterized by a polyarticular joint inflammation which eventually leads to joint destruction and general disability. Besides these polyarticular manifestations, several systemic immune phenomena have been described. An increased mortality in RA patients is evident and is mainly caused by an increased cardiovascular risk. The correlation between disease activity and mortality highlighted the important role of the systemic inflammatory reaction in induction and progression of vascular damaging processes. Endothelial dysfunction and vascular inflammation are important, mechanisms in atherosclerosis and induced by conventional risk factors and systemic inflammation. It has been shown that the deleterious influence of conventional risk factors is aggravated by inflammatory mediators, mainly by pro-inflammatory cytokines. In addition, certain inflammatory mediators exert damaging effects to blood vessels. Especially CRP, merely considered as a risk indicating parameter in the past, has attracted remarkable attention. Also certain RA specific immune phenomena are of considerable proatherosclerotic potential. At least in part, they could be responsible for the excess mortality in RA patients. The newer TNFα blocking agents interfere with different mechanisms responsible for induction and perpetuation of atherosclerotic processes. Time will show whether they make a remarkable impact on the cardiovascular mortality in RA patients.

Kardiovaskuläre Manifestationen bei Rheumatoider Arthritis

ZusammenfassungDie Rheumatoide Arthritis (RA) ist eine systemische Erkrankung des Bindegewebes, die durch eine polyartikuläre Entzündung mit synovialer Hyperplasie und progredienter Gelenkzerstörung, aber auch durch extraartikuläre Manifestationen und systemische pathologische Immunphänomene charakterisiert ist. Eine erhöhte Mortalität innerhalb der RA-Patientenpopulation ist seit langem bekannt und vor allem auf ein erhöhtes kardiovaskuläres Risiko zurückzuführen. Die Korrelation der kardiovaskulären Morbidität und Mortalität mit der Erkrankungsaktivität sowie dem Ausmaß extraartikulärer Manifestationen war der Ausgangspunkt für die Suche nach entzündungs- und erkrankungsassoziierten Pathomechanismen. Endothelzelldysfunktion und vaskuläre Inflammation konnten als zentrale Mechanismen der Atheroskleroseinduktion und deren Progression charakterisiert werden. Beide Phänomene stellen eine uniforme Reaktionsweise von Gefäßen unter dem Einfluss klassischer Risikofaktoren sowie einer systemischen-Entzündung dar. Für die akzelerierte Atherosklerose von RA-Patienten sind neben den klassischen Risikofaktoren erkrankungsbedingte Faktoren wie Immobilität, medikamentöse Therapie sowie Entzündungsmediatoren zu berücksichtigen. Bei den beschriebenen entzündungsvermittelten Mechanismen der Gefäßschädigung kommt vor allem den bei RA-Patienten als Folge der Synovialitis exzessiv gebildeten pro-inflammatorischen Zytokinen eine Bedeutung zu. Die Frage, ob der Entzündungsmarker CRP gleichzeitig einen kardiovaskulären Risikoindikator und einen Mediator atherosklerotischer Gefäßschädigung darstellt, bedarf noch endgültiger Beantwortung durch weitere Studien. Neben diesen unspezifischen entzündungsassoziierten Mechanismen können bei der Rheumatoiden Arthritis zusätzlich krankheitsspezifische Immunphänomene, wie die klonal expandierten autoreaktiven T-Zellen für die kardiovaskuläre Morbidität und Mortalität von Bedeutung sein. Die neueren TNFα-hemmenden Basistherapeutika interferieren auf unterschiedlichen Ebenen mit pro-atherosklerotischen Prozessen. Die Zukunft wird zeigen, wie sich diese Medikamente auf die kardiovaskuläre Morbidität und Mortalität auswirken.SummaryRheumatoid arthritis (RA) is a chronic inflammatory disease, characterized by a polyarticular joint inflammation which eventually leads to joint destruction and general disability. Besides these polyarticular manifestations, several systemic immune phenomena have been described. An increased mortality in RA patients is evident and is mainly caused by an increased cardiovascular risk. The correlation between disease activity and mortality highlighted the important role of the systemic inflammatory reaction in induction and progression of vascular damaging processes. Endothelial dysfunction and vascular inflammation are important, mechanisms in atherosclerosis and induced by conventional risk factors and systemic inflammation. It has been shown that the deleterious influence of conventional risk factors is aggravated by inflammatory mediators, mainly by pro-inflammatory cytokines. In addition, certain inflammatory mediators exert damaging effects to blood vessels. Especially CRP, merely considered as a risk indicating parameter in the past, has attracted remarkable attention. Also certain RA specific immune phenomena are of considerable proatherosclerotic potential. At least in part, they could be responsible for the excess mortality in RA patients. The newer TNFα blocking agents interfere with different mechanisms responsible for induction and perpetuation of atherosclerotic processes. Time will show whether they make a remarkable impact on the cardiovascular mortality in RA patients.

