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1.
Osteoarthritis Cartilage ; 20(12): 1500-6, 2012 Dec.
Article in English | MEDLINE | ID: mdl-22944522

ABSTRACT

OBJECTIVES: (1) Test the hypothesis that walking poles decrease the external knee adduction moment during gait in patients with varus gonarthrosis, and (2) explore potential mechanisms. DESIGN: Thirty-four patients with medial compartment knee osteoarthritis (OA) and varus alignment underwent three dimensional (3D) gait analysis with and without using walking poles. Conditions were randomized and walking speed was maintained ±5% of the self-selected speed of the initial condition. The pole held in the hand of the unaffected side was instrumented with a compression load cell. RESULTS: Student's t tests for paired samples indicated small but statistically significant increases (P < 0.001) in knee adduction moment (calculated from inverse dynamics) for its first peak, second peak and angular impulse when using the poles; mean increases (95% confidence interval - CI) were 0.17%BW*Ht (0.08, 0.27), 0.17%BW*Ht (0.04, 0.30) and 0.15%BW*Ht*s (0.09, 0.22), respectively. There was a decrease (P = 0.015) in vertical ground reaction force (-0.02 BW (-0.04, -0.01)), yet increase (P < 0.001) in its frontal plane lever arm about the knee (0.30 cm (0.15, 0.44)), at the time of the first peak knee adduction moment. Pole force in the vertical direction was inversely related (r = -0.34, P = 0.05) to the increase in first peak adduction moment. CONCLUSION: Although results are variable among patients, and may be related to individual technique, these overall findings suggest that walking poles do not decrease knee adduction moments, and therefore likely do not decrease medial compartment loads, in patients with varus gonarthrosis. Decreases in knee joint loading should not be used as rationale for walking pole use in these patients.


Subject(s)
Canes , Gait , Knee Joint/physiopathology , Osteoarthritis, Knee/physiopathology , Range of Motion, Articular/physiology , Walking/physiology , Weight-Bearing/physiology , Biomechanical Phenomena , Female , Humans , Male , Middle Aged , Osteoarthritis, Knee/rehabilitation
2.
J Mal Vasc ; 36(1): 3-8, 2011 Feb.
Article in French | MEDLINE | ID: mdl-21145677

ABSTRACT

OBJECTIVES: To analyze in-hospital thromboprophylaxis in patients at risk for venous thromboembolism. To evaluate compliance with heparin-induced thrombocytopenia screening recommendations in these patients. PATIENT AND METHODS: We performed a cross-sectional study of 395 patients hospitalized in our tertiary care center at risk for venous thromboembolism. We collected data regarding thromboprophylaxis (risk factors for thrombosis, type of prophylaxis, bleeding risk, demographic data, and hospitalization data). RESULTS: Three hundred and twenty patients were included in the study; 183 patients were hospitalized on medical wards and 137 patients on surgical wards. Thromboprophylaxis was indicated in 57% of the patients according to the American College of Chest Physicians' clinical practice guidelines. Adequate venous thrombosis prophylaxis was prescribed for 83.7% of these patients (76.1% of medical cases and 90.6% of the surgical cases). In contrast, only 47.1% of at risk patients on the family medicine wards received adequate prophylaxis. 79.3% of patients for whom it was indicated underwent appropriate platelet count monitoring. CONCLUSION: The use of thromboprophylaxis is well established in our institution. After having reviewed these data we instituted measures to improve our rate of appropriate thromboprophylaxis and platelet count monitoring. This type of evaluation could be considered by other centers in order to evaluate their performance and institute measures to improve their quality of care.


Subject(s)
Fibrinolytic Agents/administration & dosage , Venous Thromboembolism/prevention & control , Aged , Aged, 80 and over , Female , Fibrinolytic Agents/adverse effects , Hospitalization , Hospitals , Humans , Male , Middle Aged , Platelet Count , Practice Guidelines as Topic , Practice Patterns, Physicians' , Risk Factors , Thrombocytopenia/chemically induced , Thrombocytopenia/prevention & control
3.
Clin Microbiol Infect ; 15(2): 193-9, 2009 Feb.
Article in English | MEDLINE | ID: mdl-19196260

