Journal of Allergy Disorders & Therapy Category: Clinical Type: Case Report
Seasonal Allergy Induced Back Pain: A Report of Two Cases
- Sue Killian1*, John McMichael1
- 1 The Institute For Therapeutic Discovery, Westfall Road, Delanson, NY, United States
*Corresponding Author:Sue Killian
The Institute For Therapeutic Discovery, Westfall Road, Delanson, NY, United States
Received Date: Mar 25, 2015 Accepted Date: Aug 25, 2015 Published Date: Sep 10, 2015
Cases: These case studies illustrate a co-occurrence of seasonal allergies and back pain for which there is no obvious cause. Two patient cases were tested and treated using the provocation- neutralization method of allergy treatment and experienced pain relief using this method.
Discussion: The allergic cascade produces inflammatory, pain-producing cytokines and neuropeptides which may exacerbate other chronic conditions.
Conclusion: By controlling the allergic response through appropriate immunotherapy, co-occurring back pain often diminishes.
Theron Randolph, described the co-occurrence of allergy and muscle spasms in a patient whose family harbored an apple allergy. In a 1976 publication, Randolph pleaded for physicians to consider the connection between allergy and myalgia. “The most important point in making a tentative working diagnosis of allergic myalgia is to think of it. The fact remains that this possibility is rarely ever considered and is even more rarely approached by means of diagnostico-therapeutic measures capable of identifying and avoiding the most common environmental incitants and perpetuants of this condition - namely, specific foods addictants, environmental chemical exposures and house dust".
Dr. AH Rinkel and colleagues listed symptoms of allergy as “low back pain, muscle tightness and muscles pulling” with discomfort in nuchal and hamstring muscles with the sharp pain often resembling that of sciatica . Allergist Joseph Miller wrote, “Physicians interested in food allergy are very familiar with the ability of foods to cause muscle spasms and joint pain in various parts of the body. We frequently see food-allergic patients suffering from muscle and joint pains of the chest, back, abdomen, arms, legs or the back of the neck” .
Epidemiologists Hurwitz and Morgenstern interviewed a large population between 20 and 39 years of age and found that patients with a history of allergy were 50% more likely to report suffering from back pain and depression . More recently, a 2009 study in the Journal of Pain concluded that women with incontinence or allergy were at a greater risk for developing back pain than women without those conditions. They suggested that back pain in allergic individuals was a result of changes in the trunk muscles and the muscles of respiration (diaphragm and transverses abdominis) resulting in “compromised postural control”. They also noted that sneezing and coughing are associated with trunk muscle co-contraction and “increased spinal loading” adding to the “development of pain” .
Physicians observed that allergy and muscle pain were not only related but that muscle and joint symptoms could be diminished by successfully treating allergies [3,6]. The purpose of this paper is to report two cases of allergy and back pain and to discuss how allergy desensitization using the method of provocation neutralization (PN) of allergy testing and treatment might impact that pain.
An explanation of the PN method is a prerequisite to the unexpected immediate response found observed in these two case studies. Provocation-neutralization allergy testing and treatment is a method developed in 1957 by Carleton H Lee  which refines intradermal skin testing  to determine the level which will relieve the patients reactivity to a particular allergen while being tested.
Each concentrate of antigen is diluted into 9 or more vials (9 serial dilutions). Each elevation in number is a five-fold dilution (a 5x dilution) therefore the most concentrated is a #1, and #2 is 5x more dilute than #1 etc. The highest number is the greatest dilution.
As with traditional allergy testing, a positive wheal indicates a localized allergic reaction. Different dilutions of the same antigen are injected intradermally to produce a wheal, but the neutralizing dilution will produce a negative wheal. The strongest negative wheal produced is associated with the proper dilution of antigen, the neutralizing level, which is used to create the patients individualized therapeutic formulation.
