Nickel allergy

Nickel allergy
SpecialtyAllergology, immunology 
Edit this on Wikidata

Nickel allergy or nickel allergic contact dermatitis (Ni-ACD) is a form of allergic contact dermatitis (ACD) caused by exposure to the chemical element nickel. It typically causes a rash that is red and itchy and that may be bumpy or scaly. The main treatment is avoiding contact with nickel-releasing metals, such as wearing inexpensive jewelry.

Signs and symptoms

The most common sign of nickel allergy is inflammation of the skin at an area that comes into regular contact with nickel.[1] This often takes the form of a reddened patch of skin with raised bumps (papules) or small blisters (vesicles), and edema.[1] People with chronic dermatitis tend to have dry, scaly, and cracked skin at the site of contact.[1] These sites of inflammation (called "primary eruptions") can occur anywhere on the skin that contacts nickel, but are most common on the hands, face, or anywhere that contacts metal objects such as jewelry or metal clothes buttons.[1] Particularly high levels of nickel exposure can cause irritated patches of skin to appear at other sites on the body (called "secondary eruptions"). These typically occur at as blistering rashes on the hands, eyelids, and at the inside of flexing joints (inside the elbow, back of the knee, etc.).[1]

Ingestion of nickel may cause a systemic reaction, which can result in generalized inflammation of the skin across the body, small blisters in the hands, irritation inside the flexing joints (flexural eczema), and redness and irritation of both buttocks.[1]

Systemic contact dermatitis (SCD) is defined as a dermatitis occurring in an epi-cutaneously contact-sensitized person when exposed to haptens systemically such as orally, per rectum, intravesically, transcutaneously, intrauterinely, intravenously, or by inhalation.[2]

The pathophysiology of systemic nickel allergy syndrome (SNAS) is not well understood. The clinical course is determined by an immunological interplay between two types of T cells (Th1 and Th2 responses). SCD is often considered a subset of SNAS, but with only skin manifestations.[3] SNAS presents with an array of symptoms ranging from respiratory to generalized skin rash to gastrointestinal symptoms[4] A meta review evaluating SNAS found that 1% of patients sensitized to nickel reacted to the nickel content of a 'normal' diet, and with increasing doses of nickel more individuals reacted[5] SNAS is a multilayered immunological response demonstrating variance between individuals and doses of nickel exposure.

Causes

Nickel exposure

Nickel is both naturally abundant – it is the fifth most common element on earth – and widely used in industry and commercial goods.[1] Workplace nickel exposure is common in many industries, and the performance of normal work tasks can result in nickel skin levels sufficient to elicit dermatitis.[1] Within the workplace, individuals may be exposed to significant amounts of nickel, airborne from the combustion of fossil fuels or from contact with tools that are nickel plated.[6] Historically, workplaces where prolonged contact with soluble nickel has been high have shown high risks for allergic contact nickel dermatitis. For example, nickel dermatitis was common in the past among nickel platers.[7] Outbreaks of nickel allergy from consumer goods have been documented throughout the 20th century, with jewelry, stocking suspenders, and metallic buttons on blue jeans each resulting in dermatitis at the point of contact.[1] Nickel can also be present in food and drinking water; ingestion of increased nickel is not associated with systemic allergic disease, but is associated with flare-ups of dermatitis or aggravation of vesicular hand eczema.[1] Similarly, aggravation of dermatitis has been reported in response to nickel-containing surgical implants or dental gear.[1]

The risk of an object eliciting nickel allergy is linked to the amount of nickel released by its surface (and not to its total nickel content).[1] Suspected objects can be screened by wiping the surface with a 1% dimethylglyoxime solution that turns pink if more than 0.5 μg/cm2 per week is released by the surface.[1] Various methods exist to test the skin or nails for nickel exposure, typically relying on wiping the skin, then quantifying the nickel on the wipe via mass spectrometry.[1]

Physiology

Nickel allergy results in a skin response after the skin comes in contact with an item that releases a large amount of nickel from its surface. It is commonly associated with nickel-containing belt buckles coming into prolonged contact with the skin.[8][9][10] The skin reaction can occur at the site of contact, or sometimes spread beyond to the rest of the body. Free (released) nickel that is able to penetrate the skin is taken up by scavenger (dendritic) cells and then presented to the immune system T-Cells. With each subsequent exposure to nickel these T cells become stimulated and duplicate themselves. With enough exposure to nickel, the amassing clones of T-cells reach “threshold” and the skin develops a rash. The rash can appear as acute, subacute, or chronic eczema-like skin patches, primarily at the site of contact with the nickel (e.g., earlobe from nickel earrings). From the time of exposure, the rash usually appears within 12–120 hours and can last for 3–4 weeks or for the continued duration of nickel contact/exposure.[8]