ABSTRACT

Whether antiplatelet therapy is associated with better outcomes among patients with infective endocarditis (IE) remains controversial. A retrospective study was conducted concerning all patients with IE, treated in a tertiary-care centre of Canada between 1991 and 2006, who satisfied the modified Duke criteria for a definite or possible IE. The primary outcome was all-cause mortality within 90 days of diagnosis. A secondary outcome was the development of major systemic embolism. In total, 241 patients satisfied the inclusion criteria, 75 of whom had been on chronic antiplatelet therapy prior to developing endocarditis. Seventy-one (29.5%) patients died. According to multivariate analysis, age, a high Charlson score, aortic valve involvement, myocardial infarction and presence of a perivalvular abscess were strongly associated with mortality. Undergoing valvular replacement (adjusted OR (AOR) 0.28, 95% CI 0.09-0.84) and chronic antiplatelet therapy before IE (AOR 0.27, 95% CI 0.11-0.64) correlated with lower mortality. There was a trend for lower mortality among patients started on antiplatelet drugs after admission (AOR 0.29, 95% CI 0.08-1.13). The effect of aspirin on mortality was much the same in patients who received 325 or 80 mg daily. Chronic antiplatelet therapy was not associated with a significantly lower risk of major embolism. In conclusion, chronic antiplatelet therapy was associated with lower mortality among patients with IE, independently of any effect on major embolism. Whether or not a beneficial effect could be replicated by initiating antiplatelet therapy at the time of diagnosis remains unproven.


Subject(s)
Endocarditis/drug therapy , Endocarditis/mortality , Platelet Aggregation Inhibitors/therapeutic use , Adult , Aged , Aged, 80 and over , Canada , Embolism/prevention & control , Female , Hospitals , Humans , Male , Middle Aged , Risk Factors , Treatment Outcome , Young Adult
4.
Biochim Biophys Acta ; 1765(1): 25-37, 2006 Jan.
Article in English | MEDLINE | ID: mdl-16168566

ABSTRACT

Endocan, previously called endothelial cell specific molecule-1, is a soluble proteoglycan of 50 kDa, constituted of a mature polypeptide of 165 amino acids and a single dermatan sulphate chain covalently linked to the serine residue at position 137. This dermatan sulphate proteoglycan, which is expressed by the vascular endothelium, has been found freely circulating in the bloodstream of healthy subjects. Experimental evidence is accumulating that implicates endocan as a key player in the regulation of major processes such as cell adhesion, in inflammatory disorders and tumor progression. Inflammatory cytokines such as TNF-alpha, and pro-angiogenic growth factors such as VEGF, FGF-2 and HGF/SF, strongly increased the expression, synthesis or the secretion of endocan by human endothelial cells. Endocan is clearly overexpressed in human tumors, with elevated serum levels being observed in late-stage lung cancer patients, as measured by enzyme-linked immunoassay, and with its overexpression in experimental tumors being evident by immunohistochemistry. Recently, the mRNA levels of endocan have also been recognized as being one of the most significant molecular signatures of a bad prognosis in several types of cancer including lung cancer. Overexpression of this dermatan sulphate proteoglycan has also been shown to be directly involved in tumor progression as observed in mouse models of human tumor xenografts. Collectively, these results suggest that endocan could be a biomarker for both inflammatory disorders and tumor progression as well as a validated therapeutic target in cancer. On the basis of the recent successes of immunotherapeutic approaches in cancer, the preclinical data on endocan suggests that an antibody raised against the protein core of endocan could be a promising cancer therapy.


Subject(s)
Antineoplastic Agents/administration & dosage , Biomarkers, Tumor/metabolism , Drug Delivery Systems , Endothelial Cells/metabolism , Neoplasm Proteins/metabolism , Proteoglycans/metabolism , Amino Acid Sequence , Animals , Cell Line, Tumor , Cell Transformation, Neoplastic/drug effects , Cell Transformation, Neoplastic/metabolism , Gene Expression Regulation , Humans , Lung Neoplasms/drug therapy , Lung Neoplasms/metabolism , Lung Neoplasms/pathology , Molecular Sequence Data , Neoplasm Proteins/chemistry , Neoplasm Proteins/genetics , Protein Conformation , Proteoglycans/chemistry , Proteoglycans/genetics , Transcription, Genetic
5.
J Biol Chem ; 276(51): 48341-9, 2001 Dec 21.
Article in English | MEDLINE | ID: mdl-11590178