Tie2 as a novel key factor of microangiopathy in systemic sclerosis

BackgroundThe angiopoietin(Ang)/Tie2 system is a key regulator of vascular biology. The expression of membrane bound (mb) Tie2 and Ang-1 ensures vessel stability, whereas Ang-2, inducible by vascular endothelial growth factor (VEGF), hypoxia, and inflammation, acts as an antagonist. Tie2 signalling is also attenuated by soluble Tie2 (sTie2), the extracellular domain of the receptor, which is shed upon stimulation with VEGF. Herein, we investigate the role of Ang/Tie2 in the peripheral vasculopathy in systemic sclerosis (SSc) including animal models.MethodsThe expression of Ang-1/-2 and Tie2 in skin/serum of SSc patients was compared with healthy controls by immunohistochemistry (IHC)/ELISA. Expression of Ang/Tie2 was analysed in different animal models: VEGF transgenic (tg) mice, hypoxia model, bleomycin-induced skin fibrosis, and tight skin 1 (TSK1) mice.ResultsIn SSc, dermal microvessels abundantly expressed Ang-2, but not Ang-1 compared with healthy controls. The percentage of mbTie2+ microvessels was profoundly decreased whereas the levels of sTie2 were increased already in early disease. Both in skin and sera of SSc patients, the Ang1/2 ratio was reduced, being lowest in patients with digital ulcers indicating vessel destabilizing conditions. We next studied potential influencing factors in animal models. The VEGF tg mouse model, the hypoxia, and the inflammation-dependent bleomycin model all showed a similar dysregulation of Ang/Tie2 as in SSc, which did not apply for the non-inflammatory TSK1 model.ConclusionPeripheral microvasculopathy in SSc results from a complex dysregulation of angiogenic signalling networks including the VEGF and the Ang/Tie2 system. The profoundly disturbed Ang-/Tie-2 balance might represent an important target for vascular therapeutic approaches in SSc.

Angiogenesis. Possibilities for therapeutic intervention in rheumatic diseases

In contrast to vasculogenesis, angiogenesis is defined as the formation of new vessels from preexisting ones. Physiologically, this multistep process occurs in adults during the reproductive cycle and during pregnancy, pathophysiologically it can be found in wound healing, inflammation and carcinogenesis. The underlying mechanisms are vasodilatation and increasing permeability, destabilization of vessel walls and degradation of extracellular matrix, followed by the proliferation and migration of endothelial cells. Migrated endothelial cells form vascular tubes at sites of ischemia and these tubes are finally stabilized by pericytes and smooth muscle cells. This process is controlled by a complex interaction of angiogenic and angiostatic factors. In contrast to carcinogenesis, the role of angiogenesis for the pathogenesis and therapy of rheumatic diseases is less understood. Two examples for pathologically disturbed angiogenesis, rheumatoid arthritis and systemic sclerosis, are discussed in this review with respect to therapeutic options.ZusammenfassungIm Gegensatz zur Vaskulogenese bedeutet Angiogenese die Formation neuer Blutgefäße aus bereits bestehenden Gefäßen. Dieser vielschrittige Prozess tritt beim Erwachsenen physiologisch nur während des Reproduktionszyklus und der Schwangerschaft auf, pathophysiologisch bei Wundheilung und Entzündung, aber auch bei Tumorwachstum und Metastasierung. Zugrunde liegende Mechanismen sind Vasodilatation und Steigerung der Gefäßpermeabilität, gefolgt von einer Destabilisierung der Gefäßwände und der extrazellulären Matrix mit anschließender Endothelzellproliferation und -migration, die zur Bildung eines neuen Gefäßsystems führt, das schließlich durch Perizyten und glatte Muskelzellen stabilisiert wird. Dieser Ablauf wird durch ein komplexes Zusammenspiel proangiogener und angiostatischer Faktoren kontrolliert. Im Gegensatz zur Karzinogenese ist die Bedeutung der Angiogenese für die Pathogenese und Therapie rheumatischer Erkrankungen bisher weniger gut untersucht.In diesem Übersichtsartikel werden verschiedene Aspekte pathologischer Angiogenese im Hinblick auf therapeutische Optionen bei der rheumatoiden Arthritis (RA) und der systemischen Sklerose (SSc) diskutiert.AbstractIn contrast to vasculogenesis, angiogenesis is defined as the formation of new vessels from preexisting ones. Physiologically, this multistep process occurs in adults during the reproductive cycle and during pregnancy, pathophysiologically it can be found in wound healing, inflammation and carcinogenesis. The underlying mechanisms are vasodilatation and increasing permeability, destabilization of vessel walls and degradation of extracellular matrix, followed by the proliferation and migration of endothelial cells. Migrated endothelial cells form vascular tubes at sites of ischemia and these tubes are finally stabilized by pericytes and smooth muscle cells. This process is controlled by a complex interaction of angiogenic and angiostatic factors. In contrast to carcinogenesis, the role of angiogenesis for the pathogenesis and therapy of rheumatic diseases is less understood. Two examples for pathologically disturbed angiogenesis, rheumatoid arthritis and systemic sclerosis, are discussed in this review with respect to therapeutic options.

