this post was submitted on 17 Mar 2025
1301 points (98.7% liked)

Science Memes

13440 readers
2739 users here now

Welcome to c/science_memes @ Mander.xyz!

A place for majestic STEMLORD peacocking, as well as memes about the realities of working in a lab.



Rules

  1. Don't throw mud. Behave like an intellectual and remember the human.
  2. Keep it rooted (on topic).
  3. No spam.
  4. Infographics welcome, get schooled.

This is a science community. We use the Dawkins definition of meme.



Research Committee

Other Mander Communities

Science and Research

Biology and Life Sciences

Physical Sciences

Humanities and Social Sciences

Practical and Applied Sciences

Memes

Miscellaneous

founded 2 years ago
MODERATORS
 
top 50 comments
sorted by: hot top controversial new old
[–] [email protected] 3 points 5 hours ago* (last edited 4 hours ago) (3 children)

To all the commenters saying this guy was a saint for doing what he did, would you say the same thing had the outcome been disastrous? Babies born without HIV, but with constant excruciating pain or mental deficiency?

He took an extraordinarily reckless and permanently life-altering, for good or bad, risk with children's lives.

edit: spelling

[–] [email protected] 0 points 2 minutes ago

Sure lets just torture all the poor people so a handfull of rich fucks can afford stem-cell-zinfandel, never mind that 100,000 people were tortured and killed, at least we discovered a new anti-wrinkle cream. If you don't think that's what it always is in practice you're delusional. Shit like that is just as likely to cause mass disease or our extinction than it is to discover something useful, perhaps even more so

[–] [email protected] 1 points 16 minutes ago* (last edited 15 minutes ago)

He also did actual time for it and everyone involved was banned from practicing medicine in China, even despite the fact they are the core of CRISPR technology at the moment, they still care enough about ethics to not support this.

Seems like a case of one rogue team of people deciding what they where doing was for the moral good and then the state checking them.

We can still see the initial intentions as being morally good, and the outcome of it being gray but punished; its a balanced perspective; a lot of people here seem to have the impression it was approved by the CPC when it wasnt.

[–] [email protected] 0 points 34 minutes ago

This is the moral dilemma.

The whole Grimdank universe of just randomly testing things on people to make humans genetically more superior will absolutely improve life for future humans. No question. On paper anyways.

[–] [email protected] 10 points 10 hours ago* (last edited 10 hours ago) (2 children)

Just so you all know what his horrible crime was...

"Formally presenting the story at the Second International Summit on Human Genome Editing at the University of Hong Kong (HKU) three days later, he said that the twins were born from genetically modified embryos that were made resistant to M-tropic strains of HIV.[48] His team recruited 8 couples consisting each of HIV-positive father and HIV-negative mother through Beijing-based HIV volunteer group called Baihualin China League. During in vitro fertilization, the sperms were cleansed of HIV. Using CRISPR/Cas9 gene-editing, they introduced a natural mutation CCR5-Δ32 in gene called CCR5, which would confer resistance to M-tropic HIV infection."

So imagine a couple where one has HIV but they really want to have a baby. So instead of condemn the child to potentially a short miserable HIV life, he basically made it so their children were healthy. In all my Crispr research, this is the story that most caused me to feel the science system had wronged a good person. Literally Lulu and Nana can grow up healthy now. Science community smashed him, but to the real people he helped he is basically a saint. I love now seeing him again and seeing he still has his ideals. Again, fuck all those science boards and councils that attacked him. Think of the actual real couple that just wants a kid without their liferuining disease. Those science boards rather their kids suffer and die. Nah. Help the people. Also I love how he isnt some rightwing nutjob nor greedy capitalist. See his statement about this tech should be free for all people and he will never privately help billionaires etc etc.

anyway, ideals. i recognized them when i first came across him; i recognize them now. I know enough about him that I will savagely defend this guy. He isn't making plagues or whatever. He is helping real people.

[–] [email protected] -1 points 7 hours ago

But this is what's wrong with the world. They'd rather make a life, genetically modify it, which by the way will serve the rich, then adopt? OK I guess....

