Publications by authors named "Balazs Petrovich"

Article Synopsis
  • - Immune checkpoint inhibitors, particularly anti-PD-1 monoclonal antibodies, can enhance T-cell activity against cancer but may also cause heart issues like myocarditis and cardiotoxicity, prompting research into their effects on cardiac function.
  • - In experiments using mice, anti-PD-1 treatment led to cardiac dysfunction and increased inflammation in the thymus, particularly with heightened IL-17A levels, while other inflammatory markers remained mild.
  • - Notably, blocking IL-17A prevented the cardiac dysfunction associated with PD-1 inhibition, suggesting that targeting IL-17A could mitigate the heart-related side effects of immune checkpoint therapy in cancer treatment.
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Introduction: Signal detection yields confirmed signals in only 2.1%, which imposes a heavy burden on the pharmacovigilance system in the European Union.

Objectives: We aimed to develop a network theoretical metric to increase the confirmed signal ratio of individual case safety report (ICSR) networks.

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(1) Background: Ischemia reperfusion (IR) is the leading cause of acute kidney injury (AKI) and results in predisposition to chronic kidney disease. We demonstrated that delayed contralateral nephrectomy (Nx) greatly improved the function of the IR-injured kidney and decelerated fibrosis progression. Our aim was to identify microRNAs (miRNA/miR) involved in this process.

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Although myocardial ischemia-reperfusion injury (I/R) and its pathological consequences are the leading cause of morbidity and mortality worldwide, cardioprotective therapeutics are still not on the market. Oxidative stress, a major contributing factor to myocardial I/R, changes transcription of coding and non-coding RNAs, alters post-transcriptional modulations, and regulate protein function. MicroRNA (miRNA) expression can be altered by oxidative stress and microRNAs may also regulate cytoprotective mechanisms and exert cardioprotection againts I/R.

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