Evidence map›Paper›PMID 24484236›Full record

ArticleAmerican journal of respiratory and critical care medicine2014

Presence of B cells in tertiary lymphoid structures is associated with a protective immunity in patients with lung cancer.

Claire Germain, Sacha Gnjatic, Fella Tamzalit, Samantha Knockaert, Romain Remark, Jérémy Goc, Alice Lepelley, Etienne Becht, Sandrine Katsahian, Geoffray Bizouard and 9 more

Registry-linked trialAbstract read
PubMed Publisher
In one paragraph

Article in American journal of respiratory and critical care medicine, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04525859 (Direct Injection of Poly-ICLC), which is not on this map. Cited by 545 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
545citing papers in PubMed, 1 pooled it
12.7field-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.

NCT04525859 phase1completednot on this mapstarted 2020, after this paper: background citation

Direct Injection of Poly-ICLC (Hiltonol®) Vaccine In Malignant Pleural Mesothelioma

TypeinterventionalSponsorOncovir, Inc.Ran2020 to 2025Enrolled19ConditionsMalignant Pleural MesotheliomaArmsSafety, Expansion Cohort
3 · Its place in the literature

Who cites it

545 citing papers in PubMed, 1 synthesis or guideline pooled it, 788 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Review
  5. B cells in cancer: functions, mechanisms and therapeutic advances.Signal transduction and targeted therapy · 2026
    Review
  6. Review
  7. Review
  8. Humoral immunity in cancer.Signal transduction and targeted therapy · 2026
    Review
  9. Review
  10. Review
  11. Review
  12. Review
  13. Article
  14. Review
  15. Review
  16. Review
  17. Article
  18. Article
  19. Article
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485 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

19 authors at 6 institutions in 2 countries.

Claire Germain1 Laboratory "Immune Microenvironment and Tumors" and.
Sacha Gnjatic
Fella Tamzalit
Samantha Knockaert
Romain Remark
Jérémy Goc
Alice Lepelley
Etienne Becht
Sandrine Katsahian
Geoffray Bizouard
Pierre Validire
Diane Damotte
Marco Alifano
Pierre Magdeleinat
Isabelle Cremer
Jean-Luc Teillaud
Wolf-Herman Fridman
Catherine Sautès-Fridman
Marie-Caroline Dieu-Nosjean
Délégation Paris 5 · FRAssistance Publique – Hôpitaux de Paris · FRHôpitaux Universitaires Henri-Mondor · FRInserm · FRInstitute Mutualiste Montsouris · FRMemorial Sloan Kettering Cancer Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

rationaleIt is now well established that immune responses can take place outside of primary and secondary lymphoid organs. We previously described the presence of tertiary lymphoid structures (TLS) in patients with non-small cell lung cancer (NSCLC) characterized by clusters of mature dendritic cells (DCs) and T cells surrounded by B-cell follicles. We demonstrated that the density of these mature DCs was associated with favorable clinical outcome.

objectivesTo study the role of follicular B cells in TLS and the potential link with a local humoral immune response in patients with NSCLC.

methodsThe cellular composition of TLS was investigated by immunohistochemistry. Characterization of B-cell subsets was performed by flow cytometry. A retrospective study was conducted in two independent cohorts of patients. Antibody specificity was analyzed by ELISA. MEASUREMENTS AND MAIN

resultsConsistent with TLS organization, all stages of B-cell differentiation were detectable in most tumors. Germinal center somatic hypermutation and class switch recombination machineries were activated, associated with the generation of plasma cells. Approximately half of the patients showed antibody reactivity against up to 7 out of the 33 tumor antigens tested. A high density of follicular B cells correlated with long-term survival, both in patients with early-stage NSCLC and with advanced-stage NSCLC treated with chemotherapy. The combination of follicular B cell and mature DC densities allowed the identification of patients with the best clinical outcome.

conclusionsB-cell density represents a new prognostic biomarker for NSCLC patient survival, and makes the link between TLS and a protective B cell-mediated immunity.

Indexed as

Immunity, HumoralBiomarkersB-Lymphocyte SubsetsCarcinoma, Non-Small-Cell LungCohort StudiesDendritic CellsEnzyme-Linked Immunosorbent AssayFemaleFlow CytometryHumansImmunohistochemistryLung NeoplasmsMalePrognosisRetrospective StudiesBiomarkers

Identifiers

PMID24484236
OpenAlexW2099900951

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.