Implant Raises Cellular Army To Attack Cancer
holy_calamity writes "New Scientist reports on a sneaky new approach to getting the immune system to fight cancer. An implant releases a 'molecular perfume' irresistible to messenger immune cells, which enter the implant where they are given a sample of the cancer's 'scent' and a disperse signal that sends them scurrying to the nearest lymph node. There they convince other immune cells to start attacking anything that matches the sample they picked up."
this is pretty amazing to a layman such as myself..
You're nothing; like me.
...until we end up with Will Smith running around a post-apocalyptic New York hitting on mannequins.
to see progress on fighting cancer.
Response from messenger cell: "not ur personal army"
There they convince other immune cells to start attacking anything that matches the sample they picked up.
"We have bad news. We accidentally gave a sample of your husband's reproductive organs. On the bright side, he won't be needing a vasectomy at any point in the future"
I am not a doctor, however -- isn't the main problem with cancer cells being that they have the same protein coating as normal cells that identify them to the immune system as "yours" versus "other"? The only way to kill a cancer cell that way would be with something that actually enters the cell and can then interact with the malignant protein. On the outside, cancer cells "look" the same to the immune system. Or is there a protein that expresses in cancer cells that can be differentiated from non-cancer cells?
#fuckbeta #iamslashdot #dicemustdie
... may be a problem if our immune system starts attacking the healthy cells instead.
What about long term life expectancy? It isn't everyday that we trigger a revolution inside of us!
But this is indeed an outstanding discovery.
Incorporate this in bullets and you get 100% lethality.
"cellular army bullet" enters body, tip takes sample of nearby healthy cells, programs immune system to attack own body, person dies horrible death to both his own immune system and the pathogens which are now left alone by the distracted immune system.
VLC FOR MAC IS DYING! IF YOU DEVELOP, PLEASE SAVE IT!!
The human immune system is a pretty potent beast to unleash. Getting it to attack cancer cells is genius. I would be worried about side effects, specifically the immune system getting confused or over-stimulated and attacking other things, but that's just speculation and surely for highly aggressive cancers like the ones they tested in the mice the risk would be more than worth it. We already use 'cures as bad as the disease' to treat cancer.
On the same note, though, I was encouraged by the teaser at the end where they suggest using similar techniques to 'reprogram' the immune system to correct auto-immune disorders. Learning how to put the immune system back in its cage could be just as useful as being able to send it after a target.
The enemies of Democracy are
If watching three seasons of Dexter has taught me anything, it's that once someone gets a taste for killing, they have a need to kill again. What happens with this army after it kills the cancer? Who does it kill next? You're going to have a mercenary army running loose in your system desperate for another kill....
all your lymph node are belong to us! WHAT YOU SAY!
However after RTA I did see that all of the control group died and the mice with the implant 90% were cured.
I hate to say it, but that's over-interpreting. This appears to have warded off imminent death in the mice, which is a result that is very encouraging. Unfortunately, it likely did not -cure- the mice. When we see data indicating these mice have a 5-year survival which is greater than the control (uh... or whatever the equivalent is since even healthy mice maybe don't live 5 years) then I too will be celebrating.
The immune system would sort of be vaccinated against markers on the cancer cells, but there's no guarantee that every cancer cell will have the marker and will keep it. You can imagine that if 99% of the cells in a tumor do have it, the tumor may be killed by the primed cells, but that 1% that doesn't will repopulate a while later.
Of course, this may have a feedback effect. I'm no immunologist, but I would hazard a guess that if a tumor were being attacked in this manner, the increased activity in the area may start targeting that 1% too. Maybe. That could also be a downside, as you can imagine if the immune system is primed but learns the wrong marker, you suddenly have an autoimmune disease on top of the cancer. Once again, I'm not an immunologist, so I don't know whether that's pure crap or not.
So it's another good finding, and of course a way to fight tumors is a miracle to a patient even if it's not a complete cure. It might be a total cure, but let's not set ourselves up for dissapointment.
I'm sure I'm about to show my ignorance here (and the fact that I did not RTFA) but couldn't this approach work against anything the body needs to fight? I'm thinking HIV/AIDS, hospital drug-resistant bacteria, Ebola, etc.? Although, in the case of AIDS, I guess the immune system itself is already ineffective. I can see this as a much better alternative to the current method of introducing toxins into the body in the hopes that it kills the disease before the host.
"terrorism" and "pedophilia" are the root passwords to the Constitution
Obviously a long way from use in humans. But I am impressed with the out of the box thinking in this approach. It seems dramatic changes in health care are coming in then next decade.
http://pbrewer.blogspot.com/2008/12/dec-18th-lunch.html
Think Deeply.
