|
by
Ward Dean, MD and Jim English
The
key to a healthy, functioning immune system rests largely with the
thymus gland, a small organ lying just beneath the breast- bone
(Fig. 1). Weighing less than half of an ounce at birth, by puberty,
the thymus will grow to its maximum size of about 10 ounces. After
age 20, the thymus begins to shrink (atrophy) and thymic cells progressively
die off to be replaced by fat and connective tissue. (1)
This
age-related atrophy of the thymus gland and the subsequent
decline of thymic hormones gradually robs the body of its
ability to fight off infectious diseases, autoimmune diseases, and
cancer. As immunologist Keith Kelly noted: "The involution
[shrinkage] of the thymus gland is one of the cardinal bio-markers
of aging." (2)

As discussed previously in the Neuroendocrine Theory of Aging, (Part
IV, The Immune Homeostat) the thymus gland interacts with the
rest of the endocrine system (the Hypothalamus-Pituitary-Thymus
axis) to maintain a healthy immune system. (3) The primary role
of the thymus is to assist in the proliferation and differentiation
of mature T-lymphocytes cells that attack and kill viruses
and bacteria.
T-lymphocytes
(T-cells) and B-lymphocytes (B-cells) are both white blood cells
that are produced in bone marrow. B-cells emerge from bone marrow
fully mature and ready to go about the business of recognizing invaders
(antigens) and signaling the production of antibodies. By contrast,
T-cells emerge from marrow in an incomplete state. Before they can
begin to function properly, the "immature" T-cells must
first migrate to the thymus gland (Fig. 2.) where they "incubate"
and are programmed to transform into one of three types of specialized
T-cells:
- T-4 Helper cells work to orchestrate the immune response
by activating other immune cells and stimulating the production
of antibodies by the B-cells.
- T-8 Killer cells are directed by the T-4 Helper
cells to attack and destroy invading viruses and cancer cells.
- The T-8 Suppressor cells suppress killer cells by signaling
the termination of an attack.
In our early twenties we have an abundance
of well-functioning T-cells that regulate the immune system and help
the body fight off pathogens and disease. But with the inexorable
shrinking of the thymus gland over time, by about age forty the output
of thymic hormones has decreased significantly and the T-cells have
begun to lose their effectiveness. It is this gradual loss of functioning
T-cells that is thought to be responsible for many of the age-related
changes in the immune system.Restoring Thymic Function
A number
of animal extracts and synthetic thymic hormones have demonstrated
the ability to dramatically reverse thymic atrophy and restore levels
of immunity to much more youthful levels. In addition to being among
the most effective immune-enhancing agents known, thymic extracts
and thymic hormones are among the few agents that are documented
to extend the life span of experimental animals. (4,5) Many processed
thymus extracts generally consists of ground up thymus glands. These
products contain a conglomeration of biologically inactive thymus
tissues, cell debris, fragments of thymus proteins and thymus by-products.
Terry Beardsley, Ph.D., is an immunologist
and experimental biologist from Baylor College of Medicine in Texas.
He has been the principal scientist in the Monoclonal Antibody Facility
at Smith Kline Beckman; Assistant Professor of research at the University
of California at San Diego; Research Associate at Scripps Clinic,
La Jolla; and Assistant Research Professor at UCLA's Laboratory of
Nuclear Medicine.
Dr.
Beardsley has spent most of his career researching the thymus gland,
and is considered one of the leading experts in the world on this
subject. In the early 1980s, Dr. Beardsley established the first
continuously growing line of thymic stromal cells (cells producing
immune-regulating substances such as IL-2) in his laboratory. (6)
Dr. Beardsley also succeeded in proving that his cultures possessed
higher levels of immune stimulatory activity than seen in previously
known cultures. However, his results were less effective than he
desired due to the presence of unwanted competing biological activities.
(7)
Dr.
Beardsley spent the next eight years working tediously with one
cell at a time until he isolated a single purified protein that
produced all of the immune activity of the mixed thymic cultures
without the presence of any of the other cell types. What
Dr. Beardsley had discovered was a complete, biologically "intact"
500-amino chain protein that fits into the receptor sites on T-4
cells to "turn on" and program the cells for their disease-fighting
functions. Dr. Beardsley named the peptide Thymic Protein A (TPA).
