424 results match your criteria: "Joint Research Center for Human Retrovirus Infection.[Affiliation]"

Facilitating cholangiocarcinoma inhibition by targeting CD47.

Exp Mol Pathol

December 2024

Division of Hematopoiesis, Joint Research Center for Human Retrovirus Infection and Graduate School of Medical Sciences, Kumamoto University, Kumamoto 860-0811, Japan. Electronic address:

Immune evasion is one of the mechanisms by which cancer cells acquire immunity during cancer development and progression. One of these is the increased expression of cluster of differentiation 47 (CD47), a transmembrane glycoprotein that protects cells from phagocytic elimination. The interaction between CD47 and signal regulatory protein alpha (SIRPα) on macrophages alleviates the phagocytic signal.

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Article Synopsis
  • * A new vaccine, ChAdOx1.COVconsv12, was created to enhance the immune response by targeting conserved viral regions, aiming to provide broader protection against various sarbecoviruses, including new variants of SARS-CoV-2.
  • * In studies with mice and Syrian hamsters, while ChAdOx1.COVconsv12 alone didn't prevent SARS-CoV-2 infection, it improved recovery and reduced viral load when given alongside a smaller dose of the spike vaccine, indicating potential benefits
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Evaluating the Use of Sacran, a Polysaccharide Isolated from , as a Possible Microbicide for Preventing HIV-1 Infection.

Viruses

September 2024

Division of Hematopoiesis, Joint Research Center for Human Retrovirus Infection, Kumamoto University, 2-2-1 Honjo, Chuo-ku, Kumamoto 860-0811, Japan.

Article Synopsis
  • Sacran is a special substance that comes from a type of blue-green algae and can help protect against HIV, a virus that causes AIDS.
  • Since a new treatment for HIV was created, fewer people are dying from AIDS, but the virus is still spreading through sexual contact.
  • The study showed that sacran can stop HIV from spreading and might work even better when used with other HIV medicines.
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  • Overexpression of acetyl-CoA carboxylase 1 (ACC1) is linked to poor outcomes in cholangiocarcinoma (CCA) patients, and reducing ACC1 levels impairs cell growth in lab models.
  • The study investigated how inhibiting ACC1 leads to increased protein acetylation, revealing that both genetic knockdown and pharmacological inhibition resulted in hyperacetylated proteins that hindered cell growth and migration.
  • The research identified HSP90 as a key acetylated protein and established a connection between protein hyperacetylation and the AKT/GSK3β/Snail pathway, indicating that targeting ACC1 and lysine deacetylases could be effective in treating CCA.
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Background: Data are limited on the protective role of the Omicron BA bivalent vaccine, previous infection, and their induced neutralizing antibodies against Omicron XBB.1.16 and EG.

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  • - HTLV-1 can quickly transform CD4+ T cells in a lab setting, but most infected people remain asymptomatic, indicating a balance between the virus and the host's immune response.
  • - The study found a variant in the HTLV-1 Tax301-309 viral antigen in individuals with a specific HLA-A24 type, which affected the detection of anti-Tax cytotoxic T cells (CTLs).
  • - More than half of the T-cell receptors (TCRs) from these anti-Tax CTLs failed to recognize the mismatched Tax301-309 peptides, underlining the need for precise matching of viral antigens in T-cell therapy for adult T-cell leukemia (ATL).
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Induced lactation in a transgender woman: case report.

Int Breastfeed J

September 2024

The Nippon Foundation Human Milk Bank, Tokyo, Japan.

Background: Breastfeeding offers significant health benefits, but its practice and success can vary. While research on induced lactation in cisgender women has been documented, there is limited research on lactation induction in transgender women.

Case Presentation: A 50-year-old transgender woman undergoing hormone therapy and living with a pregnant partner sought to co-feed using induced lactation.

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Development of a sensor to detect methylmercury toxicity.

Sci Rep

September 2024

Department of Basic Medical Sciences, National Institute for Minamata Disease, 4058-18 Hama, Minamata, Kumamoto, 867-0008, Japan.

Methylmercury (MeHg) is a well-known neurotoxicant that induces various cellular functions depending on cellular- and developmental-specific vulnerabilities. MeHg has a high affinity for selenol and thiol groups, thus impairing the antioxidant system. Such affinity characteristics of MeHg led us to develop sensor vectors to assess MeHg toxicity.

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Molecular and structural insights into SARS-CoV-2 evolution: from BA.2 to XBB subvariants.

mBio

October 2024

Division of Systems Virology, Department of Microbiology and Immunology, The Institute of Medical Science, The University of Tokyo, Tokyo, Japan.

Due to the incessant emergence of various SARS-CoV-2 variants with enhanced fitness in the human population, controlling the COVID-19 pandemic has been challenging. Understanding how the virus enhances its fitness during a pandemic could offer valuable insights for more effective control of viral epidemics. In this manuscript, we review the evolution of SARS-CoV-2 from early 2022 to the end of 2023-from Omicron BA.

