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'''Enzyme potentiated desensitization''', or EPD, is a treatment for allergies developed in the [[1960s]] by Dr. Len McEwen in the [[United Kingdom]]. EPD uses much lower doses of antigens than conventional treatment, with the addition of an enzyme, beta glucuronidase. EPD is available in the United Kingdom and [[Canada]] for the treatment of [[hay fever]], [[food allergy and intolerance]] and environmental allergies, and was available in the [[United States]] until [[2001]], when the [[Food and Drug Administration]] revoked approval for an investigative study which it had previously sanctioned which had allowed EPD to be imported into the USA without being licensed. The reason cited for revoking approval were:-
'''Enzyme potentiated desensitization''', or EPD, is a treatment for allergies developed in the [[1960s]] by Dr. Len McEwen in the [[United Kingdom]]. EPD uses much lower doses of antigens than conventional treatment, with the addition of an enzyme, beta glucuronidase. EPD is available in the United Kingdom and [[Canada]] for the treatment of [[hay fever]], [[food allergy and intolerance]] and environmental allergies, and was available in the [[United States]] until [[2001]], when the [[Food and Drug Administration]] revoked approval for an investigative study which it had previously sanctioned which had allowed EPD to be imported into the USA without being licensed. The reason given for revoking approval was that complex mixtures of allergens used in EPD treatments were not allowed under FDA rules. Since then the FDA has banned importation of EPD<ref>[http://www.fda.gov/ora/fiars/ora_import_ia5715.html FDA Import Alert]</ref> for the following reasons:-.
* EPD is not licensed.
* that complex mixtures of allergens such as used in EPD treatments were not allowed under FDA rules
* the labeling of the medicine does not contain adequate directions for use. See <ref>[http://www.fda.gov/ora/fiars/ora_import_ia5715.html FDA Import Alert]</ref>. (EPD is only supplied to doctors who have been through a one week training course, and instructions supplied with the medicine would not be adequate)
* the labeling of the medicine does not contain adequate directions for use. (EPD is only supplied to doctors who have been through a one week training course, and instructions supplied with the medicine would not be adequate)

* EPD is not licensed. See <ref>[http://www.fda.gov/ora/fiars/ora_import_ia5715.html FDA Import Alert]</ref>
EPD is under development for the treatment of [[autoimmune disease]] by a United Kingdom company called Epidyme<ref>[http://www.epidyme.com Epidyme website] use of EPD to treat autoimmune diseases.</ref> which has been granted a United Kingdom [[patent]]. There are encouraging results <ref>[http://www.epidyme.com/ra.html EPD treatment of rheumatoid arthritis proof of concept results on Epidyme website] use of EPD to treat autoimmune diseases.</ref> in an experimental model of [[rheumatoid arthritis]] and work on treatments for further [[autoimmune diseases]] is planned. Suitable autoimmune diseases for possible future EPD research include [[multiple sclerosis]], [[type 1 diabetes]] and [[myasthenia gravis]].
EPD is under development for the treatment of [[autoimmune disease]] by a United Kingdom company called Epidyme<ref>[http://www.epidyme.com Epidyme website] use of EPD to treat autoimmune diseases.</ref> which has been granted a United Kingdom [[patent]]. There are encouraging results <ref>[http://www.epidyme.com/ra.html EPD treatment of rheumatoid arthritis proof of concept results on Epidyme website] use of EPD to treat autoimmune diseases.</ref> in an experimental model of [[rheumatoid arthritis]] and work on treatments for further [[autoimmune diseases]] is planned. Suitable autoimmune diseases for possible future EPD research include [[multiple sclerosis]], [[type 1 diabetes]] and [[myasthenia gravis]].


Revision as of 11:49, 29 July 2007

Enzyme potentiated desensitization, or EPD, is a treatment for allergies developed in the 1960s by Dr. Len McEwen in the United Kingdom. EPD uses much lower doses of antigens than conventional treatment, with the addition of an enzyme, beta glucuronidase. EPD is available in the United Kingdom and Canada for the treatment of hay fever, food allergy and intolerance and environmental allergies, and was available in the United States until 2001, when the Food and Drug Administration revoked approval for an investigative study which it had previously sanctioned which had allowed EPD to be imported into the USA without being licensed. The reason given for revoking approval was that complex mixtures of allergens used in EPD treatments were not allowed under FDA rules. Since then the FDA has banned importation of EPD[1] for the following reasons:-.

