posted on 2015-12-16, 20:31authored byFelix
L. Yeh, Yiming Zhu, William H. Tepp, Eric A. Johnson, Paul J. Bertics, Edwin R. Chapman
Botulinum neurotoxin (BoNT) A and B are used to treat
neuropathic
disorders; if retargeted, these agents could be used to treat medical
conditions that involve secretion from nonneuronal cells. Here, we
report novel strategies for successfully retargeting BoNTs, and also
tetanus neurotoxin (TeNT), to primary human blood monocyte-derived
macrophages where BoNT/B inhibited the release of tumor necrosis factor-α,
a cytokine that plays a key role in inflammation. Furthermore, mice
treated with retargeted BoNT/B exhibited a significant reduction in
macrophage (MΦ) recruitment, indicating that these toxins can
be used to treat chronic inflammation.