HLA gene variations and mycotoxin toxicity: Four case reports
- PMID: 38198040
- DOI: 10.1007/s12550-023-00517-y
HLA gene variations and mycotoxin toxicity: Four case reports
Abstract
Mycotoxins are produced by certain molds that can cause many health effects. We present four human cases of prolonged consistent mycotoxins exposure linked to genetic variations in human leukocyte antigen (HLA) alleles. The HLA-DR/DQ isotype alleles are linked to mycotoxins susceptibility due to the lack of proper immune response; individuals with these alleles are poor eliminators of mycotoxins from their system. Four subjects with variations in their HLA-DR alleles were exposed to mycotoxins from living in mold-infested houses and experienced persistent mold-related symptoms long after moving out from the mold-infested houses and only exposed to the levels of molds found in the ambient air. From one of the subjects, two urine samples were collected ~ 18 months apart after the cessation of exposure. Urinary elimination rate was extremely slow for two of the mycotoxins (ochratoxin A [OTA] and mycophenolic acid [MPA]) detected in both samples. In 18 months, decline in OTA level was only ~ 3-fold (estimated t½ of ~ 311 days) and decline in MPA level was ~ 11-fold (estimated t½ of ~ 160 days), which was ~ 10- and ~ 213-fold slower than expected in individuals without HLA-DR alleles, respectively. We estimated that ~ 4.3 and ~ 2.2 years will be required for OTA and MPA to reach < LLQ in urine, respectively. Three other subjects with variations in HLA-DR alleles were members of a family who lived in a mold-infested house for 4 years. They kept experiencing mold-related issues >2 years after moving to a non-mold-infested house. Consistent exposure was confirmed by the presence of several mycotoxins in urine >2 years after the secession of higher than background (from outdoor ambient air) exposure. This was consistent with the extremely slow elimination of mycotoxins from their system. Variations in HLA-DR alleles can, consequently, make even short periods of exposure to chronic exposure scenarios with related adverse health effects. It is, therefore, important to determine genetic predisposition as a reason for prolonged/lingering mold-related symptoms long after the cessation of higher than background exposure. Increased human exposure to mycotoxins is expected from increased mold infestation that is anticipated due to rising CO2, temperature, and humidity from the climate change with possibly increased adverse health effects, especially in individuals with genetic susceptibility to mold toxicity.
Keywords: HLA alleles linked to mycotoxins susceptibility; Mold toxicity; Mycotoxin elimination and presence of HLA alleles variations; Role of human leukocyte antigen (HLA) in mold toxicity.
© 2024. The Author(s) under exclusive licence to Society for Mycotoxin (Research Gesellschaft für Mykotoxinforschung e.V.) and Springer-Verlag GmbH Germany, part of Springer Nature.
References
-
- Angelo LS, Kurzrock R (2007) Vascular endothelial growth factor and its relationship to inflammatory mediators. Clin Cancer Res 13(10):2825–2830. https://doi.org/10.1158/1078-0432.CCR-06-2416 - DOI - PubMed
-
- Ansari RA, Alfuraih S, Abbas A, Shekh K, Omidi Y, Javed S, Saghir SA (2023) Endocrine disruptors: Genetic, epigenetic and related pathways. In: Sahu SC (ed) Impact of engineered nanomaterials in genomics and epigenomics. John Wiley & Sons, Inc, pp 41–81
-
- Apter AJ, Schelleman H, Walker A, Addya K, Rebbeck T (2008) Clinical and genetic risk factors of self-reported penicillin allergy. J Allergy Clin Immunol 122(1):152–158. https://doi.org/10.1016/j.jaci.2008.03.037 - DOI - PubMed
-
- Arbour NC, Lorenz E, Schutte BC, Zabner J, Kline JN, Jones M, Frees K, Watt JL, Schwartz DA (2000) TLR4 mutations are associated with endotoxin hyporesponsiveness in humans. Nat Genet 25(2):187–191. https://doi.org/10.1038/76048 - DOI - PubMed
-
- Armendáriz CR, Fernández ÁJG, Gironés MCLR, de la Torre AH (2014) Mycotoxins. In: Wexler P (ed) Encyclopedia of Toxicology, 3rd edn. Academic Press, Oxford, pp 424–427 - DOI
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Research Materials
