Tea tree oil: contact allergy and chemical composition
Summary In this article, contact allergy to, and the chemical composition of, tea tree oil (TTO) are reviewed. This essential oil is a popular remedy for many skin diseases, and may be used as neat oil or be present in cosmetics, topical pharmaceuticals and household products. Of all essential oils,...
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| Published in: | Contact dermatitis Vol. 75; no. 3; pp. 129 - 143 |
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| Main Authors: | , |
| Format: | Journal Article |
| Language: | English |
| Published: |
Oxford, UK
Blackwell Publishing Ltd
01.09.2016
Wiley Subscription Services, Inc |
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| ISSN: | 0105-1873, 1600-0536, 1600-0536 |
| Online Access: | Get full text |
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| Abstract | Summary
In this article, contact allergy to, and the chemical composition of, tea tree oil (TTO) are reviewed. This essential oil is a popular remedy for many skin diseases, and may be used as neat oil or be present in cosmetics, topical pharmaceuticals and household products. Of all essential oils, TTO has caused most (published) allergic reactions since the first cases were reported in 1991. In routine testing, prevalences of positive patch test reactions have ranged from 0.1% to 3.5%. Nearly 100 allergic patients have been described in case reports and case series. The major constituents of commercial TTO are terpinen‐4‐ol, γ‐terpinene, 1,8‐cineole, α‐terpinene, α‐terpineol, p‐cymene, and α‐pinene. Fresh TTO is a weak to moderate sensitizer, but oxidation increases its allergenic potency. The major sensitizers appear to be ascaridole, terpinolene, α‐terpinene, 1,2,4‐trihydroxymenthane, α‐phellandrene, and limonene. The clinical picture of allergic contact dermatitis caused by TTO depends on the products used. Most reactions are caused by the application of pure oil; cosmetics are the culprits in a minority of cases. Patch testing may be performed with 5% oxidized TTO. Co‐reactivity to turpentine oil is frequent, and there is an overrepresentation of reactions to fragrance mix I, Myroxylon pereirae, colophonium, and other essential oils. |
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| AbstractList | In this article, contact allergy to, and the chemical composition of, tea tree oil (TTO) are reviewed. This essential oil is a popular remedy for many skin diseases, and may be used as neat oil or be present in cosmetics, topical pharmaceuticals and household products. Of all essential oils, TTO has caused most (published) allergic reactions since the first cases were reported in 1991. In routine testing, prevalences of positive patch test reactions have ranged from 0.1% to 3.5%. Nearly 100 allergic patients have been described in case reports and case series. The major constituents of commercial TTO are terpinen-4-ol, γ-terpinene, 1,8-cineole, α-terpinene, α-terpineol, p-cymene, and α-pinene. Fresh TTO is a weak to moderate sensitizer, but oxidation increases its allergenic potency. The major sensitizers appear to be ascaridole, terpinolene, α-terpinene, 1,2,4-trihydroxymenthane, α-phellandrene, and limonene. The clinical picture of allergic contact dermatitis caused by TTO depends on the products used. Most reactions are caused by the application of pure oil; cosmetics are the culprits in a minority of cases. Patch testing may be performed with 5% oxidized TTO. Co-reactivity to turpentine oil is frequent, and there is an overrepresentation of reactions to fragrance mix I, Myroxylon pereirae, colophonium, and other essential oils. In this article, contact allergy to, and the chemical composition of, tea tree oil (TTO) are reviewed. This essential oil is a popular remedy for many skin diseases, and may be used as neat oil or be present in cosmetics, topical pharmaceuticals and household products. Of all essential oils, TTO has caused most (published) allergic reactions since the first cases were reported in 1991. In routine testing, prevalences of positive patch test reactions have ranged from 0.1% to 3.5%. Nearly 100 allergic patients have been described in case reports and case series. The major constituents of commercial TTO are terpinen-4-ol, [gamma]-terpinene, 1,8-cineole, [alpha]-terpinene, [alpha]-terpineol, p- cymene, and [alpha]-pinene. Fresh TTO is a weak to moderate sensitizer, but oxidation increases its allergenic potency. The major sensitizers appear to be ascaridole, terpinolene, [alpha]-terpinene, 