Low molecular weight heparin synergistically enhances the efficacy of adoptive and anti-PD-1-based immunotherapy by increasing lymphocyte infiltration in colorectal cancer

• Published in: Journal for immunotherapy of cancer Vol. 11; no. 8; p. e007080
• Main Authors: Quan, Yibo, He, Jie, Zou, Qi, Zhang, Liuxi, Sun, Qihui, Huang, Hongli, Li, Wanglin, Xie, Keping, Wei, Fang
• Format: Journal Article
• Language: English
• Published: London BMJ Publishing Group LTD 01.08.2023; BMJ Publishing Group
• Series: Original research
• Subjects: Anticoagulants; Apoptosis; Basic Tumor Immunology; Cancer; Cancer therapies; Cells; Chemotherapy; Cloning; Colorectal cancer; Hypoxia; Immunotherapy; Laboratory animals; Liver; Lymphocytes; Medical prognosis; Metastasis; Molecular weight; Surgery; Tumors; Vascular endothelial growth factor; China
• ISSN: 2051-1426; 2051-1426
• DOI: 10.1136/jitc-2023-007080

Background Immunotherapy, including adoptive cell therapy (ACT) and immune checkpoint inhibitors (ICIs), has a limited effect in most patients with colorectal cancer (CRC), and the efficacy is further limited in patients with liver metastasis. Lack of antitumor lymphocyte infiltration could be a major cause, and there remains an urgent need for more potent and safer therapies for CRC. Methods In this study, the antitumoral synergism of low molecular weight heparin (LMWH) combined with immunotherapy in the microsatellite stable (MSS) highly aggressive murine model of CRC was fully evaluated. Results Dual LMWH and ACT objectively mediated the stagnation of tumor growth and inhibition of liver metastasis, neither LMWH nor ACT alone had any antitumoral activity on them. The combination of LMWH and ACT obviously increased the infiltration of intratumor CD8 + T cells, as revealed by multiplex immunohistochemistry, purified CD8 + T-cell transfer assay, and IVIM in vivo imaging. Mechanistically, evaluation of changes in the tumor microenvironment revealed that LMWH improved tumor vascular normalization and facilitated the trafficking of activated CD8 + T cells into tumors. Similarly, LMWH combined with anti-programmed cell death protein 1 (PD-1) therapy provided superior antitumor activity as compared with the single PD-1 blockade in murine CT26 tumor models. Conclusions LMWH could enhance ACT and ICIs-based immunotherapy by increasing lymphocyte infiltration into tumors, especially cytotoxic CD8 + T cells. These results indicate that combining LMWH with an immunotherapy strategy presents a promising and safe approach for CRC treatment, especially in MSS tumors.