Álvarez Paula, Molina Juan, Bernardo Raquel, González Rafael, Manzanares Bárbara, Aguado Rocío, Carrero Laura, Jurado Aurora, Ruiz-León Berta, Navas Ana
Department of Immunology and Allergy, Reina Sofía University Hospital, 14004 Córdoba, Spain.
Maimonides Biomedical Research Institute of Córdoba (IMIBIC)/Reina Sofía University Hospital, University of Córdoba, 14004 Córdoba, Spain.
Int J Mol Sci. 2025 Aug 11;26(16):7755. doi: 10.3390/ijms26167755.
Concomitant sensitisation to non-specific lipid transfer proteins (nsLTPs) from olive pollen (Ole e 7) and peach (Pru p 3) has been observed in the south of Spain. In the search for reasons to explain this observation, we studied a potential causal relationship between Human Leukocyte Antigen (HLA) molecules and nsLTP sensitisation. For this purpose, eighteen Ole e 7-monosensitised (MONOLE) patients, 22 Pru p 3-monosensitised (MONPRU) patients, and 22 bisensitised (BI) patients were genotyped for HLA class II alleles. Complementarily, T-cell epitopes were predicted with the Immune Epitope Database analysis tool to test HLA epitope presentation. Our results showed a significant increase in DRB111 and DQB103 frequencies in MONPRU patients and DRB104 frequency in MONOLE patients. Additionally, T-cell epitope analysis revealed high binding affinity between the predicted Pru p 3 epitopes and DRB111 and between the predicted Ole e 7 epitopes and DRB104, suggesting that presentation of these epitopes may be favoured and predisposing individuals to sensitisation. Conversely, low DQB105 frequency and poor binding ability of predicted epitopes from both nsLTPs postulated this allele as a possible protective factor to sensitisation. Variations in the binding affinity between nsLTP epitopes and HLA molecules may underlie individual susceptibility to nsLTP allergy.
在西班牙南部,已观察到对来自橄榄花粉(Ole e 7)和桃子(Pru p 3)的非特异性脂质转移蛋白(nsLTPs)的伴随致敏现象。为探寻这一现象的原因,我们研究了人类白细胞抗原(HLA)分子与nsLTP致敏之间的潜在因果关系。为此,对18名仅对Ole e 7致敏(MONOLE)的患者、22名仅对Pru p 3致敏(MONPRU)的患者以及22名双重致敏(BI)的患者进行了HLA II类等位基因分型。作为补充,使用免疫表位数据库分析工具预测T细胞表位,以测试HLA表位呈递情况。我们的结果显示,MONPRU患者中DRB111和DQB103的频率显著增加,MONOLE患者中DRB104的频率增加。此外,T细胞表位分析显示,预测的Pru p 3表位与DRB111之间以及预测的Ole e 7表位与DRB104之间具有高结合亲和力,这表明这些表位的呈递可能更受青睐,并使个体易致敏。相反,DQB105频率较低以及两种nsLTP预测表位的结合能力较差,表明该等位基因可能是致敏的一个保护因素。nsLTP表位与HLA分子之间结合亲和力的差异可能是个体对nsLTP过敏易感性的基础。