Publications by authors named "Yohei Uchida"

Purpose: Trastuzumab-pertuzumab (HP) plus taxane is a current standard first-line therapy for recurrent or metastatic human epidermal growth factor 2 (HER2)+ breast cancer (BC). We investigated noninferiority of eribulin to a taxane when combined with dual HER2 blockade as first-line systemic treatment for locally advanced/metastatic HER2+ BC.

Methods: In the phase III EMERALD trial (target sample size, 480; ClinicalTrials.

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Respiratory syncytial virus (RSV) is a leading cause of upper and lower respiratory tract infection, especially in children and the elderly. Various vaccines containing the major transmembrane surface proteins of RSV (proteins F and G) have been tested; however, they have either afforded inadequate protection or are associated with the risk of vaccine-enhanced disease (VED). Recently, F protein-based maternal immunization and vaccines for elderly patients have shown promising results in phase III clinical trials, however, these vaccines have been administered by injection.

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Article Synopsis
  • Cationic cholesteryl-group-bearing pullulan nanogel (cCHP-nanogel) is a promising carrier for nasal vaccines, but concerns arise about its potential to reach the central nervous system due to proximity in the nasal cavity.
  • Previous studies showed no vaccine antigens deposited in the cerebrum or olfactory bulbs after administration in mice and NHPs.
  • In this study, positron emission tomography (PET) confirmed that the cCHP-nanogel remained safe and did not accumulate in the brains or eyes of either species after nasal delivery.
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Passive administration of neutralizing antibodies (Abs) is an attractive strategy for the control of gastrointestinal infections. However, an unanswered practical concern is the need to assure the stability of sufficient amounts of orally administered neutralizing Abs against intestinal pathogens (e.g.

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Article Synopsis
  • Nontypeable Haemophilus influenzae (NTHi) is a significant cause of ear infections in children, and there is currently no licensed vaccine against it.
  • Researchers developed a nasal vaccine using a cationic cholesteryl pullulan-based nanogel (cCHP) that contains a conserved surface protein, P6, which is found in 90% of NTHi strains.
  • Immunizing mice with this vaccine resulted in the production of specific antibodies (IgA) that effectively inhibited NTHi biofilm formation and colonization, showing promise for preventing various NTHi-related respiratory infections.
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Background: There are an estimated 1·3-4·0 million cases of cholera and 20 000-140 000 cholera-related deaths worldwide each year. The rice-based cholera toxin B subunit (CTB) vaccine, MucoRice-CTB, is an oral candidate vaccine that does not require a cold chain, has shown efficacy in animal models, and could be of benefit in places where there is a paucity of medical infrastructure. We aim to assess the safety, tolerability, and immunogenicity of MucoRice-CTB in humans.

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Current polysaccharide-based pneumococcal vaccines are effective but not compatible with all serotypes of Streptococcus pneumoniae. We previously developed an adjuvant-free cationic nanogel nasal vaccine containing pneumococcal surface protein A (PspA), which is expressed on the surfaces of all pneumococcal serotypes. Here, to address the sequence diversity of PspA proteins, we formulated a cationic nanogel-based trivalent pneumococcal nasal vaccine and demonstrated the vaccine's immunogenicity and protective efficacy in macaques by using a newly developed nasal spray device applicable to humans.

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Article Synopsis
  • The study describes the development of a nasal vaccine delivery system using a nanosized hydrogel (nanogel) to encapsulate pneumococcal surface protein A (PspA) for immunization.
  • Various methods (PAGE and ELISA) were used to characterize the encapsulation and release of PspA from the nanogel, revealing that heat treatment negatively affected the vaccine's immunologic activity.
  • The trivalent nanogel-PspA formulation effectively internalized into nasal mucosa in mice, maintaining strong immunogenic potential when not heat-treated, highlighting the importance of proper handling for vaccine efficacy.
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Our current study focused on elucidating the role of specific chemokine-receptor interactions in antigen (Ag)-specific immune cell migration from nasal to genital mucosal tissues. This cellular migration is critical to induce effective Ag-specific immune responses against sexually transmitted genital infections. In this study, nasal immunization with live attenuated HSV-2 TK induced the upregulation of CCR5 expression in effector immune cells, including CD4 T cells, in Ag-priming sites and vaginal tissue.

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Aberrant Wnt/β-catenin signaling is implicated in tumorigenesis and the progression of human colorectal cancers, and mutations in the components of the Wnt/β-catenin signaling pathway are observed in the majority of patients. Therefore, extensive studies on the Wnt signaling pathway and its target genes are crucial to understand the molecular events of tumorigenesis and develop an efficacious therapy. In this study, we showed that the stress response gene ATF3 is transcriptionally activated by the binding of β-catenin and TCF4 to the redundant TCF4 site at the proximal promoter region of the ATF3 gene, indicating that ATF3 is a direct target of the Wnt/β-catenin pathway.

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Elongin A was shown previously to be capable of potently activating the rate of RNA polymerase II (RNAPII) transcription elongation in vitro by suppressing transient pausing by the enzyme at many sites along DNA templates. The role of Elongin A in RNAPII transcription in mammalian cells, however, has not been clearly established. In this report, we investigate the function of Elongin A in RNAPII transcription.

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