Network


Latest external collaboration on country level. Dive into details by clicking on the dots.

Hotspot


Dive into the research topics where Brigitte Kaiser is active.

Publication


Featured researches published by Brigitte Kaiser.


Proceedings of the National Academy of Sciences of the United States of America | 2003

Expanding expression of the 5-lipoxygenase pathway within the arterial wall during human atherogenesis

Rainer Spanbroek; Rolf Gräbner; Katharina Lötzer; Markus Hildner; Anja Urbach; Katharina Rühling; Michael P. W. Moos; Brigitte Kaiser; Tina U. Cohnert; Thorsten Wahlers; Arthur W. Zieske; Gabriele Plenz; Horst Robenek; Peter Salbach; Hartmut Kühn; Olof Rådmark; Bengt Samuelsson; Andreas J.R. Habenicht

Oxidation products of low-density lipoproteins have been suggested to promote inflammation during atherogenesis, and reticulocyte-type 15-lipoxygenase has been implicated to mediate this oxidation. In addition, the 5-lipoxygenase cascade leads to formation of leukotrienes, which exhibit strong proinflammatory activities in cardiovascular tissues. Here, we studied both lipoxygenase pathways in human atherosclerosis. The 5-lipoxygenase pathway was abundantly expressed in arterial walls of patients afflicted with various lesion stages of atherosclerosis of the aorta and of coronary and carotid arteries. 5-lipoxygenase localized to macrophages, dendritic cells, foam cells, mast cells, and neutrophilic granulocytes, and the number of 5-lipoxygenase expressing cells markedly increased in advanced lesions. By contrast, reticulocyte-type 15-lipoxygenase was expressed at levels that were several orders of magnitude lower than 5-lipoxygenase in both normal and diseased arteries, and its expression could not be related to lesion pathology. Our data support a model of atherogenesis in which 5-lipoxygenase cascade-dependent inflammatory circuits consisting of several leukocyte lineages and arterial wall cells evolve within the blood vessel wall during critical stages of lesion development. They raise the possibility that antileukotriene drugs may be an effective treatment regimen in late-stage disease.


Nature Medicine | 2004

The 5-lipoxygenase pathway promotes pathogenesis of hyperlipidemia-dependent aortic aneurysm

Lei Zhao; Michael P. W. Moos; Rolf Gräbner; Frédérique Pédrono; Jinjin Fan; Brigitte Kaiser; Nicole John; Sandra Schmidt; Rainer Spanbroek; Katharina Lötzer; Li Huang; Jisong Cui; Daniel J. Rader; Jilly F. Evans; Andreas J.R. Habenicht; Colin D. Funk

Activation of the 5-lipoxygenase (5-LO) pathway leads to the biosynthesis of proinflammatory leukotriene lipid mediators. Genetic studies have associated 5-LO and its accessory protein, 5-LO-activating protein, with cardiovascular disease, myocardial infarction and stroke. Here we show that 5-LO-positive macrophages localize to the adventitia of diseased mouse and human arteries in areas of neoangiogenesis and that these cells constitute a main component of aortic aneurysms induced by an atherogenic diet containing cholate in mice deficient in apolipoprotein E. 5-LO deficiency markedly attenuates the formation of these aneurysms and is associated with reduced matrix metalloproteinase-2 activity and diminished plasma macrophage inflammatory protein-1α (MIP-1α; also called CCL3), but only minimally affects the formation of lipid-rich lesions. The leukotriene LTD4 strongly stimulates expression of MIP-1α in macrophages and MIP-2 (also called CXCL2) in endothelial cells. These data link the 5-LO pathway to hyperlipidemia-dependent inflammation of the arterial wall and to pathogenesis of aortic aneurysms through a potential chemokine intermediary route.


Arteriosclerosis, Thrombosis, and Vascular Biology | 2005

The Lamina Adventitia Is the Major Site of Immune Cell Accumulation in Standard Chow-Fed Apolipoprotein E–Deficient Mice

Michael P. W. Moos; Nicole John; Rolf Gräbner; Silke Noßmann; Bernd Günther; Rüdiger Vollandt; Colin D. Funk; Brigitte Kaiser; Andreas J.R. Habenicht

