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Comment by willmeyers

12 hours ago

As slow as it may be to adopt, it's a welcome change to how people should do research. Why induce suffering on an animal when the potential for failure and or miscalculation is so high? It seems from the article a model/chip can be more insightful on how something will affect humans.

It should be a tiered system, IMO.

1) Where possible, don't test in animals.

2) When testing in animals, first ensure that there is reasonable confidence the risk and severity of harm from the testing will be minimal. Only begin initial in vivo testing after this has first been achieved.

3) For test animals that are or aren't harmed, allow them to live happy, (relatively) normal, natural lives. Don't end their life early unnecessarily, with exceptions for humane euthanasia if the testing has unexpectedly caused significant, persistent suffering. Treat them as a pet owner would treat their beloved pet rat.

Some may consider it extreme, but, in my view, in an ideal world, people would treat testing in animals almost like testing in humans. The researcher should first ask "would I feel comfortable testing this in a voluntary human test subject?" Non-human animals would still be the first line of testing, since harm/death in a rat/mouse/chimpanzee is less morally bad than in a human, but I think this should be the mindset.

  • Most of what you said is already how it's done today, at least in the pharmaceutical industry.

    > Some may consider it extreme, but, in my view, in an ideal world, people would treat testing in animals almost like testing in humans.

    I don't consider it an extreme view, as lots of people share that view. But within the scope of pharmaceuticals, as opposed to cosmetics, I disagree with it because I think that's an impractical guideline to follow. Animal testing happens because there aren't good alternative ways to get safety data (on a per-treatment basis) without putting human lives at risk, and it's already a tiered system designed to balance scientific need against animal welfare. This is also why in standard medical trials proving safety comes before proving efficacy.

    > The researcher should first ask "would I feel comfortable testing this in a voluntary human test subject?" Non-human animals would still be the first line of testing, since harm/death in a rat/mouse/chimpanzee is less morally bad than in a human, but I think this should be the mindset.

    The problem is: how do you as a researcher become comfortable testing on a voluntary human test subject? You need safety data. How do you get the safety data? Right now, the main way is a tiered system that starts on a petri dish and eventually passes through mice, monkeys, etc. before humans.

    • > The problem is: how do you as a researcher become comfortable testing on a voluntary human test subject?

      I don't think you and GP are actually saying anything different. I interpreted their statement 'The researcher should first ask "would I feel comfortable testing this in a voluntary human test subject?"' not to mean don't test on animals if you wouldn't on a human, but to use your reaction and feelings to that to guide your judgement, and help judge what type of animal testing you're at, not to be a binary switch of whether any animal testing at all should be done.

  • > It should be a tiered system, IMO.

    It is a tiered system, at least if you look at big pharma. There are many stages in the pharmaceutical drug development process.

    Also human testing (clinical trials) have different stages/tiers to maximize learning and minimize risk at every stage. A lot of companies trying to innovate here.

    I’m exited what more AI can bring to this space.

  • I do feel bad for medical mice, especially things like SCID Mice https://en.wikipedia.org/wiki/Severe_combined_immunodeficien..., which are basically only born to be infected with something, and then die. Even more so in a recent case of academic fraud I've seen involving cancer testing, where the data was obviously faked, but mice still died for the data.

    But yes, it's hard to test immune responses without hurting a living animal, since you'd have to somehow have a non-alive immune system to test on otherwise

  • No matter how many checks, there's a human trial, and that may not go to plan either: http://news.bbc.co.uk/1/hi/england/london/4811626.stm

    --

    Two men who fell seriously ill following a clinical drugs trial remain in a critical condition but four others are showing signs of improvement.

    All six are still in intensive care in Northwick Park Hospital, north-west London, after falling ill on Monday.

    TeGenero, which manufactures the anti-inflammatory drug, says it has apologised to the men's families.

    • Okay, so let's not do the human trials. Just be content with the modelling (which is known to be imprecise especially where it matters most), and just approve the drug. What would that even solve? Instead of 6 volunteers getting injured, all the customers/patients who bought and took the drug would get harmed.

      There is always human trial — the whole history/timeline of people taking a particular medicine is effectively a decades-long human trial. That's actually the only way we learn about long-term side effects, see paracetamol for instance. All you're proposing is we remove a smaller, controlled pre-trial before releasing the medicine into the wilder population. Sorry, but that won't solve anything except for your feeling of moral indignation.