Following
several favorable clinical studies involving both animal (Feline
AIDS and distemper) and human (chronic fatigue syndrome [CFIDS]
and Epstein-Barr [EBV]) subjects, Dr. Beardsley developed a unique
oral delivery system for his formulation which avoided the degradation
of the thymic protein in the stomach a significant problem
with other over-the-counter oral thymic preparations.
The
scientific data gathered from these studies resulted in the awarding
of a US patent to Dr. Beardsley in 1997 for both the Thymic protein
A molecule and its method of production.
In
the five-and-a-half years since Thymic Protein A was introduced
as an oral nutritional supplement, thousands of individuals have
consumed this product. Hundreds of medical doctors are using it
for a variety of immune-related illnesses with no adverse reactions
from this highly purified, extremely safe, low-dose protein molecule.
Thymic Protein A is produced at only one site in the world, under
the personal control and supervision of Dr. Beardsley. Based on
his commitment to maintaining the highest scientific standards,
utmost purity is assured.
The immune system is clearly an integral
component of the neuroendocrine system, which exhibits typical age-related
decrements. Previous research with a number of nutritional and/or
pharmacological substances has proven that aspects of impaired immune
function can be restored to more youthful, healthy levels. Fabris
noted that, "age-related thymic involution is not an irreversible
process
functional recovery can be achieved even in old age
[and]
thymus regrowth can be induced in old age." (8)
Thymic
Protein A has been demonstrated to have immune-enhancing properties.
A dose of a mere 4 micrograms of Thymic Protein A may make a major
difference in strengthening the immune system through its T-cell
"programming" role. The more T-cells that are functioning
properly, the greater the immune response against infections and
pathogenic agents. The reported benefits of Thymic Protein A include
increased stamina, energy, well-being and ability to ward off infections.
Dr.
Julian Whitaker states that Thymic protein A "is likely the
most powerful natural stimulant of the immune system ever discovered."
(9) Many other physicians such as Drs. Robert Atkins, Abram Ber,
Jonathan Wright, Lee Cowden and Serefina Corsello, are using it
regularly in their practices and for themselves. Dr. Whitaker recommends
one to three packets a day, taken sublingually when sick (I have
known cancer patients and very debilitated patients who took six
packets daily. WD). Dr. Whitaker also recommends that a maintenance
dosage be taken on a daily basis to support age-impaired immune
systems. Thymic Protein A is extremely safe, with no adverse effects
noted in any dose.
References
1. South, James, "Thymus Gland, Its Overlooked
But Vital Role," Vitamin Research News, November 1999, Vol. 13:11,
pp 1-5.
2. K. Kelly et al. "A pituitary-Thymus Connection During Aging."
Ann. N.Y. Acad. Sci. 521, 88-98, 1988.
3. Dean, Ward, MD. "The Neuroendocrine Theory of Aging Part IV
The Immune Homeostat." Vitamin Research News, October
1999, Vol. 13:10, pp 1-11.
4. Fabris, N., Mocchegiani, E., Muzzioli, M., and Provinciali, M.
Neuroendocrine-thymus interactions: Perspectives for intervention
in aging. In: Neuroimmunomodulation: Interventions in Aging and Cancer,
Ann NY Acad Sci, Vol 621, by Pierpaoli, W. and Spector, N.H., (eds).
NY Acad Sci, New York, 1988, 72-87.
5. Cardarelli, Nate. The role of a thymus-pineal axis in an immune
mechanism of aging. J Theor Biol, 1990, 145: 397-405.
6. Beardsley TR, Pierschbacher M, Wetzel GD, Hays EF. Induction of
T-cell maturation by a cloned line of thymic epithelium (TEPI). Proc
Natl Acad Sci USA 1983 Oct;80(19):6005-9.
7. Hays EF, Beardsley TR. Immunologic effects of human thymic stromal
grafts and cell lines. Clin Immunol Immunopathol 1984 Dec;33(3):381-90.
8. Fabris, N., Mocchegiani, E., Muzzioli, M., and Provinciali, M.
Role of zinc in neuroendocrine-immune interactions during aging. In:
Physiological Senescence and Its Postponement, Ann New York Acad Sci,
Vol 621, by Walter Pierpaoli and Nicola Fabris, (eds.),1991, NY Acad
Sci, New York, 314-326.
9. Whitaker, Julian. Give your immune cells a natural 'shot in the
arm.' Dr. Julian Whitaker's Health & Healing, March, 1997, Vol 7,
No. 3, 1-2. |