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Nguyen, Y. N.

Publications and source records attributed to Nguyen, Y. N..

2 recordsLinked to original sources

Immuno-functionomics reveals geographical variation and a role for TLR8 in mRNA vaccine responses

The innate immune system plays a pivotal role in pathogen defense via pattern recognition receptor sensing, initiating responses upon infection or vaccination. Understanding its functional capacity is crucial for deciphering correlates of vaccine efficacy and understanding responses to infection. In this study, we developed a holistic approach to study immune function, generating >3100 readouts across 16 cell types, 18 pattern recognition receptors and 11 produced cytokines using spectral flow cytometry. To explore geographical variation, we studied the immune system of Europeans, urban, and rural Indonesians. We found differences in immune responses, such as increased IL1{beta} production in rural Indonesians and impaired IFN{gamma} production by innate lymphocytes after TLR8 stimulation. In Europeans vaccinated with mRNA-1273, baseline IFN{gamma} production by innate lymphocytes correlated with SARS-CoV-2 Spike-specific immune responses. In vitro mRNA vaccine stimulation also induced IFN{gamma} production, which was TLR8-dependent and reduced in rural Indonesians. This study highlights functional immune diversity and TLR8s potential role in mRNA vaccine responses. SummaryWe developed an approach to study the function capacity of the immune system, exploring geographical variation and mRNA vaccine responses. This revealed TLR8s potential role in responding to mRNA vaccines, and an impairment in this pathway in rural Indonesians.

immunology↗

Cytotoxic activity against human leukemia cells of Kaempferol-3-O-rhamnoside from Vietnamese Schima wallichii (DC.) Korth: A combination of in vitro and in silico insights

In the investigation of the cytotoxic activity against leukemia cells of Vietnamese medicinal plants, we identified the extract of Schima wallichii (DC.) Korth as capable of inhibiting several leukemia cell lines. In this study, we isolated a main compound as kaempferol-3-O-rhamnoside, marking the first report of this compound being isolated from the stem of Schima wallichii collected in Vietnam. In in vitro experiments, kaempferol-3-O-rhamnoside exhibited cytotoxic effects on three leukemia cell lines, HL-60 and KG-1. Regarding its mechanism of action, the compound effectively inhibited growth of HL-60 and KG-1 leukemia cell lines by activating caspase-3 and caspase-9 in both cell lines. Additionally, kaempferol-3-O-rhamnoside upregulated the pro-apoptotic protein Bax while downregulating the anti-apoptotic protein Bcl-2 in these cell lines. In silico experiments revealed that docking simulations showed kaempferol-3-O-rhamnoside binds to both the allosteric site of procaspase-3 and the active site of PARP1, with binding energies of -7.36 and -10.76 kcal/mol, respectively. Kaempferol-3-O-rhamnoside demonstrated stable binding affinity with PARP1, characterized by significant hydrogen bonding, hydrophobic interactions, and pi-stacking in the molecular dynamic simulations. These results suggest that kaempferol-3-O-rhamnoside has the potential PARP1 inhibitor, making it a promising candidate for targeting leukemia cells. Moreover, it provides evidence for considering this compound in drug discovery and development targeting PARP1-related pathways.

pharmacology and toxicology↗