The strength of the immune response changes based on
several variables such as diet, stress, and mood.
Thus, around the holidays, when people are more
prone to eat sugary foods and refined carbohydrates,
there is a direct and unfavorable effect on immune
function. In addition, the stress of the holiday
season can also have detrimental effects on the
immune response. Adults average 2-4 colds per year,
with increased occurrence during the fall and winter
when the air is colder with decreased humidity.
1
Consequently, many people have an increased
susceptibility to colds and flu during the holiday
season.
Sugar and the Immune System
Animal models have shown that increasing sucrose
intake increases the neurotransmitter serotonin,
important for mood balancing, suggesting that eating
sugar can make us feel better when depressed.2
Although consuming sugar may result in enhanced
mood, anyone who experiences this “sugar high” must
pay a steep price. This is because numerous studies
have shown that increased sugar intake dramatically
decreases the immune response.
Short-term hyperglycemia (elevated blood sugar)
affects all major components of innate immunity and
impairs the ability of the individual to fight
infection.3 The white blood cells are the
primary mediators of the immune response.
Neutrophils are a type of white blood cell that act
as an important first-line-of-defense in the immune
system by engulfing (phagocytizing) pathogens.
Hyperglycemia has been shown to decrease neutrophil
activity in numerous studies.4 One study showed that
increased glucose levels decreased neutrophils’
ability to engulf several pathogens such as
Staphylococcus epidermidis, Staphylococcus
aureus, and Escherichia coli.5
A similar study showed that poor blood sugar control
in diabetic patients decreased neutrophil activity
against Klebsiella pneumoniae.6
Specifically, neutrophils experienced a decrease in
their movement and their ability to engulf and kill
pathogens, an increase in leukocyte apoptosis
(programmed cell death), and a reduction in lymph
node retention capacity. Additionally, lowering of
blood glucose has been shown to significantly
improve neutrophil activity.7
Sugar’s harmful effect on the immune system was
further demonstrated in a study that showed a
significant decrease in neutrophil activity in blood
samples from healthy adults at 30 and 60 minutes
following ingestion of 75 grams of glucose.8
Another similar study examined the activity of
neutrophils after a 100 gram dose of various simple
carbohydrates including glucose, fructose, sucrose,
honey, and orange juice in humans. The results
indicated that all simple carbohydrates tested
significantly decreased the capacity of neutrophils
to engulf bacteria. The greatest effects occurred
between 1 and 2 hours after ingestion of the
carbohydrates, and the values were still
significantly below the fasting control values five
hours after glucose ingestion.9 Thus,
increasing intake of sugary foods will have a
profound impact on the immune response.
Stress and the Immune System
Around the holidays, not only do individuals
increase their consumption of sugary foods, they
also often experience increased stress levels.
Stress, through the hypothalamic-pituitary-adrenal (HPA)
axis, can modulate the immune system. Cortisol,
released from the adrenal glands, is the primary
hormone that mediates the stress response. Cortisol,
in response to stress, suppresses the immune
response.10 Research has shown that
stress can affect the immune system in several ways
such as reduced neutrophil activity, changes in
types of chemical mediators (cytokines) produced by
the white blood cells, and decreased cytotoxic
T-lymphocytes and natural killer cell activities.11-12
Studies suggest that an elevated cortisol:DHEA ratio
is a contributing factor to this reduced immunity,
particularly in elderly patients. DHEA (dehydroepiandrosterone)
is a steroid hormone secreted from the adrenal
glands). More specifically, an elevated
cortisol:DHEA ratio significantly decreases
neutrophil activity.
One particularly interesting study evaluated the
perceived life stress and risk of upper respiratory
infections (URI). The study found that those
individuals with high levels of negative life events
and who showed high cortisol reactivity had
increased numbers of URIs. Also this study showed
that during times of increased perceived stress,
lower reactivity of natural killer cells and CD8
T-lymphocytes were also correlated with increased
URIs.13
In addition, studies have shown that anxiety
affects immune function. Anxious subjects were found
to have increased cortisol levels with impaired
immune function and changes in cytokines released
from the white blood cells.14
When Defenses are Down
EpiCor® is widely used for its ability to act as
a potent immune system modulator. It has been shown
to modulate the number and activity of immune cells
known as lymphocytes including T-lymphocytes and
natural killer cells, as well as antibody
production.15 Additionally, EpiCor has
been shown to significantly decrease the duration
and number of reported symptoms in individuals
suffering from colds and flu in a clinical trial.16
However, under times of increased vulnerability and
decreased resistance to infection, such as during
the holidays, pathogens may gain the upper hand.
