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臍帶血含有豐富造血幹細胞,可以分化成各種血球細胞,是重建血液與免疫系統重要關鍵;臍帶含有間葉幹細胞,可以分化各種組織細胞,還具有調節免疫反應與輔助造血功能,在組織工程及再生醫學應用發展相當被看好

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  • 2月 28 週一 201121:41
  • 間葉幹細胞治療帕金森氏症 非侵入性療法


德國的研究團隊利用大鼠的動物實驗發現一個非侵入性的幹細胞療法,能治療帕金森氏症.將間葉幹細胞從鼻腔打入,讓細胞移至大腦中,釋放多巴胺的神經傳導物質,改善運動神經功能. 
這項動物實驗證實能改善高達68%的帕金森氏症老鼠的運動神經功能,並且由鼻腔進到腦中的幹細胞能存活六個月之久
鼻腔運送(intranasal delivery)的幹細胞治療法能避免幹細胞移植手術所引起的創傷和發炎現象,並可不斷補充所需的幹細胞,因此更為安全和有效.此項發現已刊登在回春研究(Rejuvenation Research)的期刊
Non invasive Parkinson's treatment 'reduces symptoms'
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  • 個人分類:間葉幹細胞(MSC)
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  • 2月 25 週五 201118:24
  • 胚胎幹細胞新技術 已取得專利

通過美國食品藥物管理局(FDA)兩項胚胎幹細胞臨床試驗的先進生物科技公司(advance cell techology),日前發表最新的幹細胞專利技術--單胚芽細胞技術(single-blastmere technology),此技術為不需破壞胚胎就可取得胚胎幹細胞.
先進生物科技公司在2010年11月22日率先通過FDA核准,利用胚胎幹細胞治療眼底黃斑變性症(Stargardt's Macular Degeneration);2011年1月3日又再次獲得批准,進行乾性老年黃斑變性症(Dry Age-Related Macular Degeneration)的臨床試驗.目前擁有超過150項關於幹細胞治療和再生醫學的專利和相關證照.
單胚芽細胞技術類似體外受精的技術,且不會干擾胚胎發育的過程,並達到歐洲藥物管理局(European Medicines Agency)和FDA規範的標準.這項專利技術已發表在自然(Nature)和細胞之幹細胞(Cell Stem Cell)期刊中.
先進生物科技公司將這項專利技術運用在通過FDA審核的兩件臨床試驗中,希望藉此可以幫助更多需要幹細胞治療的病患.
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  • 個人分類:胚胎幹細胞
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  • 2月 23 週三 201115:13
  • 臍帶血幹細胞 加速糖尿病病患的傷口癒合

韓國科學家日前發現,人類臍帶血幹細胞可以分化成內皮前驅細胞(endothelial progenitor cells; EPC),將內皮細胞移植到患有糖尿病的老鼠身上,可以加速傷口的癒合
糖尿病病患一旦有傷口通常難以癒合,這是因為病患的血糖過高,導致周邊血流量減少,血中帶有較少的生長因子(growth factor)和細胞激素(cytokine),因此血管新生速度較慢,傷口難以癒合
臍帶血幹細胞分化的內皮前驅細胞,可以促進血管新生,因此可以幫助傷口的癒合,這項發現已在動物實驗中被證實,並發表在細胞移植期刊中(Cell Transplantation)
Human umbilical cord blood cells accelerate diabetic wound healing
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  • 個人分類:臍帶血幹細胞(HSC)
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  • 2月 21 週一 201116:56
  • 等待幹細胞的捐贈 如同器官和血液 有日益增加的趨勢

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每個人一生中都有機會拯救至少一個人的生命,透過器官,血液,骨髓,甚至臍帶血的捐贈,可以拯救數萬人脫離嚴重的疾病,但是等待被捐贈的病人往往還是比捐贈者來的多很多

根據美國健康資源與服務管理局的統計,結至今年2月10日全球已有110324人等待器官的捐贈,比起十年前的59862人,增加80%需求量
為了正視捐贈者與受贈者的比例差距,美國衛生機構在2月14日的世界捐贈日(National Donor Day)上,宣導民眾以下四點:
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  • 個人分類:臍帶血幹細胞(HSC)
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  • 2月 18 週五 201123:12
  • 幹細胞 治療骨質疏鬆症與椎間盤退化已現曙光

中時
    
  以「幹細胞」治療骨質疏鬆症與椎間盤退化已現曙光,因為國內的動物實驗發現:幹細胞對治療老鼠骨質疏鬆症與豬隻的椎間盤退化,具有顯著療效。


 


