Evidence map›Paper›PMID 35552285›Full record

ArticleJCI insight2022

CXCL13-producing CD4+ T cells accumulate in the early phase of tertiary lymphoid structures in ovarian cancer.

Masayo Ukita, Junzo Hamanishi, Hiroyuki Yoshitomi, Koji Yamanoi, Shiro Takamatsu, Akihiko Ueda, Haruka Suzuki, Yuko Hosoe, Yoko Furutake, Mana Taki and 8 more

Open access · goldAbstract read
In one paragraph

Article in JCI insight, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 145 papers.

0numbers the graph read from it
0cells of the map it votes in
145citing papers in PubMed
13.8field-weighted citation impact, top 1% of its field
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

145 citing papers in PubMed, 177 citations in OpenAlex.

  1. CXCL13-expressing CD4Oncoimmunology · 2026
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85 more citing papers are in PubMed but not listed here.

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

18 authors at 4 institutions in 1 country.

Masayo UkitaDepartment of Gynecology and Obstetrics and.
Junzo HamanishiDepartment of Gynecology and Obstetrics and.
Hiroyuki YoshitomiDepartment of Immunology, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Koji YamanoiDepartment of Gynecology and Obstetrics and.
Shiro TakamatsuDepartment of Gynecology and Obstetrics and.
Akihiko UedaDepartment of Gynecology and Obstetrics and.
Haruka SuzukiDepartment of Gynecology and Obstetrics and.
Yuko HosoeDepartment of Gynecology and Obstetrics and.
Yoko FurutakeDepartment of Gynecology and Obstetrics and.
Mana TakiDepartment of Gynecology and Obstetrics and.
Kaoru AbikoDepartment of Obstetrics and Gynecology, National Hospital Organization Kyoto Medical Center, Kyoto, Japan.
Ken YamaguchiDepartment of Gynecology and Obstetrics and.
Hidekatsu NakaiDepartment of Obstetrics and Gynecology, Kindai University Faculty of Medicine, Osaka, Japan.
Tsukasa BabaDepartment of Obstetrics and Gynecology, Iwate Medical University, Iwate, Japan.
Noriomi MatsumuraDepartment of Obstetrics and Gynecology, Kindai University Faculty of Medicine, Osaka, Japan.
Akihiko YoshizawaDepartment of Diagnostic Pathology, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Hideki UenoDepartment of Immunology, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Masaki MandaiDepartment of Gynecology and Obstetrics and.
Kyoto University · JPKindai University · JPIwate Medical University · JPKyoto Medical Center · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tertiary lymphoid structures (TLS) are transient ectopic lymphoid aggregates whose formation might be caused by chronic inflammation states, such as cancer. However, how TLS are induced in the tumor microenvironment (TME) and how they affect patient survival are not well understood. We investigated TLS distribution in relation to tumor infiltrating lymphocytes (TILs) and related gene expression in high-grade serous ovarian cancer (HGSC) specimens. CXCL13 gene expression correlated with TLS presence and the infiltration of T cells and B cells, and it was a favorable prognostic factor for patients with HGSC. Coexistence of CD8+ T cells and B cell lineages in the TME significantly improved the prognosis of HGSC and was correlated with the presence of TLS. CXCL13 expression was predominantly coincident with CD4+ T cells in TLS and CD8+ T cells in TILs, and it shifted from CD4+ T cells to CD21+ follicular DCs as TLS matured. In a mouse ovarian cancer model, recombinant CXCL13 induced TLS and enhanced survival by the infiltration of CD8+ T cells. These results suggest that TLS formation was associated with CXCL13-producing CD4+ T cells and that TLS facilitated the coordinated antitumor response of cellular and humoral immunity in ovarian cancer.

Indexed as

Ovarian NeoplasmsTertiary Lymphoid StructuresAnimalsCD4-Positive T-LymphocytesChemokine CXCL13FemaleHumansLymphocytes, Tumor-InfiltratingMicePrognosisTumor MicroenvironmentChemokine CXCL13CXCL13 protein, humanCxcl13 protein, mouseAdaptive immunityCancerImmunologyObstetrics/gynecologyOncology

Identifiers

PMID35552285
PMCPMC9309049
OpenAlexW4280519874

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.