FRI0434 TIE2 As a Novel Key Factor of Microangiopathy in Systemic Sclerosis

Background The angiopoietin (ang)/Tie2 system is a key regulator of vascular biology. However, its impact on SSc-associated microangiopathy has not yet been addressed in detail. Objectives To assess the role of ang/Tie2 in SSc-associated dermal microangiopathy ex vivo and in four different animal models. Methods The expression of Ang1/2 and Tie2 in the serum/dermis of SSc patients (n=24/10) was compared with healthy donors (n=20/8) by ELISA/immunohistochemistry (IHC). Hypoxia exposed C57BL/6 mice (n=3) were compared with normoxic controls (n=9). Mono- and double (n=9/8) VEGF transgenic (tg) mice were compared with wild type controls (n=6/9). The impact of inflammatory and non-inflammatory conditions were evaluated in the bleomycin and TSK1 model (n=4 each). For statistical analysis, GraphPad Prism software was employed. Parametric non-related data were expressed as mean ± SEM, nonparametric non-related data as median(Q1,Q3). P-values <0.05 were considered statistically significant. Results In dermal microvessels of SSc patients Ang2, but not Ang1 was more abundantly expressed compared with healthy controls (p=0.004) indicating vessel destabilizing conditions. Most interestingly, in SSc, membrane bound (mb) Tie2 was nearly undetectable in dermal microvessels (p<0.001). Tie2+ microvessels occurred in 90% of healthy controls but only in 5.5% of SSc patients. In context with the remarkably lower microvascular density in SSc patients (p=0.05), this supports previous observations that deficiency of Tie2 protein results in microvasculopathy. To evaluate whether the loss of mbTie2 might be due to shedding, we assessed the serum levels of soluble (s) Tie2. Interestingly, sTie2 levels of SSc patients were higher than those of healthy controls (p=0.001). As in skin, the ang1/ang2 ratio was substantially reduced in SSc sera (p<0.001). These findings suggest that the competitive binding of sTie2 and Ang2 prevents Tie2 activation with anti-angiogenic effects. Next, we evaluated the in vivo effects of angiogenic factors on the expression of ang/Tie2. In VEGF tg mice, similar to SSc, reduction of mbTie2 (p=0.002), increase of Ang2 (p=0.05) and decrease of Ang1 (p=0.07) occurred in the dermis. These results indicate that a dysregulation of ang/Tie2 might contribute to the anti-angiogenic effects of chronically elevated VEGF levels in SSc. In the hypoxia model, Tie2-mRNA was increased (p=0.042) which underlines that chronic hypoxia and VEGF exposure induce reduction of Tie2 protein by shedding. Similar to VEGF tg mice, the reduced Ang1/Ang2 ratio in the hypoxia model indicated anti-angiogenic effects. In the bleomycin model, the pro-inflammatory conditions had no effect on the dermal expression ang/Tie2. Interestingly, in the TSK1 model, our findings supported interactions of extracellular matrix (ECM) and angiogenesis. Membrane bound Tie2 was increased (p<0.0001) whereas Ang1/2 were decreased which is in line with previous studies showing that α5β1 integrin activates Tie2 at low Ang-1 concentrations. Conclusions Our data derived from SSc patients and 4 different SSc animal models give evidence of an alteration of the ang/Tie2 system towards vessel destabilization in which VEGF, hypoxia and ECM interactions might play a major role. Disclosure of Interest B. Maurer: None declared, F. Moritz Grant/research support from: Articulum Fellowship Pfizer, Speakers bureau: Roche, Lilly, Medac, J. Distler: None declared, B. Michel: None declared, R. Gay: None declared, S. Gay: None declared, O. Distler Grant/research support from: 4D Science, Actelion, Active Biotec, Bayer-Schering, Biogen, Biovitrium, BMS, Boehringer Ingelheim Pharma, EpiPharm, Ergonex, GSK, Inventiva, Medac, Novartis, Pfizer, Pharmacyclics, Roche/Genentech, Sanofi/Genzyme, Serodapharm, Sinoxa and United BioSource Corporation.