The patient may be neutralized to ragweed at level 5, to oak pollen at level 6 and to a particular mold at level 4. The specific level of each antigen is used to create a custom-made, unique vial of antigens which can be administered as injections or sublingual drops. In addition to the long term effect expected to occur with traditional immunotherapy, there is a yet scientifically unexplained symptom relief in 30 minutes to 2 hours.
CASE STUDY 1
At a visit to his chiropractor, he was asked if he realized that this was the fourth time he had sought help and each of these visits occurred in February. The cyclical and apparent seasonal occurrence made him wonder if his neck and back pain were triggered by tree pollen.
He underwent provocative or challenge testing with mountain cedar tree pollen, a predominant pollen in his geographical area from early December to February. A few minutes after cedar pollen antigen was injected, this physician noted relief from his chronic neck and back pain. This quick response of allergy relief is often observed when PN is used for testing and treatment. Taking the specific dilution of mountain cedar twice weekly completely relieved his seasonal pain.
Of interest, this patient’s history revealed that as a college student and episodically during his early years in the navy he had acute onset of severe back pain, so severe he had difficulty even taking a deep breath. Treatment for these attacks was with analgesics and trigger point injections. In retrospect the patient remembered that these acute muscular skeletal episodes were always in the spring.
CASE STUDY 2
The patient underwent comprehensive allergy testing and was found to be sensitive to trees, grasses, weeds, dusts and molds. Testing individually with these allergens provoked symptoms of rhinitis but during testing for grasses she exacerbated overt pain in the area of her reported intermittent back aches attacks. Since beginning tree, grass, weed, dust and mold allergy extract treatment, she has demonstrated much improvement and also recognizes a relationship between exacerbation of back pain in grass pollinating seasons if she stops taking her allergy extracts.
This case demonstrates the principle of the previously injured organ or tissue becoming the target of the allergic response. (Personal communication. Allan D Lieberman, MD, COEM).
The allergic cascade begins with either mast cells or basophils, each having receptors for the antibody usually associated with allergy, IgE, and both cell types store mediators which will be involved in the allergic cascade .
The cascade begins with two Y - shaped antibodies, their Y - base sitting on the edge of a single mast cell. The arms of the two adjacent Y’s must be connected by an allergen for cascade initiation. This is described in immunology texts as two IgE antibodies becoming cross-linked, inducing degranulation and releasing mediators which cause the allergic reaction .
The mediators in allergy can be divided into early response mediators (Table 1) and late response mediators (Tables 2 and 3). Reviewing these tables underscores the complexity of the allergic reaction and belies the notion that the condition is “just allergy” and not a major concern.
Early response mediators are produced before degranulation of mast cells of basophils and are stored in the granules .
Late response mediators are produced after degranulation of mast cells or basophils .
One can easily visualize Dr. Joseph Miller’s simplification of the allergic process. He describes capillaries as a one - cell thick jigsaw puzzle of cells forming tubes with mast cells clinging to the outer sides of the tubes. When an allergen is introduced, each mast cell can “sting” its adjacent capillary cell. Chemical mediators from the mast cell force the local capillary cells to separate slightly, leaking both mediators and antigens into the blood stream. These newly formed gaps between the capillary cells now allow serum to leak into other tissues. The mediators can then cause symptoms by stimulating sensitive stress organs such as the brain, lungs, stomach, colon or the complex association of tissues in the lower back .
|Histamine||Increased vascular permeability; smooth muscle contraction|
|Serotonin||Increased vascular permeability; smooth muscle contraction|
|ECF-A||Eosinophil chemotaxis factor-A. Leukocyte migration|
|NCF-A||Neutrophil chemotactic factor. Neutrophil chemotaxis|
Degranulation of blood-vessel basement membrane; generation of complement split products
|PAF||Platelet activating factor affects platelet aggregation and degranulation; contraction of pulmonary smooth muscles.|
|SRS-A||Leukotrienes. Slow-reacting substance of anaphylaxis affects vasodilation; contraction of pulmonary smooth muscles; platelet aggregation.|
|Prostaglandins||Vasodilation; contraction of pulmonary smooth muscles; platelet aggregation.|
|Bradykinin||Increased vascular permeability; smooth muscle contraction.|
A cytokine whose action is initiated hours after the allergic insult.Activates macrophages, granulocytes, cytotoxic cells, and leukocytes .
