Evidence map›Paper›PMID 21715317›Full record

ArticleBlood2011

Differential and tumor-specific expression of CD160 in B-cell malignancies.

Timothy W Farren, Jerome Giustiniani, Feng-Ting Liu, Dimitris A Tsitsikas, Marion G Macey, James D Cavenagh, Heather E Oakervee, David Taussig, Adrian C Newland, Maria Calaminici and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

25 citing papers in PubMed, 53 citations in OpenAlex.

  1. MutantFrontiers in immunology · 2026
    Article
  2. Aberrant Expression ofCancers · 2025
    Article
  3. Article
  4. Effect ofInternational journal of molecular sciences · 2024
    Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Expanded antigen-experienced CD160Journal for immunotherapy of cancer · 2021
    Article
  10. Measurable residual disease in the treatment of chronic lymphocytic leukemia.Journal of clinical and experimental hematopathology : JCEH · 2020
    Review
  11. Article
  12. CD160 expression on CD8Cancer immunology, immunotherapy : CII · 2020
    Article
  13. Article
  14. Article
  15. Consistency of the Moreau CLL score.Journal of clinical laboratory analysis · 2018
    Article
  16. Review
  17. Inhibitory receptors as targets for cancer immunotherapy.European journal of immunology · 2015
    Review
  18. Article
  19. Tumor necrosis factor superfamily in innate immunity and inflammation.Cold Spring Harbor perspectives in biology · 2014
    Review
  20. 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

14 authors at 5 institutions in 2 countries.

Timothy W FarrenDivision of Haemato-Oncology and Immunophenotyping Section, Department of Haematology, Barts and The London National Health Service (NHS) Trust, London, UK.
Jerome Giustiniani
Feng-Ting Liu
Dimitris A Tsitsikas
Marion G Macey
James D Cavenagh
Heather E Oakervee
David Taussig
Adrian C Newland
Maria Calaminici
Armand Bensussan
Michael Jenner
John G Gribben
Samir G Agrawal
Queen Mary University of London · GBNational Health Service · GBBarts Health NHS Trust · GBInserm · FRInstitut Jean Godinot · FR

Funding

Tissue CoreP01CA081534 · NCI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI KIPPS, THOMAS J · 2000 to 2016
$59.5M
6 · The paper itself

Abstract

CD160 is a human natural killer (NK)-cell-activating receptor that is also expressed on T-cell subsets. In the present study, we examined 811 consecutive cases of B-cell lymphoproliferative disorders (B-LPDs), and demonstrated CD160 expression in 98% (590 of 600) of chronic lymphocytic leukemia (CLL) cases, 100% (32 of 32) of hairy cell leukemia (HCL) cases, 15% (5 of 34) of mantle cell lymphoma (MCL) in the leukemic phase, and 16% (23 of 145) of other B-LPD cases. CD160 transcript and protein were absent in the normal B-cell hierarchy, from stem cells, B-cell precursors, maturing B cells in the germinal center, and circulating B cells, including CD5(+)CD19(+) B1 cells in umbilical cord. CD160 positivity was significantly higher in CLL and HCL in terms of percentage (65.9% and 67.8%, respectively, P < .0001) and median fluorescence intensity (552 and 857, respectively, P < .0001) compared with all other B-LPD cases. Lymph node CLL samples were also CD160(+). Using the disease-specific expression of CD5, CD23, and CD160, a score of 3 characterized CLL (diagnostic odds ratio, 1430); a score of 0 excluded CLL, MCL, and HCL; and the CD23/CD5 ratio differentiated CLL from leukemic CD23(+) MCL. In the B-cell lineage, CD160 is a tumor-specific antigen known to mediate cellular activation signals in CLL, and is a novel target for therapeutic manipulation and monitoring of minimal residual disease.

Indexed as

Antigens, CDBase SequenceBiomarkers, TumorB-LymphocytesCohort StudiesDNA, NeoplasmDNA PrimersGene ExpressionGPI-Linked ProteinsHumansImmunohistochemistryLeukemia, Hairy CellLeukemia, Lymphocytic, Chronic, B-CellLymphocytosisLymphoma, Mantle-CellLymphoproliferative DisordersAntigens, CDBiomarkers, TumorCD160 protein, humanDNA, NeoplasmDNA PrimersGPI-Linked ProteinsReceptors, Immunologic

Identifiers

PMID21715317
PMCPMC5292591
OpenAlexW1996416214

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.