Been fairly busy lately so I haven't had the time to collect my thoughts and do the reading into the subject that I wanted until now. Yeah, I worked in a biochem lab for a couple of years, at present I'm just a tech at a hospital while waiting on medical school applications and such, though obviously I still try to keep up with research developments because it's interesting.
Gene therapy is essentially the current cutting edge of genetic modification. Contrary to what I was saying about pre-birth GM being easier than post, gene therapy is pretty much exclusively somatic (that is, done to the non sex-cells of the patient, which means that any modifications will not be passed on to their children). That said, there's a bevy of issues with our current methods: the (typically viral) vectors used for gene insertion carry risks (cancer, immune response, difficulty with insertion of longer sequences, etc.), current methods are typically not permanent and therefore require multiple sessions of therapy (which thereby adds the chance of the patient developing resistance to the method), we aren't currently really able to deal with conditions involving the contribution of multiple genes (e.g. Alzheimers, diabetes) and so on and so forth. I can elaborate on the reasons for these issues if you'd like but it gets fairly technical fairly quickly. Simplistically I think we can say that current methods can accomplish a lot of interesting things but they're fairly limited because they tend to involve
insertion of a gene rather than
direct modification of the genome - That is to say, our current way of doing things is to simply "drown out" the effects of an undesired mutation by introducing the "normal" version of the gene elsewhere and hoping its expression will compensate for the effects of the mutated one, rather than going in and editing the mutated gene so that it does what we want it to do (which seems much simpler in theory but is much more difficult to accomplish in practice).
Last edited by hanz0; Feb 16, 2015 at 09:19 PM.