Evidence map›Paper›PMID 41048011›Full record

ReviewClinical and translational medicine2025

Role of tertiary lymphoid structures in the tumour microenvironment and immunotherapy response of renal cell carcinoma.

Lin Yang, Wentai Shangguan, Weijia Li, Wenxue Huang, Zhuohang Li, Boyuan Sun, Cunzhen Ma, Xunguo Yang, Bisheng Cheng, Peng Wu

Abstract readReview
In one paragraph

Review in Clinical and translational medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

10 citing papers in PubMed.

  1. Review
  2. Review
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  4. Strategies to target PD-1/PD-L1 in the tumor microenvironment.Cellular oncology (Dordrecht, Netherlands) · 2026
    Review
  5. Article
  6. Review
  7. Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Lin YangNanfang Hospital, Southern Medical University, Guangzhou, China.ORCID 0009-0007-4275-1135
Wentai ShangguanNanfang Hospital, Southern Medical University, Guangzhou, China.
Weijia LiNanfang Hospital, Southern Medical University, Guangzhou, China.
Wenxue HuangNanfang Hospital, Southern Medical University, Guangzhou, China.
Zhuohang LiNanfang Hospital, Southern Medical University, Guangzhou, China.
Boyuan SunNanfang Hospital, Southern Medical University, Guangzhou, China.
Cunzhen MaNanfang Hospital, Southern Medical University, Guangzhou, China.
Xunguo YangNanfang Hospital, Southern Medical University, Guangzhou, China.
Bisheng ChengNanfang Hospital, Southern Medical University, Guangzhou, China.
Peng WuNanfang Hospital, Southern Medical University, Guangzhou, China.

Funding

President Foundation of Nanfang Hospital, Southern Medical University 2024A028the Guangzhou Key Research and Development Program SL2022B03J00592The National Natural Science Foundation of China 82173304The National Natural Science Foundation of China 82370782The National Natural Science Foundation of China 82503289
6 · The paper itself

Abstract

In the tumour microenvironment (TME) of renal cell carcinoma (RCC), tertiary lymphoid structures (TLS) play a crucial role in anti-tumour immune responses. Resembling secondary lymphoid organs, TLS comprises B cells, T cell zones, high endothelial venules, and antigen-presenting cells, facilitating local immune activation. While TLS has shown correlations with improved immune checkpoint inhibitors (ICIs) outcomes in other cancers, its role in RCC is still under investigation. Emerging evidence indicates that mature TLS enhances anti-tumour activity by activating T and B cells, whereas immature TLS may contribute to immune suppression. The RCC TME is highly immunosuppressive, marked by regulatory T cells, myeloid-derived suppressor cells, and elevated pro-angiogenic and immunosuppressive cytokines. In this context, TLS, particularly mature TLS, can counteract immunosuppression, boost local immune responses, and improve ICIs efficacy. However, TLS in RCC is heterogeneous, with their formation and function affected by factors like CXCL13 expression. The presence, maturity, and functionality of TLS may serve as valuable predictors of ICIs response and patient prognosis. Further research is required to understand TLS regulation and leverage their potential to enhance personalised immunotherapy for RCC.

Indexed as

Carcinoma, Renal CellImmunotherapyKidney NeoplasmsTertiary Lymphoid StructuresTumor MicroenvironmentHumansimmune checkpoint inhibitorsindividualised therapyrenal cell carcinomatertiary lymphoid structurestumour microenvironment

Identifiers

PMID41048011
PMCPMC12498089

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.