Genetic Insights Into Allergic Contact Dermatitis: Reassessing the Role of LCE3C_LCE3B Deletion
Zeineb Ben Lamine, Amen Moussa, Marwa Bouhoula, Razene Gerisha, Sarra Sabbagh, Imen Kacem, Asma Aloui, Souheil Chatti, Aicha Brahem, Ramzi Zemni, Foued Ben Hadj Slama

TL;DR
This study investigated the genetic link between a specific deletion and allergic skin reactions in Tunisia but found no significant connection.
Contribution
The study provides new population-specific insights into the LCE3C_LCE3B deletion's role in allergic contact dermatitis in Tunisians.
Findings
The LCE3C_LCE3B deletion was not significantly associated with allergic contact dermatitis in Tunisian patients.
No link was found between the deletion and hypersensitivity to multiple unrelated allergens.
The deletion showed no significant association with metal sensitization in the studied population.
Abstract
Allergic contact dermatitis (ACD) is a multifactorial inflammatory skin disorder. Polysensitisation, defined as hypersensitivity to ≥ 3 unrelated allergens, reflects a more severe clinical form. The LCE3C_LCE3B deletion, implicated in skin barrier dysfunction, has a yet unclear role in the susceptibility to ACD and polysensitisation. This study aims to evaluate the association between LCE3C_LCE3B deletion and susceptibility to ACD and polysensitisation in the Tunisian population. A case–control study included 94 confirmed ACD patients and 125 age‐ and sex‐matched controls without immune‐related diseases. Patch testing followed the European Baseline Series. LCE3C_LCE3B genotyping was performed using conventional three‐primer PCR after DNA extraction by the salting‐out method. Polysensitisation was observed in 33% of ACD cases. Genotyping of the LCE3C_LCE3B deletion did not reveal…
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Taxonomy
TopicsContact Dermatitis and Allergies · Dermatology and Skin Diseases · Skin and Cellular Biology Research