    • All patients recovered, the final patient left hospital after 3 months. Not ideal. The company went bankrupt and the outcome was better regulation in the UK and Germany; great wiki article here: https://en.wikipedia.org/wiki/Theralizumab including the relevant:

          Critics of animal testing have cited the case to argue that experiments on nonhuman animals, even in species closely related to humans, are not necessarily predictive of human responses, and cannot justify the harm inflicted on animals or the resultant risks to humans

  • this is already what they do, you have to justify usage of animals and meet standards for quality of life to do any research at a real institution

    also animal research is a huge pain in the ass, nobody is doing it unless they have to

    • That's a naive understanding of academia.

      Meeting standards is nothing but a formality, a form to fill. The PhDs and lab staff doing the killing, if they have any qualms about the act itself or just the purpose of the killing, generally justify it away as being what they have to do to keep the job. The "humane" killing methods are learned on the job through trial and error, and such errors keep happening regularly to experienced staff.

      Prior to lockdowns, many/most lab animals just got killed: interesting quality of life standard.

      What's written in lab policies is not at all how it happens in reality.

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    • > Treat them as a pet owner would treat their beloved pet rat.

      They do that already? Then how come an estimated 192 million mice are killed each year?

  • That's already how it works.

    FWIW, just watching a few pigs in an existing herd without interacting with them in any active way requires an extensive ethical approval process. Nobody would go through even that if they could gather the same data from a computer model.

  • I agree. If it’s a question of just cost - (animals being cheaper to just test on quickly and faster) animal testing shouldn’t be allowed.

    • I feel like "just a question of cost" is a heavy lifter here though.

      Cost core to our resource allocation system, for better or worse, and if something costs a lot it usually means we can't do it as much. In this framing, cutting out animal testing would (often) mean medical research is slower. In this framing it's a question of where people are willing to put the dial on ethics vs results, and of course pumping the breaks in one place without universal buy-in just means the cruelty moves elsewhere.

      I don't think the above 1-dimensional framing is the whole story though. You could imagine more standardized data sharing, so that the data that cost the lives of a few thousand rats could be used by others. And of course you could require (as drug trials do) that the study be registered before any experiment happened, and that the results be published regardless of the outcome. Some of these changes could actually make the science better, in addition to more ethical.

      2 replies →

    • It’s not just a question of cost. Our biological mechanisms are so complex, there is no single system that can tell us whether a drug is 100% safe or not. That’s why drugs are eventually also “tested” in humans during clinical trials. How amazing would it be if we could throw any drug/compound into a computer, then also spit in it, and get a personalized efficacy score as a response…?

    • Animals are NOT cheaper. Pharma companies do everything to avoid animal testing.

      For most drugs the only reasonable test animals are mice and rats. And they LOVE to naturally get cancer and other diseases, so you need to use large groups to get even a semblance of statistical significance.

      Oh, and don't forget that it takes a lot of time to run the tests. And time IS money for pharma.

    • Even within animal testing, the cost and convenience of animal testing could vary tremendously. Working in animal testing intrinsically means running a death-camp for mice. The mice aren't are barely even raw materials, they're basically stationery, more treated more like a mobile pH test-strip then a living creature.

      There are ways that animal testing could be made far more humane (like birth control to prevent the kind of overbreeding that demands mass culling), but those, themselves, would be costly.

      And in order to test cures, you must first inflict the animals with the disease. How many do you need? Are you sure? Because waiting to produce more later would also create costs. Cheaper just to breed a huge batch now and then cull the surplus.

      ... so how many extra do you want?

Potential for failure is high, of course, an experiment might not have the desired outcome and a death of a few hundred mice would not lead to a cure of some disease, sure. But without trying for millions of times, scientists won’t find the one drug that works. If it saves at least person, isn’t the risk and cost of not trying to find the cure by all mean possible even higher?

  • > But without trying for millions of times, scientists won’t find the one drug that works.

    well isn't it mostly other way around? millions of times to LOOK FOR hidden SIDE-EFFECTS?

    animal testing is mostly for answering 'is it safe?'

    • Sacrificial animals are used to answer nearly all questions in medicine. I would be surprised if you could find a single therapeutic out of the last 3,000 that entered Phase I that didn't cite mouse experiments in its preclinical studies for efficacy.

It’s far more scalable too

I can see more biomed researchers being able to run bigger batteries of tests with this tech vs the alternative of animal testing.. which tarnishes companies needlessly like with Neuralink

>Why induce suffering on an animal when the potential for failure and or miscalculation is so high?

Because that's drug testing in general, even with human subjects.