ABSTRACT

Proteoglycans that modulate the activities of growth factors, chemokines, and coagulation factors regulate in turn the vascular endothelium with respect to processes such as inflammation, hemostasis, and angiogenesis. Endothelial cell-specific molecule-1 is mainly expressed by endothelial cells and regulated by pro-inflammatory cytokines (Lassalle, P., Molet, S., Janin, A., Heyden, J. V., Tavernier, J., Fiers, W., Devos, R., and Tonnel, A. B. (1996) J. Biol. Chem. 271, 20458-20464). We demonstrate that this molecule is secreted as a soluble dermatan sulfate (DS) proteoglycan. This proteoglycan represents the major form either secreted by cell lines or circulating in the human bloodstream. Because this proteoglycan is specifically secreted by endothelial cells, we propose to name it endocan. The glycosaminoglycan component of endocan consists of a single DS chain covalently attached to serine 137. Endocan dose-dependently increased the hepatocyte growth factor/scatter factor (HGF/SF)-mediated proliferation of human embryonic kidney cells, whereas the nonglycanated form of endocan did not. Moreover, DS chains purified from endocan mimicked the endocan-mediated increase of cell proliferation in the presence of HGF/SF. Overall, our results demonstrate that endocan is a novel soluble dermatan sulfate proteoglycan produced by endothelial cells. Endocan regulates HGF/SF-mediated mitogenic activity and may support the function of HGF/SF not only in embryogenesis and tissue repair after injury but also in tumor progression.


Subject(s)
Hepatocyte Growth Factor/physiology , Mitogens/physiology , Neoplasm Proteins , Proteoglycans/physiology , Amino Acid Sequence , Animals , Blood Coagulation/physiology , CHO Cells , Cell Line , Chondroitinases and Chondroitin Lyases/metabolism , Chromatography, Gel , Cricetinae , Glycosylation , Humans , Molecular Weight , Polysaccharide-Lyases/metabolism , Proteoglycans/chemistry
6.
J Immunol ; 167(6): 3099-106, 2001 Sep 15.
Article in English | MEDLINE | ID: mdl-11544294

ABSTRACT

ICAMs are ligands for LFA-1, a major integrin of mononuclear cells involved in the immune and inflammatory processes. We previously showed that endothelial cell specific molecule-1 (ESM-1) is a proteoglycan secreted by endothelial cells under the control of inflammatory cytokines. Here, we demonstrate that ESM-1 binds directly to LFA-1 onto the cell surface of human blood lymphocytes, monocytes, and Jurkat cells. The binding of ESM-1 was equally dependent on Ca(2+), Mg(2+), or Mn(2+) divalent ions, which are specific, saturable, and sensitive to temperature. An anti-CD11a mAb or PMA induced a transient increase in binding, peaking 5 min after activation. Direct binding of ESM-1 to LFA-1 integrin was demonstrated by specific coimmunoprecipitation by CD11a and CD18 mAbs. A cell-free system using a Biacore biosensor confirmed that ESM-1 and LFA-1 dynamically interacted in real time with high affinity (K(d) = 18.7 nM). ESM-1 consistently inhibited the specific binding of soluble ICAM-1 to Jurkat cells in a dose-dependent manner. These results suggest that ESM-1 and ICAM-1 interact with LFA-1 on binding sites very close to but distinct from the I domain of CD11a. Through this mechanism, ESM-1 could be implicated in the regulation of the LFA-1/ICAM-1 pathway and may therefore influence both the recruitment of circulating lymphocytes to inflammatory sites and LFA-1-dependent leukocyte adhesion and activation.


Subject(s)
CD18 Antigens/metabolism , Endothelium, Vascular/physiology , Intercellular Adhesion Molecule-1/metabolism , Lymphocyte Function-Associated Antigen-1/metabolism , Neoplasm Proteins , Proteins/metabolism , Proteoglycans , Biosensing Techniques , Cell Adhesion/physiology , Cell Movement/physiology , Cell-Free System , Computer Systems , Humans , Inflammation , Jurkat Cells/metabolism , Lymphocyte Activation/physiology , Protein Binding/drug effects , Protein Structure, Tertiary , Proteins/pharmacology , Temperature , Tetradecanoylphorbol Acetate/pharmacology
7.
J Vasc Res ; 37(5): 417-25, 2000.
Article in English | MEDLINE | ID: mdl-11025405