Objective—Cells of adaptive immunity have been implicated in atherogenesis. Though substantial information is available on immune cells in atherosclerotic lesions of the lamina intima, cells in the lamina adventitia have received less attention. Methods and Results—The composition of immune cells in the innominate artery and abdominal aorta was examined in young, adult, and old apolipoprotein (apo) E−/− and wild-type mice on standard mouse chow. In the innominate artery of apoE−/− mice, adventitial T cells increased at 32, 52, and 78 weeks exceeding those of the intima by 6-, 24-, and 85-fold. Single T cells dominated in young mice, later T/B cell clusters emerged, and lymphoid-like structures reminiscent of inflammatory follicles formed preferentially in the abdominal aorta of old mice. Follicles contained organized sets of immune response-regulating cells: Interdigitating dendritic cells, T cell effectors, proliferating B cells, and plasma cells. Adventitial T cell inflammation was associated with a marked increase in transcripts of the chemokine MIP-1&agr; in the aorta but not in spleen or liver. Conclusions—Adventitial lymphocyte infiltration and formation of inflammatory follicle-like structures in the abdominal aorta of old apoE−/− mice point to the adventitia as a site of local adaptive immune reactions during atherogenesis in hyperlipidemic mice.


Thrombosis Research | 1989

Studies on antithrombotic effects of recombinant hirudin

Fritz Markwardt; Brigitte Kaiser; G. Nowak

Recombinant desulfato hirudin (rH) was studied with regard to its effects on various models of thrombosis, its pharmacokinetic behaviour as well as its influence on primary haemostasis in rats. The pharmacological behaviour of rH proved to be similar to that of native hirudin. Depending on the different models of experimental thrombosis different dosages of rH were required to prevent thrombus formation. This corresponds to rH plasma concentrations of 0.5-1.5 micrograms/ml. Primary haemostasis is influenced only after excess dosages and plasma concentrations of 4 micrograms/ml and above.


Expert Opinion on Investigational Drugs | 2001

Tissue factor pathway inhibitor: an update of potential implications in the treatment of cardiovascular disorders

Brigitte Kaiser; Debra Hoppensteadt; Jawed Fareed

Tissue factor (TF) plays a crucial role in the pathogenesis of thrombotic, vascular and inflammatory disorders. Thus, the inhibition of this membrane protein provides a unique therapeutic approach for prophylaxis and/or treatment of various diseases. Tissue factor pathway inhibitor (TFPI), the only endogenous inhibitor of the TF/Factor VIIa (FVIIa) complex, has recently been characterised biochemically and pharmacologically. Studies in patients demonstrated that both TF and TFPI may be indicators for the course and the outcome of cardiovascular and other diseases. Based on experimental and clinical data, TFPI might become an important drug for several clinical indications. TFPI is expected to inhibit the development of post-injury intimal hyperplasia and thrombotic occlusion in atherosclerotic vessels as well as to be effective in acute coronary syndromes, such as unstable angina and myocardial infarction. Of special interest is the inhibition of TF-mediated processes in sepsis and disseminated intravascular coagulation (DIC), which are associated with the activation of various inflammatory pathways as well as of the coagulation system. A Phase II trial of the efficacy of TFPI in patients with severe sepsis showed a mortality reduction in TFPI- compared to placebo-treated patients and an improvement of organ dysfunctions. TFPI can be administered exogenously in high doses to suppress TF-mediated effects, alternatively high amounts of TFPI can be released from intravascular stores by other drugs, such as heparin and low molecular weight heparins (LMWH). Using this method high concentrations of the inhibitor are provided at sites of tissue damage and ongoing thrombosis. At present, clinical studies with TFPI are rather limited so that the clinical potential of the drug cannot be assessed properly. However, TFPI and its variants are expected to undergo further development and to find indications in various clinical states.


Thrombosis Research | 1991

In vitro studies on thrombin generation in citrated, r-hirudinized and heparinized whole blood

