Evidence map›Paper›PMID 41669970›Full record

ReviewRespirology (Carlton, Vic.)2026

T-Cell Immunity and Lung Cancer.

Kotaro Yamada, Yosuke Togashi

Abstract readReview
In one paragraph

Review in Respirology (Carlton, Vic.), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. T-Cell Immunity and Lung Cancer.Respirology (Carlton, Vic.) · 2026
    Review
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

2 authors.

Kotaro YamadaDepartment of Respiratory Medicine, Okayama University Hospital, Okayama, Japan.
Yosuke TogashiDepartment of Respiratory Medicine, Okayama University Hospital, Okayama, Japan.ORCID 0000-0001-9910-0164

Funding

AMED JP23ama221325h0001AMED JP25ck0106001h0001Fusion Oriented REsearch for disruptive Science and Technology, FOREST JPMJFR2049Japan Society for the Promotion of Science JP24K02549
6 · The paper itself

Abstract

Lung cancer remains a leading cause of cancer mortality worldwide. Although immune checkpoint inhibitors (ICIs) have reshaped therapeutic strategies in lung cancer, their benefits remain limited. ICIs exert their therapeutic efficacy by activating T-cell effector functions, underscoring the central role of T cells in antitumor immunity. Thus, this review focuses on the role of T cells in lung cancer and summarises recent advances. Tumour-specific CD8

Indexed as

Lung NeoplasmsT-LymphocytesAnimalsCD8-Positive T-LymphocytesHumansImmune Checkpoint InhibitorsT-Cell ExhaustionT-Lymphocytes, RegulatoryTumor MicroenvironmentImmune Checkpoint Inhibitorsimmune checkpoint inhibitorslung neoplasmsT‐cell exhaustionT follicular helper cellsT‐lymphocytes cytotoxicT‐lymphocytes regulatorytumour microenvironment

Identifiers

PMID41669970
PMCPMC12963705

What Socratic 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 Socratic graph.