ABSTRACT

Endothelial-cell-specific molecule 1 (ESM-1) is a recently identified endothelial cell molecule. As ESM-1 mRNA is preferentially expressed in human lung and kidney tissues, and as ESM-1 mRNA expression is regulated by inflammatory cytokines, ESM-1 is thought to play a role in the vascular contribution to organ-specific inflammation. In order to define its behavior, mouse anti-ESM-1 monoclonal antibodies were developed, and three distinct epitopes were mapped, which allowed development of a specific ELISA assay, immunohistological staining and immunoblot analysis. Here, we demonstrate that ESM-1 is present in cell lysates of human endothelial cells (human umbilical vein endothelial cells) with an apparent molecular weight of 20 kD. In contrast, the secreted form of ESM-1 is shifted to an apparent molecular weight of 50 kD, indicating that the secreted form of ESM-1 is posttranslationally modified. By ELISA, we show that the secretion of ESM-1 is significantly enhanced in the presence of TNFalpha. In contrast, the spontaneous as well as TNFalpha-induced secretion of ESM-1 is strongly inhibited by IFNgamma. Moreover, ESM-1 was detected in the serum of healthy subjects at an average concentration of 1.08 ng/ml, and we demonstrated that the serum level of ESM-1 is dramatically increased in patients presenting a septic shock. Analysis of ESM-1 expression in normal human tissues by immunohistochemistry showed that ESM-1 is localized in the vascular network, but also in the bronchial and renal epithelia. Our results demonstrate that ESM-1 is mainly expressed in the vascular endothelium both in vitro and in vivo, but also by different epithelia. ESM-1 may represent a new marker of endothelial cell activation, and may have a functional role in endothelium-dependent pathological disorders.


Subject(s)
Neoplasm Proteins , Proteins/analysis , Proteoglycans , Adult , Animals , Antibodies, Monoclonal , Antibody Specificity , Blotting, Western , Endothelium, Vascular/chemistry , Enzyme-Linked Immunosorbent Assay , Epithelium/chemistry , Epitope Mapping , Female , Graft Rejection , Humans , Immunosorbent Techniques , Kidney/blood supply , Kidney Transplantation , Male , Mice , Middle Aged , Proteins/immunology , Sepsis/blood , Umbilical Veins
8.
Exp Cell Res ; 253(2): 413-21, 1999 Dec 15.
Article in English | MEDLINE | ID: mdl-10585264

ABSTRACT

In Xenopus eggs, metaphase II arrest is due to the cytostatic factor that maintains a high level of MPF activity. Kinases are important in this phenomenon since p39(mos) and MAPK play a part in the cytostatic activity whereas p34(cdc2) is the catalytic subunit of MPF. Fertilization induces a rise in intracellular calcium leading to egg activation that can be mimicked by calcium-increasing agents such as calcium ionophore. We have performed on Xenopus eggs a biochemical comparison of the effects of the kinase inhibitor 6-DMAP and the calcium ionophore. Both drugs were able to induce pronucleus formation but the underlying molecular events were different. The inactivation of MAPK occurred earlier in eggs exposed to 6-DMAP. Cyclins B1 and B2 were stable and p39(mos) was proteolysed in 6-DMAP-treated eggs while the three proteins underwent degradation in A23187-treated ones. These results suggest a differential regulation of ubiquitin-dependent proteolysis of cyclin B and p39(mos).


Subject(s)
Adenine/analogs & derivatives , Cyclin B/metabolism , Enzyme Inhibitors/pharmacology , Oocytes/enzymology , Proto-Oncogene Proteins c-mos/metabolism , Adenine/pharmacology , Animals , CDC2 Protein Kinase/analysis , CDC2 Protein Kinase/metabolism , Calcimycin/pharmacology , Calcium/metabolism , Cell Nucleus/enzymology , Cyclin B/analysis , Female , Ionophores/pharmacology , Metaphase/physiology , Mitogen-Activated Protein Kinase 1/analysis , Mitogen-Activated Protein Kinase 1/metabolism , Oocytes/cytology , Oocytes/drug effects , Proto-Oncogene Proteins c-mos/analysis , Xenopus laevis
9.
FEBS Lett ; 457(2): 175-8, 1999 Aug 27.
Article in English | MEDLINE | ID: mdl-10471773

ABSTRACT

We have studied the effect of a protein tyrosine phosphatases (PTP) inhibitor on calcium-induced activation of Xenopus laevis oocytes arrested at metaphase II. Ammonium molybdate microinjection blocked pronucleus formation following A23187 treatment while cortical granules still underwent exocytosis. Pronuclei still occurred in ammonium molybdate-injected oocytes following 6-DMAP addition. Changes that usually occurred following A23187 exposure were inhibited in the presence of ammonium molybdate in the oocyte: MAPK dephosphorylation, p34(cdc2) rephosphorylation and cyclin B2 and p39(mos) proteolysis. These results suggest that a PTP is involved in the activation of the ubiquitin-dependent degradation machinery.


