Drugs of the future
Small-chemical drugs will be the principal
pharmaceutical tools for the foreseeable future, though with
monoclonal antibodies and proteins making an increasing
impact.
Other approaches are also being researched:
Gene therapy
In the 1980s, there were high hopes that gene therapy would open
up a wealth of new treatments, particularly for inherited
conditions. The idea is that a gene is delivered into cells and
begins to make a therapeutic protein. So people with cystic
fibrosis, who lack a working version of a protein known as CFTR,
would receive a copy of the CFTR gene.
Unfortunately, the promise has yet to be realised. It has proved
difficult to get active DNA into the nucleus and stably active.
Progress has been slower than expected, and also suffered after the
death of a patient, Jesse Gelsinger, in a clinical trial in 1999. A
further setback came in 2003, when French patients developed cancer
linked to the integration of a viral vector into their DNA.
Nevertheless, clinical trials are underway in a number of
conditions, including muscular dystrophy and Parkinson's disease.
Gene therapy is also being tested in some cancers, though the aim
is to kill cells rather than repair them. Routine use, however,
remains a long way off.
RNAi
RNA interference (RNAi), which gained a Nobel Prize for its
discoverers in 2006, is a new and highly promising strategy. RNAi
is used to eliminate (or 'knock down') specific proteins from a
cell, such as those causing a disease. It is based on an unusual
phenomenon: short RNA molecules triggering highly specific
destruction of messenger RNA molecules containing the same RNA
sequence. Its normal role is probably to protect against viruses
invading the cell.
The medical possibilities are very broad. Examples include
knocking down the receptor for a virus, or an overactive protein
causing cancer or messenger molecules promoting inflammation.
A small number of clinical trials have begun, for example for
macular degeneration (a form of blindness). But it is early days.
As in gene therapy, it is difficult to deliver the RNA and there
are worries that other, useful proteins might be eliminated. One
study in mice led to severe liver damage in animals, possibly
because large doses of RNA were used.
Nanotechnology
As discussed in
'Big Picture on Nanoscience', nanotechnology-based solutions
are being tested in a variety of conditions.
Some applications depend on the unusual properties of materials
at the nanoscale. Nanoscale silver is toxic to bacteria and is
being used in wound dressings (silver-impregnated pyjamas have been
suggested for hospitals). Gold nanoparticles can convert some
wavelengths of light into intense heat, and are being tested as a
possible cancer treatment (a 'thermal scalpel').
Critical to many applications will be targeting. Antibodies
could target a toxin-linked nanoparticle to a cancer cell.
More generally, because they are so small, weight-for-weight
nanoparticles have a very high surface area. There is interest in
using this property for controlled release of drugs.
Nanobased structures are being explored as molecular scaffolds
for tissue repair. Some exciting applications combine a physical
support role for nanomaterials with bioactive molecules attached to
a nanoscale scaffold. This approach could be used to encourage bone
or nerve growth following tissue damage.
Nanotechnologies also show significant promise in diagnostics
(for example, through 'lab-on-a-chip' technologies, or by detection
of very low concentrations of key metabolites) and medical imaging.
Another exciting possibility is to link detection to treatment - so
a diagnostic device automatically delivers the required medication.
In animal studies, nanoparticles have been used both to detect
blood glucose levels and to release insulin.
Nanotechnologies are undoubtedly an area of great promise. Given
the diversity of approaches they encompass, they could have a
profound impact on healthcare. Initially they may enhance current
treatments, but entirely new agents could soon become
available.
However, nanotechnologies also raise challenging regulatory
issues - the properties of nanomaterials differ fundamentally from
their everyday counterparts; can they be considered the same
substance? And there are concerns about the possible environmental
impact of nanoparticles.
A living thing
As well as chemically produced agents, researchers are also
looking at living organisms. In doing so, they are reviving a long
and colourful medical history.
Leeches may not be everyone's cup of tea, but they produce a
very useful anti-blood-clotting agent (hirudin) and are very
effective at draining blood. They are used clinically in
microsurgery, helping to improve blood flow when digits are
reattached.
Maggots may be similarly repellent to most, but they have long
been medicinally useful. In World War I, infections with maggots
kept bacterial infections in check. Experiments have been carried
out with maggots to clean wounds; they also seem to secrete
compounds that promote wound healing. They have been shown to be
just as good (and cost-effective) as conventional medications for
chronic wounds, and greenbottle larvae are commercially available
for use in medicine. The main obstacle to their wider use is
patient squeamishness…
An area of growing interest is the use of parasites or their
secretions or eggs to manipulate the immune response. There is a
school of thought that the current high incidence of asthma,
inflammation and allergy in the West is due to a lower parasite
burden. In parts of the world where parasites are common, asthma is
rare. Various trials have been carried out of parasitic worm eggs
for inflammatory bowel disease, with some success. In the UK,
hookworms are being tested as a treatment for asthma.
Much effort is being put into identifying the active substances
produced by parasites, so that they can be given medicinally
without a patient having to be infected with the real thing.