Release of LL-37 by activated human Vgamma9Vdelta2 T cells: a microbicidal weapon against Brucella suis.
Dudal. Sherri S; Turriere. Chrystell C; Bessoles. Stephanie S; Fontes. Pascaline P; Sanchez. Françoise F; Liautard. Janny J; Liautard. Jean-Pierre JP; Lafont. Virginie V
Key Findings
- Activated Vγ9Vδ2 T cells produce and release the peptide LL‑37.
- LL‑37 has direct antibacterial activity against Brucella suis in lab tests.
- LL‑37 contributes to the overall bactericidal effect of these T cells.
Practical Outcomes
- The study confirms that LL‑37 is an innate antimicrobial factor, but it does not provide dosing, safety, or supplementation guidelines. For biohackers, the finding suggests LL‑37 could be a target for future anti‑infection strategies, yet more research is needed before it can be used in real‑world protocols.
Summary
When a special type of immune cell (Vγ9Vδ2 T cell) gets activated, it releases a natural antimicrobial protein called LL‑37, which can kill the bacteria Brucella suis. This shows that LL‑37 is part of the body’s own weaponry against certain infections.
Abstract
Human Vgamma9Vdelta2 T cells play a crucial role in early immune response to intracellular pathogens. Moreover, in brucellosis, these cells are drastically increased in the peripheral blood of patients during the acute phase of infection. In vitro, Vgamma9Vdelta2 T cells are capable of inhibiting Brucella growth and development through a combination of mechanisms: 1) cytotoxicity, 2) macrophage activation and bactericidal activity through cytokine and chemokine secretion, and 3) antibacterial effects. We previously described that antibacterial factors were found in supernatants from activated Vgamma9Vdelta2 T cells. In this study, we show that Vgamma9Vdelta2 T cells express the human cathelicidin hCAP18 and its mature form, known as LL-37, is released upon activation of Vgamma9Vdelta2 T cells. We also show that LL-37 has an antibacterial effect on Brucella suis. Overall, our results demonstrate that LL-37 is a soluble factor responsible for a part of the bactericidal activity of Vgamma9Vdelta2 T cells.
Study Information
pubmed
2006
2006-10-15T00:00:00.000Z
10.4049/jimmunol.177.8.5533
45
38