Subject(s)
Calcium/metabolism , Metaphase/physiology , Protein Tyrosine Phosphatases/metabolism , Animals , Anti-Bacterial Agents/pharmacology , Calcimycin/pharmacology , Calcium-Calmodulin-Dependent Protein Kinases/metabolism , Enzyme Inhibitors/pharmacology , Maturation-Promoting Factor/analysis , Metaphase/drug effects , Molybdenum/pharmacology , Oocytes/cytology , Oocytes/drug effects , Protein Tyrosine Phosphatases/antagonists & inhibitors , Proto-Oncogene Proteins c-mos/analysis , Xenopus laevis
11.
Shock ; 1(5): 343-6, 1994 May.
Article in English | MEDLINE | ID: mdl-7743336

ABSTRACT

Septic shock is characterized by surges of tumor necrosis factor-alpha (TNF-alpha) along with myocardial dysfunction and systemic hypotension. TNF-alpha promotes the release of immunoreactive endothelin (ET). Because TNF-alpha is elevated in septic shock, we hypothesized that elevated levels of endothelin can contribute to cardiac dysfunction and hypotension. We infused live Pseudomonas aeruginosa into anesthetized, hemodynamically monitored young swine and measured ET and TNF-alpha. Septic swine developed systemic arterial hypotension and had significantly elevated TNF-alpha (4.15 +/- .41 U/ml at 1 h versus .40 +/- .13 U/ml at time zero) compared to control animals. ET levels were significantly elevated at 4 h (52.38 +/- 12.88 pg/ml vs. 10.45 +/- 1.82 pg/ml at time zero) and correlated negatively with the decline in cardiac output. We then passively immunized swine using anti TNF-alpha prior to the induction of sepsis to examine if TNF played a central role in the release ET. The anti TNF-alpha effectively removed circulating TNF-alpha bioactivity in septic animals. Anti-TNF-alpha-treated animals did not develop significant systemic arterial hypotension and had significant attenuation in endothelin (19.01 +/- 4.18 pg/ml at 4 h compared to 52.38 +/- 12.88 pg/ml in septic animals at 4 h) which correlated with preservation of cardiac output. TNF-alpha may cause cardiac dysfunction in sepsis syndrome through increased release of ET.


Subject(s)
Endothelins/blood , Pseudomonas Infections/metabolism , Pseudomonas aeruginosa , Shock, Septic/metabolism , Tumor Necrosis Factor-alpha/metabolism , Animals , Antibodies, Monoclonal/immunology , Disease Models, Animal , Endothelins/agonists , Hemodynamics/drug effects , Immunization , Infusions, Intravenous , Shock, Septic/microbiology , Swine , Tumor Necrosis Factor-alpha/immunology
12.
Chest ; 103(5): 1625-6, 1993 May.
Article in English | MEDLINE | ID: mdl-8486065

ABSTRACT

A 29-year-old woman experienced overwhelming rubeola pneumonia requiring endotracheal intubation and mechanical ventilation. Treatment with high-dose corticosteroids and vitamin A was accompanied by a prompt clinical response. Further investigation of this novel therapy is needed.


Subject(s)
Measles/drug therapy , Methylprednisolone/administration & dosage , Pneumonia, Viral/drug therapy , Vitamin A/administration & dosage , Adult , Drug Therapy, Combination , Female , Humans
16.
Surgery ; 110(2): 205-11; discussion 211-2, 1991 Aug.
Article in English | MEDLINE | ID: mdl-1677491