Not saying this treatment won't work, just saying don't get your hopes up.
Mice don't usually live longer than 2 or 3 years, whereas humans do. The human body might already be doing stuff like that or even superior stuff.
So there's a high chance that what works for mice for age related problems won't work for humans.
Analogy: Researcher says, "hey I've just found that steel and concrete allows us to make bigger and taller mud huts", and then saying "We should use steel and concrete to make skyscrapers bigger and taller". When what we might need is something better than the usual steel and concrete.
As opposed to the nonmolecular kind?
Yo dawg, I heard you like the Ackermann function, so OH GOD OH GOD OH GOD
No wait, I have something even better! Make bullets with a BOMB attached! Then you kill not only your target, but everyone around them as well! You wouldn't even have to aim! I think I'll name this invention after my favorite type of video game, the RPG.
When my father had lung cancer, I did a lot of research on cancer treatments and came to believe that the best possible treatment for cancer was to get the body's immune system to attack it. Especially for cancer that has spread, you need a systemic treatment that targets the cancer cells while not damaging the healthy ones and nothing will ever be as effective at doing that as the body's own immune system. This treatment is very encouraging and is on the right track. There are also several cancer vaccines under development that train the immune system to fight cancer before it takes hold. In the future, you may be able to get vaccinated against the kind of cancers that you are genetically vulnerable to.
Vaccines work much the same way, I'm surprised it took until now to come up with this.
Of course, one has to wonder what the reprogrammed cells go after once the cancer's been eaten, since "cancer" is defined as the abnormal growth rate of otherwise-normal (at least for the location they were supposed to be in) cells. I could see an immune reconstitution-style problem popping up. Point a bunch of 'redirected' immune cells at lung cancer, for example, and there's a possibility they will "finish" the cancerous cells and decide the healthy lung tissue is "close enough" for a snack afterwards.
"In tests, the researchers implanted cylinders with a diameter of 8.5 millimetres into mice and two weeks later injected the animals with highly aggressive melanoma cells."
This sounds ok for research, but in real life you would detect the cancer first and then implant the capsule.
The logical way to carry that experiment would be to implant the cancerous cells first and then, after some time, implant the capsule. I guess they would have done it first that way and if it is not on the report, that means that it didn't work as expected. That also means that this is just (very good) research, but they will need a lot more to come up with a working therapy.
When his defense asked, "Which computer has Jon Johansen trespassed upon?" the answer was: "His own."
I know, right? The Visitors would have given us their cancer cure ages ago, if it wasn't for that stupid Donovan guy.
Did anyone else think of the latest movie version of /I AM LEGEND/ when reading about this miracle cure for cancer?
I'll begin hording food and guns now.
Reading TFA, it seems that they're dealing with a melanoma.
IANAMD (I Am Not A Medical Doctor), but since my wife was recently diagnosed with a malignant melanoma, I've learned a few things about cancer.
Melanoma is one of the few cancers that the immune system responds to. Immunotherapy is part of standard treatment for melanoma, but not for most other cancers. There is a good chance that this research will lead to helpful treatments of a few types of cancer, but very little chance it will help with most.
How the heck did this get to 60 something post without the obligatory tie in to a similar product to attract super models to the geeks posting on /.???
Geez .. is there a subliminal message imbedded in the posts trying to get all our minds of the geek and girls dilema?
Always remember, even if you have to bribe the MegaCops, you always want to be taken to the Hoosegow, never the Clink.
--The FNP
with apologies to N.S.
tnx
Mmm Tranny. Can I have the buttseks with you. I am pretty good and I know how to fuck a she he. We could play prison and I can be the guard. I am 14 I hope thats okay
Fascinating. Could this technique be used with a 'good signal' to stop the body rejecting donor tissue?
:wq
Background info....Think of these antigens the article is referring to as extremely unique binding sites ("locks"). A cell can have a variety of locks on the cell surface. Some exist to bind to only one other molecule or binding site of another specific cell. So for anything to bind this lock, it must work like an incredibly precise lock and key mechanism. Our immune's adaptive systems (that is, T cells) go around with their "set of keys"** to every cell they come across and see if they fit into the "cell's lock" (remember, that's the antigen). These T cells have keys to fit the "locks" of bacteria, viruses, tumors, or any foreign, non-human cells that's there. That is why when you come across the same flu virus you were immunized against, the T cells, already having the right "key" made, can bind to the cell and cause cell death. But if it's a new flu virus, with the lock even slightly modified by a few DNA mutations, the T-cell's keys must be made to fit once again (this takes ~2 weeks and requires B cells, antibody production, etc).
