Cytotoxic granules and effector molecules from immune cells in tuberculosis: Mechanisms of host defense and therapeutic potential.
Yongwei Qin, Jianhao Xu, Qinglan Wang, Jiahai Shi
Virulence · 2025-12
Abstract
Tuberculosis (TB), a disease caused by(), remains one of the most formidable infectious diseases globally. The immune system orchestrates a complex response including, but not limited to, T lymphocytes, natural killer (NK) cells, macrophages, and dendritic cells (DCs) to control and eliminate. While these cells are well-recognized for their roles in anti-tumor immunity, their contributions to the defense againstare equally critical. This review delves into the specific mechanisms by which these immune cells release cytotoxic enzymes and effector molecules, offering new insights into their pivotal roles inclearance. A deeper understanding of these mechanisms is essential for developing more effective strategies to combat tuberculosis.
MeSH terms
- Humans
- Mycobacterium tuberculosis
- Tuberculosis
- Dendritic Cells
- Killer Cells, Natural
- Macrophages
- Animals
- T-Lymphocytes
- Cytoplasmic Granules
- Host-Pathogen Interactions