Brigitte Kaiser; Jawed Fareed; Jeanine M. Walenga; D. Hoppensteadt; F. Markwardt

The generation of thrombin in citrated, r-hirudinized and heparinized whole blood (final concentrations 10, 25, 50 micrograms/ml) was studied in the presence or absence of various activators. Whole blood from healthy volunteers was activated either by glass or dextran sulfate (contact activation; CA) as well as by thromboplastin/calcium chloride (extrinsic activation; EA) and by ellagic acid/cephaloplastin/calcium chloride (intrinsic activation; IA) and incubated 10 (CA, EA, IA) and 30 (CA) min at 37 degrees C. After the incubation period plasma levels of prothrombin fragment 1 + 2 (F1 + 2) and thrombin-antithrombin III complex (TAT) were measured utilizing ELISA methodology. After EA or IA no blood clotting occurred in all r-hirudinized samples and in heparinized blood at the highest concentration used. Despite inhibition of clotting F1 + 2 levels were increased both in r-hirudinized and in heparinized blood. However, in blood anticoagulated with heparin F1 + 2 levels after EA, IA and especially after CA were markedly lower than in r-hirudinized blood. Furthermore, in r-hirudinized blood an increase of TAT levels was found. The enhancement of F1 + 2 and TAT levels by r-hirudin was concentration-dependent and was lower in the higher r-hirudin concentration. The results indicate that in r-hirudinized whole blood significant amounts of thrombin can be generated which may elicit thrombin-mediated feedback mechanisms.


Thrombosis Research | 1994

Inhibitory effects of TFPI on thrombin and factor Xa generation in vitro - modulatory action of glycosaminoglycans

Brigitte Kaiser; Debra Hoppensteadt; Walter Jeske; T.C. Wun; Jawed Fareed

The effect of tissue factor pathway inhibitor (TFPI) on thrombin and factor Xa generation was studied in an in vitro system using a prothrombin complex concentrate. It was found that TFPI, via the direct inhibition of factor Xa and the tissue factor/factor VIIa complex, inhibited both the further generation of factor Xa and the generation of thrombin in a concentration-dependent manner. The generation of thrombin (IC50 255 ng/ml) was more pronounced than that of factor Xa (IC50 684 ng/ml). The inhibitory activity of TFPI was significantly enhanced when unfractionated heparin was present in the assay system at a concentration of 10 micrograms/ml which did not show any inhibitory effects on protease generation in the same system. Furthermore, the influence of TFPI at subthreshold concentrations (100 ng/ml and 200 ng/ml, resp.) on the inhibitory action of unfractionated heparin (UFH), a low molecular weight heparin (LMWH), heparan sulfate (HS) and the synthetic heparin pentasaccharide (PS) was investigated. Whereas in the concentration range used (0.3-40 micrograms/ml) these glycosaminoglycans did not inhibit thrombin and factor Xa generation, after supplementation of the system with TFPI a concentration-dependent inhibition of the generation of the proteases up to 40-50% was seen for UFH, LMWH and HS. TFPI did not increase the activity of PS.


Thrombosis Research | 1996

Flow cytometric evaluation of the effect of various thrombin inhibitors on platelet activation in whole blood

Brigitte Kaiser; Michael Koza; Jeanine M. Walenga; Jawed Fareed

In an in vitro study the effect of various thrombin inhibitors (argatroban, efegatran, DuP 714, recombinant hirudin and PEG-hirudin) on platelet activation in whole blood was investigated. Blood was drawn from normal human volunteers using the double syringe technique without use of a tourniquet to avoid autoaggregation of platelets. Blood was anticoagulated with either argatroban, efegatran, DuP 714, hirudin or PEG-hirudin at final concentrations of 10 micrograms/ml. Blood samples were then incubated at 37 degrees C either with saline, r-tissue factor, arachidonic acid, adenosine diphosphate or collagen. At definite times (1, 2.5, 5, 10 min) aliquots were taken and after various steps of fixative procedure the percentage of platelet activation was measured using fluorescent monoclonal antibodies to platelet surface receptors GPIIIa (CD-61) and P-selectin (CD-62). Flow cytometric analysis showed a platelet activation after all agonists used. All thrombin inhibitors studied caused a nearly complete inhibition of r-tissue factor-mediated platelet activation. In contrast, after activation with the other agonists an increased percent CD-62 expression was found with a maximum after 2.5 to 5 min. The results show that in whole blood thrombin inhibitors are effective in preventing platelet activation induced by r-tissue factor. The formation of active serine proteases including thrombin may be effectively inhibited by these agents. The observations further suggest that while thrombin inhibitors may control serine proteases, these agents do not inhibit the activation of platelets mediated by other agonists.