Now to get to the tumor part....Tumors with tumor-specific antigens (TSAs) will fit the keys of T-cells once the keys are made. I recall someone asking "what if the immune cells kill healthy tissue?" There are "locks" called TAAs (tumor associated antigens) that are present on normal and tumor cells...they will all be destroyed. (Thankfully you can regenerate most of your healthy tissue--the rationale behind using toxic chemotherapeutics that target healthy and cancer tissue).
Now to actually explain the article's research....So effectively what this research is trying to accomplish IS THIS: release a barrel of locks around the tumor that will ONLY bind to the tumor. ALLOW your T-cells and other immune cells to use their "keys" to BIND the huge number of locks and activate cell death of the tumor cells. Currently, most research of biologic cancer drug development is focused on producing the right "key" for the naturally occurring "locks" that are present on cancer cells. Let me say that this research is a great approach--why not make and put the locks there?
Side note and extra info for fun....It's easy to think that one method of research is going to replace another. But the new trend is hitting cancer cells with EVERYTHING at once. That is, chemotherapy + biologic + barrel of "locks" + whatever else is out there. In addition, another trend that may occur is treating cancer like a CHRONIC illness, like diabetes. You've all seen how at best we can only kill 90-99% of tumor cells (at least, our imaging technology can only pick up small malignancy, not individual tumor cells)....so imagine getting cancer treatment intermittently every 2-5 years, but never experiencing symptoms of cancer (ie sickness, death)...I just thought I'd share that extra stuff. Now that I'm done with my essay I guess I should get back to my cancer research. Thanks for reading all the way through, and please comment.
**For the science geek: Yes Yes, I know the role antibodies play as the "set of keys" T-cells use...I think it would compromise the easy of explanation if I got into all that
"Engineering. Where the noble, semi-skilled laborers execute the vision of those who think and dream." -Sheldon
This reminds me of the star trek episode where these genetically enhanced children had an immune system that could not only fight off infection within themselves, but also seek out and destroy any infectious agents in the vicinity. Of course these super-immune systems went haywire. It started attacking regular people causing them to age at an advanced rate.
> WooHoo! I DON'T need to quit smoking!
Y'know, my Grandpa didn't die from cancer, but he did die from smoking. They had to put him on Prednizone (a steroid) so that he'd have enough strength to breathe. Unfortunately, that steroid also makes your bones brittle. He broke his back picking up a gallon of milk. Eventually, he got so feeble that he yelled at Grandma for having called an ambulance to save him (he wanted to die).
So, feel free to continue smoking. But don't pretend that cancer is the only worry. There are a lot of horrible ways to die, but after seeing what happened to him, I don't even want to touch a tobacco product.
welcome our new cellular overlords.
Fascism starts when the efficiency of the government becomes more important than the rights of the people.
There's a good reason they have to implant the device before injecting the cancer cells. The immune response isn't instantaneous, it takes some time, 2 weeks or so, for the immune system to reach it's full response. But this particular cancer kills untreated mice in about 20 days, which doesn't really leave the immune system much time to really do it's job. Fortunately, most types of cancer aren't lethal in 20 days, and for a more "normal" cancer that could take months or years to be fatal, the immune system would have more than enough time to fully respond. But, it's not really practical to use a slowly growing tumor for this kind of basic research. If you use a tumor that would kill the mouse in 6 months, it would just take too long.
Once you get past the misleading science-journalist talk of "scents" and so on, this sounds an awful lot like the "antibody-based therapeutics" that have been around for decades. But I'm no scientist, and I only even know of this stuff because my dad's an immunologist who works on it. Could anyone out there explain if/how this is anything new or different?
It'll be interesting to see how human trials go. The last time I saw cytokines referenced, it was in relation to this drug:
http://en.wikipedia.org/wiki/TGN1412
Looked great in animal studies; not so great for the humans involved.
To quote the article, "the researchers implanted cylinders with a diameter of 8.5 millimeters into mice". To be honest, if they can survive that, I'm not overly surprised cancer didn't kill them. What kind of super mice are we breeding here?
I think this might be a case of the cure being worse than the disease. If you take 10cm as the average size of a lab mouse, and scale that implant up to people size (160cm), that treatment means implanting a cylinder with a 13.6 centimeter diameter.
13.6 centimeters? Holy fuck. If I ever get testicular cancer you can count me out of this cure...
Are you thick?
I'm over three times as old as you, and, even if I was interested in guys, I don't do kids.
I am legally, physically, mentally, COMPLETELY female. I just arrived at womanhood through a different route. I am not a 'she-he'. I am not a fucking drag queen.
Unless you have tits and a cunt yourself, I'm not interested. I'm confirmed lesbian.
Now go back to your keyboard wanking, little boy.