Evidence map›Paper›PMID 17617631›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2007

Tumor-associated embryonic antigen-expressing vaccines that target CCR6 elicit potent CD8+ T cell-mediated protective and therapeutic antitumor immunity.

Arya Biragyn, Roberta Schiavo, Purevdorj Olkhanud, Kenya Sumitomo, Alan King, Megan McCain, Fred E Indig, Giovanni Almanzar, Dolgor Baatar

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

19 citing papers in PubMed, 34 citations in OpenAlex.

  1. Review
  2. A distinct population of CD8Nature aging · 2025
    Article
  3. MIP3α-RelVaccine · 2025
    Article
  4. Article
  5. CD8Brain, behavior, and immunity · 2024
    Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Sperm-derived SPANX-B is a clinically relevant tumor antigen that is expressed in human tumors and readily recognized by human CD4+ and CD8+ T cells.Clinical cancer research : an official journal of the American Association for Cancer Research · 2009
    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

9 authors at 2 institutions in 1 country.

Arya BiragynLaboratory of Immunology, National Institute on Aging, National Institutes of Health, Baltimore, MD 21224, USA. biragyna@mail.nih.gov
Roberta Schiavo
Purevdorj Olkhanud
Kenya Sumitomo
Alan King
Megan McCain
Fred E Indig
Giovanni Almanzar
Dolgor Baatar
National Institute on Aging · USPulse Biosciences (United States) · US

Funding

Chemoattractant-based vaccines which modulate APCsZ01AG000770 · NIA · NATIONAL INSTITUTE ON AGING · PI BIRAGYN, ARYA · 2004 to 2008
$1.0M
NIA/RRB Confocal Imaging FacilityZ01AG000615 · NIA · NATIONAL INSTITUTE ON AGING · PI BECKER, KEVIN · 2008 to 2008
$445k
Intramural NIH HHS Z01 AG000770
6 · The paper itself

Abstract

Despite its potency, the wider use of immunotherapy for B cell malignancies is hampered by the lack of well-defined tumor-specific Ags. In this study, we demonstrate that an evolutionarily conserved 37-kDa immature laminin receptor protein (OFA-iLRP), a nonimmunogenic embryonic Ag expressed by a variety of tumors, is rendered immunogenic if targeted to the APCs using the CCR6 ligands MIP3alpha/CCL20 and mDF2beta. The CCR6 targeting facilitated efficient Ag cross-presentation and induction of tumor-neutralizing CTLs. Although the Ag targeting alone, without activation of dendritic cells (DCs), is proposed to induce tolerance, and MIP3alpha does not directly activate DCs, the MIP3alpha-based vaccine efficiently induced protective and therapeutic antitumor responses. The responses were as strong as those elicited by the OFA-iLRP fusions with moieties that activated DCs and Th1-type cytokine responses, mDF2beta, or mycobacterial Hsp70 Ag. Although the same cDNA encodes the dimerized high-affinity mature 67-kDa mLRP that is expressed in normal tissues to stabilize the binding of laminin to cell surface integrins, the vaccines expressing OFA-iLRP elicited long-term protective CD8(+) T cell-mediated memory responses against syngeneic B cell lymphoma, indicating the potential application of these simple vaccines as preventive and therapeutic formulations for human use.

Indexed as

AnimalsAntigen PresentationAntigen-Presenting CellsAntigens, NeoplasmCancer VaccinesCD8-Positive T-LymphocytesChemokine CCL20Chemokines, CCCloning, MolecularCytotoxicity, ImmunologicFemaleLymphoma, B-CellMacrophage Inflammatory ProteinsMiceMicroscopy, ConfocalReceptors, CCR6Antigens, NeoplasmCancer VaccinesCCL20 protein, mouseCCR6 protein, mouseChemokine CCL20Chemokines, CCMacrophage Inflammatory Proteinsoncofetal antigensReceptors, CCR6Receptors, ChemokineReceptors, Laminin

Identifiers

PMID17617631
PMCPMC2365706
OpenAlexW2147366609

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.