270073835 0 1 Santos David Elementary Number Theory Notes pdf. 5 Nov 2011 – Download 270073835 0 1 Santos David Elementary Number Theory Notes pdf documents from. British Bookshop [ Specimen with photos of Jewish information control and censorship ] Freemasons [ Example of Jews and Freemasons—this example is Neville Nagler.

Can capitalism and citizenship co-exist? Advocates of the third way have championed the idea of public-spirited capitalism as the antidote to the many problems confronting the modern world. This book develops a multi-disciplinary theory of citizenship, exploring the human abilities needed for its practice. It then argues that capitalism impedes the nurturing of these abili Can capitalism and citizenship co-exist? Advocates of the third way have championed the idea of public-spirited capitalism as the antidote to the many problems confronting the modern world.

This book develops a multi-disciplinary theory of citizenship, exploring the human abilities needed for its practice. It then argues that capitalism impedes the nurturing of these abilities. In advancing these arguments, Kathryn Dean draws on the work of a wide range of thinkers including Freud, Marx, Lacan, Habermas and Castells.

Adobe Flash Player is required to view this feature. If you are using an operating system that does not support Flash, we are working to bring you alternative formats. Original Article Brief Report Cytokine Storm in a Phase 1 Trial of the Anti-CD28 Monoclonal Antibody TGN1412 Ganesh Suntharalingam, F.R.C.A., Meghan R. Perry, M.R.C.P., Stephen Ward, F.R.C.A., Stephen J. Brett, M.D., Andrew Castello-Cortes, F.R.C.A., Michael D. Brunner, F.R.C.A., and Nicki Panoskaltsis, M.D., Ph.D.

N Engl J Med 2006; 355:1018-1028 DOI: 10.1056/NEJMoa063842. Six healthy young male volunteers at a contract research organization were enrolled in the first phase 1 clinical trial of TGN1412, a novel superagonist anti-CD28 monoclonal antibody that directly stimulates T cells. Within 90 minutes after receiving a single intravenous dose of the drug, all six volunteers had a systemic inflammatory response characterized by a rapid induction of proinflammatory cytokines and accompanied by headache, myalgias, nausea, diarrhea, erythema, vasodilatation, and hypotension. Within 12 to 16 hours after infusion, they became critically ill, with pulmonary infiltrates and lung injury, renal failure, and disseminated intravascular coagulation. Severe and unexpected depletion of lymphocytes and monocytes occurred within 24 hours after infusion.

All six patients were transferred to the care of the authors at an intensive care unit at a public hospital, where they received intensive cardiopulmonary support (including dialysis), high-dose methylprednisolone, and an anti–interleukin-2 receptor antagonist antibody. Prolonged cardiovascular shock and acute respiratory distress syndrome developed in two patients, who required intensive organ support for 8 and 16 days. Despite evidence of the multiple cytokine-release syndrome, all six patients survived.

Documentation of the clinical course occurring over the 30 days after infusion offers insight into the systemic inflammatory response syndrome in the absence of contaminating pathogens, endotoxin, or underlying disease. On March 13, 2006, eight healthy male volunteers participated in a double-blind, randomized, placebo-controlled phase 1 study of the safety of TGN1412 (TeGenero), a novel monoclonal antibody. The study drug is a recombinantly expressed, humanized superagonist anti-CD28 monoclonal antibody of the IgG4κ subclass that stimulates and expands T cells independently of the ligation of the T-cell receptor. In contrast to other antibodies in clinical use or in clinical trials, TGN1412 directly stimulates the immune response in vivo. In preclinical models, the stimulation of CD28 with TGN1412 (or with murine-antibody counterparts) preferentially activated and expanded type 2 helper T cells and, in particular, CD4+CD25+ regulatory T cells, resulting in transient lymphocytosis with no detectable toxic or proinflammatory effects. On the day of the trial, six of the eight volunteers received TGN1412 and two received placebo. Subsequently, the six volunteers in the treatment group, who had multiorgan failure with an unknown mechanism and an unpredictable severity, were all admitted to the on-site critical care unit at Northwick Park and St.

Mark's Hospital, a National Health Service (NHS) hospital in London. We detail the clinical and pathological findings during the first 30 days after the infusion. Trial Conduct TeGenero sponsored the trial of the monoclonal antibody TGN1412, which was manufactured by Boehringer Ingelheim.

