Anx5 Therapy - Ashley Davis

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Recombinant Human Annexin A5 Therapy – Inhibition of Proinflammatory Response with Improved Cardiac Function and Survival Rate in Mice with Endotoxemia Ashley Davis University of North Florida

Transcript of Anx5 Therapy - Ashley Davis

Page 1: Anx5 Therapy - Ashley Davis

Recombinant Human Annexin A5 Therapy – Inhibition of Proinflammatory Response with Improved Cardiac Function and Survival Rate

in Mice with Endotoxemia

Ashley DavisUniversity of North Florida

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Collaborative Research• Paul Arnold & Fatemeh Armirahmadi – Department of

Physiology and Pharmacology at the University of Western Ontario, London, Canada

• Xiangru Lu MD - Center of Critical Illness Research at the Lawson Health Research Institute ON, Canada

• Katharina Brandl PhD – Department of Genetics at the The Scripps Research Institute La Jolla, California

• Qingpin Feng MD, PhD – Department of Medicine at the University of Western Ontario, London, Canada

• Dr. Feng is a career investigator at Heart and Stroke Foundation of Canada

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Endotoxemia✧ Bacteria enter bloodstream and release endotoxins

✧ WBCs react to the presence of bacteria and release inflammatory substances – excessive cytokine production

✧ 18 million cases annually

✧ Increased endothelial permeability• Stage (II) - Severe Sepsis

• Organ dysfunction

• Mortality rate: 30-40%

• Stage (III) - Septic shock

• Myocardial depression

• Mortality rate: 40-80%

NIAID/RML, Science 2002

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Host’s Immunity✧ Host’s innate immunity activated

✧ TLR2 = Gram-positive

✧ TLR4 = Gram-negative

✧ Activation of TLR4 via LPS binding

✧ Initiates signaling pathway that leads to

✧ activation of MAPKs (mitogen-activated protein kinases)

✧ production of inflammatory cytokines - tumor necrosis factor (TNF-α) and Interleukin (IL-β)

Celeste Thorpe MD 2004

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Roll of Toll-like Receptors

Modlin, Nature 2000

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LPS• Lipopolysaccharide

• From Gram-negative bacteria

• LPS binds to TLR4 in CD14

• Binding of LPS activations signaling pathway that leads to activation of MAPKs and production of inflammatory cytokines

• Necrosis factor alpha (TNF-α)

• Leading cause of cardiac dysfunction

• Interleukin-1 beta (IL-β)

Feng et al. Crit Care Med, 2014

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Previous Treatment• Xigris = Activated Protein C

• Indications: for severe sepsis & septic shock

• Acute organ failure

• Properties: Anticoagulant, Anti-inflammatory, Profibrinolytic

• Side Effect: Serious Bleeding

• Was the only approved therapy by the U.S Food and Drug Administration

• No longer used due to severe bleeding risk

• Results from trial showed no survival benefit over placebo

• Xigris was voluntarily withdrawn from market in 2011

FDA Medwatch, 2011

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Annexin A5• A 35-kDa phospholipid binding protein

• High affinity binding to negatively charged phospholipids

• Has antiapoptotic and anticoagulant properties – by forming 2D crystallized shield over the surface of cells

• Shield decreases ability to initiate phagocytosis or thrombosis

• Anx5 interacts with cell receptors to inhibit their function in binding to leucine-rich repeats

• LPS binds to extracellular domain of TLR4 at leucine-rich repeats

• Anx5 inhibits LPS binding to TLR4 and thus decreases downstream MAPK signaling

HTI Inc, 2009

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Results• Anx5 improved cardiac function and survival rate during

endotoxemia by inhibiting LPS binding to TLR4/myeloid differentiation factor 2 (MD-2) receptor complex

• Anx5 decreased myocardial TNF-α and IL-βexpression

• Anx5 restored cardiac function to control levels

• via the inhibition of activation of NF-kB

Feng et al. Crit Care Med, 2014

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Anx5 decreases myocardial MAPKs and NK-κB

Feng et al. Crit Care Med, 2014

CardiacTissue

MAPK

Side Pathway

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Treatment with Anx5 significantly decreased myocardial TNF-αand IL-1β

Feng et al. Crit Care Med, 2014

mRNA

Protein

Plasma

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Anx5 Improves Cardiac Function

Feng et al. Crit Care Med, 2014

Measuring meanarterial pressure

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Improved Survival Rates5 day animal survival was significantly improved by either the immediate or 4-hour delayed

Anx5 treatment following LPS challenge.

