Publications by authors named "Cui Yimin"

Background: The development of bivalent or multivalent vaccines offers a promising strategy for combating SARS-CoV-2 mutations.

Research Design And Methods: In this phase 2 trial, conducted from 1 December 2021, to 25 July 2023, 392 unvaccinated adults aged ≥18 years were randomized to receive a primary series of two doses and a booster dose of SCTV01C, a bivalent protein SARS-CoV-2 vaccine.

Results: Geometric mean titers (GMTs) of neutralizing antibodies (nAb) against live Alpha, Beta, Delta, and Omicron showed 85.

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Background: This study aimed to provide a comprehensive review of adverse events (AEs) associated with factor Xa (FXa) inhibitors in pediatric patients.

Methods: We searched PubMed, Embase, Cochrane Library, ClinicalTrials.gov, and the European Union Clinical Trials Register for English-language records from the establishment of the database up to October 17, 2023.

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Atherosclerosis (AS) is a prevalent inflammatory vascular disease characterized by plaque formation, primarily composed of foam cells laden with lipids. Despite lipid-lowering therapies, effective plaque clearance remains challenging due to the overexpression of the CD47 molecule on apoptotic foam cells, inhibiting macrophage-mediated cellular efferocytosis and plaque resolution. Moreover, AS lesions are often associated with severe inflammation and oxidative stress, exacerbating disease progression.

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Article Synopsis
  • Platelets play a key role in blood clotting and are increasingly recognized for their involvement in immune-mediated inflammatory diseases.
  • Resting platelets can be activated by immune complexes and other stimuli, leading to interactions with various immune cells and the release of immune activators.
  • Targeting platelet activation and their interactions with immune and endothelial cells is a promising area for developing new therapeutic strategies.
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Background: is a member of the lactic acid bacterium group commonly found in many salt-fermented foods. Strains of isolated from high-salinity environments have been shown to tolerate salt stress to some extent. However, the specific responses and mechanisms of under salt stress are not fully understood.

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The binding of viruses to host-entry factor receptors is an essential step for viral infection. Many studies have shown that macrophages can internalize viruses and degrade them in lysosomes for clearance in vivo. Inspired by these natural behaviors and using SARS-CoV-2 as a testbed, we harvest lysosomes from activated macrophages and anchor the protein-receptor ACE2 as bait, thus constructing a lysosomal "TRAP" (lysoTRAP) that selectively captures, internalizes, and eventually degrades SARS-CoV-2.

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Liver metastasis is the major cause of death in colorectal cancer (CRC) due to the lack of effective treatment. To explore novel drivers of CRC liver metastasis, the transcriptomes of primary paracancerous, colorectal tumors and metastases from human patients are profiled. It is found that SLIT- and NTRK-like family member 4 (SLITRK4) is the top upregulated gene in liver metastases and is associated with worse overall survival of CRC patients.

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Article Synopsis
  • The study aims to enhance the understanding of how genetic and nongenetic factors influence the pharmacokinetics and pharmacodynamics (PK/PD) of apixaban to enable personalized medication prescriptions for future patients.* -
  • Researchers created an integrated PK/PD model based on data from 181 healthy Chinese volunteers, analyzing various biological markers and genetic factors, with a total of 2877 observations used for the modeling process.* -
  • The final PK model indicates key variables like clearance rate and absorption rate, while the PD model successfully simulates the effects of apixaban on relevant blood markers, supporting the idea that individual dosing can be tailored effectively.*
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Background And Hypothesis: Sensory gating deficit is considered a pathophysiological feature of schizophrenia, which has been linked to N-methyl-d-aspartate receptor (NMDAR) hypofunction as one of the potential underlying mechanisms. Here, we hypothesize that higher levels of NMDAR antibody (Ab) may contribute to the sensory gating deficits in schizophrenia.

Study Design: We enrolled 72 non-smoking inpatients with first-episode schizophrenia (FES), most of them with only a relatively short duration of exposure to antipsychotic medications, and 51 non-smoking healthy controls (HC).

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Background: Pulmonary tuberculosis (PTB), as a respiratory infectious disease, poses significant risks of covert transmission and dissemination. The high aggregation and close contact among students in Chinese schools exacerbate the transmission risk of PTB outbreaks.

Objective: This study investigated the epidemiological characteristics, geographic distribution, and spatiotemporal evolution of student PTB in Chongqing, Southwest China, aiming to delineate the incidence risks and clustering patterns of PTB among students.

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Background: Recently, cyclin-dependent kinase 4/6 inhibitors (CDK4/6i) have emerged as a novel treatment strategy for breast cancer. However, increasing reports of CDK4/6i-associated venous thromboembolism (VTE) have garnered attention. This study assessed CDK4/6i-associated VTE in breast cancer, and examined the effect of CDK4/6i on platelet/coagulation function for the first time in vitro.