The trial was conducted by Parexel International, a contract research organization that operates an independent clinical trials unit in leased space on the premises of Northwick Park and St. Mark's Hospital. The authors of this report are a group of NHS clinicians who assumed clinical responsibility for the secondary care of these patients after they were transferred to the NHS (between 12 hours [one patient] and 16 hours [five patients] after infusion). The authors have no contractual or operational relationship with either Parexel International or TeGenero. Patients and Sources of Data All six patients provided written informed consent to the NHS for the publication of data obtained during clinical case management. Clinical data obtained before admission to the NHS, and selected laboratory data obtained before the complications were observed, are reproduced here with permission from TeGenero.

The trial was suspended owing to the serious adverse events, and no further tests were performed for research purposes. There was full disclosure of drug information, scientific data, and trial documentation by TeGenero and Parexel International, in order to assist in clinical management decisions at the time of the incident. Results All six patients who received the trial drug were male, with a median age of 29.5 years (range, 19 to 34) ( Table 1 Data for All Six Affected Patients on Transfer to the Intensive Care Unit (ICU).

None had a notable medical history, and all were clinically well during the 2 weeks before the study; baseline laboratory values were normal ( Table 2 Median Results of Blood Tests for the Six Patients before Infusion and 8 and 16 Hours after Infusion of TGN1412. Anaconda 1 Full Movie In Hindi Free Download 3gp here. Beginning at 8 a.m. On day 1, each volunteer received an intravenous infusion, 10 minutes apart, of either the study drug or placebo. Each infusion lasted 3 to 6 minutes. The six volunteers in the treatment group each received 0.1 mg of TGN1412 per kilogram of body weight, infused at a rate of 2 mg per minute; the remaining two volunteers received a similar volume of saline. Initial Response after Infusion of TGN1412 A series of adverse effects began in the treatment group after infusion, starting with the onset of severe headache in five patients after a median of 60 minutes (range, 50 to 90), accompanied by lumbar myalgia in all six patients after a median of 77 minutes (range, 57 to 95) ( Figure 1 Summary Timeline of the Main Events after Infusion of TGN1412.

The course is divided into four phases: cytokine storm, reactive, recovery, and steady state. ALT denotes alanine aminotransferase. Dashed lines represent the responses of Patients 5 and 6 (who were the most seriously ill). Subsequently, during this early phase, the patients were restless and had varying degrees of nausea, vomiting, bowel urgency, or diarrhea ( ). Five subjects had short amnestic episodes associated with severe pyrexia, restlessness, or both.

All patients had a systemic inflammatory response that included erythema and peripheral vasodilatation (the timing of which was undocumented), with recorded rigors in four patients at a median of 59 minutes (range, 58 to 120) after infusion. Hypotension (defined by a decline in systolic blood pressure of 20 mm Hg or more) developed in all patients a median of 240 minutes (range, 210 to 280) after infusion, accompanied by tachycardia, with maximal heart rates of 110 to 145 beats per minute. All patients received intravenous lactated Ringer's solution during this time. Body temperatures of 39.5 to 40.0°C were recorded a median of 280 minutes (range, 240 to 390) after infusion. At 300 minutes after infusion, Patient 1 had signs of respiratory failure, with tachypnea and a partial pressure of arterial oxygen (PaO 2) of 52 mm Hg while breathing ambient air; the PaO 2 increased with the addition of supplemental oxygen. Chest radiography revealed pulmonary infiltrates; these findings were not consistent with the expected response of a fit young man to the infusion of less than 4 liters of fluid at this stage. There was no clinical evidence of bronchospasm or laryngeal edema.

All patients were initially empirically treated in the independent clinical trials unit. A dose of 200 mg of hydrocortisone was administered intravenously in divided doses (with the initial 100-mg bolus a median of 331 minutes [range, 315 to 346] after infusion), in addition to 10 mg of chlorpheniramine intravenously, 1 g of acetaminophen intravenously, 4 to 8 mg of ondansetron intravenously, and 0.5 to 3.0 mg of metaraminol intravenously (in divided doses, titrated to effect). Blood samples were analyzed 8 hours after infusion at an off-site private laboratory (according to the study protocol) and therefore were not available as the situation evolved; the results were abnormal ( ).