Feng et al. Crit Care Med, 2014

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References1. Angus DC, Linde-Zwirble WT, et al. Epidemiology of severe sepsis in the United States:

Analysis of incidence, outcome, and associated costs of care. Critical Care Medicine 2001; 29:1303-1310.

2. Zhang T, Feng Q: Nitric oxide and calcium signaling regulate myocardial tumor necrosis factor- expression and cardiac function in sepsis. Can J Physiol Pharmacol 2010;88;92-104.

3. Parrillo JE, Parker MM, Natanson C, et al: Septic shock in humans. Advances in the understanding of pathogenesis, cardiovascular dysfunction, and therapy. Ann Intern Med 1990; 113:227-242.

4. Toussaint S, Gerlach H: Activated protein C for sepsis. N Engl J Med 2009;361:2646-2652.

5. Gentry CA, Gross KB, Sub B, et al: Adverse outcomes associated with the use of drotrecogin alfa (activated) in patients with severe sepsis and baseline bleeding precautions. Crit Care Med 2009; 37:19-25

6. Gerke V, Moss SE: Annexins: From structure to function. Physiol Rev 2002; 82:331-371 

7. Reutelingsperger CP, van Heerde QL: Annexin V, the regulator of phosphatidylserine-catalyzed inflammation and coagulation during apoptosis. Cell Mol Life Sci 1997;53:527-532

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References8. Markoff A, Bogdanova N, Knop M, et al: Annexin A5 interacts with polycystin-1 and interferes with

polycystin-1 stimulated recruitment of E-cadherin into adherens junctions. J Mol Biol 2007;369:954-966

9. Bell JK, Mullen GE, Leifer CA, et al: Leucine-rich repeats and pathogen recognition in Toll-like receptors, Trends Immunol 2003; 24:528-533

10. Peng T, Lu X, Lei M, et al: Inhibition of p38 MAPK decreased myocardial TNF-alpha expression and improves myocardial function and survival during acute endotoxemia in mice. Cardiovasc Res 2003;59: 123-134

11. Ranieri VM, Thompson BT, Sarie PS, et al: PROWESS-SHOCK Study Group: Drotrecogin alfa (activated) in adults with septic shock. N Engl J Med 2012;366:2055-2064

12. US Food and Drug Administration: Voluntary market withdrawal of Xigris [drotrecogin alfa (activated)] due to failure to show a survival benefit. 2011.

13. Xiang FL, Lu X, Hammoud L, et al: Cardiomyocyte-specific overexpression of human stem cell factor improves cardiac function and survival post myocardial infarction in mice. Circulation 2009; 120: 1065-1074

14. Zhang T, Lu X, Beier F, et al: Rac1 activation induces tumor necrosis factor- expression and cardiac dysfunction in endotoxemia. J Cell Mol Med 2011; 15:1109-1121

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References15. Cour O, Kumar A, Parrillo JE, et al: Clinical review: Myocardial depression in sepsis and septic shock. Crit

Care 2002; 6:500-508

16. Peng T, Lu X, Lei M, et al: Endothelial nitric-oxide synthase enhances lipopolysaccharide-stimulated tumor necrosis factor-alpha expression via cAMP-mediated p38 MAPK pathway in cardiomyocytes. J Biol Chem 2003; 278:8099-8105

17. Grandel U, Fink L, Blum A, et al: Endotoxin-induced myocardial tumor necrosis factor-alpha synthesis depressed contractility of isolated rat hearts: Evidence for a role of sphingosine and cyclooxygenase-2-derived thromboxane production. Circulation 2000; 102:2758-2764

18. Damazo AS, Yona S, D’Acquisto F, et al: Critical protective role for annexin 1 gene expression in the endotoxemic murine microcirculation. Am J Pathol 2005; 166:1607-1617

19. Bouter A, Gounou C, Berat R, et al: Annexin-A5 assembled into two-dimensional arrays promotes cell membrane repair. Nat Commun 2011; 2:270

20. Lee WL, Liles WC: Endothelial activation, dysfunction, and permeability during severe infections. Curr Opin Hematol 2011; 18: 191-196

21. Romisch J, Seiffge D, Reiner G, et al: In-vivo antithrombotic potency of placenta protein 4 (annexin V). Thromb Res 1991; 61; 93-104