Three simultaneous conditions must occur to trigger Ni-ACD:

  1. Direct skin contact with nickel-releasing item
  2. Prolonged skin contact with nickel-releasing item
  3. A sufficient amount of nickel is released and absorbed into the skin to cause a reaction[11]

The pathophysiology is divided into induction elicitation phases. Induction is the critical phase (immunological event) when skin contact to nickel results in antigen presentation to the T cells, and T cell duplication (cloning) occurs. The metal cation Ni++ is a low molecular weight hapten that easily penetrates the stratum corneum (top layer of skin). Nickel then binds to skin protein carriers creating an antigenic epitope.[12] The determining factor in sensitization is exposure of significant amounts of “free nickel”.[13] This is important because different metal alloys release different amounts of free nickel. The antigenic epitope is collected by dermal dendritic cells and Langerhans cells, the antigen-presenting cells (APC) of the skin, and undergo maturation and migration to regional lymph nodes. The complex is predominantly expressed on major histocompatibility complex (MHC) II, which activates and clonally expands naive CD4+ T cells.[14] Upon re-exposure these now primed T cells will be activated and massively recruited to the skin, resulting in the elicitation phase and the clinical presentation of Ni-ACD.

Although ACD has been considered a Th1 predominate process, recent studies highlight a more complex picture. In Ni-ACD other cells are involved including: Th17, Th22, Th1/IFN and the innate immune responses consistent with toll-like receptor 4.[15] [16]

Prevention

Nickel has a wide utility of application in manufactured metals because it is both strong and malleable, leading to ubiquitous presence and the potential for consumers to be in contact with it daily. However, for those who have the rash of allergic contact dermatitis (ACD) due to a nickel allergy, it can be a challenge to avoid. Foods, common kitchen utensils, cell phones, jewelry, and many other items may contain nickel and be a source of irritation due to the allergic reaction caused by the absorption of free released nickel through direct and prolonged contact. The most appropriate measure for nickel-allergic persons is to prevent contact with the allergen.

In 2011, researchers showed that applying a thin layer of glycerine emollient containing nanoparticles of either calcium carbonate or calcium phosphate on an isolated piece of pig skin (in vitro) and on the skin of mice (in vivo) prevents the penetration of nickel ions into the skin. The nanoparticles capture nickel ions by cation exchange, and remain on the surface of the skin, allowing them to be removed by simple washing with water. Approximately 11-fold fewer nanoparticles by mass are required to achieve the same efficacy as the chelating agent ethylenediamine tetraacetic acid. Using nanoparticles with diameters smaller than 500 nm in topical creams may be an effective way to limit the exposure to metal ions that can cause skin irritation'.[17]

Pre-emptive avoidance strategies (PEAS) might ultimately lower the sensitization rates of children who would suffer from ACD[18] It is theorized that prevention of exposure to nickel early on could reduce the number of those that are sensitive to nickel by one-quarter to one-third. Identification of the many sources of nickel is vital to understanding the nickel sensitization story, food like chocolate and fish, zippers, buttons, cell phones and even orthodontic braces and eyeglass frames might contain nickel. Items that contain sentimental value (heirlooms, wedding rings) could be treated with an enamel or rhodium plating.[19]

Sensitized individuals may check product labels or contact the manufacturer or retailer regarding possible nickel content.[20] The Dermatitis Academy has created an educational website to provide more information about nickel, including information about prevention, exposure, sources, and general information about nickel allergy. These resources provide guidance in a prevention initiative for children worldwide.

Diagnosis

Nickel allergy it typically diagnosed by patch testing – applying a patch with 2.5% (in North America) or 5% (in Europe) nickel sulfate to the upper back and looking for irritation on the skin.[1] As with other causes of allergic contact dermatitis, patches containing several common allergens are typically applied to the back for 48 hours, removed, then the spots examined for allergic reactions 2 to 5 days later.[21]

Treatment

Once a nickel allergy is detected, the best treatment is avoidance of nickel-releasing items. The top 13 categories that contain nickel include beauty accessories, eyeglasses, money, cigarettes, clothes, kitchen and household, electronics and office equipment, metal utensils, aliment, jewelry, batteries, orthodontic and dental appliances, and medical equipment.[22] Other than strict avoidance of items that release free nickel, there are other treatment options for reduction of exposure. The first step is to limit friction between skin and metallic items. Susceptible people may try to limit sweating while wearing nickel items, to reduce nickel release and thus decrease chances for developing sensitization or allergy. Another option is to shield electronics, metal devices, and tools with fabric, plastic, or acrylic coverings.[22]

There are dimethylglyoxime test kits that can be very helpful to check for nickel release from items prior to purchasing.[23] The American Contact Dermatitis Society 'find a provider' resource can help identify clinicians with training in providing guidance lists of safe items.[24] In addition to avoidance, healthcare providers may prescribe additional creams or medications to help relieve the skin reaction.