Subsequent Events After an initial recovery, Patient 6 became hypotensive (blood pressure, 65/40 mm Hg), and 12 hours after infusion, he had metabolic acidosis and marked respiratory distress with hypoxemia that was refractory to treatment with supplemental oxygen. He underwent intubation and mechanical ventilation, after which he was admitted to the intensive care unit (ICU) at Northwick Park and St. Mark's Hospital. He had severely abnormal hemodynamics, coagulation, and pulmonary function, with a PaO 2 of 84 mm Hg while breathing 100% oxygen (ratio of PaO 2 to the fraction of inspired oxygen, 84) ( ).

Because there was concern that all patients would follow a similar course of rapid deterioration, all remaining patients were transferred to NHS ICU facilities 16 hours after infusion. Supportive Management Patients 1 through 4 received continuous positive airway pressure of 10 cm H 2O by means of a tight-fitting face mask. Patients 5 and 6 underwent mechanical ventilation, with tidal volumes limited to 6 to 8 ml per kilogram of dry body weight and positive end-expiratory pressure maintained at 15 to 20 cm H 2O. All six patients had oliguria, metabolic acidosis, and increasing creatinine levels; they therefore received renal support by means of continuous venovenous hemodiafiltration with the use of a standard polyacrylonitrile membrane (Gambro Hospal U.K.) within 36 hours after their exposure to TGN1412. Dialysate rates were set to 1 liter per hour and were subsequently increased to 4 liters per hour. All patients required the replacement of blood components by means of the infusion of fresh-frozen plasma and cryoprecipitate to correct coagulopathy. Owing to their severe lymphopenia, the patients were treated according to a protocol of infusions of irradiated red cells and platelets, as required, to prevent possible graft-versus-host disease.

Clinical Progression Patients 1, 2, 3, and 4 continued to have intermittent fever, myalgia, and diffuse erythematous flushing for 48 hours, at which point their clinical symptoms and signs diminished markedly. Immunomodulatory treatment in these four patients was reduced to a tapering dose of intravenous hydrocortisone followed by oral prednisolone (total duration of corticosteroid treatment in each case, 21 days).

Continuous venovenous hemodiafiltration was stopped after a median of 28 hours (range, 22 to 35), and continuous positive airway pressure was stopped after 4 hours in Patient 1 and after a median of 77 hours (range, 57 to 82) in Patients 2, 3, and 4 (Figure 4A and 4B through 7A and 7B in the ). Patient 2 was also successfully treated for presumed nosocomial Klebsiella pneumoniae bacteremia, isolated on day 6 after TGN1412 infusion. Patients 5 and 6 had a more complex course, as detailed in the. Although both patients initially had diminished erythema and fever 48 hours after infusion, they subsequently had recurrent fever, increased peripheral vascular permeability, and episodes of diffuse erythematous flushing lasting several days. Both patients required intubation and mechanical ventilation. Peripheral ischemia was observed in a glove-and-stocking distribution in Patient 6.

It fluctuated over time, independently of the changing vasopressor dose. Most of the peripheral ischemia slowly resolved, except in patches of necrosis on the fingers of both hands and all the toes. Over the next 30 days, all patients had generalized desquamation (most marked in Patients 5 and 6) and muscle weakness on discharge from the ICU. Five patients had late myalgia, headache after the discontinuation of corticosteroids, difficulties with concentration, and short-term difficulties in finding words (particularly names).

Three patients had delayed hyperalgesia, and two had peripheral numbness. None had documented lymphadenopathy or splenomegaly while in the ICU or after discharge.

Simple Plan Rar Get Your Heart On. Hematologic and Immunologic Progression The laboratory values for the six patients are summarized in Figure 3 Summary of Laboratory Results for the Six Patients during the First 30 Days (Panels A and B) and the First 5 Days (Panel C) after Infusion of TGN1412. Panel A shows that C-reactive protein and serum creatinine levels increased rapidly during the first 48 hours after infusion, with a concomitant decline in the platelet count starting within the first 8 hours and persisting for at least 5 days. Alanine aminotransferase levels increased slowly, starting within the first 48 hours, and peaked between 10 and 25 days after infusion, when the patients had recovered from the acute illness.