執行這項動物實驗的北醫生醫材料暨工程研究所所長鄧文炳表示:骨質疏鬆症的好發對象是老年人與停經婦女,因此在實驗設計上,是將提早老化的老鼠去除其卵巢,以模擬老年及停經狀態,隨後注入骨前驅細胞的幹細胞進行治療兩個月,結果發現老鼠體內的骨骼與正常骨骼相近,顯示幹細胞對於老鼠的骨質疏鬆症具有修復功能,且應用分子造影可以看到幹細胞在骨髓內之移動,移向受損之處,並已發表在分子造影領域領先之雜誌(J Nucl Med 2009, IF: 6.662)。


另一項針對25頭豬隻的實驗則可發現幹細胞在治療椎間盤退化的應用。鄧文炳教授表示,該項成果已發表在關節炎領域領先之雜誌(Arthritis & Rheumatism, IF: 7.677),以及生醫材料領域領先之雜誌(Biomaterials, IF: 7.365)。


本文由臺北醫學大學研發處副研發長鄧文炳教授提供)


 



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  • 2月 16 週三 201115:57
  • 間葉幹細胞進入臨床試驗 治療慢性疾病





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歷經15個月的審查,印度的藥物管控衛生機構(Drug Controller General of India: DCGI)日前一次同意四個慢性疾病的間葉幹細胞臨床試驗,包括慢性阻塞性肺病(chronic obstructive pulmonary disease: COPD),第二型糖尿病(diabetes type 2),酒精性肝纖維化(alcoholic liver cirrhosis)和關節炎(osteoarthritis),於四月在印度的五個城市進行,完整試驗將為期三年,預計2014會有結果報告出爐.

 

Stempeutics Research 幹細胞公司負責這次的臨床試驗,於去年曾向國家藥物管理局申請間葉幹細胞對心臟病的臨床試驗,一年多來已完成安全性的評估.因此這次針對慢性疾病的臨床試驗直接進入第二期的階段

   

第二期的臨床試驗是針對小規模病患進行治療性的評估,預計在慢性阻塞性病患有30人;糖尿病病患30人;肝硬化病患60人;關節炎病患45人,一共近200人進行這次的臨床試驗.治療方式是抽取健康捐贈者的骨髓,分離出間葉幹細胞並進行培養,增殖後的間葉幹細胞再打入病患受損的位置,直接進行修補

      

間葉幹細胞經實驗證實,可分化出三個胚層的細胞,例如肺臟,胰島,肝臟,骨骼,心肌等細胞,因此打入受損位置可以因分化而再生新的組織

     

間葉幹細胞不只分布於骨髓,在剛出生嬰兒的臍帶組織中,也富含間葉幹細胞.這些間葉幹細胞經萃取培養後能進行儲存,以提供未來的疾病治療

     

看似保守的印度政府已同意並進行間葉幹細胞的臨床試驗,相信我國衛生機關在不久之後,也能開放間葉幹細胞的人體臨床試驗,讓我國醫療能與國際接軌,並越來越進步

 

First nod for stem cell clinical trial









New Delhi, Feb. 15: India’s first set of government-approved clinical trials of stem cells on patients with chronic obstructive lung disease, diabetes, liver cirrhosis and osteoarthritis are likely to begin in five cities in April this year.


A Bangalore-based company, Stempeutics Research, has received approval from the country’s drug regulatory agency to evaluate the efficacy of its stem cells on these four incurable diseases after safety assessments over the past year on patients with cardiovascular disease.


The efficacy — Phase II —trials are likely to begin on small groups of volunteer patients offered the experimental treatment in collaborating hospitals in Bangalore, Kochi, Delhi, Mangalore and Manipal, a senior Stempeutics official said.


Each volunteer patient will receive a dose of mesenchymal stem cells derived from the bone marrow of healthy persons. The stem cells, coaxed to proliferate in a broth of laboratory biochemicals, will be injected at the site of illness — the pancreas, the liver, the lungs, or the bone — where they are expected to stimulate resident stem cells and regenerate the damaged or lost tissue.


While private and even government hospitals have in the past offered stem cell therapy to patients with intractable conditions, the proposal by Stempeutics is the first with formal approval from regulators for chronic obstructive pulmonary disease (COPD), diabetes, liver cirrhosis and osteoarthritis.


The Phase II trials will involve testing the mesenchymal stem cells on 30 patients with COPD, 30 with diabetes, 45 with osteoarthritis, and 60 with liver cirrhosis, distributed across the five cities, Stempeutics chief executive B.N. Manohar told The Telegraph.


The proposal for the trials was screened by a panel of experts of the Indian Council of Medical Research. The evaluation of the results is expected to take several months, and Manohar cautions that a commercial therapy may emerge only by early 2014.


