Comments
tms102 t1_isb6g9u wrote
Great to see more techniques around crispr keep being developed.
No-Philosopher2573 t1_isexad6 wrote
If you say so
TemetN t1_isbbe8m wrote
Normally I'd raise an eyebrow and wonder if we never heard of this again or if it became an integral technology, but given the 'delivery, delivery, delivery' mantra we see in the area this could be more likely to be significant than most.
styxboa t1_isid25u wrote
What do you mean delivery delivery delivery mantra? Not familiar with the space
TemetN t1_isiez70 wrote
This is kind of a what it says on the tin case, basically one of the biggest problems being tackled in this field is successfully targeting and integrating treatments. As a result, even if this method turns out to be problematic down the line, it has a better than average chance of being significant.
ihateshadylandlords t1_isbjh0c wrote
Excited to see what therapies come up over the next century.
!RemindMe 10 years
ISnortBees t1_isdanst wrote
They still haven’t figured out hair growth or penis enlargement - future you
Jk jk
explicitlyimplied t1_iu9mufs wrote
Burnt
RemindMeBot t1_isbjk7i wrote
I will be messaging you in 10 years on 2032-10-14 18:27:25 UTC to remind you of this link
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Danuer_ t1_isd5mhv wrote
>!RemindMe 10 years
!RemindMe 2 years
Rakshear t1_isbb8dv wrote
So could this cure eye issues? When can my asthma be fixed?
mli t1_isbmaw8 wrote
Do anyone actually know someone who has had crispr-based therapy?
MrDreamster t1_isc9ww8 wrote
That's exactly what I was wondering. I've been hearing about Crispr for I think more than 10 years, but I am yet to hear about Crispr being actually used as a treatment. Why is that ?
Ezekiel_W OP t1_isd7i7p wrote
We need those 10 or so years for more research and development. Humans have had CRISPR used on them many times already, but it's still early days for human trials. Most of the good stuff with CRISPR probably won't start appearing until the late 2020s.
-ZeroRelevance- t1_isdy95i wrote
It’s probably just that medical technologies take a long time to be approved.
SWATSgradyBABY t1_isffgqs wrote
This has always been true. Increasingly we are able to use biological modeling in virtual space to simulate trials as we did with the COVID-19 vaccine. In that instance bringing the development time down from 5 to 10 years to one year.
Remember exponential not linear
breloomislaifu t1_isdyvnp wrote
TLDR: drugs in a nutshell.
Its because we don't know what effects a drug will have until we actually inject it. You have to realize that our entire body is a diffusion prone liquid chamber of a billion moving parts but we need to deliver soluble drugs to a very specific target number of cogs. That's physically impossible btw.
So we end up having unknown side effects, and every drug has them. We just have to be persistent and select the ones that are effective at curing yet tolerable enough, but this process can take upwards to a decade in clinical trials.
In practice this means we have a decade long backlog of drugs that we think are promising but haven't had the time or resources to check. We'll get to testing CRISPR in maybe a few more years.
One more thing, as a scientist who has used CRISPR systems in cell cultures, its not that 'robust' yet. If I had to choose between successful CRISPR and fliiping a coin in a game of russian roulette, I'd still take the coin lol.
AsuhoChinami t1_isdz6ld wrote
But... we are already testing CRISPR. I think the first human trials were 5 or 6 years ago.
Baron_Samedi_ t1_isef1zr wrote
It takes about a generation to go from technological breakthrough to large scale deployment of these types of innovation.
There are a lot of nuts-and-bolts R&D, medical safety testing, manufacturing, supply, and logistics issues to consider when looking at how new discoveries will broadly impact society.
So, from the initial Crispr breakthrough to actually seeing the effects of this revolutionary tech, you are looking at 15 - 25 years for some of the most important innovations to be noticeable for those of us outside the laboratory.
[deleted] t1_isccwqp wrote
[deleted]
Ezekiel_W OP t1_isd75wu wrote
CRISPR wast invented in 2012.
[deleted] t1_iscdz7p wrote
[deleted]
kmtrp t1_isec6nl wrote
Blame the FDA and... realize biology is a fucking mess. Specially with novel therapeutic vectors. We've rushed before in clinical trials that have maimed and killed humans.
I remember one of those, guess what happened? The field was frozen for almost 10 years. Nobody wanted to put money or political face on and have the same thing happen again.
So it takes years and years of mountains of paperwork and money and tests and more paperwork to prove safety first and then efficacy. I'd rather do most of these by compassionate use, but... I'm not in charge.
