Evidence map›Paper›PMID 31100936›Full record

ArticleCancers2019

Immunoprofiling of Breast Cancer Antigens Using Antibodies Derived from Local Lymph Nodes.

Anna Rachel Young, Jessica Da Gama Duarte, Rhiannon Coulson, Megan O'Brien, Siddhartha Deb, Alex Lopata, Andreas Behren, Suresh Mathivanan, Elgene Lim, Els Meeusen

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

4 citing papers in PubMed, 12 citations in OpenAlex.

  1. Review
  2. Article
  3. High Numbers and Densities of PD1International journal of molecular sciences · 2020
    Article
  4. 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

10 authors at 3 institutions in 1 country.

Anna Rachel YoungLa Trobe Institute for Molecular Science (LIMS), La Trobe University, Melbourne 3086, Australia. a.young@latrobe.edu.au.
Jessica Da Gama DuarteOlivia Newton-John Cancer Research Institute, Level 5, ONJ Centre, Heidelberg Vic 3084, Australia. Jessica.Duarte@onjcri.org.au.
Rhiannon CoulsonGarvan Institute of Medical Research, St Vincent's Clinical School, Darlinghurst, NSW 2010, Australia. r.coulson@garvan.org.au.
Megan O'BrienOlivia Newton-John Cancer Research Institute, Level 5, ONJ Centre, Heidelberg Vic 3084, Australia. megan.obrien@onjcri.org.au.
Siddhartha DebConsultant Pathologist, Anatpath. 120 Gardenvale Rd, Gardenvale Melbourne 3185, Australia. deb_siddhartha@hotmail.com.
Alex LopataCancerProbe Pty Ltd, PO Box 2237, Prahran 3181, Australia. alex.lopata15@gmail.com.
Andreas BehrenOlivia Newton-John Cancer Research Institute, Level 5, ONJ Centre, Heidelberg Vic 3084, Australia. Andreas.Behren@onjcri.org.au.
Suresh MathivananLa Trobe Institute for Molecular Science (LIMS), La Trobe University, Melbourne 3086, Australia. s.mathivanan@latrobe.edu.au.
Elgene LimGarvan Institute of Medical Research, St Vincent's Clinical School, Darlinghurst, NSW 2010, Australia. e.lim@garvan.org.au.
Els MeeusenLa Trobe Institute for Molecular Science (LIMS), La Trobe University, Melbourne 3086, Australia. elza.meeusen@gmail.com.
La Trobe University · AUGarvan Institute of Medical Research · AUReef Ecologic · AU

Funding

National Breast Cancer Foundation IN-16-014
6 · The paper itself

Abstract

Tumor antigens are responsible for initiating an immune response in cancer patients, and their identification may provide new biomarkers for cancer diagnosis and targets for immunotherapy. The general use of serum antibodies to identify tumor antigens has several drawbacks, including dilution, complex formation, and background reactivity. In this study, antibodies were generated from antibody-secreting cells (ASC) present in tumor-draining lymph nodes of 20 breast cancer patients (ASC-probes) and were used to screen breast cancer cell lines and protein microarrays. Half of the ASC-probes reacted strongly against extracts of the MCF-7 breast cancer cell line, but each with a distinct antigen recognition profile. Three of the positive ASC-probes reacted differentially with recombinant antigens on a microarray containing cancer-related proteins. The results of this study show that lymph node-derived ASC-probes provide a highly specific source of tumor-specific antibodies. Each breast cancer patient reacts with a different antibody profile which indicates that targeted immunotherapies may need to be personalized for individual patients. Focused microarrays in combination with ASC-probes may be useful in providing immune profiles and identifying tumor antigens of individual cancer patients.

Indexed as

antibody secreting cellbiomarkerbreast cancerimmune profileimmunotherapylymph nodemicroarraytumor antigen

Identifiers

PMID31100936
PMCPMC6562983
OpenAlexW2946228635

What OpenQuestion 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 OpenQuestion graph.