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A bioengineered probiotic for the oral delivery of a peptide Kv1.3 channel blocker to treat rheumatoid arthritis
被引:11
|作者:
Wang, Yuqing
[1
]
Zhu, Duolong
[2
,3
]
Ortiz-Velez, Laura C.
[4
]
Perry, Jacob L.
[2
,3
]
Pennington, Michael W.
[5
]
Hyser, Joseph M.
[1
,2
,3
]
Britton, Robert A.
[2
,3
]
Beeton, Christine
[1
,6
,7
]
机构:
[1] Baylor Coll Med, Dept Integrat Physiol, Houston, TX 77030 USA
[2] Baylor Coll Med, Dept Mol Virol & Microbiol, Houston, TX 77030 USA
[3] Baylor Coll Med, Alkek Ctr Metagen & Microbiome Res, Houston, TX 77030 USA
[4] Pana Bio Inc, Houston, TX 77051 USA
[5] Ambiopharm Inc, North Augusta, SC 29842 USA
[6] Baylor Coll Med, Biol Inflammat Ctr, Houston, TX 77030 USA
[7] Baylor Coll Med, Ctr Drug Discovery, Houston, TX 77030 USA
来源:
关键词:
synthetic biology;
Kv1;
3;
channel;
drug delivery;
MEMORY T-CELLS;
KV1.3-BLOCKING PEPTIDE;
KCA1.1;
CHANNELS;
K+ CHANNELS;
RAT MODELS;
BONE LOSS;
EXPRESSION;
TOXIN;
IMMUNOMODULATION;
SECRETION;
D O I:
10.1073/pnas.2211977120
中图分类号:
O [数理科学和化学];
P [天文学、地球科学];
Q [生物科学];
N [自然科学总论];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
Engineered microbes for the delivery of biologics are a promising avenue for the treat-ment of various conditions such as chronic inflammatory disorders and metabolic dis-ease. In this study, we developed a genetically engineered probiotic delivery system that delivers a peptide to the intestinal tract with high efficacy. We constructed an inducible system in the probiotic Lactobacillus reuteri to secrete the Kv1.3 potassium blocker ShK-235 (LrS235). We show that LrS235 culture supernatants block Kv1.3 currents and preferentially inhibit human T effector memory (TEM) lymphocyte proliferation in vitro. A single oral gavage of healthy rats with LrS235 resulted in sufficient functional ShK-235 in the circulation to reduce inflammation in a delayed-type hypersensitivity model of atopic dermatitis mediated by TEM cells. Furthermore, the daily oral gavage of LrS235 dramatically reduced clinical signs of disease and joint inflammation in rats with a model of rheumatoid arthritis without eliciting immunogenicity against ShK-235. This work demonstrates the efficacy of using the probiotic L. reuteri as a novel oral delivery platform for the peptide ShK-235 and provides an efficacious strategy to deliver other biologics with great translational potential.
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页数:9
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