Panel B shows that levels of CD3+, CD4+, and CD8+ T-cell subgroups were undetectable within the first 24 hours after infusion, followed by a first peak at day 5 and a second peak at day 15, with a leveling off to near-preinfusion levels by day 30. Monocyte numbers also fell in the short term but increased to above the normal range 10 to 16 days after infusion.

Neutrophil counts were relatively constant immediately after infusion and then increased, as expected, with increasing stress and corticosteroid use. Panel C shows that, during the first 4 hours after infusion, the first cytokine to increase substantially was TNF-α (2.8 pg per milliliter at 0 hour, 1760.1 at 1 hour, and 4675.9 at 4 hours), followed by interferon-γ (7.1 pg per milliliter at 0 hour, 43.9 at 1 hour, and ≥5000 at 4 hours) and interleukin-10, 8, 6, 4, 2, 1β, and 12p70. All data are medians. I bars represent interquartile ranges. Dashed lines represent the upper limit of the normal reference range (where only one dashed line is shown) or both the upper and lower limits. Time points with single values were excluded.

To convert values for creatinine to milligrams per deciliter, divide by 88.4.; data on the clinical course of each patient are provided in the. Severe thrombocytopenia was observed, initially accompanying disseminated intravascular coagulation but persisting even after the other clotting values normalized (, and Figure 4A and 4B through 9A and 9B in the ). All patients had mild normocytic anemia that persisted beyond discharge from the ICU, followed by a slow recovery.

Neutrophil numbers initially were preserved and then increased in response to corticosteroids ( ), but they were dysplastic in appearance ( ), a feature that eventually resolved. By contrast, marked lymphopenia and monocytopenia were noted in all patients 8 hours after TGN1412 infusion ( ). Lymphocyte numbers were too low to allow for the measurement of cell subgroups 1 day after infusion. Subsequent blood tests showed increasing levels of CD4+ and CD8+ T cells (Figure 3 through 9 in the ), CD19+ B cells, and CD16+ presumed natural killer cells, starting 48 hours after infusion. In Patients 1, 2, 3, and 4, who recovered the most rapidly, T-cell recovery occurred in a CD4+:CD8+ ratio of 1:1, with a temporary rise to levels just above normal in two patients (Figure 4D and 7D in the ). Patients 5 and 6, the two who were most severely ill, had a slower recovery, with lower overall numbers of T cells (Figure 8 and Figure 9 in the ) and a CD4+:CD8+ ratio of 2:1. The lymphocyte and monocyte nadirs in each patient occurred within 24 hours after TGN1412 infusion, overlapping with the cytokine storm (, and Figure 4C through 9C in the ).

A dramatic increase in the level of tumor necrosis factor α (TNF-α) was observed in all patients within an hour after TGN1412 infusion, followed by elevations in the level of interleukin-2, 6, and 10 and interferon-γ within the first 4 hours after infusion (, and Figure 4C through 9C and 10 in the ). This cytokine release resolved after the first doses of hydrocortisone and methylprednisolone, and in Patients 1, 2, 3, and 4 the values normalized within 2 days. By contrast, in Patients 5 and 6, the cytokine storm was prolonged by 1 to 2 days; discrete elevations in the interleukin-6 and interleukin-4 levels, out of proportion to those noted in the other patients, were observed. Discussion The intravenous infusion of TGN1412 in healthy persons produced a sudden and rapid release of proinflammatory cytokines.

These unexpected clinical data provide insight into the natural course of the cytokine storm and the systemic inflammatory response syndrome (SIRS) in the absence of contaminating organic factors. Regulatory authorities, who tested TGN1412 from the same batch as the infused drug, found no errors in its manufacture, formulation, or administration and found no contamination with endotoxin, pyrogen, or microbiologic or other agents. This type of cytokine release had not been observed in the preclinical studies of TGN1412, and it is currently unclear whether the severe effects of this type of cytokine release in vivo in humans is caused by the direct ligation of CD28 on T cells or by the ligation and activation of other cell types, leading to the release of preformed TNF-α, which then triggers the remainder of the cascade.

The Secretary of State for Health has convened an expert scientific group to study the events of the clinical trial in greater detail. Clinically, the most striking phenomenon in the cohort was the stereotypical response to the study drug in all six patients and in all organ systems affected (albeit to varying degrees) ( Table 3 Common Features after Infusion of TGN1412. All six patients initially had clinical signs that fit the criteria for SIRS. Subsequently, the most prominent clinical feature was the early appearance of respiratory distress and pulmonary infiltrates, accompanied by renal impairment and profound disseminated intravascular coagulation.

