Evidence map›Paper›PMID 38629072›Full record

ArticleFrontiers in immunology2024

Neoadjuvant chemotherapy is associated with suppression of the B cell-centered immune landscape in pancreatic ductal adenocarcinoma.

Luise Rupp, Ina Dietsche, Maximilian Kießler, Ulrich Sommer, Alexander Muckenhuber, Katja Steiger, Casper W F van Eijck, Leonard Richter, Rouzanna Istvanffy, Carsten Jäger and 5 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.5field-weighted citation impact, top 9% 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

11 citing papers in PubMed, 9 citations in OpenAlex.

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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

15 authors at 5 institutions in 2 countries.

Luise Rupp *Institute of Immunology, Faculty of Medicine Carl Gustav Carus, Technical University Dresden, Dresden, Germany.
Ina Dietsche *Institute of Immunology, Faculty of Medicine Carl Gustav Carus, Technical University Dresden, Dresden, Germany.
Maximilian KießlerDepartment of Surgery, Klinikum rechts der Isar, Technical University of Munich, Munich, Germany.
Ulrich SommerInstitute of Pathology, University Hospital Carl Gustav Carus, Technical University Dresden, Dresden, Germany.
Alexander MuckenhuberInstitute of Pathology, School of Medicine and Health, Technical University of Munich, Munich, Germany.
Katja SteigerInstitute of Pathology, School of Medicine and Health, Technical University of Munich, Munich, Germany.
Casper W F van EijckDepartment of Surgery, Erasmus University Medical Center, Rotterdam, Netherlands.
Leonard RichterDepartment of Surgery, Klinikum rechts der Isar, Technical University of Munich, Munich, Germany.
Rouzanna IstvanffyDepartment of Surgery, Klinikum rechts der Isar, Technical University of Munich, Munich, Germany.
Carsten JägerDepartment of Surgery, Klinikum rechts der Isar, Technical University of Munich, Munich, Germany.
Helmut FriessDepartment of Surgery, Klinikum rechts der Isar, Technical University of Munich, Munich, Germany.
Casper H J van EijckDepartment of Surgery, Erasmus University Medical Center, Rotterdam, Netherlands.
Ihsan Ekin DemirDepartment of Surgery, Klinikum rechts der Isar, Technical University of Munich, Munich, Germany.
Carmen Mota ReyesDepartment of Surgery, Klinikum rechts der Isar, Technical University of Munich, Munich, Germany.
Marc SchmitzInstitute of Immunology, Faculty of Medicine Carl Gustav Carus, Technical University Dresden, Dresden, Germany.
Klinikum rechts der Isar · DETechnical University of Munich · DEUniversity Hospital Carl Gustav Carus · DEErasmus MC · NLHeidelberg University · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pancreatic ductal adenocarcinoma (PDAC) is typically diagnosed at advanced stages and associated with early distant metastasis and poor survival. Besides clinical factors, the tumor microenvironment (TME) emerged as a crucial determinant of patient survival and therapy response in many tumors, including PDAC. Thus, the presence of tumor-infiltrating lymphocytes and the formation of tertiary lymphoid structures (TLS) is associated with longer survival in PDAC. Although neoadjuvant therapy (NeoTx) has improved the management of locally advanced tumors, detailed insight into its effect on various TME components is limited. While a remodeling towards a proinflammatory state was reported for PDAC-infiltrating T cells, the effect of NeoTx on B cell subsets, including plasma cells, and TLS formation is widely unclear. We thus investigated the frequency, composition, and spatial distribution of PDAC-infiltrating B cells in primary resected (PR) versus neoadjuvant-treated patients using a novel multiplex immunohistochemistry panel. The NeoTx group displayed significantly lower frequencies of pan B cells, GC B cells, plasmablasts, and plasma cells, accompanied by a reduced abundance of TLS. This finding was supported by bulk RNA-sequencing analysis of an independent fresh frozen tissue cohort, which revealed that major B cell pathways were downregulated in the NeoTx group. We further observed that plasma cells frequently formed aggregates that localized close to TLS and that TLS

Indexed as

Carcinoma, Pancreatic DuctalPancreatic NeoplasmsB-LymphocytesHumansNeoadjuvant TherapyT-LymphocytesTumor MicroenvironmentB cellsneoadjuvant chemotherapypancreatic ductal adenocarcinomaplasma cellstertiary lymphoid structurestumor immune contexture

Identifiers

PMID38629072
PMCPMC11018975
OpenAlexW4393443754

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.