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Role of HLA-B*58:01-restricted CD8+ T cells in HIV-1 subtype AE infection.

J Infect Dis

September 2024

Division of International Collaboration Research and Tokyo Joint Laboratory, Joint Research Center for Human Retrovirus Infection, Kumamoto University, Kumamoto/Tokyo, Japan.

HLA-B*58:01 and HLA-B*57 are protective alleles against HIV-1 subtype B or C infection whereas these HLA alleles have not been reported as protective in HIV-1 subtype AE infection. Although HLA-B*58:01-restricted and HLA-B*57-restricted HIV-1-specific CD8+ T cells have been thoroughly analyzed in subtype B or C infection, they have only been partially analyzed in subtype AE infection. We identified six HLA-B*58:01-restricted subtype AE epitopes in Vietnamese individuals infected with subtype AE.

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Histoplasmosis is caused by Histoplasma capsulatum and is prevalent in areas of the world where H. capsulatum is endemic. We herein report a patient diagnosed with HIV-1 who developed histoplasmosis from a non-H.

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Article Synopsis
  • Cholangiocarcinoma (CCA) is a challenging cancer with poor outcomes due to late diagnosis and resistance to chemotherapy, making effective treatments scarce.
  • Dinaciclib, a small molecule that inhibits cyclin-dependent kinases (CDKs), has shown promise in reducing growth and inducing cell death in CCA cells resistant to standard chemotherapy, like gemcitabine.
  • The study demonstrates that dinaciclib not only hinders the proliferation of CCA cells but also enhances the effectiveness of gemcitabine, highlighting its potential as a new therapeutic option for treating CCA.
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Human immunodeficiency virus 1 (HIV-1) infection is characterized by a dynamic and persistent state of viral replication that overwhelms the host immune system in the absence of antiretroviral therapy (ART). The impact of prolonged treatment on the antiviral efficacy of HIV-1-specific CD8 T cells has nonetheless remained unknown. Here, we used single-cell technologies to address this issue in a cohort of aging individuals infected early during the pandemic and subsequently treated with continuous ART.

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Unraveling T-cell dynamics using fluorescent timer: Insights from the Tocky system.

Biophys Physicobiol

February 2024

Department of Life Sciences, Imperial College London, London, SW7 2AZ, United Kingdom.

Understanding the temporal dynamics of T-cell transcription is crucial for insights into immune cell function and development. In this study, we show the features of the Timer-of-Cell-Kinetics-and-Activity (Tocky) system, which enables analysis of temporal dynamics of cell activities and differentiation, leveraging Fluorescent Timer protein, which spontaneously changes its emission spectrum from blue to red fluorescence in known kinetics, as reporters. The current study examines the properties of the Tocky system, highlighting the Timer-Angle approach, which is a core algorithm of Tocky analysis and converts Timer Blue and Red fluorescence into Timer Angle and Intensity by trigonometric transformation.

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A heterocyclic compound inhibits viral release by inducing cell surface BST2/Tetherin/CD317/HM1.24.

J Biol Chem

September 2024

Department of Microbiology, Faculty of Life Sciences, Kumamoto University, Kumamoto, Japan; Collaboration Unit for Infection, Joint Research Center for Human Retrovirus Infection, Kumamoto University, Kumamoto, Japan. Electronic address:

The introduction of combined antiretroviral therapy (cART) has greatly improved the quality of life of human immunodeficiency virus type 1 (HIV-1)-infected individuals. Nonetheless, the ever-present desire to seek out a full remedy for HIV-1 infections makes the discovery of novel antiviral medication compelling. Owing to this, a new late-stage inhibitor, Lenacapavir/Sunlenca, an HIV multi-phase suppressor, was clinically authorized in 2022.

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Virological characteristics of the SARS-CoV-2 KP.3.1.1 variant.

Lancet Infect Dis

October 2024

Division of Systems Virology, Department of Microbiology and Immunology, The University of Tokyo, Tokyo 113-0033, Japan; International Research Center for Infectious Diseases, The University of Tokyo, Tokyo 113-0033, Japan; International Vaccine Design Center, The Institute of Medical Science, The University of Tokyo, Tokyo 113-0033, Japan; Graduate School of Medicine, The University of Tokyo, Tokyo, Japan; Department of Computational Biology and Medical Sciences, Graduate School of Frontier Sciences, The University of Tokyo, Kashiwa, Japan; Collaboration Unit for Infection, Joint Research Center for Human Retrovirus Infection, Kumamoto University, Kumamoto, Japan; MRC-University of Glasgow Centre for Virus Research, Glasgow, Scotland, UK. Electronic address:

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HIV viral suppression in the era of dolutegravir use: Findings from a national survey in Tanzania.

PLoS One

August 2024

Collaboration Unit for Infection, Joint Research Center for Human Retrovirus Infection, Kumamoto University, Kumamoto, Japan.

Background: Tanzania has made significant progress in improving access to HIV care and treatment. However, virologic suppression among people living with HIV (PLHIV) has not been fully realized. In March 2019, Tanzania introduced a World Health Organization (WHO)-recommended dolutegravir-based regimen as the default first-line regimen.