|IL-1||A cytokine released by mast cells. Principal targets: T-cells, B-cells, macrophages, endothelium, tissue cells [7,10].|
A cytokine released by mast cells. Secreted by TH cells TH2 subset, macrophages,monocytes, fibroblasts and endothelial cells. Increases secretion of antibodies by plasmacells, togetherwithIL-1co-stimulates T-cell activation .
|SP||Substance P. A pain-producing neuropeptide produced by nerve cells .|
ALLERGY AND THE NERVOUS SYSTEM
The nervous and immune systems are coordinated so that dysregulation of one may affect the other. Some neuropeptides involved in this coordination are the neurotransmitters acetylcholine, serotonin, and substance P .
IL-1 is an inflammatory cytokines excreted in plasma and tissue fluids. It increases the production of substance P, a pain sensitivity mediator released from the terminals of some sensory nerves (Table 3) . Substance P not only amplifies nerve pain signals  but also induces histamine release from mast cells , muscles and joints . In addition it increases the production of TNF-α, which in association with substance P activates immune monocytes and macrophages .
IL-1 is associated with interactions in the Hypothalamic Pituitary Adrenal axis (HPA axis). The hypothalamus has the role to connect the nervous system and the endocrine system via the pituitary gland. Allergy sufferers secrete pro-inflammatory cytokines, including IL-1, in greater quantities than non-allergic patients. IL-1 activates the HPA axis, “firing the immune response” .
The mast cells involved in allergy contain preformed TNF-α granules . After tissue injury occurs, TNF-α, which is the primary inflammatory mediator in nerve injury, is also released by macrophages and nerve cells. This TNF-α release increases inflammation and prostaglandin formation which in turn increases the release of the neurotransmitter glutamate, enhancing nerve communication and pain .
IL-6 is synthesized in response to IL-1 and TNF-α  and acts at the site of inflammation by sensitizing afferent fibers and stimulating their release of prostaglandins . IL-6 is the primary chemical mediator involved in bone inflammation and pain .
Prostaglandins are inflammatory mediators which are released both during the allergic cascade and more generally by any inflammatory response, sensitize peripheral nociceptor terminals and generate local pain. Tissues adjacent to inflamed tissues may also become painful due to increased sensitization in the spinal cord [12,19].
THE BACK AS A TARGET ORGAN OF ALLERGY
Many unmyelinated nerve terminals are embedded in the interstitial sheaths of the intramuscular blood vessels in the lumbar system. The muscular nociceptive system is perivascular and involves both arteries and veins. These nociceptive receptors are irritated by either mechanical or chemical stimuli to the tissues in which they are embedded. If a chemical, such as histamine, achieves a critical concentration, it can irritate the nociceptive receptor system resulting in lower back pain .
Biochemical mediators are both cytokines and neuropeptides. Bradykinin, serotonin, histamine, acetylcholine, prostaglandins, and leukotrienes produced by the immune cells [21,22] as well as substance P produced by nerve cells , cause inflammation which in turn causes pain. While research has focused on single mediators such as a prostaglandin, Dr. Omoigui states the need to address instead the “inflammatory soup of biochemical mediators” that are present in all pain conditions, including back pain. After the inflammatory mediators are released they affect motor nerves that travel from the spinal cord to the muscles and can cause muscle tension, spasm and pain. Inhibition or suppression of the production of inflammatory mediators suppresses motor transmission. The result of less inflammation is less pain .
STOPPING THE PAIN
Written consent for publication was obtained from the patients or their relatives. Funding was provided by The Institute for Therapeutic Discovery, www.tiftd.org
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Citation:Killian S, McMichael J (2015) Seasonal Allergy Induced Back Pain: A Report of Two Cases. J Allergy Disord Ther 2: 005.
Copyright: © 2015 Sue Killian, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.