1,2,4-trihydroxymenthane, [alpha]-phellandrene, and limonene. The clinical picture of allergic contact dermatitis caused by TTO depends on the products used. Most reactions are caused by the application of pure oil; cosmetics are the culprits in a minority of cases. Patch testing may be performed with 5% oxidized TTO. Co-reactivity to turpentine oil is frequent, and there is an overrepresentation of reactions to fragrance mix I, Myroxylon pereirae , colophonium, and other essential oils. In this article, contact allergy to, and the chemical composition of, tea tree oil ( TTO ) are reviewed. This essential oil is a popular remedy for many skin diseases, and may be used as neat oil or be present in cosmetics, topical pharmaceuticals and household products. Of all essential oils, TTO has caused most (published) allergic reactions since the first cases were reported in 1991. In routine testing, prevalences of positive patch test reactions have ranged from 0.1% to 3.5%. Nearly 100 allergic patients have been described in case reports and case series. The major constituents of commercial TTO are terpinen‐4‐ol, γ‐terpinene, 1,8‐cineole, α‐terpinene, α‐terpineol, p‐ cymene, and α‐pinene. Fresh TTO is a weak to moderate sensitizer, but oxidation increases its allergenic potency. The major sensitizers appear to be ascaridole, terpinolene, α‐terpinene, 1,2,4‐trihydroxymenthane, α‐phellandrene, and limonene. The clinical picture of allergic contact dermatitis caused by TTO depends on the products used. Most reactions are caused by the application of pure oil; cosmetics are the culprits in a minority of cases. Patch testing may be performed with 5% oxidized TTO . Co‐reactivity to turpentine oil is frequent, and there is an overrepresentation of reactions to fragrance mix I , M yroxylon pereirae , colophonium, and other essential oils. Summary In this article, contact allergy to, and the chemical composition of, tea tree oil (TTO) are reviewed. This essential oil is a popular remedy for many skin diseases, and may be used as neat oil or be present in cosmetics, topical pharmaceuticals and household products. Of all essential oils, TTO has caused most (published) allergic reactions since the first cases were reported in 1991. In routine testing, prevalences of positive patch test reactions have ranged from 0.1% to 3.5%. Nearly 100 allergic patients have been described in case reports and case series. The major constituents of commercial TTO are terpinen‐4‐ol, γ‐terpinene, 1,8‐cineole, α‐terpinene, α‐terpineol, p‐cymene, and α‐pinene. Fresh TTO is a weak to moderate sensitizer, but oxidation increases its allergenic potency. The major sensitizers appear to be ascaridole, terpinolene, α‐terpinene, 1,2,4‐trihydroxymenthane, α‐phellandrene, and limonene. The clinical picture of allergic contact dermatitis caused by TTO depends on the products used. Most reactions are caused by the application of pure oil; cosmetics are the culprits in a minority of cases. Patch testing may be performed with 5% oxidized TTO. Co‐reactivity to turpentine oil is frequent, and there is an overrepresentation of reactions to fragrance mix I, Myroxylon pereirae, colophonium, and other essential oils. In this article, contact allergy to, and the chemical composition of, tea tree oil (TTO) are reviewed. This essential oil is a popular remedy for many skin diseases, and may be used as neat oil or be present in cosmetics, topical pharmaceuticals and household products. Of all essential oils, TTO has caused most (published) allergic reactions since the first cases were reported in 1991. In routine testing, prevalences of positive patch test reactions have ranged from 0.1% to 3.5%. Nearly 100 allergic patients have been described in case reports and case series. The major constituents of commercial TTO are terpinen-4-ol, γ-terpinene, 1,8-cineole, α-terpinene, α-terpineol, p-cymene, and α-pinene. Fresh TTO is a weak to moderate sensitizer, but oxidation increases its allergenic potency. The major sensitizers appear to be ascaridole, terpinolene, α-terpinene, 1,2,4-trihydroxymenthane, α-phellandrene, and limonene. The clinical picture of allergic contact dermatitis caused by TTO depends on the products used. Most reactions are caused by the application of pure oil; cosmetics are the culprits in a minority of cases. Patch testing may be performed with 5% oxidized TTO. Co-reactivity to turpentine oil is frequent, and there is an overrepresentation of reactions to fragrance mix I, Myroxylon pereirae, colophonium, and other essential oils.In this article, contact