  • EPD is not licensed.
  • the labeling of the medicine does not contain adequate directions for use. (EPD is only supplied to doctors who have been through a one week training course, and instructions supplied with the medicine would not be adequate)

EPD is under development for the treatment of autoimmune disease by a United Kingdom company called Epidyme[2] which has been granted a United Kingdom patent. There are encouraging results [3] in an experimental model of rheumatoid arthritis and work on treatments for further autoimmune diseases is planned. Suitable autoimmune diseases for possible future EPD research include multiple sclerosis, type 1 diabetes and myasthenia gravis.

EPD treatment

The enzyme beta glucuronidase appears to potentiate the desensitizing effect of a small dose of allergen. The quantities of both are smaller than those occurring naturally in the body, but not so small that they can be regarded as homeopathic. Intradermal injections are used. The treatment takes 3-4 weeks before any effect is seen. For food and environmental allergies and intolerances treatments are typically given at two monthly intervals at first, but the interval between treatments is gradually lengthened. Hay fever is treated with two shots of EPD outside the pollen season.

Mechanism for EPD

The treatment uses dilutions of allergen and enzyme to which T-regulatory lymphocytes are believed to respond by favouring desensitization, or down-regulation, rather than sensitization. Once activated these lymphocytes travel to lymph nodes and reproduce or stimulate similar T-lymphocytes.

Evidence for the Effectiveness of EPD

EPD is considered experimental by some doctors and allergists. However, there is evidence for the efficacy of EPD in the treatment of hay fever and other conditions as a result of nine placebo-controlled, double-blind trials (the gold standard of proof) involving 271 patients. These trials showed a significant improvement in the symptoms with probabilities of 0.001 to 0.01 (a chance of one in a thousand to one in a hundred that the results of the trial would be seen by chance alone assuming EPD had no effect),[4] [5] [6] [7] [8] [9] [10] [11]. However, one trial involving 183 patients published in the British Medical Journal showed no overall effect.[12]. Dr Len McEwen, inventor of EPD, speculated [13] that the reason for the failure might have been that the beta glucuronidase enzyme preparation was inadvertently heated or frozen during storage in the hospital pharmacy, as it is sensitive to the storage temperature and enzyme from the same manufactured batch had been used to treat a number of patients successfully. However, there is no evidence available after the event to test this theory as the remaining trial materials were destroyed immediately the trial ended.

Safety of EPD

While the efficacy of EPD is sometimes the subject of controversy among the medical community, the safety of EPD is demonstrated in one study under the control of an Investigational Review Board and reported by the American EPD Society. 5,400 patients received at least 3 doses of EPD with no severe reactions reported [14]. No serious complications have been reported in more than 300,000 doses of EPD given since 1966.

Comparison of EPD with conventional escalating-dose immunotherapy (hyposensitization)

By contrast uncontrolled use of conventional (escalating dose) immunotherapy (hyposensitization not EPD) for general allergic conditions was believed to be responsible for at least 29 deaths in the UK, and is now banned in the United Kingdom except in hospital under close observation.[15]. A working party of the British Society for Allergy and Clinical Immunology reviewed the role of conventional high dose specific allergen immunotherapy (not EPD) in the treatment of allergic disease and recommends high dose specific allergen immunotherapy for treating summer hay fever uncontrolled by conventional medication and for wasp and bee venom hypersensitivity. For the recommended indications the risk:benefit ratio was found to be acceptable for conventional immunotherapy provided patients are carefully selected; in particular, patients with asthma should be excluded and injections should be given only by allergists experienced in this form of treatment in a clinic where resuscitative facilities are available and patients remain symptom free for an observation period after injection which is sufficient to detect all serious adverse reactions.[16]

Conventional escalating-dose immunotherapy (not EPD) has been used to treat tens of millions of people in the United States with a death rate of less than one in one million according to the American Academy of Allergy, Asthma, and Immunology [citation needed].

