A variant of the CXCL11 gene may influence susceptibility to contact allergy, particularly in polysensitized patients
BACKGROUND: Hereditary factors may influence individual susceptibility to contact allergy. OBJECTIVES: To investigate genetic variants with impacts on early inflammatory reactions and T cell functions that possibly increase the risk of contact allergy. PATIENTS AND METHODS: Three hundred and seventy...
Gespeichert in:
| Hauptverfasser: | , |
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| Dokumenttyp: | Article (Journal) |
| Sprache: | Englisch |
| Veröffentlicht: |
28 April 2016
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| In: |
Contact dermatitis
Year: 2016, Jahrgang: 75, Heft: 5, Pages: 303-307 |
| ISSN: | 1600-0536 |
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| Verfasserangaben: | Götz A. Westphal, Hans-Peter Rihs, Antje Schaffranek, Thomas Zeiler, Thomas Werfel, Annice Heratizadeh, Heinrich Dickel, Elke Weisshaar, Andrea Bauer, Sibylle Schliemann, Kristian Reich, Kristine Breuer, Claudia Schröder-Kraft, Margitta Worm, Sonja Molin, Richard Brans, Knut Schäkel, Hilmar Schwantes, Claudia Pföhler, Christiane Szliska, Burkhard Kreft, Harald Löffler, Jürgen Bünger, Thomas Brüning, Johannes Geier andAxel Schnuch |
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| 245 | 1 | 2 | |a A variant of the CXCL11 gene may influence susceptibility to contact allergy, particularly in polysensitized patients |c Götz A. Westphal, Hans-Peter Rihs, Antje Schaffranek, Thomas Zeiler, Thomas Werfel, Annice Heratizadeh, Heinrich Dickel, Elke Weisshaar, Andrea Bauer, Sibylle Schliemann, Kristian Reich, Kristine Breuer, Claudia Schröder-Kraft, Margitta Worm, Sonja Molin, Richard Brans, Knut Schäkel, Hilmar Schwantes, Claudia Pföhler, Christiane Szliska, Burkhard Kreft, Harald Löffler, Jürgen Bünger, Thomas Brüning, Johannes Geier andAxel Schnuch |
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| 520 | |a BACKGROUND: Hereditary factors may influence individual susceptibility to contact allergy. OBJECTIVES: To investigate genetic variants with impacts on early inflammatory reactions and T cell functions that possibly increase the risk of contact allergy. PATIENTS AND METHODS: Three hundred and seventy two patients undergoing patch testing were recruited from the Information Network of Departments of Dermatology (IVDK). Of these, 133 were monosensitized and 239 were polysensitized, defined as reacting to three or more unrelated sensitizers. Within the polysensitized individuals, a subgroup with at least one particularly strong patch test reaction (strong reactors; n = 194) was considered. Three hundred and forty-seven blood bank donors served as controls. Fifteen genetic variants in 13 genes were analysed. RESULTS: The homozygous variant CXCL11 AA genotype (rs6817952) was significantly more frequent among polysensitized patients (10 of 239 = 4.2%; p = 0.0048; odds ratio 7.49; 95%CI: 1.7-36.1) than among monosensitized patients (2.2%) and in the control group (0.6%). None of the remaining genetic variants investigated were characterized by similarly strong associations. However, the significance was lost after correction for multiple comparisons. CONCLUSIONS: The homozygous variant CXCL11 genotype is associated with an increased risk of contact allergy. To confirm this exploratory finding, further independent studies are needed. | ||
| 650 | 4 | |a Aged | |
| 650 | 4 | |a Female | |
| 650 | 4 | |a Humans | |
| 650 | 4 | |a Male | |
| 650 | 4 | |a Middle Aged | |
| 650 | 4 | |a Adult | |
| 650 | 4 | |a Cytokines | |
| 650 | 4 | |a Young Adult | |
| 650 | 4 | |a Adolescent | |
| 650 | 4 | |a Case-Control Studies | |
| 650 | 4 | |a Chemokine CXCL11 | |
| 650 | 4 | |a contact allergy | |
| 650 | 4 | |a CXCL11 | |
| 650 | 4 | |a Dermatitis, Allergic Contact | |
| 650 | 4 | |a Genetic Predisposition to Disease | |
| 650 | 4 | |a Homozygote | |
| 650 | 4 | |a Odds Ratio | |
| 650 | 4 | |a Patch Tests | |
| 650 | 4 | |a Polymorphism, Single Nucleotide | |
| 650 | 4 | |a polysensitization | |
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