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Frequently Asked Questions
Q What is the difference between your stem cell technology and other currently available stem cell technologies?
A The stem cells are produced from human blood in relatively large quantities, cost-effectively and the method avoids current political and ethical problems. No invasive surgical procedure or anaesthetic is required. The patient can act as his/her own donor (autologous) reducing the risk of immune rejection.
Q Retrodifferentiation, sounds funky, what does it mean with respect to pluripotent stem cells?
A Essentially, the technology we are proposing has the ability to reprogramme mature adult blood cells to a more primitive stage (i.e. pluripotent stem cell). This stem cell is then able to develop along one of several different pathways into a variety of tissue types (e.g. muscle, cartilage, neurons).
Q Are you sure what you have isolated is really pluripotent stem cells and how? 
A Yes, (i) because they have been characterized using standard in vitro assay methods such as clonal assay, flow cytometry, long-term culture and molecular biological techniques e.g. PCR, RT-PCR and Southern blotting; and (ii) functionally evaluated in established rodent models ( NOD/SCID & Rnu/Rnu) where they were shown to re-constitute the bone marrow, spleen, thymus and heart.
Q How long does it take to generate the pluripotent stem cells?
A Pluripotent stem cells are generated within hours of apheresis and processing the blood samples.
Q Can the technology be applied to both healthy and leukaemic patients to source stem cells?
A Yes. In both cases there is an abundant supply of mononuclear cells within the blood.
Q What are the implications and potential of the technology in terms of its therapeutic use?
A Many diseases (e.g. Parkinson's, Alzheimer's, heart, diabetes) result from the dysfunction of a single cell type. With TriStem's technology, the introduction of healthy cells of a particular type in large quantities into a patient could potentially restore a lost or compromised function. In addition, the retrodifferentiation process can also help us to understand better, and possibly treat, cancer and AIDS.
Q Is this technological process like cloning/genetic engineering?
A No. It does not involve the use of human embryos or foetal tissue nor does it involve any genetic manipulation.
Q How long will it be before your technology is available to patients? 
A Prior to a novel technology such as this being made available it must go through a rigorous regulatory approval process which involves a series of trials. Assuming satisfactory discussions with the appropriate regulators and successful clinical trials, we would hope that TriStem's technology can be rolled out for general application from early 2006.
Q Have you been able to produce neural stem cells?
A Yes. Images of neural stem cells produced from retrodifferentiation can be found on our website. These stems cells have also been confirmed to secrete neurotransmitters such as dopamine, serotonin and GABA.
Q Has stem cell therapy been used to treat 'liquid' cancers such as leukaemia?
A Yes. Autologous and allogeneic stem cell transplants have been used to treat leukaemia, lymphoma and myeloma, including some solid tumours such as breast and ovarian cancers.
Q What is the risk of using a leukaemia patient's own blood cells to create stem cells?
A There is no conceivable additional risk to using the patient's own blood cells. Any risk of immune rejection is nullified because of a perfect tissue match. In certain cases, an allogeneic stem cell transplant is preferred to deliberately mount an immune response against host tumour cells. This latter process is facilitated by TriStem's technology because the technology enables the production of stem cells from healthy blood donors without the need for invasive surgical procedures or anaesthesia. Consequently, this technology is donor-friendly, and increases the options available for the transplant recipient to locate a viable donor in a relatively short period of time.
Q How can you control conversion from stem cell to a specific mature cell type?
A Stem cells are cultured in a rigorously controlled environment that determines the redifferentiation pathway they follow. Stem cells may become new cell types ('transdifferentiation') or they may mature along their original pathway (re-ontogeny). The technology also exists to identify the type of cell resulting from the differentiation of stem cells in the laboratory.
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