SARS-CoV-2 tropism and immunomodulation in salivary gland

  • Funded by National Institutes of Health (NIH)
  • Total publications:0 publications

Grant number: 1R21DE033795-01A1

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Key facts

  • Disease

    COVID-19
  • Start & end year

    2025
    2027
  • Known Financial Commitments (USD)

    $401,500
  • Funder

    National Institutes of Health (NIH)
  • Principal Investigator

    ASSISTANT PROFESSOR Taichiro Nonaka
  • Research Location

    United States of America
  • Lead Research Institution

    LOUISIANA STATE UNIV HSC SHREVEPORT
  • Research Priority Alignment

    N/A
  • Research Category

    Pathogen: natural history, transmission and diagnostics

  • Research Subcategory

    Immunity

  • Special Interest Tags

    N/A

  • Study Type

    Non-Clinical

  • Clinical Trial Details

    N/A

  • Broad Policy Alignment

    Pending

  • Age Group

    Not Applicable

  • Vulnerable Population

    Not applicable

  • Occupations of Interest

    Not applicable

Abstract

Project Summary/Abstract SARS-CoV-2 has been detected in a variety of human tissues, including the salivary gland. While its behavior in the respiratory tract has been widely studied, relatively little is known about how this virus interacts with oral tissues and the local immune environment. The salivary gland may serve as a unique site of viral presence and immunological modulation, particularly through pathways involving non-classical major histocompatibility complex (MHC) class I molecules. This project aims to investigate fundamental aspects of the innate immune response to SARS-CoV-2 within the salivary gland, with a focus on the molecular interactions between virus- or host-derived peptides and components of the mucosal immune system. In particular, we will explore how antigen presentation mechanisms may shape or reflect local immune activity in this tissue. Identifying such mechanisms will advance our understanding of tissue-specific immune regulation and viral tropism. The proposed research is designed to clarify basic molecular and cellular processes that underlie host-pathogen interactions in the oral cavity. By studying immunological dynamics in the salivary gland, this work will contribute to a framework for understanding mucosal immunity and may reveal foundational principles of immune surveillance in non-respiratory tissues.