allergy to, and the chemical composition of, tea tree oil (TTO) are reviewed. This essential oil is a popular remedy for many skin diseases, and may be used as neat oil or be present in cosmetics, topical pharmaceuticals and household products. Of all essential oils, TTO has caused most (published) allergic reactions since the first cases were reported in 1991. In routine testing, prevalences of positive patch test reactions have ranged from 0.1% to 3.5%. Nearly 100 allergic patients have been described in case reports and case series. The major constituents of commercial TTO are terpinen-4-ol, γ-terpinene, 1,8-cineole, α-terpinene, α-terpineol, p-cymene, and α-pinene. Fresh TTO is a weak to moderate sensitizer, but oxidation increases its allergenic potency. The major sensitizers appear to be ascaridole, terpinolene, α-terpinene, 1,2,4-trihydroxymenthane, α-phellandrene, and limonene. The clinical picture of allergic contact dermatitis caused by TTO depends on the products used. Most reactions are caused by the application of pure oil; cosmetics are the culprits in a minority of cases. Patch testing may be performed with 5% oxidized TTO. Co-reactivity to turpentine oil is frequent, and there is an overrepresentation of reactions to fragrance mix I, Myroxylon pereirae, colophonium, and other essential oils. Summary In this article, contact allergy to, and the chemical composition of, tea tree oil (TTO) are reviewed. This essential oil is a popular remedy for many skin diseases, and may be used as neat oil or be present in cosmetics, topical pharmaceuticals and household products. Of all essential oils, TTO has caused most (published) allergic reactions since the first cases were reported in 1991. In routine testing, prevalences of positive patch test reactions have ranged from 0.1% to 3.5%. Nearly 100 allergic patients have been described in case reports and case series. The major constituents of commercial TTO are terpinen-4-ol, [gamma]-terpinene, 1,8-cineole, [alpha]-terpinene, [alpha]-terpineol, p-cymene, and [alpha]-pinene. Fresh TTO is a weak to moderate sensitizer, but oxidation increases its allergenic potency. The major sensitizers appear to be ascaridole, terpinolene, [alpha]-terpinene, 1,2,4-trihydroxymenthane, [alpha]-phellandrene, and limonene. The clinical picture of allergic contact dermatitis caused by TTO depends on the products used. Most reactions are caused by the application of pure oil; cosmetics are the culprits in a minority of cases. Patch testing may be performed with 5% oxidized TTO. Co-reactivity to turpentine oil is frequent, and there is an overrepresentation of reactions to fragrance mix I, Myroxylon pereirae, colophonium, and other essential oils. |
| Author | Schmidt, Erich de Groot, Anton C. |
| Author_xml | – sequence: 1 givenname: Anton C. surname: de Groot fullname: de Groot, Anton C. email: antondegroot@planet.nl organization: Acdegroot Publishing, 8351 HV, Wapserveen, The Netherlands – sequence: 2 givenname: Erich surname: Schmidt fullname: Schmidt, Erich organization: 86720, Nördlingen, Germany |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/27173437$$D View this record in MEDLINE/PubMed |
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| Keywords | contact allergy antimicrobial tea tree oil aromatherapy allergic contact dermatitis Melaleuca alternifolia essential oil chemical composition |
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| PublicationDecade | 2010 |
| PublicationPlace | Oxford, UK |
| PublicationPlace_xml | – name: Oxford, UK – name: England – name: Malden |
| PublicationTitle | Contact dermatitis |
| PublicationTitleAlternate | Contact Dermatitis |
| PublicationYear | 2016 |
| Publisher | Blackwell Publishing Ltd Wiley Subscription Services, Inc |
| Publisher_xml | – name: Blackwell Publishing Ltd – name: Wiley Subscription Services, Inc |
| References | Brophy J J, Craven L A, Doran J C. Melaleucas: their Botany, Essential Oils and Uses. ACIAR Monograph No. 156: Canberra, Australian Centre for International Agricultural Research, 2013. Available at: http://aciar.gov.au/publication/mn156. (last accessed 15 January 2016). Lawless J. The Encyclopedia of Essential Oils, 2nd edition: London, Harper Thorsons, 2014. Hammer K A. Treatment of acne with tea tree oil (melaleuca) products: a review of efficacy, tolerability and potential modes of action. Int J Antimicrob Agents 2015: 45: 106-110. Apted J H. Contact dermatitis associated with the use of tea-tree oil. Australas J Dermatol 1991: 32: 177. Warshaw E M, Belsito D V, DeLeo V A et