Epidemiology

Nickel allergy is the most common contact allergy in industrialized countries, affecting around 8% to 19% of adults and 8% to 10% of children.[1] women are affected 4–10 times as frequently as men.[1]

Regulation

As nickel can be harmful to skin, its use in daily products must be regulated. A safety directive has been in place in Europe since 2004. Denmark in 1980, and then shortly after the European Union (EU), enacted legislation that limited the amount of free nickel in consumer products that come in contact with the skin. This resulted in significantly decreased rates of sensitization among Danish children 0 to 18 years of age from 24.8% to 9.2% between 1985 and 1998, with similar reductions in sensitization throughout the EU.[25][26]

No such directive exists in the United States, but efforts are under way to mandate safe use guidelines for nickel. In August 2015, the American Academy of Dermatology (AAD) adopted a nickel safety position paper.[27] The exact prevalence of Ni-ACD in the general population in the US is largely unknown. However, current estimates gauge that roughly 2.5 million US adults and 250,000 children suffer from nickel allergy, which costs an estimated $5.7 billion per year for treatment of symptoms.[28] Loma Linda University, Nickel Allergy Alliance, and Dermatitis Academy created the first open access self-reported patient registry to record nickel allergy prevalence data in the US.[ref 23]

History

In the 17th century, copper miners in Saxony, Germany, began to experience irritation caused by a "dark red ore". Since the substance, which would later be called nickel, led to many ailments, they believed it to be protected by "goblins", and called it "Goblin's Copper".[29] Josef Jadassohn described the first case of metal contact dermatitis in 1895, to a mercury-based therapeutic cream, and confirmed the cause by epi-cutaneous patch testing.[30] In the next century nickel began to be mass-produced for jewelry worldwide due to its cheap cost, resistance to corrosion and high supply.

In 1979 a large comprehensive study of healthy US volunteers found that 9% had been unknowingly sensitized to nickel.[31] As of 2008, that number has tripled.[32] Most importantly, nickel allergy among children is increasing, with an estimated 250,000 children sensitized to nickel.[33]

Published literature shows an exponential increase in reported nickel allergy cases.[34] The North American Contact Dermatitis Group (NACDG) patch tested 5,085 adults, presenting with eczema-like symptoms, showing 19.5% had a positive reaction to nickel.[35] Nickel allergy is also more prevalent in women (17.1%) than men (3%), possibly due to cultural norms related to jewelry and ear piercings and therefore increased exposure to nickel.[36] In order to investigate the current prevalence of nickel, Loma Linda University, Nickel Allergy Alliance, and Dermatitis Academy,[37] are conducting a self-reporting nickel allergy-dermatitis survey.[38]


