Analysis of HLA Alleles in Different Cohorts of Patients Infected by L. infantum from Southern Spain

Leishmaniasis is an infectious disease caused by protozoa of the genus , which is endemic in certain areas of Europe, such as southern Spain. The disease manifests in various clinical phenotypes, including visceral, cutaneous, mucosal, or asymptomatic leishmaniasis. This diversity in clinical outcom...

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Veröffentlicht in:International journal of molecular sciences 2024-08, Vol.25 (15), p.8205
Hauptverfasser: Gutiérrez-Bautista, Juan Francisco, Sampedro, Antonio, Ballesta-Alcaraz, Lucia, Aguilera-Franco, María, Olivares-Durán, María José, Cobo, Fernando, Reguera, Juan Antonio, Rodríguez-Granger, Javier, Torres-Llamas, Andrés, Martín-Sánchez, Joaquina, Aznar-Peralta, Inés, Vilchez, Jose Ramon, López-Nevot, Miguel Ángel, Sampedro-Martínez, Antonio
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Sprache:eng
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Zusammenfassung:Leishmaniasis is an infectious disease caused by protozoa of the genus , which is endemic in certain areas of Europe, such as southern Spain. The disease manifests in various clinical phenotypes, including visceral, cutaneous, mucosal, or asymptomatic leishmaniasis. This diversity in clinical outcomes may be influenced by the host immune response, with human leukocyte antigen (HLA) molecules playing a crucial role in determining susceptibility and progression of the infection. This study explores the association between specific HLA variants and infection. We recruited four cohorts: a control group, asymptomatic individuals, patients with symptomatic disease, and cohabitants of infected individuals. HLA typing was performed for all participants, followed by an association analysis with infection status and disease progression. Our findings indicate that the HLA-B*38 and HLA-C*03 alleles are associated with protection against infection. These results contribute to a better understanding of the disease's progression, offer potential for new therapeutic approaches such as vaccines, and expand the existing knowledge in the literature.
ISSN:1422-0067
1661-6596
1422-0067
DOI:10.3390/ijms25158205