Allergic disorders are characterized by potentially harmful reactions to extrinsic materials or allergens. They include allergic rhinitis (hay fever), atopic dermatitis, anaphylaxis, hives, and blood transfusion reactions.(1)
The immune response is the bodys defense mechanism which identifies and destroys harmful foreign organisms. Allergic reactions are an overreaction of the bodys defense mechanism. This overreaction can lead to swelling, itching and many other symptoms all with varying degrees of severity.
It is important to remember that the immune response is vital for protecting the body from foreign invaders and when working correctly its importance cannot be understated. Asthma and allergies are among the most common health problems, with as many as 50 million Americans afflicted with asthma, hay fever or other allergy-related conditions.
The preponderance of food allergies are caused by eggs, milk, wheat, fish, shellfish, nuts, peanuts, soybeans and rice.
One of the most severe allergic reactions is anaphylaxis, which is "marked by the sudden onset of rapidly progressive urticaria (a vascular reaction of the skin) and respiratory distress." (2)
Causes
The reasons that the body overreacts to a particular antigen are not well understood. It is known that it takes time and repeated exposure to an antigen for an allergic response to take place. There is also evidence that susceptibility to allergies have a hereditary component.
At Risk
There is a genetic predisposition for atopic allergies, but not for any particular allergy itself. (3)
Prevention and Management
General: Avoid the materials or organisms that initiate the allergic reaction. This may mean avoiding certain foods or environments.
Nutritional Influences:
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AbstractsMeydani SN, Meydani M, Blumberg JB, Leka LS, Siber G, Loszewski R, Thompson C, Pedrosa MC, Diamond RD, Stollar BD. Vitamin E supplementation and in vivo immune response in healthy elderly subjects. A randomized controlled trial. JAMA 1997 May 7;277(17):1380-6.OBJECTIVE: To determine whether long-term supplementation with vitamin E enhances in vivo, clinically relevant measures of cell-mediated immunity in healthy elderly subjects. DESIGN: Randomized, double-blind, placebo-controlled intervention study. SETTING AND PARTICIPANTS: A total of 88 free-living, healthy subjects at least 65 years of age. INTERVENTION: Subjects were randomly assigned to a placebo group or to groups consuming 60, 200, or 800 mg/d of vitamin E for 235 days. MAIN OUTCOME MEASURES: Delayed-type hypersensitivity skin response (DTH); antibody response to hepatitis B, tetanus and diphtheria, and pneumococcal vaccines; and autoantibodies to DNA and thyroglobulin were assessed before and after supplementation. RESULTS: Supplementation with vitamin E for 4 months improved certain clinically relevant indexes of cell-mediated immunity in healthy elderly. Subjects consuming 200 mg/d of vitamin E had a 65% increase in DTH and a 6-fold increase in antibody titer to hepatitis compared with placebo (17% and 3-fold, respectively), 60-mg/d (41% and 3-fold, respectively), and 800-mg/d (49% and 2.5-fold, respectively) groups. The 200-mg/d group also had a significant increase in antibody titer to tetanus vaccine. Subjects in the upper tertile of serum alpha-tocopherol (vitamin E) concentration (>48.4 micromol/L [2.08 mg/dL]) after supplementation had higher antibody response to hepatitis B and DTH. Vitamin E supplementation had no effect on antibody titer to diphtheria and did not affect immunoglobulin levels or levels of T and B cells. No significant effect of vitamin E supplementation on autoantibody levels was observed. CONCLUSIONS: Our results indicate that a level of vitamin E greater than currently recommended enhances certain clinically relevant in vivo indexes of T-cell-mediated function in healthy elderly persons. No adverse effects were observed with vitamin E supplementation.
References
1 Diseases. Springhouse (PA): Springhouse Corporation;1993. p 52-66.
2 Diseases. Springhouse (PA): Springhouse Corporation;1993. p 52.
3 Tabers Cyclopedic Medical Dictionary. 16th ed. Philadelphia:FA Davis Company; 1985. p 120.
4 Wiedermann U, Chen XJ, Enerblack L, Hanson LA, Kahu H, Dahlgren UI. Vitamin A deficiency increases inflammatory responses. Scand J Immunolo 1996 Dec;44(6):58-84.
5 Kosogorova LS, Kovalenko NN, Liubenko VA, Novosad FI. Recovery of immunological responsiveness in patients with bronchial asthma during nicotinamide treatment. Probl Tuberk 1996;(5):41-4.
6 Martin W. On treating allergic disorders. Letter. Townsend Letter for Doctors 1991 Aug/Sep:671-1.
7 Cohen HA, Neuman I, Nahum H. Blocking effect of vitamin C in exercise-induced asthma. Arch Pediatr Adolese Med 1997 Apr;151(4):367-70.
8 Meydani SN, Meydani M, Blumberg JB, Leka LS, Siber G, Loszewski R, Thompson C, Pedrosa MC, Diamind RD, Stollar BD. Vitamin E supplementation and in vivo immune response in healthy elderly subjects. A randomized controlled trial. JAMA 1997 May 7;277(17):1380-6.
9 Kadrabova J, Madaric A, Kovacikova Z, Podivinsky F, Ginter E, Gazdik F. Selenium status is decreased in patients with intrinsic asthma. Biol Trace Elem Res 1996 Jun;52(3):241-8.
10 Ojuawo A, Lindley KJ, Milla PJ. Serum zinc, selenium and copper concentration in children with allergic colitis. East Afr Med J 1996 Apr;73(4):236-8.
11 Greene LS. Asthma and oxidant stress: nutritional, environmental, and genetic risk factors. J Am Coll Nutr 1995 Aug;14(4):317-24.
12 Read MA. Flavonoids: naturally occurring anti-inflammatory agents [comment]. Am J Pathol 1995;147(2):235-7.
Source: USANA Health Sciences