al. North American Contact Dermatitis Group patch-test results, 2003-2004 study period. Dermatitis 2008: 19: 129-136. Veien N K, Rosner K, Skovgaard G L. Is tea tree oil an important contact allergen? Contact Dermatitis 2004: 50: 378-379. Southwell I, Freeman S, Rubel D M. Skin irritancy of tea tree oil. J Essent Oil Res 1997: 9: 47-52. Enshaieh S, Jooya A, Siadat A H, Iraji F. The efficacy of 5% topical tea tree oil gel in mild to moderate acne vulgaris: a randomized, double-blind placebo-controlled study. Indian J Dermatol Venereol Leprol 2007: 73: 22-25. Hackzell-Bradley M, Bradley T, Fischer T. Kontaktallergi av 'tea tree-oil'. Lakartidningen 1997: 94: 4359-4361 (article in Swedish). Hausen B M. 'Wundermittel' mit Tücken: Teebaumöl. Ärzt Prax Dermatol 1999: 27: 9-10. Beckmann B, Ippen H. Teebaum-Öl. Dermatosen 1998: 46: 120-124. Rubel D M, Freeman S, Southwell I. Tea tree oil allergy: what is the offending agent? Report of three cases of tea tree oil allergy and review of the literature. Australas J Dermatol 1998: 39: 244-247. Dharmagunawardena B, Takwale A, Sanders K J et al. Gas chromatography: an investigative tool in multiple allergies to essential oils. Contact Dermatitis 2002: 47: 288-292. Tranchida P Q, Shellie R A, Purcaro G et al. Analysis of fresh and aged tea tree essential oils by using GCxGCC-qMS. J Chromatogr Sci 2010: 48: 262-266. Rudbäck J, Andresen Bergström M, Börje A et al. α-Terpinene, an antioxidant in tea tree oil, autoxidizes rapidly to skin allergens on air exposure. Chem Res Toxicol 2012: 25: 713-721. Sasseville D, Saber M, Lessard L. Allergic contact dermatitis from tincture of benzoin with multiple concomitant reactions. Contact Dermatitis 2009: 61: 358-360. Carson C F, Hammer K A, Riley T V. Melaleuca alternifolia (tea tree) oil: a review of antimicrobial and other medicinal properties. Clin Microbiol Rev 2006: 19: 50-62. Coutts I, Shaw S, Orton D. Patch testing with pure tea tree oil - 12 months experience. Br J Dermatol 2002: 147 (Suppl. 62): 70. Selvaag E, Holm J, Thune P. Allergic contact dermatitis in an aromatherapist with multiple sensitizations to essential oils. Contact Dermatitis 1995: 33: 354-355. Harkenthal M, Reichling J, Geiss H K, Saller R. Oxidationsprodukte als mögliche Ursache von Kontaktdermati-tiden. Pharmazeut Z 1998: 47: 4092. Lisi P, Meligeni L, Pigatto P et al. The prevalence of sensitivity to melaleuca essential oil. Ital Ann Clin Exp Allergol Dermat 2000: 54: 141-144. Toholka R, Wang Y-S, Tate B et al. The first Australian baseline series: recommendations for patch testing in suspected contact dermatitis. Australas J Dermatol 2015: 56: 107-115. Belsito D V, Fowler J F Jr, Sasseville D et al. Delayed-type hypersensitivity to fragrance materials in a select North American population. Dermatitis 2006: 17: 23-28. Calcabrini A, Stringaro S, Toccacieli L et al. Terpinen-4-ol, the main component of Melaleuca alternifolia (tea tree) oil inhibits the in vitro growth of human melanoma cells. J Invest Dermatol 2004: 122: 349-360. Crawford G H, Sciacca J R, James W D. Tea tree oil: cutaneous effects of the extracted oil of Melaleuca alternifolia. Dermatitis 2004: 15: 59-66. Pazyar N, Yaghoobi R, Bagherani N, Kazerouni A. A review of applications of tea tree oil in dermatology. Int J Dermatol 2013: 52: 784-790. Pirker C, Hausen B M, Uter W et al. Sensitization to tea tree oil in Germany and Austria. A multicenter study of the German Contact Dermatitis Group. J Dtsch Dermatol Ges 2003: 1: 629-634. Thomson K F, Wilkinson S M. Allergic contact dermatitis to plant extracts in patients with cosmetic dermatitis. Br J Dermatol 2000: 142: 84-88. de Groot A C, Weijland J W. Systemic contact dermatitis from tea tree oil. Contact Dermatitis 1992: 27: 279-280. Bhushan M, Beck M H. Allergic contact dermatitis from tea tree oil in a wart paint. Contact Dermatitis 1997: 36: 117-118. Perrett C M, Evans A V, Russell-Jones R. Tea tree oil dermatitis associated with linear IgA disease. Clin Exp Dermatol 2003: 28: 167-170. Brophy J J, Davies N W, Southwell I A. Gas chromatographic quality control for oil of Melaleuca terpinen-4-ol type (Australian tea tree). J Agric Food Chem 1989: 37: 1330-1335. Fransway A F, Zug K A, Belsito D V et al. North American Contact Dermatitis Group patch test results for 2007-2008. Dermatitis 2013: 24: 10-21. Zug K A, Warshaw E M, Fowler J F Jr et al. Patch-test results of the North American Contact Dermatitis Group 2005-2006. Dermatitis 2009: 20: 149-160. Kränke B. Allergisierende Potenz von Teebaumöl. Hautarzt 1997: 48: 203-204. Knight T E, Hausen B M. Melaleuca oil (tea-tree oil) dermatitis. J Am Acad Dermatol 1994: 30: 423-427. Santesteban R, Loidi L, Agulló A et al. Allergic contact dermatitis to tea tree oil. Contact Dermatitis 2014: 70 (Suppl. 