Stem cells are progenitor cells that have the capacity to turn into other cell types, such as liver cells, insulin-secreting pancreatic cells, bone cells, lung cells or even cells of the heart muscle.


Stempeutics has already conducted safety tests of mesenchymal stem cells on patients who have suffered damage to their heart muscles from heart attacks. These trials, which began more than a year ago, have shown that the stem cell injections are safe.





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  • 個人分類:間葉幹細胞(MSC)
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  • 2月 10 週四 201108:52
  • 幹細胞新培養 無需動物血清培養液

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再生醫學為目前醫療的新趨勢,FDA已核准三例胚胎幹細胞的人體試驗.幹細胞要進入人體,培養上需安全無疑與穩定,才能放心進行移植.

傳統的幹細胞培養是將細胞培養在一層滋養層(feeder cells)上,滋養層主要為老鼠的纖維母細胞(mouse fibroblasts),並加入含胎牛血清的培養液.因為胎牛血清含牛的白蛋白,生長激素,抗體,甚至病毒,對人體細胞來說是外來的抗原,可能產生排斥的過敏反應和病毒感染的可能.
美國加州大學洛杉磯分校(UCLA)的幹細胞研究團隊日前發表研究成果,利用三個小分子抑制物(3 small molecule inhibitors)與纖維母細胞生長因子(bFGF;basic fibroblast growth factor)的組合,成功讓幹細胞能長期在無滋養層與無動物血清培養液下生長.
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  • 個人分類:胚胎幹細胞
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  • 1月 30 週日 201110:15
  • 港大突破 全新誘導式多功能幹細胞技術

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港大研究團隊最近成功在不須使用動物生物成分的情況下,製造出誘導式多功能幹細胞,這種新的誘導式多功能幹細胞和胚胎幹細胞一樣,可轉化成為不同的組織的細胞,包括心臟、腦、血管、肝等,研究結果已刊登於科學期刊《Cellular Reprogramming》。 
負責這次研究的香港大學李嘉誠醫學院研究人員(左起):內科學系高級技術主任黎永漢先生、內科學系臨床助理教授蕭頌華醫生、內科學系心臟學科謝鴻發教授及內科學系及眼科研究所助理教授連祺周博士
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  • 個人分類:多功能幹細胞(iPSC)
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  • 1月 27 週四 201114:25
  • 史丹佛大學加入由FDA首例核准的胚胎幹細胞臨床試驗





 


2010年10月,FDA首例核准的胚胎幹細胞臨床試驗,治療脊髓損傷的病患在美國亞特蘭大的Shepherd中心開始進行.芝加哥的西北大學也於後續開始進行病人的蒐集,成為第二個臨床試驗的參與機構.而加州的史丹佛大學於1月24日宣布,將成為第三個醫療機構參與此項胚胎幹細胞的臨床試驗.


這項臨床試驗是由傑龍公司(Geron)所發起與執行,利用胚胎幹細胞誘導成寡狀樹突的前驅神經細胞(Oligodendrocyte precursors),再打入脊髓損傷的病患,首要目標是進行病患安全試驗的評估.


史丹佛大學的第一期臨床試驗對象為10名病患,其條件為兩個星期內首次的脊髓受損患者或是近期的創傷經醫師評估後被推薦的病患.


手術的流程為:由Geron公司製造並提供前驅神經細胞(GRNOPC1),送至史丹佛大學實驗室進行解凍與處理準備,最後在合作醫院-聖克拉拉醫療中心(Santa Clara Valley Medical Center:SCVMC)進行移植試驗.


SCVMC醫療中心為西岸最大的神經損傷治療與復健中心,每年有150名病患因車禍,摔落,運動等意外造成嚴重的脊髓損傷.參與此項臨床試驗的史丹佛大學教授-Gary Steinberg也是醫療中心的神經科醫師,將為病患進行這次的移植手術.


Steinberg表示,過去對於中風,腦瘤和阿茲海默症等的脊髓損傷,神經的修復與再生是不抱有任何希望,但是現在幹細胞研究已走向臨床試驗,跳脫過去限有的動物實驗結果,直接進行人體移植作觀察,對未來醫療是個很大的進展.


第一期的人體試驗安全評估結果如果順利,下一步目標是就是要達到神經修復的療效,希望未來脊髓損傷的患者能再站起來,迎向新的人生.

























 


Stanford joins first embryonic-stem-cell therapy clinical trial


The first clinical trial of cells derived from human embryonic stem cells began in October 2010 in a paralyzed patient at the Shepherd Center in Atlanta. Today, Stanford University School of Medicine and Santa Clara Valley Medical Center became the third site to participate in the trial, which will enroll up to 10 patients with spinal cord injuries at up to seven institutions nationwide.