Restrictions on EPD

EPD has not been developed for treatment of allergy to insect stings (for which convenventional immunotherapy is recommended), nor for contact dermatitis and allergy to drugs.[17]. It is not FDA approved.

References

  1. ^ FDA Import Alert
  2. ^ Epidyme website use of EPD to treat autoimmune diseases.
  3. ^ EPD treatment of rheumatoid arthritis proof of concept results on Epidyme website use of EPD to treat autoimmune diseases.
  4. ^ Brostoff J., Fell P. (1990). "A single dose desensitisation for summer hay fever". Eur. J. Clin Pharmacol. 38: 77–79.
  5. ^ Astarita C., Scala G., Spoviero S., Franseze A. (1996). "Effect of enzyme potentiated desensitisation in the treatment of pollenosis : A double-blind placebo-controlled trial". J. Invest. Allergol. Clin. lmmunol. 6 (4): 248–255.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  6. ^ Longo G., PoIi F., Bertoli G. (1992). "Clinical efficacy of a new hyposensitising treatment, EPD (Enzyme Potentiated Desensitisation) in the therapy of pollenosis". Riforma Med. (107): 171–176.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  7. ^ Angelini G., Curatoli G., D’Argento V., Vena G. A. Pollinosi (1993). "Una nuova metodica di immunoterapia. Med. J. Surg. Med": 253-256. {{cite journal}}: Cite journal requires |journal= (help)CS1 maint: multiple names: authors list (link)
  8. ^ Di Stanislao C.. Di Berardino L., Bianchi I., Bologna G. (1997). "A double-blind, placebo-controlled study of preventive immunotherapy with EPD in the treatment of seasonal allergic disease". Allergie et lmmunologie. 30 (2): 39-42.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  9. ^ Caramia G., Franceschini F., Cimarelli Z.A., Ciucchi M.S., Gagliardini R., Rufllni E. (1996). "The efficacy of EPD, a new immunotherapy, in the treatment of allergic diseases in children". Allergie et lmmunologie. 28 (9): 308-310.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  10. ^ Di Stanislao C., Angelini F.; et al. (2002). "Beta glucuronidase short-term immunotherapy prevents seasonal rhinoconjunctivitis in grass pollen allergic patients by modifying dendritic cell phenotype". Allergy. 57 (Suppl 73): 76–77. {{cite journal}}: Explicit use of et al. in: |author= (help)
  11. ^ Boscolo M. A., Brivio G. "E.P.D. preventive therapy (McEwen method) vs. placebo: a double-blind trial". Poster presentation. European Congress of Allergy & Clinical Immunology. Brussels, July 1999.
  12. ^ Radcliffe M. J., Lewith G. T., Turner R. G., Prescott P., Church M. K., Holgate S. T. (2003). "Enzyme potentiated desensitisation in treatment of seasonal allergic rhinitis: double blind randomised controlled study". British Medical Journal. (327 2 August.): 251–254.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  13. ^ Epidyme website Enzyme Potentiated Desensitisation (EPD) A promising low-dose method of immunotherapy Dr. Len McEwen BM., BCh. unpublished paper.
  14. ^ Shrader, W A (2001). "The American EPD Study: 1993–2000" (PDF). White Paper for United States Senators and Representatives. Enzyme Potentiated Desensitization (EPD). p. 14. Retrieved 2006-09-16. {{cite web}}: Unknown parameter |coauthors= ignored (|author= suggested) (help); Unknown parameter |month= ignored (help)
  15. ^ JA Douglass, FC Thien and RE O'Hehir (1997). "Immunotherapy in asthma". Thorax. (52): 22–29.
  16. ^ AJ Frew (1993). "Injection immunotherapy. British Society for Allergy and Clinical Immunology Working Party". BMJ. (307): 919–23.
  17. ^ L.M. McEwen "Enzyme Potentiated Desensistization" (patient pink handbook) 1993
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