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Published Online:https://doi.org/10.2217/rme.10.5

Biocompatibles International plc is focused on the development of targeted therapies for a range of indications, including oncology, neurology and cardiology. By delivering the therapy directly to the site of a localized disease numerous benefits can be achieved, including the targeting of a very high therapeutic dose to the required location and reduced systemic toxicity. As part of this strategy the company is now a leader in the field of using locally placed stem cells to make and deliver therapeutically active peptide drugs. The encapsulated cells (CellBeads®), modified to produce a potent anti-apoptotic peptide, CM1, are currently being evaluated in a Phase I/IIa study for the treatment of stroke and in preclinical models of acute myocardial infarction.

Bibliography

  • Bamford J, Sandercock P, Dennis M, Burn J, Warlow C: A prospective study of acute cerebrovascular disease in the community: the Oxfordshire Community Stroke Project – 1981–86. 2. Incidence, case fatality rates and overall outcome at one year of cerebral infarction, primary intracerebral and subarachnoid haemorrhage. J. Neurol. Neurosurg. Psychiatry53(1),16–22 (1990).
  • Qureshi AI, Tuhrim S, Broderick JP, Batjer HH, Hondo H, Hanley DF: Spontaneous intracerebral hemorrhage. N. Engl. J. Med.344(19),1450–1460 (2001).
  • Sacco S, Marini C, Toni D, Olivieri L, Carolei A: Incidence and 10-year survival of intracerebral hemorrhage in a population-based registry. Stroke40(2),394–399 (2009).
  • Yang BY, Betz AL, Chenevert TL, Brunberg JA, Hoff JT: Experimental intracerebral hemorrhage: relationship between brain edema, blood flow, and blood–brain barrier permeability in rats. J. Neurosurg.81,93–102 (1994).
  • Fewel ME, Thompson BG, Hoff JT: Spontaneous intracerebral hemorrhage: a review. Neurosurg. Focus15(4),1–16 (2003).
  • Hankey GJ: Evacuation of intracerebral hematoma is likely to be beneficial–against. Stroke34,1568 (2003).
  • Broderick JP, Brott T, Tomsick T, Miller R, Huster G: Intracerebral hemorrhage more than twice as common as subarachnoid hemorrhage. J. Neurosurg.78(2),188–191 (1993).
  • Yoo SW, Kim SS, Lee SY et al.: Mesenchymal stem cells promote proliferation of endogenous neural stem cells and survival of newborn cells in a rat stroke model. Exp. Mol. Med.40(4),387–397 (2008).
  • Deng YB, Ye WB, Hu ZZ et al.: Intravenously administered BMSCs reduce neuronal apoptosis and promote neuronal proliferation through the release of VEGF after stroke in rats. Neurol. Res. (2009) (Epub ahead of print).
  • 10  Li Y, Perry T, Kindy MS et al.: GLP-1 receptor stimulation preserves primary cortical and dopaminergic neurons in cellular and rodent models of stroke and Parkinsonism. Proc. Natl Acad. Sci. USA106(4),1285–1290 (2009).
  • 11  Meir JJ, Nauck MA: Glucagon-like peptide 1 (GLP-1) in biology and pathology. Diabetes Metab. Res. Rev.21(2),91–117 (2005).
  • 12  Heile AMB, Wallrapp C, Klinge PM et al.: Cerebral transplantation of encapsulated mesenchymal stem cells improves cellular pathology after experimental traumatic brain injury. Neurosci. Lett.463(3),176–181 (2009).
  • 13  Taylor DA, Zenovich AG: Cardiovascular cell therapy and endogenous repair. Diabetes Obes. Metab.10(Suppl. 4),5–15 (2008).
  • 14  Krijnen PA, Nijmeijer R, Meijer CJ, Visser CA, Hack CE, Niessen HW: Apoptosis in myocardial ischaemia and infarction. J. Clin. Pathol.55(11),801–811 (2002).
  • 15  Duffy GP, Ahsan T, O’Brien T, Barry F, Nerem RM: Bone marrow-derived mesenchymal stem cells promote angiogenic processes in a time- and dose-dependent manner in vitro.Tissue Eng. Part A15(9),2459–2470 (2009).
  • 16  Nikolaidis LA, Mankad S, Sokos GG et al.: Effects of glucagon-like peptide-1 in patients with acute myocardial infarction and left ventricular dysfunction after successful reperfusion. Circulation109(8),962–965 (2004).
  • 17  Bose AK, Mocanu MM, Carr RD, Yellon DM: Myocardial ischaemia-reperfusion injury is attenuated by intact glucagon like peptide-1 (GLP-1) in the in vitro rat heart and may involve the p70s6K pathway. Cardiovasc. Drugs Ther.21(4),253–256 (2007).
  • 18  Geigle P, Wallrapp C, Lewis A et al.: Encapsulated mesenchymal stem cells for the local, long-term delivery of GLP-1 for use in the treatment of acute myocardial infarction. Presented at: World Stem Cell Summit 2009. Baltimore, MA, USA, 21–23 September 2009.
  • 19  Farrell K, Hawthorne M, Wallrapp C et al.: GLP-1 CellBeads enhance myocardial angiogenesis and improve LV function. Eur Heart J.30(Abstract Suppl.),495 (2009).