Evidence map›Paper›PMID 39120462›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2024

Rapid Autopsy to Define Dendritic Cell Spatial Distribution and T Cell Association in Lung Adenocarcinoma.

Hilal Ozakinci, Xiaofei Song, Gina S Nazario, Thomas Lila, Benjamin Chen, Tyler Simpson, Jonathan V Nguyen, Carlos M Moran Segura, Zachary J Thompson, Ram Thapa and 8 more

Abstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2024. 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. Article
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.

Hilal OzakinciThoracic Oncology Department, Moffitt Cancer Center, Tampa, FL.
Xiaofei SongBiostatistics and Bioinformatics Department, Moffitt Cancer Center, Tampa, FL.ORCID 0000-0002-6585-7318
Gina S NazarioThoracic Oncology Department, Moffitt Cancer Center, Tampa, FL.
Thomas LilaSolid Tumor Translational Medicine, Bristol Myers Squibb, Cambridge, MA.
Benjamin ChenSolid Tumor Translational Medicine, Bristol Myers Squibb, Cambridge, MA.
Tyler SimpsonSolid Tumor Translational Medicine, Bristol Myers Squibb, Cambridge, MA.
Jonathan V NguyenAdvanced Analytical and Digital Laboratory, Moffitt Cancer Center, Tampa, FL.ORCID 0000-0001-6146-2047
Carlos M Moran SeguraAdvanced Analytical and Digital Laboratory, Moffitt Cancer Center, Tampa, FL.ORCID 0000-0001-8702-0554
Zachary J ThompsonBiostatistics and Bioinformatics Department, Moffitt Cancer Center, Tampa, FL.
Ram ThapaBiostatistics and Bioinformatics Department, Moffitt Cancer Center, Tampa, FL.
Trevor A RoseDiagnostic Imaging and Interventional Radiology, Moffitt Cancer Center, Tampa, FL.
Eric B HauraThoracic Oncology Department, Moffitt Cancer Center, Tampa, FL.
Bruna PelliniThoracic Oncology Department, Moffitt Cancer Center, Tampa, FL.ORCID 0000-0003-0898-0202
Xiaoqing YuBiostatistics and Bioinformatics Department, Moffitt Cancer Center, Tampa, FL.
Brian H RuffellImmunology Department, Moffitt Cancer Center, Tampa, FL.ORCID 0000-0002-3846-6872
Dung-Tsa ChenBiostatistics and Bioinformatics Department, Moffitt Cancer Center, Tampa, FL.
Theresa A BoyleThoracic Oncology Department, Moffitt Cancer Center, Tampa, FL.ORCID 0000-0001-5950-3970
Amer A BegThoracic Oncology Department, Moffitt Cancer Center, Tampa, FL.

Funding

TRANSLATIONAL RESEARCHP30CA076292 · NCI · UNIVERSITY OF SOUTH FLORIDA · PI Christine O'Connell · 1998 to 2026
$93.5M
Bristol-Myers Squibb (BMS) 84-18843-01-02Moffitt Cancer Center (MCC)NCI NIH HHS P30 CA076292
6 · The paper itself

Abstract

Immunotherapy response is associated with the presence of conventional dendritic cells (cDCs). cDC type 1 (cDC1) is critically important for CD8+ T cell activation, cDC type 2 (cDC2) regulates CD4+ T cell responses, and mature regulatory cDCs may dampen T cell responses in the tumor microenvironment (TME). However, we lack a clear understanding of cDC distribution in the human TME, cDC prevalence in metastatic sites, and cDC differences in early- versus late-stage disease. Rapid autopsy specimens of 10 patients with lung adenocarcinoma were evaluated to detect cDCs and immune cells via multiplex immunofluorescence using 18 markers and 42 tumors. First, we found that T cells, cDC1, and cDC2 were confined to stroma, whereas mature regulatory DCs were enriched in tumor, suggesting unique localization-specific functions. Second, lung and lymph node tumors were more enriched in T cells and cDCs than liver tumors, underscoring differences in the TME of metastatic sites. Third, although the proportion of T cells and cDC1 did not differ in different stages, an increase in the proportion of cDC2 and macrophages in late stage suggests potential differences in regulation of T cell responses in different stages. Collectively, these findings provide new, to our knowledge, insights into cDC biology in human cancer that may have important therapeutic implications.

Indexed as

Adenocarcinoma of LungAutopsyDendritic CellsLung NeoplasmsTumor MicroenvironmentAdenocarcinomaAgedCD8-Positive T-LymphocytesFemaleHumansMaleMiddle Aged

Identifiers

PMID39120462
PMCPMC11404669

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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.