ABSTRACT

Activated polymorphonuclear leukocytes (PMNs) are implicated in the pathogenesis of acute lung injury (ALI) associated with sepsis. Adhesion of activated PMNs to endothelial monolayers is mediated by the CD18 adhesion-receptor complex on the PMN cell surface. Monoclonal antibody 60.3 (MoAb 60.3) blocks CD18-dependent PMN-endothelial adhesion in vitro and in vivo. This study was designed to determine the role of CD18-dependent PMN adhesion in ALI associated with gram-negative sepsis. Anesthetized, ventilated (FiO2 0.5, positive end-expiratory pressure 5 cm H2O) pigs received sterile saline (control, n = 8) or live Pseudomonas aeruginosa, 5 x 10(8) colony-forming units/ml at 0.3 ml/20 kg/min (septic, n = 9) for 1 hour. A third group (n = 7) received MoAb 60.3, 2 mg/kg intravenously, 15 minutes before Pseudomonas infusion. Animals were studied for 300 minutes. MoAb 60.3 significantly (p less than 0.05) attenuated the neutropenia seen in sepsis (15 +/- 1 vs 6 +/- 1 x 10(3) PMNs/mm3 at 300 min). Alveolar-capillary membrane injury was assessed by bronchoalveolar-lavage protein content and extravascular lung water determination. MoAb 60.3 significantly (p less than 0.05) reduced BAL protein at 300 minutes (388 +/- 75 vs 1059 +/- 216 micrograms/ml in septic animals) and attenuated the increase in extravascular lung water to 240 minutes (7.1 +/- 2 vs 14.2 +/- 1.2 ml/kg in septic animals). Systemic hypotension, decreased cardiac index, pulmonary hypertension, and relative hypoxemia, all characteristic of this model, were not altered by MoAb 60.3. These data suggest that, in this model of septic ALI, neutropenia is, in part, CD18 dependent and that blocking CD18-dependent PMN adhesion protects the alveolar-capillary membrane independently of altered hemodynamic status.


Subject(s)
Antibodies, Monoclonal , Antigens, CD/physiology , Lung Diseases/physiopathology , Neutrophils/physiology , Pseudomonas Infections/complications , Receptors, Leukocyte-Adhesion/physiology , Shock, Septic/complications , Acute Disease , Analysis of Variance , Animals , CD18 Antigens , Cell Adhesion/immunology , Endothelium, Vascular/physiopathology , Lung Diseases/immunology , Lung Diseases/microbiology , Pulmonary Alveoli/physiopathology , Swine
17.
Microvasc Res ; 41(3): 328-44, 1991 May.
Article in English | MEDLINE | ID: mdl-1649374

ABSTRACT

The microcirculation contains mononuclear phagocytes, with features characteristic of macrophages, adhered to luminal capillary surfaces by intercellular adhesion plaques. These pulmonary intravascular macrophages may play an important role in regulating lung vascular tone and capillary permeability, and may modulate capillary endothelial cell growth and replication by the secretion of soluble mediators (i.e., arachidonate metabolites, cytokines). This study describes a technique which utilizes in situ lung perfusion to remove intravascular macrophages in large numbers from the microcirculation of porcine lung (n = 26). This technique yielded 3.8 +/- 0.5 x 10(8) (mean +/- SEM) mononuclear cells which were highly phagocytic toward particulate carbon (phagocytic index, 80 +/- 6%). Harvested mononuclear phagocytes reestablished intercellular adhesion plaques when placed on small vessel porcine pulmonary artery endothelial cell monolayers and exhibited histochemical characteristics typical of monocyte/macrophage lineage cells. Mononuclear cells obtained from lung microcirculation displayed size heterogeneity varying from 10.4 to 16.5 microns in diameter. Both large and small cell populations phagocytosed particulate carbon. Morphometric studies performed on collagenase-treated lung demonstrated that in situ perfusion removed significant numbers of intravascular macrophages in lung capillaries. The technique described permits the rapid removal of anchored mononuclear phagocytes from lung capillaries with minimal postmortem delay.


Subject(s)
Cell Separation , Lung/blood supply , Macrophages , Animals , Cell Count , Cell Separation/methods , Histocytochemistry , Lung/cytology , Lung/drug effects , Macrophages/chemistry , Macrophages/physiology , Macrophages/ultrastructure , Microbial Collagenase/pharmacology , Microcirculation , Perfusion , Phagocytosis , Swine
18.
J Surg Res ; 50(4): 323-9, 1991 Apr.
Article in English | MEDLINE | ID: mdl-1673483

