Personalized cell therapy in ophthalmology. I. Method for obtaining and phenotype of autologous product
S E Avetisov , A M Subbot , A I Antochin , E A Kasparova , A A Kasparov , A S Pavliuk
Genes & Cells ›› 2011, Vol. 6 ›› Issue (2) : 38 -42.
Personalized cell therapy in ophthalmology. I. Method for obtaining and phenotype of autologous product
The method for obtaining activated in vitro by poly A:Uautologous leucocytes from peripheral blood for cornealdiseases treatment is developed. Method allows us to obtaina product with sufficient content of viable nucleated cells (upto 3106 cell/ml). Cellular composition of the product wasdetermined. Mononuclear fraction decreased in 1,3 times andgranulocyte portion is increased. Phenotype of lymphocytesin the cell product is the same as in peripheral blood, withselective loss of B-lymphocytes. The presence of CD14+/34lowcells, which are considered to be progenitors, is defined in theproduct. Using of cell product, obtained by designed technique,may be promising in clinic, because of it minimal traumatismfor the patient and simplicity.
| [1] |
Patel S.A., King C.C., Lim P.K. et al. Personalizing stem cell research and therapy: the arduous road ahead or missed opportunity? Curr. Pharmacog. Person Med. 2010; 8(1): 25-36. |
| [2] |
Romagnani P., Lasagni L., Romagnani S. Peripheral blood as a source of stem cells for regenerative medicine. Expert. Opin. Biol. Ther. 2006; 6(3): 193-202. |
| [3] |
Seta N., Kuwana M. Human circulating monocytes as multipotential progenitors. Keio. J. Med. 2007; 56(2): 41-7. |
| [4] |
Romagnani P., Annunziato F., Liotta F. et al. CD14+CD34low cells with stem cell phenotypic and functional features are the major source of circulating endothelial progenitors. Circ. Res. 2005; 97(4): 314-22. |
| [5] |
Bader A., Macchiarini P. Moving towards in situ tracheal regeneration: the bionic tissue engineered transplantation approach. J. Cell. Mol. Med. 2010; 14(7): 1877-89. |
| [6] |
Parikh C.H., Edelhauser H.F. Ocular surgical pharmacology: corneal endothelial safety and toxicity. Curr. Opin. Ophthalmol. 2003; 14(4): 178-85. |
| [7] |
Alvarado J.A., Katz L.J., Trivedi S. et al. Monocyte modulation of aqueous outflow and recruitment to the trabecular meshwork following selective laser trabeculoplasty. Arch. Ophthalmol. 2010; 128(6): 731-7. |
| [8] |
Бурунова В.В. Проблемы стандартизации при получении клеточных культур мезенхимального происхождения: эксперименталь-ный и теоретический анализ (диссертация). Москва; 2011. |
| [9] |
Sugiyama T., Hoshino K., Saito M. et al. Immunoadjuvant effects of polyadenylic:polyuridylic acids through TLR3 and TLR7. Int. Immunol. 2008; 20(1): 1-9. |
| [10] |
Суббот А.М., Каспарова Е.А., Каралкин П.А. и соавт. // Ство- ловые клетки и регенеративная медицина /под редакцией В.А. Тка- чука. М.: МАКС ПРЕСС, 2011.- С. 162-172. |
| [11] |
Ковальчук Л.В., Павлюк А.С., Синюхин В.Н. и др. Анализ фармакологических средств на модели апоптоза лимфоцитов чело- века in vitro в норме и при иммунопатологии Аллергология и имму- нология 2000; 1: 24-30. |
| [12] |
Kavai T., Akira S. TLR signaling. Cell Death Differ. 2006; 13(5): 816-25. |
| [13] |
Boyum A. Separation of lymphocytes, lymphocyte subgroups and monocytes: a review. Lymphology 1977; 10(2): 71-6. |
| [14] |
Coulson A.S., Chalmers D.G. Separation of viable lymphocytes from human blood. Lancet 1964; 1: 468-9. |
| [15] |
Zhang Z., Schluesener H.J. Mammalian toll-like receptors: from endogenous ligands to tissue regeneration. Cell Mol. Life Sci. 2006; 63(24): 2901-7. |
| [16] |
Jaremko K.M., Chen-Roetling J., Chen L. et al. Accelerated hemolysis and neurotoxicity in neuron-glia-blood clot co-cultures. J. Neurochem. 2010; 114(4): 1063-73. |
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