[–] [email protected] 4 points 8 hours ago (2 children)

On one hand, crispr isn't safe. And life is not something people have a right to create - that tremendous imposition should be met with a responsibility

On the other hand, life is treated as cheap almost everywhere. If we're going to force people to justify their right to exist, why not take a chance on their genetics to improve the species?

I mean, this was risky science, but not reckless. At some point we need to start fixing our genome, or we're just going to poison ourselves to extinction

[–] [email protected] 1 points 6 hours ago

And life is not something people have a right to create

Yes they do?

Having children is literally the one thing most of us are equipped to do, and those who cant can adopt; the children of the future are our responsibility to raise. You seem to have a pretty self centered and unrealistic idea around child rearing; people raise children through invasions, unless you want to stop people from fucking somehow you're never going to stop reproduction.

[–] [email protected] 4 points 8 hours ago (1 children)

and imagine if we had 5 more hands; we could make 5 more points.

#thefuture

[–] [email protected] 1 points 6 hours ago

Still wouldn't help people with two braincells

[–] [email protected] 8 points 10 hours ago

I think gene theraly is a miracle technology that should absolutely be explored more. The thing is, we're already at a point where we can do it in adults. So doing it on embyros, which can't consent, is simply an uncessasary moral hazard.

That said, I think the doctor here sort of has a point, which is that medical research is sometimes so concerned with doing no harm that it allows harm to happen without trying to treat it.

[–] [email protected] 5 points 11 hours ago (1 children)

my type of guy. And he still does his research to help people even with the public treating him like it does.

[–] [email protected] 1 points 7 hours ago (1 children)

HJK: Many years ago, my mother was diagnosed with Alzheimer’s disease, and unfortunately, there are no medicines available to cure it. There are many more people who are suffering from diseases that do not have a cure, so I want to do something to change it.

CT: Can you tell us about the research that you led around Lulu and Nana that was publicized in 2018? It’s been almost six years since this research was shared with the world, how are they doing now?

HJK: Lulu and Nana’s parents are HIV infected patients and they want to have a baby, a healthy baby, a baby that is not worried about HIV any more. So we took the sperm and egg from their parents during the IVF procedure, using a tiny syringe needle to inject the gene editing formula to the fertilized egg, to change one gene, and closed the door that HIV virus used to enter human cell. We then transfer the fertilized egg from the peri dish back to their mother’s uterus, and after several months, Lulu and Nana were born. Lulu and Nana are five years old now and they are healthy and happy just like any other kids in the kindergarten. I am glad that I have helped two families using my science knowledge.

CT: How did you balance the need for progressive gene editing research with ethics and general public perception?

HJK: Science research must be transparent and open, and should be approved by an ethics committee composed of medical doctors, lawyers, patient representatives, and local resident representatives.

CT: Last month, the FDA approved a new CRISPR gene editing treatment, Casgevy, by Vertex Pharmaceuticals and CRISPR Therapeutics, for sickle cell disease. To give context to the audience, sickle-cell is caused by inheriting two bad copies of one of the genes that make hemoglobin. On top of severe symptoms, life expectancy with the disease is just 53 years and it affects 1 in 4,000 people in the US. However, sources are reporting the gene editing treatment price will be $2-3m USD per patient. First, can you tell us your thoughts on this FDA approval milestone and what it means for gene-editing based medicines? And second, do you see a future where the prices for gene therapies will be lowered, making them more accessible to patients?

HJK: The approval of Casgevy is a great success for science, but not for patients. It cost more than 2 million dollars, and few patients will be able to afford it. This drug also has significant side effects including infertility.

CT: Gene therapies aside, what are your thoughts on the current state of affairs of genomics-based reproductive technologies, such as embryo gene sequencing? How do you foresee reproductive technologies being transformed by genomics in the future?

HJK: Embryo gene sequencing such as PGT-P is not ready for clinic application. Many diseases such as diabetes are influenced by hundreds of genes, and we do not have solid science to determine the risk of diabetes by genomic information.

CT:I see. So you think it's still a little bit early for clinic use.

HJK: Yes.

CT: What are your aspirations for the next chapter of your scientific career?

