Thymic Microenvironment Remodeling in Cancer Cachexia as a Determinant of Checkpoint Inhibitor Efficacy and Toxicity
ABSTRACT Background The discovery of immune checkpoints links autoimmunity and cancer, with thymus atrophy reportedly causing autoimmune multiorgan inflammation. The impact of cancer cachexia on thymic involution and its clinical significance remains unclear. This study aimed to investigate this eff...
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| Language: | English |
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Wiley
2025-08-01
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| Series: | Journal of Cachexia, Sarcopenia and Muscle |
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| Online Access: | https://doi.org/10.1002/jcsm.13874 |
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| author | Run‐Kai Huang Yan‐Fang Xing Xiang‐Yuan Wu Zhao‐Hui Shi Li Wei Xiao‐Tong Lv Lin‐Jiao Peng Xiu‐Qing Pang Qin‐Tai Yang Xing Li |
| author_facet | Run‐Kai Huang Yan‐Fang Xing Xiang‐Yuan Wu Zhao‐Hui Shi Li Wei Xiao‐Tong Lv Lin‐Jiao Peng Xiu‐Qing Pang Qin‐Tai Yang Xing Li |
| author_sort | Run‐Kai Huang |
| collection | DOAJ |
| description | ABSTRACT Background The discovery of immune checkpoints links autoimmunity and cancer, with thymus atrophy reportedly causing autoimmune multiorgan inflammation. The impact of cancer cachexia on thymic involution and its clinical significance remains unclear. This study aimed to investigate this effect and its association with immune checkpoint inhibitor (ICI) treatment. Methods Single‐cell sequencing, immunofluorescence and flow cytometry analyses were conducted to explore changes in the thymus in orthotopic hepatocellular cancer (HCC) mice with cachexia. Patients with advanced and locally advanced cancers receiving anti‐PD‐1/L1 antibody treatment were followed up to investigate the relationship between the amount of serum autoantibodies and the efficacy of ICIs. Results Single‐cell sequencing in cachexic HCC mice revealed thymic fibroblast maturity disorders characterized by elevated immature medullary fibroblasts, impaired antigen processing functions, reduced interaction with single‐positive thymocytes and decreased expression of tissue‐restricted antigen‐related genes. The thymus of mice with cancer cachexia exhibited degradation of the thymic medulla and decreased expression of LtβR, Mmp9 and Ccl19 in thymus medullary fibroblasts (mFbs). Single‐cell TCR sequencing showed that inflammatory‐related V/J TCR genes were highly used in expanded thymocyte clonotypes in cachexic HCC mice, suggesting impaired T cell negative selection. Results from coculture and cell transfer assays suggest that cancer cachexic CD45+ erythroid progenitor cells (EPCs) induce the death of CD34+ progenitor cells and decrease the number of LtβR+, Mmp9+ and Ccl19+ mFbs in tumour‐free mice. CD24+CD4+CD8− single‐positive thymocytes, typically eliminated in negative selection, did not decrease after the administration of anti‐CD3 mAb. Serum autoantibodies were markedly produced in cachexic HCC mice, cachexic HCC mice administered with anti‐PD1 and tumour‐free mice that received cancer cachexic CD45+ EPCs. Autoantibodies against tumour‐restricted antigens were found in patients with advanced and locally advanced cancer who received two cycles of ICI treatment. Univariate Cox regression analysis showed that patients with a low level of autoantibodies had a higher risk of disease progression (hazard ratio [HR]: 2.39, 95% CI [1.02–5.63], p = 0.046). Analysis of the receiver operating characteristic curve indicated that the number of autoantibodies against tumour tissues predicted treatment failure (area under the curve [AUC] 0.726, p = 0.021) and long‐term duration of treatment response (AUC 0.697, p = 0.024). Patients with high levels of serum autoantibodies against tumours had favourable progression‐free survival (HR, 0.389; 95% CI [0.158–0.960], p = 0.04). Conclusions Cancer cachexia disrupts mFbs maturity, affecting T cell negative selection and expanding the TCR repertoire against tissue‐restricted antigens. This might mediate the adverse and favourable effects of ICIs as anticancer treatments. |
| format | Article |
| id | doaj-art-77d0fe0520d64b0bbc8a2c8a6052fff6 |
| institution | Kabale University |
| issn | 2190-5991 2190-6009 |
| language | English |
| publishDate | 2025-08-01 |
| publisher | Wiley |
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| series | Journal of Cachexia, Sarcopenia and Muscle |
| spelling | doaj-art-77d0fe0520d64b0bbc8a2c8a6052fff62025-08-22T07:30:53ZengWileyJournal of Cachexia, Sarcopenia and Muscle2190-59912190-60092025-08-01164n/an/a10.1002/jcsm.13874Thymic Microenvironment Remodeling in Cancer Cachexia as a Determinant of Checkpoint Inhibitor Efficacy and ToxicityRun‐Kai Huang0Yan‐Fang Xing1Xiang‐Yuan Wu2Zhao‐Hui Shi3Li Wei4Xiao‐Tong Lv5Lin‐Jiao Peng6Xiu‐Qing Pang7Qin‐Tai Yang8Xing Li9Department of Medical Oncology The Third Affiliated Hospital of Sun Yat‐sen University Guangzhou ChinaDepartment of Neurology The Third Affiliated Hospital of Guangzhou Medical University Guangzhou ChinaDepartment of Medical Oncology The Third Affiliated Hospital of Sun Yat‐sen University Guangzhou ChinaDepartment of Allergy and Department of Otorhinolaryngology‐Head and Neck Surgery The Third Affiliated