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Messages - Renaud

Pages: 1 [2]
26
Études précliniques / Neureva - Alain Privat
« le: 09 octobre 2008 à 11:27:05 »
Bonjour, j'ai contacté la société "Neureva" et j'ai demandé si le but de leur recherche était bien d'initialiser des essais cliniques dans un futur proche.

Réponse d'Alain Privat prometteuse:


Cher Monsieur,

Votre message vient de m'être communiqué par mes collaborateurs de
Neuréva. Notre objectif est bien d'élaborer des stratégies
thérapeutiques pour les traumatismes médullaires. Nous avons depuis plus
de vingt ans exploré une série d'approches sur des modèles
expérimentaux, tant cellulaires que animaux. Aujourd'hui, nous sommes en
mesure de traduire ces travaux expérimentaux en stratégies
thérapeutiques, avec la mise en place dans les deux ans qui viennent de
plusieurs essais cliniques, visant d'une part à favoriser la repousse
des fibres nerveuses lésées à la suite du traumatisme, d'autre part à
activer des cellules souches intrinsèques pour contrôler des centres
médullaires responsables de la locomotion et de la sphère urogénitale.
je vous invite à suivre les progrès de nos travaux sur le site de l'
IRME, qui rend compte régulièrement de l'avancement de la recherche sur
les traumatismes médullaires et leurs conséquences.

Bon courage,

Alain Privat M.D. Ph.D.
Professor and head
Spinal Cord Team



27
Recherches fondamentales / cellules souches transformées
« le: 08 octobre 2008 à 20:59:09 »
Bonjour, je suis nouveau ici quoique çà fait déjà un moment que je m'informe sur le site. ALARME m'a permis de croire et de garder espoir dans la recherche. Voilà encore bonjour à tous les membres à bientôt.
J'ai trouver un article interessant sur le futur des cellules iPS.



(UWIRE.com) This story was written by June Q. Wu, Harvard Crimson
--------------------------------------------------------------------------------


Researchers at the Harvard Stem Cell Institute are one step closer to achieving the ultimate promise of stem cell research creating tissues for every part of the body without the use of harmful viruses or cancer-causing genes.



Harvard Medical School professor Konrad A. Hochedlinger and his colleagues reported last week on the Web site of the journal Science that they have created mouse induced pluripotent stem cells without permanently altering the genetic makeup of the cells.



Their technique allows scientists to genetically manipulate a patients cells typically skin cells or blood cells and reprogram them into a pluripotent state. Like embryonic stem cells, these cells are then capable of morphing into any type of body tissue.



Hochedlingers team inserted genes needed for cellular reprogramming with harmless adenoviruses.



Unlike retroviruses, which scientists have been using to createpluripotent cells, these viruses effectively disappear after a few cell divisions and do not integrate into the cells DNA. The effect of this is that adenoviruses are free from the chief adverse effect of genetic manipulation, which can turn on cancer genes and trigger malignant tumor growth.



The beauty of this is that if you want to use the cells therapeutically if you want to put them in somebody. It basically gets rid of the dangerous transcription factors that were used in the initial integration, said Gordon C. Weir, a Medical School professor who heads the diabetes program at the Stem Cell Institute. The last thing you want is to transplant a potentially malignant cell into a patient.



The findings have implications for creating body tissues safe to transplant into patients to treat diseases.



The next step, according to lead author Matthias Stadtfeld, is to increase the efficiency of creating pluripotent mouse cells and then try to reproduce the work in human cells.



Currently, the number of pluripotent cells produced using retroviruses is significantly higher than that from the harmless adenoviruses. Stadtfeld, who is a post-doctoral research fellow at Harvard-affiliated Mass. General Hospital, estimated that using the more dangerous retroviruses is 10 to 100 times more efficient than the new adenovirus method.



The recent advance in stem cell research is the latest in a stream of developments by Harvard researchers this past year.



At the third annual Stem Cell Summit held at the Medical School last week, University President Drew G. Faust cited four papers published this summer as evidence of the progress made at a time when federal funding for embryonic research has been constrained by a 2001 order by President Bush.



Among the discoveries were the creation of 10 disease-specific stem cell lines and the direct conversion of mouse pancreatic cells into insulin-producing beta cells that can be used to treat patients with Type I diabetes.



At a time when the promise of biomedical research has never been greater, our nation risks sending a signal to our best and brightest young researchers that the funds wont be there to support their hugely important career pursuits, Faust said in her welcoming remarks.



And though the next President may prove friendlier to stem cell research, funding for the National Institutes of Health has been frozen in recent years, meaning that it has declined in real terms.



Though he used money from the NIH New Innovator Award that he won last year, Hochedlingers research was not subject to federal embryonic stem cell restrictions because the cells were created from skin cells or blood cells instead of from embryos. His work was also funded in part by the Harvard Stem Cell Insttute.



While embryonic stem cell research has come under fire from those who consider it unethical, Harvard scientists involved in the work continue to say that the research is essential.



As long as we dont know that iPS cells are really as good as embryonic stem cells in generating all types of body tissues, we should be obliged to continue, Stadtfeld said. iPS stands for induced pluripotent stem.



Scientists are now able to generate iPS cells which are embraced by those who oppose embryonic stem cell research only because of previous work performed with embryonic stem cells, Stadtfeld said.




Copyright © 2008 Harvard Crimson via UWire

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