Kardiovaskuläre Manifestationen bei Rheumatoider Arthritis@@@Cardiovascular manifestations in rheumatoid arthritis

ZusammenfassungDie Rheumatoide Arthritis (RA) ist eine systemische Erkrankung des Bindegewebes, die durch eine polyartikuläre Entzündung mit synovialer Hyperplasie und progredienter Gelenkzerstörung, aber auch durch extraartikuläre Manifestationen und systemische pathologische Immunphänomene charakterisiert ist. Eine erhöhte Mortalität innerhalb der RA-Patientenpopulation ist seit langem bekannt und vor allem auf ein erhöhtes kardiovaskuläres Risiko zurückzuführen. Die Korrelation der kardiovaskulären Morbidität und Mortalität mit der Erkrankungsaktivität sowie dem Ausmaß extraartikulärer Manifestationen war der Ausgangspunkt für die Suche nach entzündungs- und erkrankungsassoziierten Pathomechanismen. Endothelzelldysfunktion und vaskuläre Inflammation konnten als zentrale Mechanismen der Atheroskleroseinduktion und deren Progression charakterisiert werden. Beide Phänomene stellen eine uniforme Reaktionsweise von Gefäßen unter dem Einfluss klassischer Risikofaktoren sowie einer systemischen-Entzündung dar. Für die akzelerierte Atherosklerose von RA-Patienten sind neben den klassischen Risikofaktoren erkrankungsbedingte Faktoren wie Immobilität, medikamentöse Therapie sowie Entzündungsmediatoren zu berücksichtigen. Bei den beschriebenen entzündungsvermittelten Mechanismen der Gefäßschädigung kommt vor allem den bei RA-Patienten als Folge der Synovialitis exzessiv gebildeten pro-inflammatorischen Zytokinen eine Bedeutung zu. Die Frage, ob der Entzündungsmarker CRP gleichzeitig einen kardiovaskulären Risikoindikator und einen Mediator atherosklerotischer Gefäßschädigung darstellt, bedarf noch endgültiger Beantwortung durch weitere Studien. Neben diesen unspezifischen entzündungsassoziierten Mechanismen können bei der Rheumatoiden Arthritis zusätzlich krankheitsspezifische Immunphänomene, wie die klonal expandierten autoreaktiven T-Zellen für die kardiovaskuläre Morbidität und Mortalität von Bedeutung sein. Die neueren TNFα-hemmenden Basistherapeutika interferieren auf unterschiedlichen Ebenen mit pro-atherosklerotischen Prozessen. Die Zukunft wird zeigen, wie sich diese Medikamente auf die kardiovaskuläre Morbidität und Mortalität auswirken.SummaryRheumatoid arthritis (RA) is a chronic inflammatory disease, characterized by a polyarticular joint inflammation which eventually leads to joint destruction and general disability. Besides these polyarticular manifestations, several systemic immune phenomena have been described. An increased mortality in RA patients is evident and is mainly caused by an increased cardiovascular risk. The correlation between disease activity and mortality highlighted the important role of the systemic inflammatory reaction in induction and progression of vascular damaging processes. Endothelial dysfunction and vascular inflammation are important, mechanisms in atherosclerosis and induced by conventional risk factors and systemic inflammation. It has been shown that the deleterious influence of conventional risk factors is aggravated by inflammatory mediators, mainly by pro-inflammatory cytokines. In addition, certain inflammatory mediators exert damaging effects to blood vessels. Especially CRP, merely considered as a risk indicating parameter in the past, has attracted remarkable attention. Also certain RA specific immune phenomena are of considerable proatherosclerotic potential. At least in part, they could be responsible for the excess mortality in RA patients. The newer TNFα blocking agents interfere with different mechanisms responsible for induction and perpetuation of atherosclerotic processes. Time will show whether they make a remarkable impact on the cardiovascular mortality in RA patients.