References

  1. 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 Ahlström MG, Thyssen JP, Wennervaldt M, Menné T, Johansen JD (October 2019). "Nickel allergy and allergic contact dermatitis: A clinical review of immunology, epidemiology, exposure, and treatment". Contact Dermatitis. 81 (4): 227–241. doi:10.1111/cod.13327. PMID 31140194.
  2. ↑ Veien NK (December 2011). "Systemic contact dermatitis". International Journal of Dermatology. 50 (12): 1445–56. doi:10.1111/j.1365-4632.2011.05104.x. PMID 22097987.
  3. ↑ Di Gioacchino M, Ricciardi L, De Pità O, Minelli M, Patella V, Voltolini S, Di Rienzo V, Braga M, Ballone E, Mangifesta R, Schiavino D (February 2014). "Nickel oral hyposensitization in patients with systemic nickel allergy syndrome". Annals of Medicine. 46 (1): 31–7. doi:10.3109/07853890.2013.861158. PMC 4673509. PMID 24256166.
  4. ↑ Matiz C, Jacob SE (2011). "Systemic contact dermatitis in children: how an avoidance diet can make a difference". Pediatric Dermatology. 28 (4): 368–74. doi:10.1111/j.1525-1470.2010.01130.x. PMID 20807367.
  5. ↑ Jensen CS, Menné T, Johansen JD (February 2006). "Systemic contact dermatitis after oral exposure to nickel: a review with a modified meta-analysis". Contact Dermatitis. 54 (2): 79–86. doi:10.1111/j.0105-1873.2006.00773.x. PMID 16487279.
  6. ↑ Grandjean P (1984). "Human exposure to nickel". IARC Scientific Publications (53): 469–85. PMID 6241927.
  7. ↑ "Knowledge of properties and safe use of substances | Nickel Institute". www.nickelinstitute.org.
  8. 1 2 Usatine R (May 2001). "A belt buckle allergy?". The Western Journal of Medicine. 174 (5): 307–8. doi:10.1136/ewjm.174.5.307. PMC 1071380. PMID 11342499.
  9. ↑ "Nickel allergy - Symptoms and causes".
  10. ↑ "Nickel Contact Dermatitis Picture Image on MedicineNet.com".
  11. ↑ "What Do You Need To Know About Nickel Allergy?" (PDF).
  12. ↑ Lu L, Vollmer J, Moulon C, Weltzien HU, Marrack P, Kappler J (March 2003). "Components of the ligand for a Ni++ reactive human T cell clone". The Journal of Experimental Medicine. 197 (5): 567–74. doi:10.1084/jem.20021762. PMC 2193829. PMID 12615898.
  13. ↑ Silverberg NB, Licht J, Friedler S, Sethi S, Laude TA (2002). "Nickel contact hypersensitivity in children". Pediatric Dermatology. 19 (2): 110–3. doi:10.1046/j.1525-1470.2002.00057.x. PMID 11994170.
  14. ↑ Girolomoni G, Gisondi P, Ottaviani C, Cavani A (April 2004). "Immunoregulation of allergic contact dermatitis". The Journal of Dermatology. 31 (4): 264–70. doi:10.1111/j.1346-8138.2004.tb00671.x. PMID 15187320.
  15. ↑ Peana M, Zdyb K, Medici S, Pelucelli A, Simula G, Gumienna-Kontecka E, Zoroddu MA (December 2017). "Ni(II) interaction with a peptide model of the human TLR4 ectodomain". Journal of Trace Elements in Medicine and Biology. 44: 151–160. doi:10.1016/j.jtemb.2017.07.006. PMID 28965571.
  16. ↑ Dhingra N, Shemer A, Correa da Rosa J, Rozenblit M, Fuentes-Duculan J, Gittler JK, Finney R, Czarnowicki T, Zheng X, Xu H, Estrada YD, Cardinale I, Suárez-Fariñas M, Krueger JG, Guttman-Yassky E (August 2014). "Molecular profiling of contact dermatitis skin identifies allergen-dependent differences in immune response". The Journal of Allergy and Clinical Immunology. 134 (2): 362–72. doi:10.1016/j.jaci.2014.03.009. PMID 24768652.
  17. ↑ Vemula PK, Anderson RR, Karp JM (2011). "Nanoparticles reduce nickel allergy by capturing metal ions". Nature Nanotechnology. 6 (5): 291–5. Bibcode:2011NatNa...6..291V. doi:10.1038/nnano.2011.37. PMID 21460828.
  18. ↑ Hill H, Goldenberg A, Golkar L, Beck K, Williams J, Jacob SE (2016). "Pre-Emptive Avoidance Strategy (P.E.A.S.) - addressing allergic contact dermatitis in pediatric populations". Expert Review of Clinical Immunology. 12 (5): 551–61. doi:10.1586/1744666X.2016.1142373. PMID 26764601.
  19. ↑ Hill H, Goldenberg A, Sheehan MP, Patel A, Jacob SE (2015). "Nickel-Free Alternatives Raise Awareness". Dermatitis : Contact, Atopic, Occupational, Drug. 26 (6): 245–53. doi:10.1097/DER.0000000000000135. PMID 26551602.
