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Matol Botanical International Distributor Robert Veliky
robert@matolproducts.com
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Matol Biomune Code 22™The Next Generation Formula
Intended for Intelligent Immunomodulation
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Matol
Biomune Code 22™ was developed in collaboration
with Robert A. Murgita,Ph.D.  [Add to Cart]
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New! Matol Biomune Code 22™
$29.75
An internationally recognized
expert in immunology and immuno-therapeutic
proteins. He has held academic and/or research
positions at the State University New York
(SUNY) at Buffalo; the Mayo Clinic in Rochester,
Minnesota; and the University of Uppsala and
Karolinska Institutet in Stockholm, Sweden. He
is a Professor at McGill University in Montreal,
Canada, and is a member of Matol's Health and
Nutrition
Board. | |
5 Key
Ingredients of Biomune Code 22™
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WHEY PROTEIN
ISOLATE:
What is it?
Whey is the protein portion of milk, and
includes molecules such as lactalbumin, albumin,
immunoglobulin, and transferrin. What does it do? It
enhances the activity of antibody
responses1, lymphocytes2,
macrophages3, and stimulates cytokine
production4,5. |
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ARABINOGALACTAN:
What is
it? Arabinogalactan is a complex
carbohydrate found in plants, especially the
Western Larch pine tree, and is a source of
dietary fiber. What does it
do? It stimulates
pro-inflammatory cytokine
production6, increases B and T cell
production7, and enhances natural
killer (NK) cell and macrophage
activity8-10. |

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ELEUTHEROCOCCUS
SENTICOSUS (ROOT):
What is
it? Eleutherococcus is a woody shrub
native to Northeastern Asia. What does it do? It
strongly stimulates macrophage
activity11-12, enhances
anti-inflammatory cytokine
activity13-15, and increases B and
T-cell
growth16-17. |
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LACTOFERRIN:
What is
it? Lactoferrin is an
iron-binding glycoprotein found in biological
fluids, including milk and blood plasma.
The 3D molecular structure of purified
lactoferrin is shown on the
left. What
does it do? It stimulates T-cell growth
and differentiation18-21, as well as
the appropriate Th1/Th2 response depending on
the disease19,21-26.
Lactoferrin also has anti-cancer
activity24,27,28. |

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MAITAKE:
What is
it? Maitake
is a mushroom native to Japan and North America,
containing biologically active polysaccharides
and is prized by oriental
herbologists. What does it
do? It
promotes cytotoxic-T “killer” cells that attack
cancerous cells29,30, stimulates
anti-inflammatory Th2 responses31,
regulates the body’s Th1/Th2
balance32, and stimulates
phagocytosis and natural killer
cytotoxicity30,33,34.
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Additional
Benefits
Some
ingredients in Biomune Code 22™ are
adaptogens, meaning they enhance the body’s
resistance to mental and physical stress, while
others have been shown to have both anti-viral and
anti-microbial activity.
Matol Code 22™ References
WHEY PROTEIN:
Enhances antibody response
1. Low, P.P.L., Rutherfurd, M.L., Cross, M.L. & Gill, H.S. Food Agric. Immunol.13, 255-264 (2001).
Enhances lymphocyte activity
2. Low, P.P.L., Rutherfurd, K.J., Gill, H.S. & Cross, M.L. Int. Immunopharmacol.
3, 393-401 (2003).
Stimulates Macrophages
3. Cross, M.L. & Gill, H.S. Immunol. Cell Biol. 77, 345-350 (1999).
Enhances cytokine production
4. Ford, J.T., Wong, C.W. & Colditz, I.G. Immunol. Cell Biol. 79, 23-28 (2001).
5. Cross, M.L. & Gill, H.S. Immunol. Cell Biol., 77, 345-350 (1999).
ARABINOGALACTAN:
Stimulates pro-inflammatory cytokine production
6. Grieshop, C.M., Flickinger, E.A. & Fahey, G.C. Jr. J. Nutr., 132, 478-482 (2002).
Increases T and B-Cell production
7. Nergard, C.S. et al. Carbohydr. Res. 340, 115-130 (2005).
Enhances NK and macrophage activity
8. Kelly, G.S. Altern. Med. Rev. 4(2), 96-103 (1999).
9. Kim, L.S., Waters, R.F.& Burkholder, P.M. Altern. Med. Rev. 7(2), 138-149 (2002).
10. Currier, N.L., Lejtenyi, D. & Miller, S.C. Phytomedicine, 10, 145-153 (2003).
ELEUTHEROCOCCUS SENTICOSUS (ROOT):
Strong stimulation of phagocytosis by macrophages
11. Kimura, Y., Sumiyoshi, M. J. Ethnopharmacol. 95, 447-453 (2004).
12. Block, K.I. & Mead, M.N. Integr. Cancer Ther. 2(3), 247-267 (2003).
Enhanced anti-inflammatroy cytokine activity
13. Altern. Med. Rev. 11(2), 151-155 (2006).
14. Panossian, A. et al. Phytomedicine, 9, 598-605 (2002).
15. Larsen, M.W., Moser, C., Hoiby, N., Song, Z. & Kharazmi, A. APMIS 112, 369-373 (2004).
Increased T and B-Cell growth
16. Deyama, T., Nishibe, S. & Nakazawa, Y. Acta Pharmacol. Sin. 22(12), 1057-1070 (2001).
17. Kormosh, N., Laktionov, K. & Antoshechkina, M. Phytother. Res. 20, 424-425 (2006).
LACTOFERRIN:
Stimulates T-Cell growth and differentiation
18. Suzuki, Y.A., Lopez, V. & Lonnerdal, B. Cell Mol. Life Sci. 62, 2560-2575 (2005).
19. Artym, J., Zimecki, M., Kruzel, M.L. Immunobiology 207, 197-205 (2003).
20. Li, K.J. et al. J. Leukoc. Biol. 80, 350-358 (2006).
21. Legrand, D., Elass, E., Carpentier, M. & Mazurier, J. Cell Mol. Life Sci. 62, 2549-2559 (2005).
Stimulates appropriate Th1/Th2 response depending on the disease
19. Artym, J., Zimecki, M., Kruzel, M.L. Immunobiology 207, 197-205 (2003).
21. Legrand, D., Elass, E., Carpentier, M. & Mazurier, J. Cell Mol. Life Sci. 62, 2549-2559 (2005).
22. Sfeir, R.M., Dubarry, M., Boyaka, P.N., Rautureau, M. & Tomé, D. Nutr. Immunol.,134, 403-409 (2004).
23. Curran, C.S., Demick, K.P., Mans eld, J.M. Cell. Immunol. 242(1), 23-30(2006).
24. Fischer, R., Debbabi, H., Dubarry, M., Boyaka, P. & Tomé, D. Biochem. Cell Biol. 84, 303-311 (2006).
25. Guillén, C. et al. J. Immunol. 168, 3950-3957 (2002).
26. Legrand, D., Elass, E., Carpentier, M. & Mazurier, J. Biochem. Cell Biol. 84(3), 282-290 (2006).
Anti-cancer activity
24. Fischer, R., Debbabi, H., Dubarry, M., Boyaka, P. & Tomé, D. Biochem. Cell Biol. 84, 303-311 (2006).
27. Shau, H., Kim, A. & Golub, S.H. J. Leukoc. Biol. 51, 343-349 (1992).
28. Nuijens, J.H., van Berkel, P.H.C. & Schanbacher, F.L. J. Mammary Gland Biol. Neoplasia, 1(3), 285-295 (1996).
MAITAKE:
Promotes CTL cells that attack cancer cells
29. Mayell M. Altern. Med. Rev. 6(1), 48-60 (2001).
30. Borchers AT, Keen CL, Gershwin ME. Mushrooms, tumors, and immunity:an update. Exp. Biol. Med. (Maywood) 229, 393-406 (2004).
Stimulates anti-inflammatory Th2 response
31. Kodama, N., Murata, Y. & Nanba, H. J. Med. Food 7(2), 141-145 (2004).
Regulates Th1/Th2 balance
32. Inoue, A., Kodama, N., Nanba, H. Biol. Pharmacol. Bull. 25(4), 536-540 (2002).
Stimulates phagocytosis and NK cytotoxicity
30. Borchers AT, Keen CL, Gershwin ME. Mushrooms, tumors, and immunity: an update. Exp. Biol. Med. (Maywood) 229, 393-406 (2004).
33. Wu, M.J. et al. J. Agric. Food Chem. 54, 2906-2914 (2006).
34. Kodama, N., Asakawa, A., Inui, A., Masuda, Y. & Nanba, H. Oncol. Rep. 13, 497-502 (2005)
The Immune
System
The human body is gifted with the
ability to keep itself free from disease-causing
invaders. Our immune system is an amazing
constellation of natural defense mechanisms that
protect the body against attacks from
disease-causing organisms. It is composed of
individual microscopic cells and molecules that
have widespread access to every part of the body
through a vast network of interconnected lymphatic
vessels.