1): 102. Homer L E, Leach D N, Lea D et al. Natural variation in the essential oil content of Melaleuca alternifolia Cheel (Myrtaceae). Biochem Syst Ecol 2000: 28: 367-382. Reindl H, Gall H, Hausen B M, Peter U. Akutes Kontaktekzem nach Anwendung von Teebaumöl. Allergo J 2000: 9: 100-103. de Groot A C. Airborne allergic contact dermatitis from tea tree oil. Contact Dermatitis 1996: 35: 304-305. Aspres N, Freeman S. Predictive testing for irritancy and allergenicity of tea tree oil in normal human subjects. Exogen Dermatol 2003: 2: 258-261. Lawrence B M. Progress in essential oils. Perfum Flavor 1989: 14 (May/June): 71-80. Rutherford T, Nixon R, Tam M, Tate B. Allergy to tea tree oil: retrospective review of 41 cases with positive patch tests over 4.5 years. Australas J Dermatol 2007: 48: 83-87. Lippert U, Walter A, Hausen B M, Fuchs T. Increasing incidence of contact dermatitis to tea tree oil. J Allergy Clin Immunol 2000: 105: S43 (abstract 127). Selvaag E, Eriksen B, Thune P. Contact allergy due to tea tree oil and cross-sensitization to colophony. Contact Dermatitis 1994: 31: 124-125. Christoffers W A, Blömeke B, Coenraads P-J, Schuttelaar M-L A. Co-sensitization to ascaridole and tea tree oil. Contact Dermatitis 2013: 69: 189-187. Nardelli A, Drieghe J, Claes L et al. Fragrance allergens in 'specific' cosmetic products. Contact Dermatitis 2011: 64: 212-219. Nardelli A, D'Hooge E, Drieghe J et al. Allergic contact dermatitis from fragrance components in specific topical pharmaceutical products in Belgium. Contact Dermatitis 2009: 60: 303-313. Harkenthal M, Hausen B M, Reichling J. 1,2,4-Trihydroxy menthane, a contact allergen from oxidized Australian tea tree oil. Pharmazie 2000: 55: 153-154. Lawrence B M. Progress in essential oils. Perfum Flavor 2006: 31(4): 52-57. Wetter D A, Yiannias J A, Prakash A V et al. Results of patch testing to personal care product allergens in a standard series and a supplemental cosmetic series: an analysis of 945 patients from the Mayo Clinic Contact Dermatitis Group, 2000-2007. J Am Acad Dermatol 2010: 63: 789-798. Shellie R, Marriott P, Zappia G et al. Interactive use of linear retention indices on polar and apolar columns with an MS-library for reliable characterization of Australian tea tree and other Melaleuca sp. oils. J Essent Oil Res 2003: 15: 305-312. Sciarrone D, Ragonese C, Carnovale C et al. Evaluation of tea tree oil quality and ascaridole: a deep study by means of chiral and multi heart-cuts multidimensional gas chromatography system coupled to mass spectrometry detection. J Chromatogr A 2010: 1217: 6422-6427. Warshaw E M, Belsito D V, Taylor J S et al. North American Contact Dermatitis Group patch test results: 2009 to 2010. Dermatitis 2013: 24: 50-59. Lindberg M, Tammela M, Bostrom A et al. Are adverse skin reactions to cosmetics underestimated in the clinical assessment of contact dermatitis? A prospective study among 1075 patients attending Swedish patch test clinics. Acta Derm Venereol 2004: 84: 291-295. Cox S D, Mann C M, Markham J L. Interactions between components of the essential oil of Melaleuca alternifolia. J Appl Microbiol 2001: 91: 492-497. Milchard M J, Clery R, Esdale R et al. Application of gas-liquid chromatography to the analysis of essential oils. Perfum Flavor 2010: 35(5): 34-42. Warshaw E M, Maibach H I, Taylor J S et al. North American Contact Dermatitis Group patch test results: 2011-2012. Dermatitis 2015: 26: 49-59. Pereira T S, Rochade Sant'Anna J, Leite Silva E et al. In vitro genotoxicity of Melaleuca alternifolia essential oil in human lymphocytes. J Ethnopharmacol 2014: 151: 852-857. Hausen B M. Kontaktallergie auf Teebaumöl und Ascaridol. Akt Dermatol 1998: 24: 60-62. Santesteban Muruzábal R, Hervella Garcés M, Larrea García M et al. Secondary effects of topical application of an essential oil. Allergic contact dermatitis due to tea tree oil. An Sist Sanit Navar 2015: 38: 163-167 (article in Spanish). van der Valk P G, de Groot A C, Bruynzeel D P et al. Allergic contact eczema due to tea tree oil. Ned Tijdschr Geneeskd 1994: 138: 823-825 (article in Dutch). Travassos A R, Claes L, Boey L et al. Non-fragrance allergens in specific cosmetic products. Contact Dermatitis 2011: 65: 276-285. Monthrope Y, Shaw J. A 'natural' dermatitis: contact allergy to tea tree oil. Univ Toronto Med J 2004: 82: 59-60. Fritz T M, Elmer P. Allergisches