 


(Media-Newswire.com) - The first clinical trial of cells derived from human embryonic stem cells began in October 2010 in a paralyzed patient at the Shepherd Center in Atlanta. Today, Stanford University School of Medicine and Santa Clara Valley Medical Center became the third site to participate in the trial, which will enroll up to 10 patients with spinal cord injuries at up to seven institutions nationwide.
The FDA-approved, phase-1 trial is meant to test only the safety of the cells, which can develop into neural support cells called oligodendrocytes found in the brain and central nervous system. If the investigational treatment is shown to be safe for use in humans, larger clinical trials will be designed to test whether the cells are better able than conventional treatments to improve a patient’s condition.
Because the cells must be administered within two weeks of the initial spinal cord injury, the trial is open only to those with very recent trauma and only upon physician referral.
The trial is run by Menlo Park-based Geron Corp., which developed and manufactures the cells for testing. The cells for this portion of the trial will be thawed and prepared at Stanford, and the surgery to implant the cells will take place at Valley Medical Center, which is one of the largest referral centers for acute spinal cord injury and rehabilitation on the West Coast. Physicians certified to conduct the procedure include Stanford neurosurgeons Gary Steinberg, MD, PhD, and Marco Lee, MD, PhD.
Steinberg is the principal investigator of the Stanford/SCVMC portion of the trial. He has been researching the use of stem cells in models of neurological injury or illness for more than a decade, and he heads a team of Stanford researchers that received a $20 million grant from the California Institute for Regenerative Medicine to study how neural stem cells could be used to treat people with ischemic stroke — a condition that occurs when a portion of the brain is deprived of blood flow.
“Until recently, we have not had any hope of restoring neurological function in people with spinal cord injury or stroke, or those with brain tumors or Alzheimer’s disease,” said Steinberg, the Bernard and Ronni Lacroute-William Randolph Hearst Professor in Neurosurgery and Neurosciences. “But now we’re moving stem cell therapy into the clinic, which I feel is a tremendously important step. People are not mice or rats, and we can learn so much from clinical trials that we can never learn by studying animals.”
Steinberg and Stanford have a strong background in stem cell biology, while Santa Clara Valley Medical Center has the patients and an extensive rehabilitation facility for spinal cord injuries.
“Valley Medical Center treats more than 150 people a year with severe spinal cord trauma, many of which are caused by motor vehicle accidents, falls and sports injuries. Patients with this kind of injury are very familiar to our staff, and we have the training and experience to help them through their recovery,” said Stephen McKenna, MD, chief of SCVMC’s Rehabilitation Trauma Center. “By collaborating with Stanford, we can evaluate and enroll patients in the trial without altering their normal referral pathway.”
During the procedure, the neurosurgeon will apply about 2 million of the special cells ( called GRNOPC1 ) directly into the injured area of the enrolled patient’s spinal cord. Following the surgery at Santa Clara Valley Medical Center, the patient will enter an intensive inpatient rehabilitation program under the supervision of specialists in spinal cord injury medicine. Researchers will then monitor the patient to confirm that the cells are safe for use in humans.
The oligodendrocyte precursors ( GRNOPC1 ) are produced from stem cells that were originally derived from a single embryo created through in vitro fertilization. Such excess embryos are usually discarded when no longer needed, but can be donated for research by the parents under informed consent. The U.S. Food and Drug Administration approved the human clinical trial in 2009 after extensive tests in laboratory animals. The first patient was treated in October at the Shepherd Center in Atlanta; Northwestern University in Chicago is also open for patient enrollment. Other participating sites have not yet been identified.








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  • 個人分類:胚胎幹細胞
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  • 1月 13 週四 201111:21
  • 細胞治療的最高認證--FACT認證

 FACT.jpg FACT(Foundation of the Accreditation of Cellular Therapy)譯為細胞治療認證協會,為目前美國小兒科醫學會指名推薦的臍帶血庫認證,資料來源:www.pediatrics.org/cgi/content/full/119/1/165                                               
FACT是1996年由ISCT(國際細胞治療學會)與ASBMT(美國血液及骨髓移植學會)合併原有規範而成立的,其目標為建立細胞治療的醫學及實驗室作業品質的高度標準。FACT認證達到甚至超過國際間對於細胞治療的相關規範。
對於細胞治療的最佳來源--臍帶血,FACT 是唯一從採集、處理、檢驗、儲存、篩選及放行,所有流程都做完整與嚴格審查的認證機構。
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