HJK: I believe embryo gene editing can help us to defeat many diseases and improve human health. I have proposed a research project, using embryo gene editing to help prevent Alzheimer’s disease, so our next generation will no longer worry about Alzheimer’s. I am going to do it slowly and cautiously, make sure we comply with all local laws and the international ethics guidelines. We are going to do it in a mouse first and we have no plan to move on to human trials. At every step, we will disclose our progress in full to the whole world and post it in my personal social account on Twitter.

CT: Why focus on Alzheimer's?

HJK: As I said, my mother has Alzheimer's. So personally, I also have some high risk for Alzheimer's when I get old, and maybe my daughters are at risk of having it in the future too, and Alzheimer's has no cure. If this project is successful, perhaps Alzheimer’s disease can be completely eliminated from future generations.

CT: Wow. That would be very powerful if it’s successful – to be able to get rid of a disease in future generations. I have another question. If you could go back in time to 2018, would you have done anything differently?

HJK: I did it too quickly. One thing I did not finish is the health insurance. In the informed consent document we signed with the parents of Lulu and Nana, we agreed to buy additional health insurance for Lulu and Nana. However, after the birth of Lulu and Nana, due to too much negative media attention, no health insurance company wanted to get involved. Now, as an alternative, I am planning to set up a charity foundation in Singapore to raise money to cover any future medical expenses of Lulu and Nana.

CT: Let me know if you have a link to donations for the charity. I'd be happy to share it with interested individuals.

HJK: Thank you. That'd be great.

CT: What are some valuable lessons that you learned over the last few years that you can share with the viewers?

HJK: In the past few years, my wife and daughters were living in a hard time. In the future, I won’t let my family get into the same situation again.

CT: I'm sorry to hear that about your family. Thank you so much for answering all of my questions, Dr. He.

HJK: Thank you.

[–] [email protected] 2 points 6 hours ago* (last edited 6 hours ago)

I applaud how nearly every time he opens his mouth it is something caring about the wellbeing of others and his goals are noble. Where I am critical of He is that he seems to be such an idealist that when he cures these big diseases he assumes the next step is to roll out the cure to all people of the world. I love how he is against the 'charge 2million per cure' mentality and thinks cures should be available to all, but imo the risk level of doing a genetic change to the entire population is unacceptable. A single wrong unforseen thing and its like zombie apocalypse. I see from his personality why he rushed ahead and did the Lulu Nana antiHIV thing. Personally I think he should be spearheading embryo science and doing his stuff since his heart is good, but watched over so he doesnt go too far. Let him go farther than anyone else, beyond lulu nana, but watch him carefully so no zombie apocalypse.

[–] [email protected] 8 points 12 hours ago

I'd like to get in to genetic engineering. When I came across his story while researching crispr, I sympathized with him. He did the experiment in what to me is a moral way. Just going on memory it was like 'take 4 embryos, edit two, keep parents in the loop and ask which embryo they want'. Complain all you want, but he did no wrong; it's the public and system that then wronged him. So yeah, of nearly anyone, he is the one who most gets to say 'ethics ruining science'. It's ironic because there are tons and tons of unethical science activities done literally every day. But for those to be ignored and instead ethics police to hit him when he did all his stuff morally and resulted probably in two extrahealthy kids... Yeah I agree with him. I think everything should be done morally, but if he is going to be hit like that under the guise of 'ethics' then nah. 'ethics' needs to be replaced by morals and decency. Literally horrifically murdering people (war) is legal and accepted while him using science, AND CORRECTLY, to protect people from liferuining diseases got the treatment it did? nah. I hope he continues growing and doing more genetic engineering and this time doesn't share a single thing with the public. He should never give the people that treated him like that a single piece of data. There are ways to bypass the patent thickets if he isn't selling what he does, especially if he shares no info about it. I support him.

prepares for 200 downvotes

[–] [email protected] 3 points 15 hours ago

Dr He's dream of baby gladiators cannot be hindered by whiny-don't-make-the-babies-fight so-called "ethics"!

Imagine what the world has lost

[–] [email protected] 4 points 15 hours ago

Watch Star Trek

[–] [email protected] 3 points 16 hours ago

I think the only thing that deserves clarification is if he broke ethics to do biomedical research. It sure seems he did. There's ethics approval in any study for a good reason.

[–] [email protected] 1 points 19 hours ago
load more comments
view more: next ›