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Background: Highly transmissible viruses including SARS-CoV-2 frequently accumulate novel mutations that are detected via high-throughput sequencing. However, there is a need to develop an alternative rapid and non-expensive approach. Here we developed a novel multiplex DNA detection method Intelli-OVI for analysing existing and novel mutations of SARS-CoV-2.

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PAX5 functions as a tumor suppressor by RB-E2F-mediated cell cycle arrest in Kaposi sarcoma-associated herpesvirus-infected primary effusion lymphoma.

Neoplasia

October 2024

Division of Hematopoiesis, Joint Research Center for Human Retrovirus Infection, Kumamoto University, Honjo, Kumamoto, Japan. Electronic address:

Primary effusion lymphoma (PEL) is a malignant B-cell lymphoma attributable to Kaposi sarcoma-associated herpesvirus (KSHV) infection. PEL is characterized by invasive behavior, showing recurrent effusions in body cavities. The clinical outcome and typical prognosis in patients with PEL are poor and potentially lethal.

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Background: Diabetes mellitus (DM) is associated with the increased risk of development and the advancement of cholangiocarcinoma (CCA). High glucose levels were previously shown for upregulating interleukin-1β (IL-1β) in CCA cells with unclear functions. The present study, thus, aimed to investigate molecular mechanisms linking DM to CCA progression, with IL-1β hypothesized as a communicating cytokine.

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Recombination as an evolutionary driver of MERS-related coronavirus emergence.

Lancet Infect Dis

September 2024

Division of Systems Virology, Department of Microbiology and Immunology, The University of Tokyo, Tokyo 113-0033, Japan; International Research Center for Infectious Diseases, The University of Tokyo, Tokyo 113-0033, Japan; International Vaccine Design Center, The Institute of Medical Science, The University of Tokyo, Tokyo 113-0033, Japan; Department of Computational Biology and Medical Sciences, Graduate School of Frontier Sciences, The University of Tokyo, Kashiwa, Japan; MRC-University of Glasgow Centre for Virus Research, Glasgow, UK; Collaboration Unit for Infection, Joint Research Center for Human Retrovirus infection, Kumamoto University, Kumamoto, Japan. Electronic address:

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Potential Role of APOBEC3 Family Proteins in SARS-CoV-2 Replication.

Viruses

July 2024

Division of Molecular Virology and Genetics, Joint Research Center for Human Retrovirus Infection, Kumamoto University, Kumamoto 860-0811, Japan.

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has acquired multiple mutations since its emergence. Analyses of the SARS-CoV-2 genomes from infected patients exhibit a bias toward C-to-U mutations, which are suggested to be caused by the apolipoprotein B mRNA editing enzyme polypeptide-like 3 (APOBEC3, A3) cytosine deaminase proteins. However, the role of A3 enzymes in SARS-CoV-2 replication remains unclear.

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Analysis of the susceptibility of refractory hepatitis C virus resistant to nonstructural 5A inhibitors.

Sci Rep

July 2024

Digestive and Lifestyle Diseases, Department of Human and Environmental Sciences, Kagoshima University Graduate School of Medical and Dental Sciences, 8‑35‑1 Sakuragaoka, Kagoshima, 890‑8544, Japan.

Article Synopsis
  • Resistance-associated substitutions (RASs) in hepatitis C virus (HCV) can significantly reduce the effectiveness of direct-acting antivirals (DAAs), particularly in patients experiencing treatment failure.
  • In a study using a subgenomic replicon system, specific RASs were found to have extremely high levels of resistance to several DAAs, showcasing the varying degrees of resistance among different mutations.
  • The research indicates that combining pibrentasvir with sofosbuvir may effectively treat HCV infections with these resistance mutations, potentially leading to successful eradication.
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Regulatory T cells (Tregs) possess unique immunosuppressive activity among CD4-positive T cells. Tregs are ubiquitously present in mammals and function to calm excessive immune responses, thereby suppressing allergies or autoimmune diseases. On the other hand, due to their immunosuppressive function, Tregs are thought to promote cancer progression.

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HLA-A*24 Increases the Risk of HTLV-1-Associated Myelopathy despite Reducing HTLV-1 Proviral Load.

Int J Mol Sci

June 2024

Division of Neuroimmunology, Joint Research Center for Human Retrovirus Infection, Kagoshima University, 8-35-1 Sakuragaoka, Kagoshima 890-8544, Japan.

Increased human T-cell leukemia virus type 1 (HTLV-1) proviral load (PVL) is a significant risk factor for HTLV-1-associated myelopathy/tropical spastic paraparesis (HAM/TSP). There is controversy surrounding whether HTLV-1-specific cytotoxic T lymphocytes (CTLs) are beneficial or harmful to HAM/TSP patients. Recently, HTLV-1 Tax 301-309 has been identified as an immunodominant epitope restricted to HLA-A*2402.

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