Have you ever wondered why some
people come down with the flu or a cold, while
others stay healthy even though they share the
same environment? The strength of the immune
system is what makes the difference between
someone who gets sick and someone who doesn’t.
To meet the challenge of protecting
the body against infection by an ever-increasing
and evolving set of pathogenic (disease-causing)
micro-organisms, your immune system is armed with
multiple mechanisms capable of recognizing and
fighting off the constant barrage of attacks.
How the Immune System Works
The immune system works by a
series of layered defenses, each more specific and
efficient than the previous. Once a pathogen
breaks the first line of defense – the skin, mucus
membranes, and lytic enzymes – the immune system
instantly reacts to the invasion by enhancing
production of a family of signaling molecules
called cytokines. These cytokines, in turn, send
messages to other cells thereby activating the two
limbs of the natural, or non-specific, immune
response: natural killer (NK) cells and
macrophages.
As shown in Figure 1 (pathway A),
once an invading pathogen breaches the first line
of defense barriers, including skin and mucus
membranes; then the short-lived, limited, and
non-specific effect of NK cells and macrophages
take over in order to attack and destroy the
invader.
Figure 1 –
How the immune system reacts to a
pathogen1.

1
For further explanation of the details of the
immune system, see Janeway, C.A. Jr., Travers, P.,
Walport, M.W. and Shlomchik M. 2001.
Immunobiology, 5th ed., Garland Publishing, New
York.
Natural immunity is immediate, but
short-lived, and serves primarily to slow
progression of disease while a more sophisticated
and effective immune response develops. This
specific response is mediated by B-cells and
T-cells, which have the ability to “remember” a
specific infectious agent they have encountered
before. When pathogens that have invaded the
body in the past are re-encountered, the immune
response is even stronger and more rapid than it
was when the pathogen was first encountered.
Subsequently, in a matter of a few
days, the pathogen is confronted with a full-blown
specific immune response (Figure 1, pathway B),
mediated by cytotoxic T-cells, which are
especially effective at killing cells infected
with viruses, and B-cells, which secrete specific
antibodies that remove extracellular pathogens and
toxins.
How the
Balance between Th1 and Th2 T-Cells Affects
Disease
In addition, there is a an overall
balance that is maintained in the body between two
sets of T-cells, called Th1 and Th2. Th1 cells
stimulate a so-called “pro-inflammatory” immune
response that is tailored to destroying
intracellular viruses, bacteria and
parasites. Th2 cells stimulate a so-called
“anti-inflammatory” immune response, which is
suited to destroying pathogens and toxins found in
fluids outside of body cells. The Th1 / Th2
balance shifts to favour the appropriate response
against a particular invading pathogen (Figure
2).
Figure 2 –
Immune response to a pathogen is regulated by the
Th1/Th2 balance2.
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Figure
2a – When the balance is tipped in the
Th1 direction, it favors the production of
T-cell mediated responses, and production of
pro-inflammatory cytokines. This results in the
destruction of intracellular viruses, bacteria,
and parasites. |
Figure
2b - When the balance is tipped in the
Th2 direction, it favors the production of
antibody responses, and production of
anti-inflammatory cytokines. This
results is the destruction of extracellular
pathogens and toxins.
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2
For further explanation, see Kidd M. Altern. Med.
Rev. 8(3), 223-246 (2003).
Supporting
Your Immune System
People with an immune system
functioning below normal are more vulnerable to
the constant environmental bombardment on the body
by toxic materials, damaging radiation, bacteria,
viruses, parasites, and other harmful sources. The
negative effects on the immune system are
compounded by various lifestyle factors including
daily stress, poor nutrition, smoking, lack of
exercise, excessive alcohol consumption, etc.
The immune system in healthy people
is robust and functions very effectively
throughout most of the course of one’s lifetime,
showing some natural age-related deterioration in
the very elderly. However, when one’s living
environment includes any combination of the
negative factors noted above, then the immune
system can become significantly weakened.
Failure to maintain a proper diet, combined with
stress factors, has been shown to weaken the
immune systems of even healthy, college-aged
adults3. Therefore, there is a need at
all ages to incorporate a healthy lifestyle in
order to maintain a fully functioning immune
system; however, even in the pursuit of a healthy
lifestyle, many of the factors mentioned above
that act to lower immune function cannot be
completely avoided.
One of the ways to maintain a
healthy immune system, for people of all ages, is
to take immune system modulators. Matol Biomune
Code 22™ contains 5 ingredients which have all
individually been shown to modulate the immune
system.
3 For further
explanation, see Ellard DR et al. Stress and
Health. 21, 245-253 (2005).

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