Hospital of Sun Yat‐sen University Guangzhou ChinaDepartment of Medical Oncology The Third Affiliated Hospital of Sun Yat‐sen University Guangzhou ChinaDepartment of Medical Oncology The Third Affiliated Hospital of Sun Yat‐sen University Guangzhou ChinaDepartment of Neurology The Third Affiliated Hospital of Guangzhou Medical University Guangzhou ChinaGuangdong Key Laboratory of Liver Disease Research The Third Affiliated Hospital of Sun Yat‐sen University Guangzhou ChinaDepartment of Allergy and Department of Otorhinolaryngology‐Head and Neck Surgery The Third Affiliated Hospital of Sun Yat‐sen University Guangzhou ChinaDepartment of Medical Oncology The Third Affiliated Hospital of Sun Yat‐sen University Guangzhou ChinaABSTRACT Background The discovery of immune checkpoints links autoimmunity and cancer, with thymus atrophy reportedly causing autoimmune multiorgan inflammation. The impact of cancer cachexia on thymic involution and its clinical significance remains unclear. This study aimed to investigate this effect and its association with immune checkpoint inhibitor (ICI) treatment. Methods Single‐cell sequencing, immunofluorescence and flow cytometry analyses were conducted to explore changes in the thymus in orthotopic hepatocellular cancer (HCC) mice with cachexia. Patients with advanced and locally advanced cancers receiving anti‐PD‐1/L1 antibody treatment were followed up to investigate the relationship between the amount of serum autoantibodies and the efficacy of ICIs. Results Single‐cell sequencing in cachexic HCC mice revealed thymic fibroblast maturity disorders characterized by elevated immature medullary fibroblasts, impaired antigen processing functions, reduced interaction with single‐positive thymocytes and decreased expression of tissue‐restricted antigen‐related genes. The thymus of mice with cancer cachexia exhibited degradation of the thymic medulla and decreased expression of LtβR, Mmp9 and Ccl19 in thymus medullary fibroblasts (mFbs). Single‐cell TCR sequencing showed that inflammatory‐related V/J TCR genes were highly used in expanded thymocyte clonotypes in cachexic HCC mice, suggesting impaired T cell negative selection. Results from coculture and cell transfer assays suggest that cancer cachexic CD45+ erythroid progenitor cells (EPCs) induce the death of CD34+ progenitor cells and decrease the number of LtβR+, Mmp9+ and Ccl19+ mFbs in tumour‐free mice. CD24+CD4+CD8− single‐positive thymocytes, typically eliminated in negative selection, did not decrease after the administration of anti‐CD3 mAb. Serum autoantibodies were markedly produced in cachexic HCC mice, cachexic HCC mice administered with anti‐PD1 and tumour‐free mice that received cancer cachexic CD45+ EPCs. Autoantibodies against tumour‐restricted antigens were found in patients with advanced and locally advanced cancer who received two cycles of ICI treatment. Univariate Cox regression analysis showed that patients with a low level of autoantibodies had a higher risk of disease progression (hazard ratio [HR]: 2.39, 95% CI [1.02–5.63], p = 0.046). Analysis of the receiver operating characteristic curve indicated that the number of autoantibodies against tumour tissues predicted treatment failure (area under the curve [AUC] 0.726, p = 0.021) and long‐term duration of treatment response (AUC 0.697, p = 0.024). Patients with high levels of serum autoantibodies against tumours had favourable progression‐free survival (HR, 0.389; 95% CI [0.158–0.960], p = 0.04). Conclusions Cancer cachexia disrupts mFbs maturity, affecting T cell negative selection and expanding the TCR repertoire against tissue‐restricted antigens. This might mediate the adverse and favourable effects of ICIs as anticancer treatments.https://doi.org/10.1002/jcsm.13874cancer cachexiaimmune checkpoint inhibitorsT cell negative selectionthymus involutionthymus medullary fibroblast |
| spellingShingle | Run‐Kai Huang Yan‐Fang Xing Xiang‐Yuan Wu Zhao‐Hui Shi Li Wei Xiao‐Tong Lv Lin‐Jiao Peng Xiu‐Qing Pang Qin‐Tai Yang Xing Li Thymic Microenvironment Remodeling in Cancer Cachexia as a Determinant of Checkpoint Inhibitor Efficacy and Toxicity Journal of Cachexia, Sarcopenia and Muscle cancer cachexia immune checkpoint inhibitors T cell negative selection thymus involution thymus medullary fibroblast |
| title | Thymic Microenvironment Remodeling in Cancer Cachexia as a Determinant of Checkpoint Inhibitor Efficacy and Toxicity |
| title_full | Thymic Microenvironment Remodeling in Cancer Cachexia as a Determinant of Checkpoint Inhibitor Efficacy and Toxicity |
| title_fullStr | Thymic Microenvironment Remodeling in Cancer Cachexia as a Determinant of Checkpoint Inhibitor Efficacy and Toxicity |
| title_full_unstemmed | Thymic Microenvironment Remodeling in Cancer Cachexia as a Determinant of Checkpoint Inhibitor Efficacy and Toxicity |
| title_short | Thymic Microenvironment Remodeling in Cancer Cachexia as a Determinant of Checkpoint Inhibitor Efficacy and Toxicity |
| title_sort | thymic microenvironment remodeling in cancer cachexia as a determinant of checkpoint inhibitor efficacy and toxicity |
| topic | cancer cachexia immune checkpoint inhibitors T cell negative selection thymus involution thymus medullary fibroblast |
| url | https://doi.org/10.1002/jcsm.13874 |
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