Open AccessThe impact of KIR/HLA genes on the risk of developing multibacillary leprosy
Author(s) -
Hugo Vicentin Alves,
Amarilis Giaretta de Moraes,
Afonso Carrasco Pepineli,
Bruna Tiaki Tiyo,
Quirino Alves de Lima Neto,
Thaís da Silva Santos,
Jorge Juarez Vieira Teixeira,
Eliane Papa AmbrosioAlbuquerque,
Ana Maria Sell,
Jeane Eliete Laguila Visentainer
Publication year - 2019
Publication title -
plos neglected tropical diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.99
H-Index - 135
eISSN - 1935-2735
pISSN - 1935-2727
DOI - 10.1371/journal.pntd.0007696
Subject(s) - leprosy , human leukocyte antigen , immunology , genotyping , mycobacterium leprae , disease , biology , case control study , receptor , medicine , antigen , genotype , gene , genetics
Background Killer-cell immunoglobulin-like receptors (KIRs) are a group of regulatory molecules able to activate or inhibit natural killer cells upon interaction with human leukocyte antigen (HLA) class I molecules. Combinations of KIR and HLA may contribute to the occurrence of different immunological and clinical responses to infectious diseases. Leprosy is a chronic neglected disease, both disabling and disfiguring, caused mainly by Mycobacterium leprae . In this case–control study, we examined the influence of KIRs and HLA ligands on the development of multibacillary leprosy. Methodology/Principal findings Genotyping of KIR and HLA genes was performed in 264 multibacillary leprosy patients and 518 healthy unrelated controls (238 healthy household contacts and 280 healthy subjects). These are unprecedented results in which KIR2DL2/KIR2DL2/C1/C2 and KIR2DL3/2DL3/C1/C1 indicated a risk for developing lepromatous and borderline leprosy, respectively. Concerning to 3DL2/A3/A11+ , our study demonstrated that independent of control group (contacts or healthy subjects), this KIR receptor and its ligand act as a risk factor for the borderline clinical form. Conclusions/Significance Our finding suggests that synergetic associations of activating and inhibitory KIR genes may alter the balance between these receptors and thus interfere in the progression of multibacillary leprosy.