The Strategies for Engineered Negligible Senescence, or SENS, is the name given to a research and advocacy program that aims to develop a cure for aging. This will take the form of a package of therapies and biotechnologies capable of repairing the known forms of cellular and molecular damage that accumulate in our bodies with age, and are thus most likely the root causes of aging. This may sound ambitious indeed, but read on: you'll find that the research community is closer to being able to realize this goal than you might imagine.
An Introduction to SENS
At present the Strategies for Engineered Negligible Senescence (SENS) are a synthesis of the following items: a scientific research program carried out under the auspices of the SENS Research Foundation and involving a number of laboratories and researchers around the world; a wide range of existing life science knowledge produced over the past decades; a call to action for the public and the scientific community; and the SENS proposals first put forward by biomedical gerontologist Aubrey de Grey.
SENS is of great importance for those of us who are interested in living much longer, healthier lives. The crucial, central point of the SENS vision is that scientists already know more than enough to be working on the development of therapies that can reverse the root causes of age-related degeneration. There is no reason or need to delay this work. SENS provides a roadmap for the near future of rejuvenation research, as well as ethical and utilitarian arguments for moving to defeat age-related degeneration as rapidly as possible. The SENS initiative has been growing over the past decade and now has the support of prominent philanthropists and life scientists.
If you'd like a complete description of SENS from top to bottom, Aubrey de Grey and Michael Rae have written Ending Aging: The Rejuvenation Breakthroughs That Could Reverse Human Aging in Our Lifetime. In that book they explain, as best we know based on the biotechnology and scientific knowledge of today, how we can band together, build a mighty research infrastructure, and greatly extend our healthy life spans soon enough to matter. Ending Aging is perhaps the best introduction to the science and rationale of SENS, and is highly recommended.
The Science of SENS
It is proposed that there are most likely only seven categories of biological process that lead to degenerative aging and age-related disease, all of which have been known for at least twenty years. That no new categories have been discovered since the late 1980s - over a time of great progress in all fields of biology and medicine - strongly suggests that there are no other significant causes of age-related degeneration and disease. Scientists can already describe potential therapies that could address each of these processes. The basic tools required for these therapies have in many cases already been demonstrated in the laboratory or in trials for more limited uses. A list follows:
1) Some tissues lose cells with advancing age, like the heart and areas of the brain. Stem cell research and regenerative medicine are already providing very promising answers to degeneration through cell loss.
2) We must eliminate the telomere-related mechanisms that lead to cancer. One possibility is to selectively modifying our telomere elongation genes by using targeted gene therapies.
3) Mitochondrial DNA is outside the cellular nucleus and accumulates damage with age that impairs its critical functions. The SENS approach is to use gene therapy to copy mitochondrial DNA into the cellular nucleus. There are other strategies for manipulating and repairing damaged mitochondrial DNA in situ some first demonstrated as early as 2005.
4) Some of the proteins outside our cells, such as those vital to artery walls and skin elasticity, are created early in our life and never recycled or recycled very slowly. These long-lived proteins are susceptible to chemical reactions that degrade their effectiveness. Scientists can search for suitable enzymes or compounds to break down problem proteins that the body cannot handle.
5) Certain classes of senescent cell accumulate where they are not wanted, such as in the joints. We could in principle use immune therapies to tailor our immune systems to destroy cells as they become senescent and thus prevent any related problems.
6) As we age, junk material known as amyloid accumulates outside cells. Immune therapies (vaccines) are currently under development for Alzheimer's, a condition featuring prominent amyloid plaques, and similar efforts could be applied to other classes of extracellular junk material.
7) Junk material builds up within non-dividing, long-life span cells, impairing functions and causing damage. The biochemistry of this junk is fairly well understood; the problem lies in developing a therapy to break down the unwanted material. The SENS approach here is to search for suitable non-toxic microbial enzymes in soil bacteria that could be safely introduced into human cells.
