Unveiling the impact of tertiary lymphoid structures on immunotherapeutic responses of clear cell renal cell carcinoma

Author:

Xu Wenhao123ORCID,Lu Jiahe1234ORCID,Tian Xi123,Ye Shiqi123ORCID,Wei Shiyin5,Wang Jun6,Anwaier Aihetaimujiang123,Qu Yuanyuan123,Liu Wangrui7ORCID,Chang Kun123ORCID,Zhang Hailiang123ORCID,Ye Dingwei123ORCID

Affiliation:

1. Department of Urology Fudan University Shanghai Cancer Center Shanghai China

2. Department of Oncology Shanghai Medical College Fudan University Shanghai China

3. Shanghai Genitourinary Cancer Institute Shanghai China

4. School of Cellular and Molecular Medicine University of Bristol Bristol UK

5. Affiliated Hospital of Youjiang Medical University for Nationalities Baise China

6. State Key Laboratory of Oncology in South China Collaborative Innovation Center for Cancer Medicine Department of Urology Sun Yat‐sen University Cancer Center Guangzhou China

7. Renji Hospital Shanghai Jiao Tong University School of Medicine Shanghai China

Abstract

AbstractTertiary lymphoid structures (TLS) are organized aggregates of immune cells that form under pathological conditions. However, the predictive value of TLS in clear cell renal cell carcinoma (ccRCC) for immunotherapies remains unclear. We comprehensively assessed the implications for prognosis and immunological responses of the TLS spatial and maturation heterogeneity in 655 ccRCC patients. A higher proportion of early‐TLS was found in peritumoral TLS, while intratumoral TLS mainly comprised secondary follicle‐like TLS (SFL‐TLS), indicating markedly better survival. Notably, presence of TLS, especially intratumoral TLS and SFL‐TLS, significantly correlated with better survival and objective reflection rate for ccRCC patients receiving anti‐Programmed Cell Death Protein‐1 (PD‐1)/Programmed Cell Death‐Ligand‐1 (PD‐L1) immunotherapies. In peritumoral TLS cluster, primary follicle‐like TLS, the proportion of tumor‐associated macrophages, and Treg infiltration in the peritumoral regions increased prominently, suggesting an immunosuppressive tumor microenvironment. Interestingly, spatial transcriptome annotation and multispectral fluorescence showed that an abundance of mature plasma cells within mature TLS has the capacity to produce IgA and IgG, which demonstrate significantly higher objective response rates and a superior prognosis for ccRCC patients subjected to immunotherapy. In conclusion, this study revealed the implications of TLS spatial and maturation heterogeneity on the immunological status and clinical responses, allowing the improvement of precise immunotherapies of ccRCC.

Funder

National Natural Science Foundation of China

Shanghai Municipal Health Bureau

Beijing Xisike Clinical Oncology Research Foundation

Publisher

Wiley

Subject

Cell Biology,Biochemistry (medical),Genetics (clinical),Computer Science Applications,Drug Discovery,Genetics,Oncology,Immunology and Allergy

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