Kontaktekzem auf Teebaumöl bei einer Patientin mit Psoriasis. Akt Dermatol 1998: 24: 7-10. Noumi E, Snoussi M, Hajlaoui H et al. Chemical composition, antioxidant and antifungal potential of Mel 2001; 91 2004; 122 2014; 70 1994; 138 2006; 31 2015; 38 2013; 69 2013; 24 1997; 48 2000; 9 1995; 33 2000; 42 2010; 1217 2014; 26 2003; 15 2007; 73 2001; 45 1996; 35 2010; 63 1997; 9 1998; 47 1998; 46 2015; 45 2002; 47 1997; 94 2001 2000; 54 2013; 50 2000; 55 2002; 147 2000; 11 2013; 52 2011; 64 2003; 2 2005; 76 2011; 65 1999; 10 2003; 1 1989; 37 2012; 25 1994; 30 2011; 165 1994; 31 2015; 56 2004; 84 2000; 28 2010; 35 2009; 20 2004; 82 2002; 30 1991; 32 2009; 61 2009; 60 1999; 27 2006; 17 2008; 19 2008 1996 2006; 19 2006 2005 2001; 26 2014; 2014 2014; 151 2011; 5 2005; 44 2007; 57 2001; 128 1998; 24 1999 2015; 26 1998; 39 2004; 50 2010; 48 2013; 78 2000; 105 2004; 14 1997; 36 2004; 15 2016 2000; 142 2003; 28 2014 2013 1992; 27 1989; 14 2014; 71 2007; 48 e_1_2_5_27_1 Harkenthal M (e_1_2_5_40_1) 2000; 55 e_1_2_5_46_1 Almeida Barbosa L C (e_1_2_5_6_1) 2013; 78 e_1_2_5_65_1 e_1_2_5_88_1 e_1_2_5_69_1 e_1_2_5_80_1 e_1_2_5_61_1 e_1_2_5_84_1 Harkenthal M (e_1_2_5_42_1) 1998; 47 e_1_2_5_15_1 Lawless J (e_1_2_5_19_1) 2014 e_1_2_5_38_1 e_1_2_5_11_1 e_1_2_5_34_1 e_1_2_5_57_1 e_1_2_5_7_1 e_1_2_5_76_1 e_1_2_5_99_1 e_1_2_5_91_1 Lawrence B M (e_1_2_5_31_1) 2006; 31 e_1_2_5_72_1 e_1_2_5_95_1 e_1_2_5_53_1 e_1_2_5_49_1 e_1_2_5_26_1 e_1_2_5_45_1 e_1_2_5_100_1 e_1_2_5_22_1 e_1_2_5_87_1 e_1_2_5_68_1 Noumi E (e_1_2_5_33_1) 2011; 5 e_1_2_5_60_1 e_1_2_5_64_1 Groot A C (e_1_2_5_3_1) 2016 Apted J H (e_1_2_5_2_1) 1991; 32 e_1_2_5_14_1 e_1_2_5_37_1 e_1_2_5_8_1 e_1_2_5_10_1 Lawrence B M (e_1_2_5_32_1) 2001; 26 e_1_2_5_4_1 Hausen B M (e_1_2_5_23_1) 1999; 27 e_1_2_5_79_1 e_1_2_5_71_1 Santesteban R (e_1_2_5_98_1) 2014; 70 e_1_2_5_94_1 e_1_2_5_75_1 e_1_2_5_52_1 e_1_2_5_48_1 e_1_2_5_21_1 e_1_2_5_44_1 e_1_2_5_29_1 Brophy J J (e_1_2_5_25_1) 2013 e_1_2_5_63_1 e_1_2_5_86_1 e_1_2_5_17_1 e_1_2_5_36_1 e_1_2_5_9_1 e_1_2_5_13_1 Beckmann B (e_1_2_5_24_1) 1998; 46 e_1_2_5_5_1 Hartford O (e_1_2_5_18_1) 2005; 76 e_1_2_5_70_1 e_1_2_5_93_1 Lisi P (e_1_2_5_56_1) 2000; 54 Reindl H (e_1_2_5_78_1) 2000; 9 van der Valk P G (e_1_2_5_90_1) 1994; 138 e_1_2_5_97_1 Milchard M J (e_1_2_5_35_1) 2010; 35 Monthrope Y (e_1_2_5_73_1) 2004; 82 e_1_2_5_28_1 e_1_2_5_47_1 e_1_2_5_43_1 e_1_2_5_66_1 e_1_2_5_89_1 e_1_2_5_81_1 e_1_2_5_62_1 Kütting B (e_1_2_5_74_1) 2004; 14 e_1_2_5_85_1 e_1_2_5_20_1 e_1_2_5_39_1 e_1_2_5_16_1 e_1_2_5_58_1 e_1_2_5_12_1 e_1_2_5_54_1 Hausen B M (e_1_2_5_41_1) 1998; 24 Fritz T M (e_1_2_5_59_1) 2001; 128 Coutts I (e_1_2_5_55_1) 2002; 147 Varma S (e_1_2_5_77_1) 2000; 42 Fritz T M (e_1_2_5_82_1) 1998; 24 Newsham J (e_1_2_5_67_1) 2011; 165 e_1_2_5_92_1 Warshaw E M (e_1_2_5_51_1) 2008; 19 e_1_2_5_96_1 Lawrence B M (e_1_2_5_30_1) 1989; 14 Hackzell‐Bradley M (e_1_2_5_83_1) 1997; 94 e_1_2_5_50_1 |
| References_xml | – reference: Hausen B M. Evaluation of the main contact allergens in oxidized tea tree oil. Dermatitis 2004: 15: 213-214. – reference: Varma S, Blackford S, Statham B N, Blackwell A. Combined contact allergy to tea tree oil and lavender oil complicating chronic vulvovaginitis. Contact Dermatitis 2000: 42: 309-310. – reference: Selvaag E, Holm J, Thune P. Allergic contact dermatitis in an aromatherapist with multiple sensitizations to essential oils. Contact Dermatitis 1995: 33: 354-355. – reference: Corazza M, Borghi A, Gallo R et al. Topical botanically derived products: use, skin reactions, and usefulness of patch tests. A multicentre Italian study. Contact Dermatitis 2014: 70: 90-97. – reference: Khanna M, Qasem K, Sasseville D. Allergic contact dermatitis to tea tree oil with erythema multiforme-like Id reaction. Dermatitis 2000: 11: 238-242. – reference: Apted J H. Contact dermatitis associated with the use of tea-tree oil. Australas J Dermatol 1991: 32: 177. – reference: van der Valk P G, de Groot A C, Bruynzeel D P et al. Allergic contact eczema due to tea tree oil. Ned Tijdschr Geneeskd 1994: 138: 823-825 (article in Dutch). – reference: Homer L E, Leach D N, Lea D et al. Natural variation in the essential oil content of Melaleuca alternifolia Cheel (Myrtaceae). Biochem Syst Ecol 2000: 28: 367-382. – reference: Kränke B. Allergisierende Potenz von Teebaumöl. Hautarzt 1997: 48: 203-204. – reference: Knight T E, Hausen B M. Melaleuca oil (tea-tree oil) dermatitis. J Am Acad Dermatol 1994: 30: 423-427. – reference: Rutherford T, Nixon R, Tam M, Tate B. Allergy to tea tree oil: retrospective review of 41 cases with positive patch tests over 4.5 years. Australas J Dermatol 2007: 48: 83-87. – reference: Hausen B M. 