AI Article Synopsis

  • Aluminium hydroxide adjuvants are widely used in vaccines for livestock and humans, but their effects on the central nervous system are not well-studied.
  • In a study, lambs were treated with various aluminium-containing vaccines, aluminium hydroxide, or mock injections over 16 months, and brain samples were analyzed for gene and miRNA expression.
  • The findings indicated that aluminium hydroxide alone significantly altered brain gene expression, impacting neurological functions and suggesting potential mitochondrial dysfunction, which may require further investigation for possible health implications.

Article Abstract

Aluminium hydroxide adjuvants are crucial for livestock and human vaccines. Few studies have analysed their effect on the central nervous system in vivo. In this work, lambs received three different treatments of parallel subcutaneous inoculations during 16 months with aluminium-containing commercial vaccines, an equivalent dose of aluminium hydroxide or mock injections. Brain samples were sequenced by RNA-seq and miRNA-seq for the expression analysis of mRNAs, long non-coding RNAs and microRNAs and three expression comparisons were made. Although few differentially expressed genes were identified, some dysregulated genes by aluminium hydroxide alone were linked to neurological functions, the lncRNA TUNA among them, or were enriched in mitochondrial energy metabolism related functions. In the same way, the miRNA expression was mainly disrupted by the adjuvant alone treatment. Some differentially expressed miRNAs had been previously linked to neurological diseases, oxidative stress and apoptosis. In brief, in this study aluminium hydroxide alone altered the transcriptome of the encephalon to a higher degree than commercial vaccines that present a milder effect. The expression changes in the animals inoculated with aluminium hydroxide suggest mitochondrial disfunction. Further research is needed to elucidate to which extent these changes could have pathological consequences.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7498608PMC
http://dx.doi.org/10.1038/s41598-020-71905-yDOI Listing

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