  20. ↑ Kerr M, Cafasso J (11 January 2016). Weatherspoon D (ed.). "Nickel Allergies Symptoms, Tests, and Treatment". Healthline.
  21. ↑ Nixon RL, Allnutt KJ, Diepgen TL (2020). "Contact Dermatitis". Middleton's Allergy: Principles and Practice (9 ed.). Elsevier. pp. 553–561. ISBN 978-0-323-54424-5.
  22. 1 2 "Be Nickel Aware" (PDF). Dermatitis Academy. Retrieved 2018-06-05.
  23. ↑ Testing For Nickel www.dermatitisacademy.com, accessed 7 October 2021
  24. ↑ Find a Provider www.contactderm.org, accessed 7 October 2021
  25. ↑ Johansen JD, Menné T, Christophersen J, Kaaber K, Veien N (March 2000). "Changes in the pattern of sensitization to common contact allergens in denmark between 1985-86 and 1997-98, with a special view to the effect of preventive strategies". The British Journal of Dermatology. 142 (3): 490–5. doi:10.1046/j.1365-2133.2000.03362.x. PMID 10735956.
  26. ↑ Thyssen JP, Uter W, McFadden J, Menné T, Spiewak R, Vigan M, Gimenez-Arnau A, Lidén C (March 2011). "The EU Nickel Directive revisited--future steps towards better protection against nickel allergy". Contact Dermatitis. 64 (3): 121–5. doi:10.1111/j.1600-0536.2010.01852.x. PMID 21226718.
  27. ↑ "Position Statement on Nickel Sensitivity" (PDF). American Academy of Dermatology.
  28. ↑ Jacob SE, Goldenberg A, Pelletier JL, Fonacier LS, Usatine R, Silverberg N (2015). "Nickel Allergy and Our Children's Health: A Review of Indexed Cases and a View of Future Prevention". Pediatric Dermatology. 32 (6): 779–785. doi:10.1111/pde.12639. PMID 26212605.
  29. ↑ Baldwin WH (1931). "The story of nickel. How "old nick's" gnomes were outwitted". Journal of Chemical Education. 8 (9): 1749. Bibcode:1931JChEd...8.1749B. doi:10.1021/ed008p1749.
  30. ↑ Jadassohn J (1895). "Zur Kenntnis der medikamentösen Dermatosen". Verhandlungen der Deutschen Dermatologischen Gesellschaft. Fünfter Kongress, Raz (in German). Berlin: Julius Springer. pp. 103–129.
  31. ↑ Prystowsky SD, Allen AM, Smith RW, Nonomura JH, Odom RB, Akers WA (August 1979). "Allergic contact hypersensitivity to nickel, neomycin, ethylenediamine, and benzocaine. Relationships between age, sex, history of exposure, and reactivity to standard patch tests and use tests in a general population". Archives of Dermatology. 115 (8): 959–62. doi:10.1001/archderm.1979.04010080023015. PMID 157103.
  32. ↑ Rietschel RL, Fowler JF, Warshaw EM, Belsito D, DeLeo VA, Maibach HI, Marks JG, Mathias CG, Pratt M, Sasseville D, Storrs FJ, Taylor JS, Zug KA (2008). "Detection of nickel sensitivity has increased in North American patch-test patients". Dermatitis. 19 (1): 16–9. doi:10.2310/6620.2008.06062. PMID 18346391.
  33. ↑ Jacob SE, Goldenberg A, Pelletier JL, Fonacier LS, Usatine R, Silverberg N (2015). "Nickel Allergy and Our Children's Health: A Review of Indexed Cases and a View of Future Prevention". Pediatric Dermatology. 32 (6): 779–85. doi:10.1111/pde.12639. PMID 26212605.
  34. ↑ Goldenberg A, Vassantachart J, Lin EJ, Lampel HP, Jacob SE (2015). "Nickel Allergy in Adults in the U.S.: 1962 to 2015". Dermatitis. 26 (5): 216–23. doi:10.1097/der.0000000000000130. PMID 26177034.
  35. ↑ Fransway AF, Zug KA, Belsito DV, Deleo VA, Fowler JF, Maibach HI, Marks JG, Mathias CG, Pratt MD, Rietschel RL, Sasseville D, Storrs FJ, Taylor JS, Warshaw EM, Dekoven J, Zirwas M (2013). "North American Contact Dermatitis Group patch test results for 2007-2008". Dermatitis. 24 (1): 10–21. doi:10.1097/der.0b013e318277ca50. PMID 23340394.
  36. ↑ Thyssen JP, Menné T (February 2010). "Metal allergy--a review on exposures, penetration, genetics, prevalence, and clinical implications". Chemical Research in Toxicology. 23 (2): 309–18. doi:10.1021/tx9002726. PMID 19831422.
  37. ↑ dermatitisacademy www.dermatitisacademy.com, accessed 7 October 2021
  38. ↑ forms Loma Linda University (restricted access site)

Further reading

This article is issued from Offline. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.