April 2011
Volume 52, Issue 14
Free
ARVO Annual Meeting Abstract  |   April 2011
Phase I Study: Injection of Allogeneic Bone Marrow Derived Mesenchymal Stem Cells in Patients with Diabetic Retinopathy and Diabetic Optical Neuropathy
Author Affiliations & Notes
  • Natalia Gavrilova
    Ophthalmology, Fyodorov Federal Institution 'Eye Microsurgery', Moscow, Russian Federation
  • Khristo Takhchidi
    Ophthalmology, Fyodorov Federal Institution 'Eye Microsurgery', Moscow, Russian Federation
  • Irina Saburina
    Institute of General Pathology, Moscow, Russian Federation
  • Nikolai Mironov
    Moscow Neurology Hospital, Moscow, Russian Federation
  • Marina Polyakova
    Ophthalmology, Fyodorov Federal Institution 'Eye Microsurgery', Moscow, Russian Federation
  • Alexei Lukashev
    Stemedica Cell Technologies, San Diego, California
  • Paul Tornambe
    Retina Consultants, San Diego, California
  • Footnotes
    Commercial Relationships  Natalia Gavrilova, Stemedica Cell Technologies (F), US 20090214485 (P); Khristo Takhchidi, None; Irina Saburina, Stemedica Cell Technologies (C), US 20090214485 (P); Nikolai Mironov, Stemedica Cell Technologies (C), US 20090214485 (P); Marina Polyakova, None; Alexei Lukashev, Stemedica Cell Technologies (E); Paul Tornambe, None
  • Footnotes
    Support  None
Investigative Ophthalmology & Visual Science April 2011, Vol.52, 1273. doi:
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      Natalia Gavrilova, Khristo Takhchidi, Irina Saburina, Nikolai Mironov, Marina Polyakova, Alexei Lukashev, Paul Tornambe; Phase I Study: Injection of Allogeneic Bone Marrow Derived Mesenchymal Stem Cells in Patients with Diabetic Retinopathy and Diabetic Optical Neuropathy. Invest. Ophthalmol. Vis. Sci. 2011;52(14):1273.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

Purpose: : Diabetic retinopathy(DP) and diabetic optical neuropathy(DON) are common complications of diabetes which are caused by abnormal development of retinal microvasculature. Initial case studies have been performed on human patients to assess the safety and efficacy of this type of cell therapy.

Methods: : Six patients (4 female, 2 male, age 42-62) with early stages of diabetic retinopathy and diabetic optical neuropathy were injected intravenously with a single dose of 100M allogeneic bone marrow derived mesenchymal stem cells (BM MSC). The cells were manufactured under the guidelines of current good manufacturing practice (cGMP). All patients were examined prior to the injection and post injection on day 1, 14, 30, 2 month, 3 month, 6 month, one, two and three years. General examination included blood and urine panel, blood coagulation test and measurements of brain derived neurotrophic factor (BDNF) in blood plasma and tear fluid. Ophthalmic examination included visual acuity and ophtalmoscopic exam, perimetry test, optical coherent tomography(OCT), eletroretinography(ERG), electrooculography(EOG), Doppler ultrasound exam, optic disk color analysis.

Results: : No adverse effects were observed or reported by all patients. During the whole period of follow up there were no changes in cardiovascular system, liver and kidney functionality. No infection growth, interstitial pneumonia or cancer was found in all patients. The positive changes in hemostatic dysfunctions and well as improvements in hemodynamic at systemic level were observed as early as two weeks after injection. Fovea sensitivity; functional activity of optic nerve, pigmented epithelium layer, outer and inner nuclear layers; BDNF content in blood plasma and tear fluids as well as optic disc inflammation were gradually improved during the first six months post injection and became stable during the whole period of follow up.

Conclusions: : The results show safety of intravenous injection of BM MSC on patients with diabetic retinopathy and diabetic optical neuropathy. Positive changes of ophthalmic parameters should be further investigated in full scale clinical trails.

Clinical Trial: : Ophthalmic Department, Moscow Medical University, Phase I Safety

Keywords: diabetic retinopathy • optic nerve • neuroprotection 
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