ABSTRACT

Sequestration of neutrophils (PMNs) in the pulmonary microvasculature and associated neutropenia are characteristic features of experimental models of septic lung injury. The etiology of altered PMN kinetics during septic lung injury is uncertain, but may be partially due to increased adhesiveness of activated PMNs to pulmonary endothelium. This study examines the relationship between the expression of PMN CD18 adhesion receptors, the evolving neutropenia, and plasma tumor necrosis factor (TNF) activity in a porcine model of septic lung injury. Acute lung injury was induced by infusion of live Pseudomonas aeruginosa (5 x 10(8) CFU/ml at 0.3 ml/20 kg/min) for 60 min (Group Ps, n = 6). Control animals (Group C, n = 3) received a 60-min infusion of sterile 0.9% saline. CD18 expression of circulating PMNs was measured by quantitative immunofluorescent flow cytometry. Plasma TNF activity was measured by L929 fibroblast cytolytic assay. Group Ps developed a significant neutropenia by 30 min (14.9 +/- 2.5 vs 23.4 +/- 3.3 x 10(3) cells/microliter at baseline, P less than 0.05, ANOVA) with circulating neutrophils exhibiting significantly increased CD18 expression by 60 min (6.34 +/- 0.72 vs 5.01 +/- 0.52 equivalent soluble fluorescence molecules (ESFM) x 10(3) at baseline, P less than 0.05, ANOVA). Group Ps demonstrated a significant increase in plasma TNF activity by 30 min (2.5 +/- 0.9 vs 0.7 +/- 0.3 U/ml at baseline). There was no significant change in PMN count, PMN CD18 expression, or plasma TNF activity in Group C. In complimentary in vitro studies, porcine PMNs stimulated with recombinant human TNF-alpha (n = 5) demonstrated a time- and dose-dependent increase in CD18 expression.(ABSTRACT TRUNCATED AT 250 WORDS)


Subject(s)
Cell Adhesion Molecules/metabolism , Lung Diseases/pathology , Neutropenia/etiology , Neutrophils/metabolism , Pseudomonas Infections/blood , Receptors, Leukocyte-Adhesion/metabolism , Tumor Necrosis Factor-alpha/physiology , Animals , CD18 Antigens , Cell Adhesion , Pseudomonas Infections/pathology , Pseudomonas aeruginosa , Swine
19.
Chest ; 97(6): 1482-3, 1990 Jun.
Article in English | MEDLINE | ID: mdl-2347237

ABSTRACT

The first fatal Cunninghamella bertholletiae infection in a clinically immunocompetent host is reported. This case differs from previously reported cases by the lack of extensive vascular invasion and thrombosis.


Subject(s)
Immunocompetence , Lung Diseases, Fungal/microbiology , Mucorales/pathogenicity , Mucormycosis/microbiology , Humans , Male , Middle Aged
20.
Eur J Cancer ; 26(10): 1074-8, 1990.
Article in English | MEDLINE | ID: mdl-2148883

ABSTRACT

Therapeutic doses of recombinant interleukin-2 (rIL-2) often result in systemic toxicity consistent with increased vascular permeability. rIL-2 activated lymphocytes (IALs) may produce endothelial dysfunction and have cytolytic potential. However, much of the data on IAL cytotoxicity comes from the use of in vitro activated IALs. Alternatively, rIL-2 may enhance permeability directly or via release of various cytokines by host effector cells. The cytotoxicity of in vivo activated lung lymph lymphocytes has been studied in an ovine model of rIL-2 toxicity. The in vivo IALs had no significant endothelial cytolysis at effector to target ratios of 100:1. However, the in vivo IALs increased endothelial monolayer permeability to albumin, dependent on the concentration of IALs. rIL-2 induced no endothelial cytolysis or permeability alterations at doses of 10(5) and 2 x 10(5) U/ml, respectively. These findings suggest that the acute endothelial dysfunction characteristic of the vascular leak syndrome is not due to rIL-2 directly, but is mediated by in vivo IALs via non-cytolytic mechanisms and/or the release of secondary cytokines in response to rIL-2.


Subject(s)
Endothelium, Vascular/cytology , Endothelium, Vascular/metabolism , Interleukin-2/pharmacology , Lung/cytology , Lymph/cytology , Lymphocyte Activation/drug effects , Lymphocytes/physiology , Albumins/pharmacokinetics , Animals , Cell Membrane Permeability , Cell Survival/drug effects , Chromium Radioisotopes , Dose-Response Relationship, Drug , Endothelium, Vascular/drug effects , Humans , Interleukin-2/administration & dosage , Iodine Radioisotopes , Lymphocytes/drug effects , Recombinant Proteins/administration & dosage , Recombinant Proteins/pharmacology , Sheep
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