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Article Synopsis
  • The study aimed to test the safety, tolerability, and pharmacokinetics of mirikizumab in 60 healthy Chinese adults, who were divided into five dosing groups receiving either the drug or a placebo.
  • No serious side effects or deaths occurred; mild treatment-emergent adverse events (TEAEs) were reported in 56% of participants receiving the drug, compared to 80% in the placebo group.
  • The pharmacokinetic results showed that higher IV doses led to a 3.5-fold increase in drug concentration metrics, while subcutaneous doses increased by 1.6-fold, with the drug remaining in the system for about 10 days.
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  • * Researchers used machine learning to find that UC patients have fewer Lactobacillus bacteria and higher oxidative stress, which is linked to more severe inflammation.
  • * They created a new probiotic treatment using Lactobacillus casei embedded with selenium dots, which improves resistance to stomach acid and helps reduce inflammation and damage in UC models in mice and non-human primates.
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  • MGL-3196 (Resmetirom) is the first approved drug for metabolic dysfunction-associated steatohepatitis (MASH), but its effectiveness varies among individuals and its impact on gut microbiota is unclear.
  • Research compared the effects of MGL-3196 and its derivative HSK31679 on MASH in germ-free versus specific-pathogen free mice to explore the role of gut microbiota.
  • HSK31679 was more effective than MGL-3196 in reducing MASH in mice with gut microbiota, indicating that gut microbiota play a crucial role in the drug's efficacy and its interaction with immune responses.
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Cell therapy, a burgeoning therapeutic strategy, necessitates a scientific regulatory framework but faces challenges in risk-based regulation due to the lack of a global consensus on risk classification. This study applies Bayesian network analysis to compare and evaluate the risk classification strategies for cellular products proposed by the Food and Drug Administration (FDA), Ministry of Health, Labour and Welfare (MHLW), and World Health Organization (WHO), using real-world data to validate the models. The appropriateness of key risk factors is assessed within the three regulatory frameworks, along with their implications for clinical safety.

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GLS4 is a first-in-class hepatitis B virus (HBV) capsid assembly modulator (class I) that is co-administered with ritonavir to maintain the anticipated concentration required for the effective antiviral activity of GLS4. In this study, the first physiologically-based pharmacokinetic (PBPK) model for GLS4/ritonavir was successfully developed. The predictive performance of the PBPK model was verified using data from 39 clinical studies, including single-dose, multiple-dose, food effects, and drug-drug interactions (DDI).

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Article Synopsis
  • - The study investigates the effects of ASC22 (a PD-1 antibody) on patients with chronic hepatitis B who are already virally suppressed using nucleos(t)ide analogs, aiming to find a potential cure for HBV by targeting the PD-1 pathway.
  • - In a phase IIb trial involving 149 patients, those receiving 1.0 mg/kg ASC22 experienced significant declines in HBsAg levels compared to the placebo group, with 30% achieving HBsAg loss among those with lower baseline levels.
  • - The treatment was found to be safe and well-tolerated, with mostly mild adverse events reported, indicating ASC22 has potential as a therapeutic option for chronic hepatitis B infection.
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Physiologically based pharmacokinetic (PBPK) models which can leverage preclinical data to predict the pharmacokinetic properties of drugs rapidly became an essential tool to improve the efficiency and quality of novel drug development. In this review, by searching the Application Review Files in Drugs@FDA, we analyzed the current application of PBPK models in novel drugs approved by the U.S.

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  • Bone metastases affect over 70% of advanced prostate cancer patients, contributing to a poor prognosis, and the study highlights the role of anoikis resistance in promoting metastasis.
  • The gene TUBB3 is identified as a significant factor in anoikis resistance, showing increased expression in bone metastatic prostate cancer, and its depletion can reverse this resistance and hinder cell invasion and migration.
  • The research also introduces bone-targeting lipid nanoparticles (BT-LNP) for effectively delivering siRNA targeting TUBB3, demonstrating potential as a novel therapy to reduce prostate cancer bone metastasis.
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Proprotein convertase subtilisin kexin type 9 (PCSK9) inhibitors are widely recognised as being able to induce a potent reduction in low‑density lipoprotein‑cholesterol. An increasing number of studies have suggested that PCSK9 also influences the haemostatic system by altering platelet function and the coagulation cascade. These findings have significant implications for anti‑PCSK9 therapy in patients with specific coagulation conditions, including expanded indications, dose adjustments and drug interactions.

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Background: Drug-induced delirium is known risk factors associated with increased morbidity and mortality in older patients. The objective was to evaluate the risk of drug-related delirium in older patients based on the FDA Adverse Event Reporting System (FAERS).

Research Design And Methods: Delirium reports in older patients (age ≥65) extracted from the FAERS database using Open Vigil 2.

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Previous studies have shown that low platelet count combined with high plasma total homocysteine (tHcy) increased stroke risk and can be lowered by 73% with folic acid. However, the combined role of other platelet activation parameters and the methylenetetrahydrofolate reductase (MTHFR) C677T genotypes on stroke risk and folic acid treatment benefit remain to be examined. This study aimed to investigate if platelet activation parameters and MTHFR genotypes jointly impact folic acid treatment efficacy in first stroke prevention.

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Background: Previous studies involving risk-benefit analysis of trastuzumab deruxtecan (DS-8201) have indicated the benefit of this treatment, although it may increase the risk of interstitial lung disease (ILD) and/or pneumonitis in certain patients. This study aimed to assess the safety of DS-8201.

Methods: A search was done for relevant articles in four electronic databases: PubMed, Embase, the Cochrane Library, and ClinicalTrials.

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Purpose: This study aimed to explore the pharmacogenetic variability associated with the pharmacokinetics (PK) and pharmacodynamics (PD) of rivaroxaban in healthy Chinese subjects.

Methods: This was a multicenter study that included 304 healthy adults aged 18 to 45 years with unknown genotypes. All participants were administered a single dose of rivaroxaban at 10 mg, 15 mg, or 20 mg.

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C-type lectin-like receptor-2 (CLEC-2) is a member of the C-type lectin superfamily of cell surface receptors. The first confirmed endogenous and exogenous ligands of CLEC-2 are podoplanin and rhodocytin, respectively. CLEC-2 is expressed on the surface of platelets, which participates in platelet activation and aggregation by binding with its ligands.

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