'Wundermittel' mit Tücken: Teebaumöl. Ärzt Prax Dermatol 1999: 27: 9-10. – reference: Nardelli A, D'Hooge E, Drieghe J et al. Allergic contact dermatitis from fragrance components in specific topical pharmaceutical products in Belgium. Contact Dermatitis 2009: 60: 303-313. – reference: Milchard M J, Clery R, Esdale R et al. Application of gas-liquid chromatography to the analysis of essential oils. Perfum Flavor 2010: 35(5): 34-42. – reference: Christoffers W A, Blömeke B, Coenraads P-J, Schuttelaar M-L A. Co-sensitization to ascaridole and tea tree oil. Contact Dermatitis 2013: 69: 189-187. – reference: de Groot A C. Airborne allergic contact dermatitis from tea tree oil. Contact Dermatitis 1996: 35: 304-305. – reference: de Groot A C, Schmidt E. Essential Oils: Contact Allergy and Cemical Ccomposition: Boca Raton, FL, CRC Press and Taylor and Francis, 2016 (ISBN 9781482246407) (expected publication date: June 2, 2016). – reference: Belsito D V, Fowler J F Jr, Sasseville D et al. Delayed-type hypersensitivity to fragrance materials in a select North American population. Dermatitis 2006: 17: 23-28. – reference: Santesteban Muruzábal R, Hervella Garcés M, Larrea García M et al. Secondary effects of topical application of an essential oil. Allergic contact dermatitis due to tea tree oil. An Sist Sanit Navar 2015: 38: 163-167 (article in Spanish). – reference: Williams J D, Nixon R L, Lee A. Recurrent allergic contact dermatitis due to allergen transfer by sunglasses. Contact Dermatitis 2007: 57: 120-121. – reference: Thomson K F, Wilkinson S M. Allergic contact dermatitis to plant extracts in patients with cosmetic dermatitis. Br J Dermatol 2000: 142: 84-88. – reference: Lawless J. The Encyclopedia of Essential Oils, 2nd edition: London, Harper Thorsons, 2014. – reference: Sciarrone D, Ragonese C, Carnovale C et al. Evaluation of tea tree oil quality and ascaridole: a deep study by means of chiral and multi heart-cuts multidimensional gas chromatography system coupled to mass spectrometry detection. J Chromatogr A 2010: 1217: 6422-6427. – reference: Tranchida P Q, Shellie R A, Purcaro G et al. Analysis of fresh and aged tea tree essential oils by using GCxGCC-qMS. J Chromatogr Sci 2010: 48: 262-266. – reference: Hausen B M, Reichling J, Harkenthal M. Degradation products of monoterpenes are the sensitizing agents in tea tree oil. Am J Cont Derm 1999: 10: 68-77. – reference: Zug K A, Warshaw E M, Fowler J F Jr et al. Patch-test results of the North American Contact Dermatitis Group 2005-2006. Dermatitis 2009: 20: 149-160. – reference: Aspres N, Freeman S. Predictive testing for irritancy and allergenicity of tea tree oil in normal human subjects. Exogen Dermatol 2003: 2: 258-261. – reference: Almeida Barbosa L C, Silva C J, Teixeira R R et al. Chemistry and biological activities of essential oils from Melaleuca L. species. Agric Conspec Sci 2013: 78: 11-23. – reference: Harkenthal M, Reichling J, Geiss H K, Saller R. Oxidationsprodukte als mögliche Ursache von Kontaktdermati-tiden. Pharmazeut Z 1998: 47: 4092. – reference: de Groot A C, Weijland J W. Systemic contact dermatitis from tea tree oil. Contact Dermatitis 1992: 27: 279-280. – reference: Carson C F, Riley T V. Safety, efficacy and provenance of tea tree (Melaleuca alternifolia) oil. Contact Dermatitis 2001: 45: 65-67. – reference: Reindl H, Gall H, Hausen B M, Peter U. Akutes Kontaktekzem nach Anwendung von Teebaumöl. Allergo J 2000: 9: 100-103. – reference: Benelli G, Canale A, Flamini G et al. Biotoxicity of Melaleuca alternifolia (Myrtaceae) essential oil against the Mediterranean fruit fly, Ceratitis capitata (Diptera: Tephritidae), and its parasitoid Psyttalia concolor (Hymenoptera: Braconidae). Ind Crops Prod 2013: 50: 596-603. – reference: Carson C F, Hammer K A, Riley T V. Melaleuca alternifolia (tea tree) oil: a review of antimicrobial and other medicinal properties. Clin Microbiol Rev 2006: 19: 50-62. – reference: Lawrence B M. Progress in essential oils. Perfum Flavor 1989: 14 (May/June): 71-80. – reference: Pirker C, Hausen B M, Uter W et al. Sensitization to tea tree oil in Germany and Austria. A multicenter study of the German Contact Dermatitis Group. J Dtsch Dermatol Ges 2003: 1: 629-634. – reference: Enshaieh S, Jooya A, Siadat A H, Iraji F. The efficacy of 5% topical tea tree oil gel in mild to moderate acne vulgaris: a randomized, double-blind placebo-controlled study. Indian J Dermatol Venereol Leprol 2007: 73: 22-25. – reference: Beckmann B, Ippen H. Teebaum-Öl. Dermatosen 