This pattern of organ impairment may be consistent with a generalized multiorgan response to inflammation or critical illness. However, the rapid onset and concordance of the lung injury among patients seemed unusual, and in the presence of high cytokine (especially interferon-γ and TNF-α) levels, these features may be consistent with immune-mediated injury that is specific to the lung. Alveolar macrophages in humans are normally inefficient in the costimulation of T cells through the CD28 pathway; thus, our data suggest that anti-CD28 agonists in vivo may be able to potentiate immune activation and therefore lung injury. Neither cytokine storm nor lung injury was observed in the preclinical studies of TGN1412. This probably indicates that the presence of high levels of proinflammatory cytokines is a requirement for the pulmonary compromise, regardless of whether CD28 is ligated in the lung.

In contrast to the pulmonary compromise that eventually ensues in SIRS, the more rapid onset of lung injury in our patients may have been due to the combination of the direct effects of the antibody and cytokines on lung tissue. Equally striking was the consistent pattern of immunologic effects and recovery in all six patients.

In particular, the severe lymphopenia observed in these patients was unexpected; a temporary lymphocytosis had been observed in preclinical studies of TGN1412 in animals. This unanticipated lymphopenia in humans may have reflected cell death or the migration of cells to other tissues such as lymph nodes, although lymphadenopathy was not detected.

Lymphopenia has been observed as part of the cytokine storm induced by other monoclonal antibodies. However, the low cell numbers observed in these studies were anticipated, given the mechanism of action and the antilymphocyte specificity of the infused antibodies. Sepsis in humans may also induce lymphopenia that is selective for B cells and CD4+ T cells over the course of several days. In contrast, the onset of lymphopenia within 8 hours after infusion of TGN1412, and the involvement of all mononuclear cells (CD4+ and CD8+ T cells and monocytes), may suggest that the depletion of cells in our patients was a response to the infused T-cell agonist drug rather than to the cytokine storm alone. The clinical progression after infusion of TGN1412 can be separated into four phases ( ). Phase 1 began within an hour after infusion, continued through days 1 and 2 (and day 3, in Patients 5 and 6), and consisted of the cytokine storm, involving the rapid induction of type 1 and type 2 cytokines (to varying degrees) and severe lymphopenia and monocytopenia.

Phase 2, the reactive phase, occurred from day 1 through day 3 (or days 1 through 8 in Patients 5 and 6, who were the most seriously ill); it consisted of renal failure, disseminated intravascular coagulation, pulmonary infiltrates, and respiratory failure. Phases 1 and 2 overlapped; phase 2 was not necessarily directly caused by the events in phase 1. The recovery phase, phase 3, occurred between day 3 and day 15 (or between day 5 and day 20, for the patients who were the sickest) and was characterized by the recovery of renal and pulmonary function. This recovery was reflected in thrombocytosis and increases in alanine aminotransferase and monocyte and lymphocyte levels (mostly in a 1:1 ratio of CD4+:CD8+ T cells). The last phase, phase 4, can be described as a plateau or steady-state phase.

It began 15 days after infusion (or 20 days after in Patients 5 and 6) and consisted of normalization of the measured variables. As compared with reactions to the infusion of other immunomodulatory agents (such as anti-CD20, anti-CD3, and anti-CD52 monoclonal antibodies ), the response to TGN1412 initially had similar kinetics, including the rapid increase in the levels of first TNF-α and then interferon-γ and interleukin-6, followed by cardiovascular instability, and disseminated intravascular coagulation. However, from phase 2 onward, features unique to the response to TGN1412 were apparent — including early acute lung injury, diffuse erythema with late desquamation, neurologic sequelae, and post-illness myalgias ( ). These events occurred during the first dosing interval in a phase 1 drug trial of a humanized immunomodulatory monoclonal antibody involving healthy subjects.

The events provide insight into an immune-mediated cytokine storm leading to multiorgan failure in the absence of infection, contamination with endotoxin, or underlying disease. The TGN1412 variant of the syndrome had some features that set it apart from a typical cytokine storm, most notably early acute lung injury and marked lymphopenia. No potential conflict of interest relevant to this article was reported. Suntharalingam can be heard at www.nejm.org. This article was published at www.nejm.org on August 14, 2006.