Consequently, even those individuals who regularly
take Epicor for immune enhancement may need
additional support this time of year. When defenses
are down and the first signs of a cold or flu are
felt, adding Fast Response™ can be a particularly
powerful tool to enhance immunity.
Fast Response supports the immune system using a
combination of vitamins and minerals with
traditional Chinese herbs. These ingredients
modulate white blood cells including B-lymphocytes,
T-lymphocytes, macrophages, and natural killer
cells, as well as decrease inflammation, which
causes many of the symptoms associated with colds
and flu.
The traditional Chinese botanicals in Fast
Response have shown efficacy in supporting immunity.
Forsythia suspense has been shown to have anti-viral
and anti-bacterial activity.17-18
Lonicera japonicus inhibits the
pro-inflammatory cyclooxygenase (COX)-2 and
5-lipoxygenase (LOX) enzymes,19 which is
important as infection with the cold virus increases
the activity of these two inflammatory enzymes.20
In traditional Chinese medicine, Platycodon
grandiflorum has been used for clearing the
lungs, resolving phlegm, and soothing the throat,21
and research has shown that constituents of
Platycodon stimulate macrophage proliferation and
activity.22 Arctium lappa
(Burdock) contains arctigenin, which has been shown
to prolong the survival time of mice infected with
influenza virus as well as inhibited lung
consolidation in mice pneumonia caused by the
influenza virus.23 Arctium lappa
decreases coughing, and was equally active as some
synthetic preparations in studies using animal
models.24 Research indicates that both
Arctium lappa and the essential oils of
Mentha arvenis inhibit the growth of several
strains of pathogenic bacteria.25-26
Constituents of Glycyrrhizae uralensis have
anti-inflammatory properties,27 can
activate macrophages,28 and have been
shown to decrease replication of coronavirus from
patients with severe acute respiratory syndrome (SARS).29
Schizonepeta tenuifolia has been shown to
regulate inflammatory responses by modulating
T-lymphocyte activity.30 This combination
of nutrients and botanicals can provide the extra
support needed during times of increased
vulnerability to colds and flu.
Taking a formula that combines the above
botanicals with immune-supporting vitamins and
minerals can be a particularly effective approach.
Vitamins A, C, B6 and the mineral zinc
are critical for optimal immune function. Vitamin A
is required for the growth and activation of
B-lymphocytes, increases macrophage activity, and is
important in maintaining a sufficient level of
natural killer cells. Deficient levels of Vitamin A
can reduce lymphocyte numbers, natural killer cells,
immunoglobulin responses, and impair T-lymphocyte
function.31 Vitamin C has been shown in
multiple studies to significantly reduce the
duration of episodes and the severity of common cold
and flu symptoms.32 Vitamin B6
is important for normal immune function as
deficiencies have been shown to alter lymphocyte
differentiation and maturation and impair antibody
production.33 Zinc is required for normal
development and function of white blood cells such
as neutrophils and natural killer cells, and zinc
deficiency adversely affects T-lymphocyte function,
B-lymphocyte development, antibody production, and
macrophage activity.34 Clinical trials
indicate that zinc supplementation can significantly
shorten the time to complete resolution of symptoms
in patients with the common cold.35
Adding a vitamin D3 supplement to the
immune-boosting regimen above also is important
during cold and flu season. Researchers have
theorized that the reason why the cold and flu
season occurs in winter is because vitamin D
deficiency is widespread during this time of year
when exposure to sunlight is minimal.36
One explanation for vitamin D’s role in immunity is
that it up-regulates an important gene called
cathelicidin, a naturally occurring broad-spectrum
antibiotic.37
Conclusion
Stress and poor dietary habits such as increasing
intake of sugary foods and refined carbohydrates
increase susceptibility to infection, particularly
this time of year. Supplements such as EpiCor
(see source link below) are ideal for general
immune support. However, under times of increased
vulnerability and decreased resistance to infection,
products such as Fast Response may be necessary for
extra immune enhancement. Adding a vitamin D3
supplement to this regimen will further strengthen
immunity and provide additional defense against
colds and influenzas.