Expert Opinion on Emerging Drugs | 2000

Tissue factor pathway inhibitor for cardiovascular disorders

Brigitte Kaiser; Debra Hoppensteadt; Jawed Fareed

The tissue factor (TF) pathway of coagulation plays a decisive role for normal haemostasis as well as in the pathophysiology of various diseases. As endogenous inhibitor of TF-mediated coagulation, the Kunitz-type proteinase inhibitor tissue factor pathway inhibitor (TFPI) is an important factor in the regulation of haemostasis and the control of clotting activation. TFPI exerts its biological effects by the binding of Factor Xa (FXa) forming a TFPI/FXa complex which then, in a second step, binds to and effectively inhibits the TF/Factor VIIa (FVIIa) complex. Due to its mechanism of action TFPI causes strong anticoagulant and antithrombotic effects under experimental conditions. Furthermore, the inhibitor was shown to be a potent antiproliferative agent both in vitro and in vivo. Based on the pathogenetic role of TF and the TF/FVIIa complex and on the effectiveness of TFPI demonstrated in preclinical studies it is assumed that TFPI might become an important drug for various clinical indications, especially for the management of acute coronary syndromes such as unstable angina and myocardial infarction. The enhanced procoagulant activity in patients with ischaemic heart diseases as documented e.g., by increased plasma levels of TF, requires an effective inhibition of clotting activation either by physiologic mechanisms or by exogenous substances. To increase circulating plasma concentrations of free TFPI, recombinant TFPI could be administered in high doses either locally or systemically, or high amounts of TFPI could be released from vascular pools by interaction with other drugs such as heparin or low molecular weight heparin derivatives. Despite the limited data on the use of TFPI in specific clinical indications, it can be concluded that TFPI and similar compounds represent a new class of drugs with a remarkable developmental potential.


Thrombosis Research | 2001

Systemic Vascular Effects of Thrombin and Thrombin Receptor Activating Peptide in Rats

Thomas Sicker; Frank Wuchold; Brigitte Kaiser; Erika Glusa

The proteolytic enzyme thrombin activates its receptor by cleavage of a peptide from the extracellular N-terminus. The newly generated N-terminus acts as a tethered ligand to activate the receptor. Receptor-mediated cellular effects of thrombin can be mimicked by synthetic peptides, which correspond to the amino acid sequence of the newly formed N-terminus. The aim of the present study was to investigate vascular effects of thrombin and the thrombin receptor activating peptide (TRAP: SFLLRN) in vitro and in vivo in rats. In precontracted rat aortic rings, both thrombin (0.3, 1, 3 U/ml) and TRAP (1, 3, 10, 20, 40 microM) induced endothelium-dependent relaxant responses. In anaesthetized rats, the mean arterial blood pressure (MAP) was measured continuously in the carotid artery by a pressure transducer. Thrombin and TRAP were administered as intravenous bolus injection via the femoral vein. Thrombin at doses of 3-100 U/kg, as well as TRAP at doses of 0.1-0.6 mg/kg i.v., caused a reversible decrease in MAP. Administration of TRAP at doses of 0.3 and 0.6 mg/kg led to a triphasic response in most of the animals treated (50% and 75%, respectively), i.e. a short drop of MAP was followed by an increase and finally a longer lasting decrease in MAP. Pretreatment with the nitric oxide (NO)-synthase inhibitor N(G)-nitro-L-arginine-methylester (L-NAME) suppressed the dose-dependent vasodilator effects of thrombin. Heparin and hirudin also inhibited the hypotensive response to thrombin. The TRAP-induced triphasic reaction on MAP was not affected by the serotonin antagonists ketanserin and tropisetron, as well as the aminopeptidase inhibitor amastatin. Pretreatment with L-NAME led to an inhibition of hypotension induced by TRAP at 0.1 mg/kg, as well as of the initial transient fall in blood pressure at doses of 0.3 and 0.6 mg/kg. The studies suggest that the thrombin- and TRAP-induced vasodilation in vitro and in vivo is in part due to the release of endothelial NO. In the blood pressure response to TRAP, additional effects seem to be involved.

Collaboration


Dive into the Brigitte Kaiser's collaboration.

Top Co-Authors

Avatar
Top Co-Authors

Avatar

Debra Hoppensteadt

Loyola University Medical Center

View shared research outputs
Top Co-Authors

Avatar

Jeanine M. Walenga

Loyola University Medical Center

View shared research outputs
Top Co-Authors

Avatar

D. Hoppensteadt

Loyola University Medical Center

View shared research outputs
Top Co-Authors

Avatar

Omer Iqbal

Anschutz Medical Campus

View shared research outputs
Top Co-Authors

Avatar

Walter Jeske

Loyola University Chicago

View shared research outputs
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Researchain Logo
Decentralizing Knowledge