[deleted] t1_isd8s61 wrote
Big Pharma
kmtrp t1_isebjuz wrote
I don't think you know about big pharma. They want these things by yesterday, because of money, you know? Always have but are heavily slowed down by the FDA's guidelines demanding all evidence in the world that this won't ever ever backfire in humans. This means more time and money spent performing safety preclinical and clinical trials and endless mountains of paperwork and years of back and forth with them.
duffmanhb t1_iscbisv wrote
There are only a small amount of super expensive custom drugs available... It's probably not going to be until the end of the decade until we start seeing it more widespread.
garden_frog t1_isdx2zc wrote
This is a good article that summarizes the state of CRISP research: [CRISPR Clinical Trials: A 2022 Update] (https://innovativegenomics.org/news/crispr-clinical-trials-2022/)
explicitlyimplied t1_iu9mxx3 wrote
Assuming crispr is involved there's only two marketable gene therapies rn. Supposed to be like 10 end of 23
ZoomedAndDoomed t1_iscioqr wrote
GPT-3 summary:
The breakthrough discussed in this article is a new platform for gene editing that could inform the future application of a near-limitless library of CRISPR-based therapeutics. This breakthrough is significant because it provides a system to deliver the cargo required for generating the gene editing machine known as CRISPR-Cas9. This breakthrough works by transforming the Cas-9 protein into a spherical nucleic acid (SNA) and loading it with critical components as required to access a broad range of tissue and cell types, as well as the intracellular compartments required for gene editing. The article discusses how this breakthrough could help gene editing technology infiltrate cells and overcome a critical limitation of CRISPR.
Ilunamie t1_isbygwj wrote
Genuine question out of curiousity: does this imply that muscular dystrophy could be treated better, and vice versa it could be used as a way to dope up for sportsman and body builders? I mean gene editting doesn't strike me as something that could be easily proven, or?
Ezekiel_W OP t1_isg0t35 wrote
The short answer is yes. Eventually, as tech progresses and our knowledge base increases you could turn a bodybuilder into a zebra if you wanted.
Ilunamie t1_isg13vz wrote
That implies that it would be possible that an ex girl of mine turns into a horse and I have to admit that I fucked her. Why you gotta scare me like that?
WaycoKid1129 t1_iscqjc6 wrote
In a decade we may be talking about the eradication of a lot of genetic disease
SuitableAd6672 t1_isg68fn wrote
The pipeline for distruttive treatments like these is much slower to reach the masses
Ok_Atmosphere_72 t1_isbot2h wrote
Can it cross the blood/brain barrier?
explicitlyimplied t1_isbq14x wrote
Therapies can ya
SteppenAxolotl t1_isbxhpw wrote
This could make it easier to design gene drives for humans. It would be the perfect birth control for unwanted populations after robot labor takes over the heavy lifting.
No-Philosopher2573 t1_isexta3 wrote
Yep. Far more concerned about the future inequality to come from crispr thsn the benefits..
Big pharma- put massive effort to cure minor genetic defects from low to middle income famalies. OR
-super engineer billionares children for huge cost and take government funding to steralize unwanted populations.
I think option 2 is much more likely unfortunately.
Ezekiel_W OP t1_isg15vl wrote
CRISPR is actually very cheap, you can order a kit online yourself if you really wanted to.
No-Philosopher2573 t1_isg1q8r wrote
Yeah and effectively modify genes? You can order iron too its not economocal for the average person to create steel and manufacture products. CRISPR is the very intro to actually applying this at any scale
r0cket-b0i t1_isdtjla wrote
To all of you who wonder it science never leaves the lab - medical takes longer than material science for example, but don't you all remember foldable displays being showcased at trade shows for like 4 years and we all thought "this never gonna go into co sumer product, it's vapor", and now we are at 4th gen consumer foldables and people aren't even surprised with those. Take Samsung flip and take it to a timeline 15 Years back - it looks and feels like a movie prop, no way it's real..
Medicine is the same we know it, in 1960, 1990 etc people were hearing about scientific concepts and those are now in the mass market from Lasik, to some Stem Cells therapies to HIV that used to be a death sentence similar to rare forms of cancer today, it not longer is....
Pace is a bit irritatingly slow compared to GPU progress and ability to simulate water in fps games (kidding) but it is also getting faster...
NoYesterday2219 t1_iscnpmi wrote
!RemindMe 10 years
[deleted] t1_isd506f wrote
Lemme guess “the researchers say it will still be years before the technique is available to humans. They hope to start clinical trials within the next 5-7 years.”
I genuinely love this science. I love that it got posted. I read thousands of pages on it. And I’ve become so bored with news articles about it.
Villad_rock t1_ish7450 wrote
Then don’t read it.
Black_RL t1_isgu2in wrote
Good, good, fix the code, fix the problem.
arebya t1_it7nm6t wrote
!RemindMe 5 years
Ezekiel_W OP t1_isaxjev wrote
>Using chemical design and synthesis, the team brought together the Nobel-prize winning technology with therapeutic technology born in their own lab to overcome a critical limitation of CRISPR. Specifically, the groundbreaking work provides a system to deliver the cargo required for generating the gene editing machine known as CRISPR-Cas9. The team developed a way to transform the Cas-9 protein into a spherical nucleic acid (SNA) and load it with critical components as required to access a broad range of tissue and cell types, as well as the intracellular compartments required for gene editing.