Introduction to promoting wound
healing with low energy laser treatment
Low energy lasers have been available for treating
wounds for nearly three decades. But, while the
basic science of their biologic effects has been
known for quite sometime, their clinical evaluation
is mired in controversy. This is so, mainly, due
to studies lacking rigor, standardization and proper
data documentation. As a result, no proper conclusions
could be drawn from these studies. Recent studies
conducted under more rigorous conditions have not
been able to rid this controversy surrounding low
energy laser treatment.
Effect of low energy lasers on cells
Earlier it was thought low energy lasers healed
wounds by some kind of photochemical reaction and
not through thermal damage. To throw more light
on the subject, many animal studies were conducted
to investigate the effect of low energy lasers
on cell function and molecular changes. The early
studies were conducted on experimentally induced
wounds on various animal species and on human skin
ulcers. These studies generated an abundance of
data making this area one of the best investigated.
Early stage investigations suggested that low
energy lasers aided wound healing. Further studies
revealed that wound healing was mainly due to collagen
formation. However there also emerged several different
views about the mechanism of action. These included
improved metabolic function of wound tissue, increased
cell proliferation, increased tensile strength
and improved proliferation phase of repair. Moreover,
different studies on the effect of low energy lasers
on the same kind of wounds showed different results.
For instance, in one study venous ulcers showed
significant improvement after low energy laser
irradiation. In contrast low energy treatment by
He: Ne lasers had no effect on the same ulcers.
In the light of these developments, it was suggested
that further studies were needed before any definite
conclusions could be drawn. It was also suggested
that, beside the exposed dermal area, the systemic
effect due to low energy laser treatment as related
to the wound should also be studied.
Effect of low energy lasers on the immune system
In an earlier study on the effects of low energy
irradiation on wound healing in humans, it was
observed that the laser irradiation not only healed
the irradiated ulcer but also similar lesions in
other parts of the body. It was concluded that
low energy laser irradiation might heal or improve
the wound condition by eliciting some response
from the immune system.
To study the effect of low energy treatment on
the immune system, both humoral and cellular immunity
were investigated. Patients irradiated by low energy
He:Ne lasers showed changes in serum complement
activity and in immunoglobin levels. When this
immunosuppressive action of these lasers were studied
in directly irradiated human lymphocytes, irradiation
by argon laser at 488nm to 501nm wave length range
was found more effective than the He:Ne laser.
Since lymphocytes are a well-known source of important
factors of wound repair, it was believed that stimulation
or inhibition of certain immune responses might
play an important role in faster wound healing,
after exposure to low energy lasers. An in vitro
study showed that low energy lasers can interact
with the immune system. It was speculated that
the same process could occur in vivo in humans,
irradiated by low energy lasers.
The role of macrophages, irradiated by low energy
lasers, in speeding up wound healing by speeding
up the proliferation phase of repair was also investigated.
It was found that irradiation by 660nm, 820nm and
870nm wave lengths caused macrophages to release
factors that triggered fibroblast proliferation
above normal levels. In contrast, 880nm wavelength
either suppressed release of these factors or triggered
the release of factors which suppressed fibroblast
production. According to the investigators, increased
fibroblast production can speed up wound healing
in the repair phase. So, some low energy laser
wave lengths can serve as useful tools to stimulate
or suppress fibroblast production.
Effect of low energy lasers on skin grafts
In a study, skin from inbred mice was allotransplanted
on mice of a genetically different strain. Both
the donor skin graft and the recipient graft beds
on the backs of mice were exposed to low energy
He:Ne laser. A similar group was given the immunosuppressant,
antithymocite treatment. A combination therapy
of laser and this immunosuppressant was also given.
While the two groups given monotherapies, showed
improved graft survival, in combined therapy, graft
survival was further improved. The investigators
inferred that combined therapy had an increased
graft- protective effect on mouse skin grafts.
Whether this benefit can be extended to humans
has to be investigated. But it raises the possibility
of successful skin grafts from foreign sources,
when the patient’s own skin is found to be
inadequate.