Evidence map›Paper›PMID 12107085›Full record

ArticleThe American journal of pathology2002

Sampling tumor-draining lymph nodes for phenotypic and functional analysis of dendritic cells and T cells.

Ronald J C L M Vuylsteke, Paul A M van Leeuwen, Sybren Meijer, Pepijn G J T B Wijnands, Markwin G Statius Muller, Dirk H Busch, Rik J Scheper, Tanja D de Gruijl

Open access · bronzeAbstract read
In one paragraph

Article in The American journal of pathology, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
0.6field-weighted citation impact, top 36% 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

17 citing papers in PubMed, 41 citations in OpenAlex.

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  8. Tolerogenic IDO1International journal of molecular sciences · 2022
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  11. Observational
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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

8 authors at 4 institutions in 3 countries.

Ronald J C L M VuylstekeDepartment of Surgical Oncology, Vrije Universiteit Medical Center, Amsterdam, The Netherlands.
Paul A M van Leeuwen
Sybren Meijer
Pepijn G J T B Wijnands
Markwin G Statius Muller
Dirk H Busch
Rik J Scheper
Tanja D de Gruijl
Vrije Universiteit Amsterdam · NLInstitute of Medical Microbiology and Hygiene · DEMolecular Oncology (United States) · USTechnical University of Munich · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Immune responses against tumor antigens will initially occur in the first tumor-draining lymph node, the sentinel node (SN). Because of extensive diagnostic procedures, obtaining a piece of SN to isolate viable immune cells for functional analyses is often impossible. For this reason an alternative method to obtain viable cells from a lymph node (LN) was investigated, ie, scraping LNs with a surgical blade, and compared with dissociation of total LNs. Tumor-draining lymph nodes were retrieved from five oncological patients. The collected dendritic cells and T cells were phenotypically and functionally characterized by flow cytometry and antigen-specific interferon (IFN)-gamma release in an ELISPOT assay. Results were compared between the two isolation methods. Viabilities and phenotypic characteristics of the collected cells were entirely comparable for both methods. T-cell functionality was also comparable between both methods, with equal T-cell expansion factors and similar frequencies of cytotoxic T cells specifically recognizing the M1 matrix protein of Influenza haemophilus or the tumor antigen Her-2/neu. In conclusion, scraping LNs to obtain cells for analysis of immune functions in LNs is feasible and presents a good alternative to dissociation of LNs. Scraping may even be applied to small LNs that a pathologist will submit entirely for histological examination and may thus prove useful in the monitoring of immune responses in SNs.

Indexed as

Breast NeoplasmsCD4-CD8 RatioCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCell SurvivalDendritic CellsErb-b2 Receptor Tyrosine KinasesFemaleHLA-A2 AntigenHumansLymph NodesNeoplasmsPhenotypeSpecimen HandlingErb-b2 Receptor Tyrosine KinasesHLA-A2 Antigen

Identifiers

PMID12107085
PMCPMC1850698
OpenAlexW2078499401

What OpenQuestion holds

Textmetadata
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.