The State of Progress in SENS
Modest philanthropic funding for SENS research commenced in 2005 under the administration of the Methuselah Foundation, and the total funds raised grew to more than $7 million by 2009 - and kept going. By 2010, the SENS Research Foundation's yearly expenditures topped $1 million, and in 2012 the annual budget was more than $3 million.
The first line of SENS research to be aggressively funded was work on intracellular aggregates that aims to discover and utilitize bacterial enzymes capable of safely degrading the accumulation of junk material inside cells. Several candidate enzymes for some of this junk material have been discovered and are undergoing further evaluation and development. This was closely followed by work on mitochondrial mutations that aims to copy the most important mitochondrial genes into the comparative safety of the cellular nucleus. By 2011, researchers had successfully accomplished this goal for three of the thirteen necessary genes. In 2012 a new and more general methodology was discovered by the broader scientific community, and is now being adapted for use - with luck it will be applicable to all thirteen genes and the job will be finished that much more rapidly.
The other lines of SENS research have followed and all are presently underway with at least a small level of funding. Far greater funds are needed in order to speed progress, however. A few million dollars a year is a tiny fraction of the resources that could be effectively deployed if they were available.
Significant progress in any one area of SENS is expected to lead to effective therapies for an entire class of age-related medical conditions, but that outcome still lies a way ahead. At this point research groups funded by the SENS Research Foundation are working at the fundamental stage of cell cultures, proving the biochemistry, and undertaking a few animal studies. Progress is outlined year by year in the SENS Research Foundation annual reports.
The Role of the Rest of the Research Community
It is not unreasonable to expect the broader research community - motivated as it is to seek cures for specific named diseases - to slowly fill in the gaps in SENS as time moves on and as the path ahead is better illuminated. For example, Alzheimer's researchers are working on immune therapies to address both amyloid plaques and other forms of junk material suspected to cause neurodegeneration. Further, at least one research group with no affiliation to the SENS Research Foundation is attempting to develop repair techniques for damaged mitochondrial DNA in order to treat certain classes of age-related illness.
It is also the case that regenerative medicine is a large and well funded field largely focused on using existing biological mechanisms to build new, replacement tissue for the body. Other researchers are also investigating the manipulation of telomeres in order to prevent or treat cancer. Yet more groups are working on compounds to break down accumulated biochemical junk outside cells.
Making gains in SENS research by way of unrelated bits and pieces is likely to be a slow path for progress towards meaningful extension of healthy life, however. Curing any one age-related condition is a wonderful thing for sufferers, but it will not increase healthy life span for anyone else - nor will it lead directly to therapies that can extend life without further investment and work. All of SENS must be implemented in order to reliably extend healthy life for all of us, and thus there must be at least some portion of the research community working directly and deliberately towards a complete implementation of the SENS vision.
The Ethics of a Cure for Aging
In many ways the hardest part of the path ahead for supporters of healthy life extension lies in convincing people that SENS and similar scientific projects should be funded in the first place. The science is much more certain than the public support. This is a strange state of affairs when you stop to look at it. As Aubrey de Grey notes: "Aging really is barbaric. It shouldn't be allowed. I don't need an ethical argument. I don't need any argument. It's visceral. To let people die is bad. I work to cure aging, and I think you should too, because I feel that saving lives is the most valuable thing anyone can spend their time doing, and since over 100,000 people die every single day of causes that young people essentially never die of, you'll save more lives by helping to cure aging than in any other way."
Many people demonstrate a certain willful blindness to the death and suffering caused by aging, a blindness that is not present for age-related disease like cancer or Alzheimer's. Yet if you support medical research to cure disease, prevent death, and relieve suffering, then you should also support medical research to prevent and rejuvenate age-related degeneration. How is suffering and death caused by the general deterioration of aging any different from suffering and death caused by a specific age-related condition we understand and have given a name?
We should all do our part to help speed development of therapies for aging. It is the right thing to do.
Last updated: May 15th 2013.