We are indebted to the NHS staff members involved in the care of the patients on the day of the event and after, for their skill and dedication and for overcoming the unprecedented clinical and logistic challenges that the event presented; and especially to the six patients for consenting to the publication of their clinical data in order to inform ongoing discussion and debate. Source Information From the Department of Intensive Care Medicine, Northwick Park and St.

Mark's Hospital (G.S., M.R.P., S.W., A.C.-C., M.D.B.); the Department of Intensive Care Medicine, Hammersmith Hospital (S.J.B.); and the Department of Haematology, Imperial College London, Northwick Park and St. Mark's Campus (N.P.) — all in London. Address reprint requests to Dr. Suntharalingam at Rm. 4J007, Department of Intensive Care Medicine, or to Dr. Panoskaltsis at the Department of Hematology — both at Northwick Park and St.

Mark's Hospital, Watford Rd., Harrow, London HA1 3UJ, United Kingdom; or. References • 1 Luhder F, Huang Y, Dennehy KM, et al.

Topological requirements and signaling properties of T cell-activating, anti-CD28 antibody superagonists. J Exp Med 2003;197:955-966 • 2 Rodriguez-Palmero M, Hara T, Thumbs A, Hunig T.

Triggering of T cell proliferation through CD28 induces GATA-3 and promotes T helper type 2 differentiation in vitro and in vivo. Eur J Immunol 19-3924 • 3 Beyersdorf N, Gaupp S, Balbach K, et al. Selective targeting of regulatory T cells with CD28 superagonists allows effective therapy of experimental autoimmune encephalomyelitis. J Exp Med 2005;202:445-455 • 4 TGN1412 investigator's brochure.

Wurzburg, Germany: TeGenero Immunotherapeutics, 2005. (Accessed August 11, 2006, at.) • 5 Offner PJ, Moore EE. Lung injury severity scoring in the era of lung protective mechanical ventilation: the PaO2/FiO2 ratio. J Trauma 2003;55:285-289 • 6 Investigations into adverse incidents during clinical trials of TGN1412. London: Medicines and Healthcare products Regulatory Agency (MHRA), 2006.

(Accessed August 11, 2006, at.) • 7 Bernard GR, Artigas A, Brigham KL, et al. The American-European Consensus Conference on ARDS: definitions, mechanisms, relevant outcomes, and clinical trial coordination.

Am J Respir Crit Care Med 1994;149:818-824 • 8 American College of Chest Physicians/Society of Critical Care Medicine Consensus Conference: definitions for sepsis and organ failure and guidelines for the use of innovative therapies in sepsis. Crit Care Med 1992;20:864-874 • 9 Hudson LD, Milberg JA, Anardi D, Maunder RJ. Clinical risks for development of the acute respiratory distress syndrome. Am J Respir Crit Care Med 1995;151:293-301 • 10 Brivet FG, Kleinknecht DJ, Loirat P, Landais PJ. Acute renal failure in intensive care units -- causes, outcome, and prognostic factors of hospital mortality: a prospective, multicenter study. Crit Care Med 1996;24:192-198 • 11 Theron M, Huang KJ, Chen YW, Liu CC, Lei HY. A probable role for IFN-gamma in the development of a lung immunopathology in SARS.

Cytokine 2005;32:30-38 • 12 Gon Y, Wood MR, Kiosses WB, et al. S1P3 receptor-induced reorganization of epithelial tight junctions compromises lung barrier integrity and is potentiated by TNF. Proc Natl Acad Sci U S A 2005;102:9270-9275 • 13 Chelen CJ, Fang Y, Freeman GJ, et al. Human alveolar macrophages present antigen ineffectively due to defective expression of B7 costimulatory cell surface molecules. J Clin Invest 19-1421 • 14 Hunig T, Dennehy K. CD28 superagonists: mode of action and therapeutic potential.

Immunol Lett 2005;100:21-28 • 15 Winkler U, Jensen M, Manzke O, Schulz H, Diehl V, Engert A. Cytokine-release syndrome in patients with B-cell chronic lymphocytic leukemia and high lymphocyte counts after treatment with an anti-CD20 monoclonal antibody (rituximab, IDEC-C2B8). Blood 19-2224 • 16.