Highly recommended
trusted source of supplements.
How
did we qualify VRP as best source?
References
1. National Institutes of Health. Common Cold.
Available at: http://www3.niaid.nih.gov/topics/commonCold/overview.htm.
Accessed on: 09-22-08.
2. Smolders I, Loo JV, Sarre S, et al. Effects of
dietary sucrose on hippocampal serotonin release: a
microdialysis study in the freely-moving rat. Br J
Nutr. 2001 Aug;86(2):151-5.
3. Turina M, Fry DE, Polk HC Jr. Acute
hyperglycemia and the innate immune system:
clinical, cellular, and molecular aspects. Crit Care
Med. 2005 Jul;33(7):1624-33.
4. Patel KL. Impact of tight glucose control on
postoperative infection rates and wound healing in
cardiac surgery patients. J Wound Ostomy Continence
Nurs. 2008 Jul-Aug;35(4):397-404.
5. Van Oss CJ. Influence of glucose levels on the
in vitro phagocytosis of bacteria by human
neutrophils. Infect Immun. 1971 Jul;4(1):54-9.
6. Lin JC, Siu LK, Fung CP, et al. Impaired
phagocytosis of capsular serotypes K1 or K2
Klebsiella pneumoniae in type 2 diabetes mellitus
patients with poor glycemic control. J Clin
Endocrinol Metab. 2006 Aug;91(8):3084-7.
7. Alba-Loureiro TC, Munhoz CD, Martins JO, et
al. Neutrophil function and metabolism in
individuals with diabetes mellitus. Braz J Med Biol
Res. 2007 Aug;40(8):1037-44.
8. Bernstein J, Alpert S, Nauss KM, et al.
Depression of lymphocyte transformation following
oral glucose ingestion. Am J Clin Nutr. 1977;30:613
(abstract).
9. Sanchez A, Reeser JL, Lau HS, et al. Role of
sugars in human neutrophilic phagocytosis. Am J Clin
Nutr. 1973 Nov;26(11):1180-4.
10. Butcher SK, Killampalli V, Lascelles D, et
al. Raised cortisol:DHEAS ratios in the elderly
after injury: potential impact upon neutrophil
function and immunity. Aging Cell. 2005
Dec;4(6):319-24.
11. Reiche EM, Morimoto HK, Nunes SM. Stress and
depression-induced immune dysfunction: implications
for the development and progression of cancer. Int
Rev Psychiatry. 2005 Dec;17(6):515-27.
12. Godbout JP, Glaser R. Stress-induced immune
dysregulation: implications for wound healing,
infectious disease and cancer. J Neuroimmune
Pharmacol. 2006 Dec;1(4):421-7.
13. Cohen S, Hamrick N, Rodriguez MS, et al.
Reactivity and vulnerability to stress-associated
risk for upper respiratory illness. Psychosom Med.
2002 Mar-Apr;64(2):302-10.
14. Arranz L, Guayerbas N, De la Fuente M.
Impairment of several immune functions in anxious
women. J Psychosom Res. 2007 Jan;62(1):1-8.
15. Jensen GS, Hart AN, Schauss AG. An
antiinflammatory immunogen from yeast culture
induces activation and alters chemokine receptor
expression on human natural killer cells and B
lymphocytes in vitro. Nutrition Research. 2007
Jun;27(6):327-335.
16. Moyad MA, Robinson LE, Zawada ET Jr, et al.
Effects of a modified yeast supplement on cold/flu
symptoms. Urol Nurs. 2008 Feb;28(1):50-5.
17. Zhang GG, Song SJ, Ren J, et al. A new
compound from Forsythia suspensa (Thunb.) Vahl with
antiviral effect on RSV. J Herb Pharmacother.
2002;2(3):35-40.
18. Kong B, Wang J, Xiong YL. Antimicrobial
activity of several herb and spice extracts in
culture medium and in vacuum-packaged pork. J Food
Prot. 2007 Mar;70(3):641-7.
19. Rall LC, Meydani SN. Vitamin B6 and immune
competence. Nutr Rev. 1993 Aug;51(8):217-25.
