T and B Cell Responses to HIV and Tuberculosis Infections/Coinfection and Vaccinations

A special issue of Vaccines (ISSN 2076-393X). This special issue belongs to the section "HIV Vaccines".

Deadline for manuscript submissions: 5 July 2025 | Viewed by 75

Special Issue Editor

Center for Biomedical Research, University of Texas Health Center at Tyler, Tyler, TX, USA
Interests: vaccine development; virus-host interaction; HIV immunology; gene editing and gene therapy; phage therapy; humanized mouse models
Special Issues, Collections and Topics in MDPI journals

Special Issue Information

Dear Colleagues,

Mycobacterium tuberculosis (Mtb) is the cause of tuberculosis (TB), which has infected an estimated 10 million people and caused 1.5 million deaths worldwide. This makes it one of the leading causes of death by a single infectious agent. Additionally, over one-third of the world's population (more than 2 billion people) has been latently infected with Mtb (LTBI). HIV is another significant pathogen responsible for the deaths of over 40 million people. Coinfection with HIV and TB leads to increased severity and higher mortality and morbidity compared to each infection alone. Currently, there are no effective vaccines for either HIV or tuberculosis, largely due to a limited understanding of HIV/Mtb-induced immunity. T cells are crucial, as they are targets for HIV infection and play a role in the immune response against both pathogens. B cell responses have also been correlated with HIV protection. Therefore, it is essential to extensively study T and B cell responses to HIV and Mtb infections, coinfection, and vaccinations in order to develop effective vaccines. Given the equal importance of T and B cell immunity in HIV/Mtb infections, coinfection, and vaccinations, the following aspects are of interest in this Special Issue:

  1. Characterization of T and B cell immunity after HIV and/or Mtb infections and coinfection using human cohorts.
  2. Develop vaccines for HIV/Mtb single infections or coinfection and test their efficacy in appropriate animal models.
  3. Characterizing T and B cell epitopes and testing their potential for vaccine development.
  4. Identify novel T cell subsets or new functions of existing T cell subsets during HIV/Mtb infections and coinfection.
  5. Profiling of TCR/BCR after infections or vaccinations using high-throughput T/B cell receptor sequencing technology.
  6. Exploration of novel techniques to characterize T and B cell immune responses to HIV/Mtb infections.

Dr. Guohua Yi
Guest Editor

Manuscript Submission Information

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Keywords

  • T cells
  • B cells
  • viral infection
  • vaccination
  • vaccine development
  • immunity
  • vaccine efficacy

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Published Papers

This special issue is now open for submission.
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