Response to Comment on “Trapping of Lipopolysaccharide to Promote Immunotherapy against Colorectal Cancer and Attenuate Liver Metastasis”

We greatly appreciate Dr. Szaryńska’s interest in our work, and appreciate her comment on our article published in Advanced Materials in 2018. In a previous publication, Dr. Szaryńska’s group reported that lipopolysaccharide (LPS) increased maturation and activation status of dendritic cells (DCs) in vitro, and hypothesized that LPS may be considered a profitable supplement before launching a DC-based immunotherapy. However, the results from our publication showed that blockade of toll-like receptor 4 (TLR4) pathway or trapping of LPS by gene delivery using lipid–protamine–DNA (LPD) nanoparticles alleviated immunosuppressive microenvironment in an orthotopic colorectal cancer (CRC) mouse model, and promoted immune checkpoint therapy in CRC. Therefore, Dr. Szaryńska commented suggesting the experimental conditions and chosen aspects should be considered in clinical applications of LPS-associated protocols.

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Publication Details

Journal
UNC Libraries
Published
2025-10-07
DOI
https://doi.org/10.17615/rbqg-ga38
Primary Topic
Immune Response and Inflammation
Type
article
Field-Weighted Citation Impact
0.00
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article

Response to Comment on “Trapping of Lipopolysaccharide to Promote Immunotherapy against Colorectal Cancer and Attenuate Liver Metastasis”

Wantong Song, Rihe Liu, Leaf Huang
UNC Libraries
Immune Response and Inflammation
article

Response to Comment on “Trapping of Lipopolysaccharide to Promote Immunotherapy against Colorectal Cancer and Attenuate Liver Metastasis”

Wantong Song, Rihe Liu, Leaf Huang
article en

Abstract

We greatly appreciate Dr. Szaryńska’s interest in our work, and appreciate her comment on our article published in Advanced Materials in 2018. In a previous publication, Dr. Szaryńska’s group reported that lipopolysaccharide (LPS) increased maturation and activation status of dendritic cells (DCs) in vitro, and hypothesized that LPS may be considered a profitable supplement before launching a DC-based immunotherapy. However, the results from our publication showed that blockade of toll-like receptor 4 (TLR4) pathway or trapping of LPS by gene delivery using lipid–protamine–DNA (LPD) nanoparticles alleviated immunosuppressive microenvironment in an orthotopic colorectal cancer (CRC) mouse model, and promoted immune checkpoint therapy in CRC. Therefore, Dr. Szaryńska commented suggesting the experimental conditions and chosen aspects should be considered in clinical applications of LPS-associated protocols.

UNC Libraries
University of North Carolina at Chapel Hill (US)
Openalex Percentile: Top 70%
Immune Response and Inflammation
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