1998: 46: 120-124. – reference: Lee L S, Brooks L O, Homer L E et al. Geographic variation in the essential oils and morphology of natural populations of Melaleuca alternifolia (Myrtaceae). Biochem Syst Ecol 2002: 30: 343-360. – reference: Bhushan M, Beck M H. Allergic contact dermatitis from tea tree oil in a wart paint. Contact Dermatitis 1997: 36: 117-118. – reference: Monthrope Y, Shaw J. A 'natural' dermatitis: contact allergy to tea tree oil. Univ Toronto Med J 2004: 82: 59-60. – reference: Nardelli A, Drieghe J, Claes L et al. Fragrance allergens in 'specific' cosmetic products. Contact Dermatitis 2011: 64: 212-219. – reference: Lindberg M, Tammela M, Bostrom A et al. Are adverse skin reactions to cosmetics underestimated in the clinical assessment of contact dermatitis? A prospective study among 1075 patients attending Swedish patch test clinics. Acta Derm Venereol 2004: 84: 291-295. – reference: Brophy J J, Craven L A, Doran J C. Melaleucas: their Botany, Essential Oils and Uses. ACIAR Monograph No. 156: Canberra, Australian Centre for International Agricultural Research, 2013. Available at: http://aciar.gov.au/publication/mn156. (last accessed 15 January 2016). – reference: Wetter D A, Yiannias J A, Prakash A V et al. Results of patch testing to personal care product allergens in a standard series and a supplemental cosmetic series: an analysis of 945 patients from the Mayo Clinic Contact Dermatitis Group, 2000-2007. J Am Acad Dermatol 2010: 63: 789-798. – reference: Lippert U, Walter A, Hausen B M, Fuchs T. Increasing incidence of contact dermatitis to tea tree oil. J Allergy Clin Immunol 2000: 105: S43 (abstract 127). – reference: Calcabrini A, Stringaro S, Toccacieli L et al. Terpinen-4-ol, the main component of Melaleuca alternifolia (tea tree) oil inhibits the in vitro growth of human melanoma cells. J Invest Dermatol 2004: 122: 349-360. – reference: Pazyar N, Yaghoobi R, Bagherani N, Kazerouni A. A review of applications of tea tree oil in dermatology. Int J Dermatol 2013: 52: 784-790. – reference: Warshaw E M, Belsito D V, Taylor J S et al. North American Contact Dermatitis Group patch test results: 2009 to 2010. Dermatitis 2013: 24: 50-59. – reference: Hammer K A. Treatment of acne with tea tree oil (melaleuca) products: a review of efficacy, tolerability and potential modes of action. Int J Antimicrob Agents 2015: 45: 106-110. – reference: Shellie R, Marriott P, Zappia G et al. Interactive use of linear retention indices on polar and apolar columns with an MS-library for reliable characterization of Australian tea tree and other Melaleuca sp. oils. J Essent Oil Res 2003: 15: 305-312. – reference: Sasseville D, Saber M, Lessard L. Allergic contact dermatitis from tincture of benzoin with multiple concomitant reactions. Contact Dermatitis 2009: 61: 358-360. – reference: Crawford G H, Sciacca J R, James W D. Tea tree oil: cutaneous effects of the extracted oil of Melaleuca alternifolia. Dermatitis 2004: 15: 59-66. – reference: Noumi E, Snoussi M, Hajlaoui H et al. Chemical composition, antioxidant and antifungal potential of Melaleuca alternifolia (tea tree) and Eucalyptus globulus essential oils against oral Candida species. 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In this article, contact allergy to, and the chemical composition of, tea tree oil (TTO) are reviewed. This essential oil is a popular remedy for many... In this article, contact allergy to, and the chemical composition of, tea tree oil ( TTO ) are reviewed. This essential oil is a popular remedy for many skin... In this article, contact allergy to, and the chemical composition of, tea tree oil (TTO) are reviewed. This essential oil is a popular remedy for many skin... Summary In this article, contact allergy to, and the chemical composition of, tea tree oil (TTO) are reviewed. This essential oil is a popular remedy for many... |
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| SubjectTerms | allergic contact dermatitis Allergies antimicrobial aromatherapy chemical composition contact allergy Cosmetics Cyclohexanols - adverse effects Cyclohexenes - adverse effects Dermatitis, Allergic Contact - etiology essential oil Humans Melaleuca Melaleuca alternifolia Menthol - adverse effects Menthol - analogs & derivatives Monoterpenes - adverse effects Oils & fats Patch Tests Peroxides - adverse effects tea tree oil Tea Tree Oil - adverse effects Tea Tree Oil - chemistry Terpenes - adverse effects |
| Title | Tea tree oil: contact allergy and chemical composition |
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