{"id":9041,"date":"2018-08-17T14:33:05","date_gmt":"2018-08-17T12:33:05","guid":{"rendered":"https:\/\/staging.futurehealthbiobank.com\/si\/?p=9041"},"modified":"2018-08-20T10:19:14","modified_gmt":"2018-08-20T08:19:14","slug":"korak-blizje-k-zdravljenju-cisticne-fibroze-z-maticnimi-celicami","status":"publish","type":"post","link":"https:\/\/staging.futurehealthbiobank.com\/si\/blog\/korak-blizje-k-zdravljenju-cisticne-fibroze-z-maticnimi-celicami\/","title":{"rendered":"Korak bli\u017eje k zdravljenju cisti\u010dne fibroze z mati\u010dnimi celicami"},"content":{"rendered":"

Pionirska raziskava Univerze Adelaide je naredila velik korak naprej pri zdravljenju bolnikov s cisti\u010dno fibrozo (CF). Raziskava ka\u017ee, da se lahko celice, ki ka\u017eejo genetske nepravilnosti, zamenja z zdravimi celicami.<\/h3>\n

<\/p>\n

Dr. Nigel Farrow, raziskovalec z Univerze Adelaide, je opisal proces, ki ga je njegov tim izvedel, da so zamenjali po\u0161kodovane celice:
\n\u00b4Na\u0161a raziskava, ki uporablja transplantacijo mati\u010dnih celic, vklju\u010duje odvzem odraslih mati\u010dnih celic iz plju\u010d bolnika z CF, ki jih nato z gensko terapijo popravimo, ter ponovno vstavimo te popravljene celice bolniku.<\/p>\n

Te na novo vstavljene odrasle mati\u010dne celice nato svoje zdrave gene predajo h\u010derinskim celicam, in na tak na\u010din se ohranjajo zdrave celice v dihalnem sistemu, kar pa tudi pomeni, da se prestavi izbruh cisti\u010dne fibroze v dihalih.\u00b4<\/p>\n

Kot je navedeno v Stem Cell Research and Therapy<\/strong><\/a> reviji, se odrasle mati\u010dne celice uporabljene v tej transplantaciji, obi\u010dajno uporabljajo za zdravljenje razli\u010dnih obolenj imunskega sistema.<\/p>\n

Na svetu je pribli\u017eno 70.000 ljudi, ki \u017eivijo z cisti\u010dno fibrozo. Bolezen – za katero trenutno ni zdravila – prizadene dihalne poti in plju\u010da, ter s tem povzro\u010di slab\u0161e zdravstveno stanje in skraj\u0161ano \u017eivljenjsko dobo. V Avstraliji, kjer je bila raziskava izvedena, je eden od 25 oseb prena\u0161alec genov za cisti\u010dno fibrozo. Ve\u010dina prena\u0161alcev genov nikoli ne zboli za boleznijo, lahko pa okvarjene gene prenesejo na svoje otroke. \u010ce sta oba star\u0161a prena\u0161alca okvarjenega gena, ima njun otrok 1 od 4 mo\u017enost, da se rodi z cisti\u010dno fibrozo.<\/p>\n

Ko bo tehnika zdravljenja, ki so jo uporabili na Univerzi Adelaide, izpopolnjena, bo zelo izbolj\u0161ala kvaliteto \u017eivljenja bolnikom z cisti\u010dno fibrozo ter pospe\u0161ila razvoj zdravila, ki bi pozdravila bolezen.<\/p>\n

Referenca:\u00a0www.ncbi.nlm.nih.gov<\/strong><\/a><\/p>\n","protected":false},"excerpt":{"rendered":"

Pionirska raziskava Univerze Adelaide je naredila velik korak naprej pri zdravljenju bolnikov s cisti\u010dno fibrozo (CF). Raziskava ka\u017ee, da se lahko celice, ki ka\u017eejo genetske nepravilnosti, zamenja z zdravimi celicami.<\/p>\n","protected":false},"author":25,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"footnotes":""},"categories":[218],"tags":[],"class_list":["post-9041","post","type-post","status-publish","format-standard","hentry","category-klinicne-posodobitve"],"acf":[],"yoast_head":"\nKorak bli\u017eje k zdravljenju cisti\u010dne fibroze z mati\u010dnimi celicami | Future Health Biobank<\/title>\n<meta name=\"description\" content=\"Pionirska raziskava Univerze Adelaide je naredila velik korak naprej pri zdravljenju bolnikov s cisti\u010dno fibrozo (CF). 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