Combinatorial leaky probiotic for anticancer immunopotentiation and tumor eradication

Combination therapies present a compelling therapeutic regimen against the immunosuppressive and heterogeneous microenvironment of solid tumors. However, incorporating separate therapeutic modalities in regimen designs can be encumbered by complex logistical, manufacturing, and pharmacokinetic considerations. Herein, we demonstrate a single-vector combinational anticancer therapy using an lpp gene knockout leaky probiotic for simultaneous secretion of immunotherapeutic and oncolytic effector molecules. Through fusion protein design and vector optimization, a Nissle1917 (EcN) bacteria vector is engineered to secrete Neoleukin-2/15 (Neo-2/15) cytokine-functionalized anti-PDL1 nanobody (aPDL1-Neo2/15) and anti-mesothelin-functionalized hemolysin E (HlyE-aMSLN). The multifunctional leaky probiotic enables synchronous immune activation and tumor-targeted cytolytic activity for effective tumor suppression, elevation of tumor immune cell infiltration, and establishment of anticancer immunological memory. lpp gene knockout is further shown to improve probiotic tolerability and intravenous applicability, offering a therapeutically viable approach for combination regimen development.

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Publication Details

Journal
Cell Reports Medicine
Published
2024-10-22
DOI
https://doi.org/10.1016/j.xcrm.2024.101793
Citations
5
Primary Topic
Cancer Research and Treatments
Type
article
Field-Weighted Citation Impact
1.93

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article

Combinatorial leaky probiotic for anticancer immunopotentiation and tumor eradication

See-Khai Lim, Yun Mou, Yi‐Chung Pan, Che‐Ming Jack Hu et al.
5 citations
Cell Reports Medicine
Cancer Research and Treatments
1.93
article

Combinatorial leaky probiotic for anticancer immunopotentiation and tumor eradication

See-Khai Lim, Yun Mou, Yi‐Chung Pan, Che‐Ming Jack Hu, Chung‐Yuan Mou, Chenghao Liu
article en
5 citations

Abstract

Combination therapies present a compelling therapeutic regimen against the immunosuppressive and heterogeneous microenvironment of solid tumors. However, incorporating separate therapeutic modalities in regimen designs can be encumbered by complex logistical, manufacturing, and pharmacokinetic considerations. Herein, we demonstrate a single-vector combinational anticancer therapy using an lpp gene knockout leaky probiotic for simultaneous secretion of immunotherapeutic and oncolytic effector molecules. Through fusion protein design and vector optimization, a Nissle1917 (EcN) bacteria vector is engineered to secrete Neoleukin-2/15 (Neo-2/15) cytokine-functionalized anti-PDL1 nanobody (aPDL1-Neo2/15) and anti-mesothelin-functionalized hemolysin E (HlyE-aMSLN). The multifunctional leaky probiotic enables synchronous immune activation and tumor-targeted cytolytic activity for effective tumor suppression, elevation of tumor immune cell infiltration, and establishment of anticancer immunological memory. lpp gene knockout is further shown to improve probiotic tolerability and intravenous applicability, offering a therapeutically viable approach for combination regimen development.

Cell Reports MedicineVol. 5(11)
National Taiwan University (TW), Institute of Biomedical Sciences, Academia Sinica (TW), Institute of Information Science, Academia Sinica (TW)
Academia Sinica, Ministry of Science and Technology, Taiwan, National Science and Technology Council
Zero hunger
Openalex Percentile: Top 15%
Cancer Research and Treatments
1.93
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