20. Seymour ML, Gilby N, Bardin PG, et al.
Rhinovirus infection increases 5-lipoxygenase and
cyclooxygenase-2 in bronchial biopsy specimens from
nonatopic subjects. J Infect Dis. 2002 Feb
15;185(4):540-4.
21. Guo L, Zhang C, Li L, et al. Advances in
studies on Platycodon grandiflorum. Zhongguo Zhong
Yao Za Zhi. 2007 Feb;32(3):181-6.
22. Choi CY, Kim JY, Kim YS, et al. Augmentation
of macrophage functions by an aqueous extract
isolated from Platycodon grandiflorum. Cancer Lett.
2001 May 10;166(1):17-25.
23. Yang Z, Liu N, Huang B, et al. Effect of
anti-influenza virus of Arctigenin in vivo. Zhong
Yao Cai. 2005 Nov;28(11):1012-4.
24. Kardosová A, Ebringerová A, Alföldi J, et al.
A biologically active fructan from the roots of
Arctium lappa L., var. Herkules. Int J Biol
Macromol. 2003 Nov;33(1-3):135-40.
25. Gentil M, Pereira JV, Sousa YT, et al. In
vitro evaluation of the antibacterial activity of
Arctium lappa as a phytotherapeutic agent used in
intracanal dressings. Phytother Res. 2006
Mar;20(3):184-6.
26. Imai H, Osawa K, Yasuda H, et al. Inhibition
by the essential oils of peppermint and spearmint of
the growth of pathogenic bacteria. Microbios.
2001;106 Suppl 1:31-9.
27. Shin EM, Zhou HY, Guo LY, et al.
Anti-inflammatory effects of glycyrol isolated from
Glycyrrhiza uralensis (Leguminosae) in LPS-induced
RAW264.7 macrophages. Int Immunopharmacol 2008 Jul
10. Published online ahead of print.
28. Nose M, Terawaki K, Oguri K, et al.
Activation of macrophages by crude polysaccharide
fractions obtained from shoots of Glycyrrhiza glabra
and hairy roots of Glycyrrhiza uralensis in vitro.
Biol Pharm Bull. 1998 Oct;21(10):1110-2.
29. Cinatl J, Morgenstern B, Bauer G, et al.
Glycyrrhizin, an active component of liquorice
roots, and replication of SARS-associated
coronavirus. Lancet. 2003 Jun 14;361(9374):2045-6.
30. Kang H, Oh YJ, Choi HY, et al.
Immunomodulatory effect of Schizonepeta tenuifolia
water extract on mouse Th1/Th2 cytokine production
in-vivo and in-vitro. J Pharm Pharmacol. 2008
Jul;60(7):901-7.
31. Food and Nutrition Board, Institute of
Medicine. Dietary Reference Intakes for Vitamin A,
Vitamin K, Arsenic, Boron, Chromium, Copper, Iodine,
Iron, Manganese, Molybdenum, Nickel, Silicon,
Vanadium, and Zinc. Washington, DC: National Academy
Press, 2002. Available at: www.nap.edu/books/0309072794/html/.
32. Gorton HC, Jarvis K. The effectiveness of
vitamin C in preventing and relieving the symptoms
of virus-induced respiratory infections. J
Manipulative Physiol Ther. 1999 Oct;22(8):530-3.
33. Rall LC, Meydani SN. Vitamin B6 and immune
competence. Nutr Rev. 1993 Aug;51(8):217-25.
34. Shankar AH, Prasad AS. Zinc and immune
function: the biological basis of altered resistance
to infection. Am J Clin Nutr. 1998 Aug;68(2 Suppl):447S-463S.
35. Mossad SB, Macknin ML, Medendorp SV, et al.
Zinc gluconate lozenges for treating the common
cold. A randomized, double-blind, placebo-controlled
study. Ann Intern Med. 1996 Jul 15;125(2):81-8.
36. Cannell JJ, Vieth R, Umhau JC, Holick MF,
Grant WB, Madronich S, Garland CF, Giovannucci E.
Epidemic influenza and vitamin D. Epidemiol Infect.
2006 Dec;134(6):1129-40.
37. Cannell JJ, Hollis BW. Use of vitamin D in
clinical practice. Altern Med Rev. 2008
Mar;13(1):6-20.