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151 Other investigators suggested that inactivation of AAT by oxidation of either Met-351 or Met-358 provides a mechanism for regulation of its activity at sites of inflammation

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Correlation analysis revealed that SLC7A11, HMOX1, G6PD, RRM2, KIF20A, HELLS, SPP1, CCR2 and DCN were positively correlated with plasma cells and CD8+ T cells, whereas GPT2, GLS2, IRF1, and IGF1 were negatively correlated with these cell subsets (Fig

Funding The author(s) declare financial support was received for the research presented in this article