Evidence map›Paper›PMID 18829565›Full record

ArticleCancer research2008

Cancer immunotherapy targeting the high molecular weight melanoma-associated antigen protein results in a broad antitumor response and reduction of pericytes in the tumor vasculature.

Paulo Cesar Maciag, Matthew M Seavey, Zhen-Kun Pan, Soldano Ferrone, Yvonne Paterson

Open access · bronzeAbstract readEvaluation Study
In one paragraph

Article in Cancer research, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed, 1 pooled it
3.2field-weighted citation impact, top 8% 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

55 citing papers in PubMed, 1 synthesis or guideline pooled it, 91 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. HarnessingArchives of Razi Institute · 2025
    Review
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  7. Article
  8. Frontiers in immunology · 2023
    Review
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  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Innate and Adaptive Immune Responses duringMicrobiology spectrum · 2019
    Article
  18. Review
  19. Vaccines · 2018
    Review
  20. 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

5 authors at 2 institutions in 1 country.

Paulo Cesar MaciagDepartment of Microbiology, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania 19104-6076, USA.
Matthew M Seavey
Zhen-Kun Pan
Soldano Ferrone
Yvonne Paterson
University of Pennsylvania · USUPMC Hillman Cancer Center · US

Funding

IMMUNOBIOLOGY OF NORMAL AND NEOPLASTIC LYMPHOCYTEST32CA009140 · NCI · UNIVERSITY OF PENNSYLVANIA · PI Malay Haldar, WARREN S PEAR · 1985 to 2026
$16.1M
Combinatorial targeting of melanoma initiating cellsR01CA138188 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI FERRONE, SOLDANO · 2008 to 2012
$1.5M
Immunotherapeutic strategies for breast cancerR01CA109253 · NCI · UNIVERSITY OF PENNSYLVANIA · PI PATERSON, YVONNE J · 2006 to 2010
$1.2M
NCI NIH HHS R01 CA109253NCI NIH HHS R01CA109253NCI NIH HHS R01 CA138188NCI NIH HHS T32 CA009140NCI NIH HHS T32CA09140
6 · The paper itself

Abstract

The high molecular weight melanoma-associated antigen (HMW-MAA), also known as melanoma chondroitin sulfate proteoglycan, has been used as a target for the immunotherapy of melanoma. This antigen is expressed on the cell surface and has a restricted distribution in normal tissues. Besides its expression in a broad range of transformed cells, this antigen is also found in pericytes, which are important for tumor angiogenesis. We generated a recombinant Listeria monocytogenes (Lm-LLO-HMW-MAA-C) that expresses and secretes a fragment of HMW-MAA (residues 2,160-2,258) fused to the first 441 residues of the listeriolysin O (LLO) protein. Immunization with Lm-LLO-HMW-MAA-C was able to impede the tumor growth of early established B16F10-HMW-MAA tumors in mice and both CD4(+) and CD8(+) T cells were required for therapeutic efficacy. Immune responses to a known HLA-A2 epitope present in the HMW-MAA(2160-2258) fragment was detected in the HLA-A2/K(b) transgenic mice immunized with Lm-LLO-HMW-MAA-C. Surprisingly, this vaccine also significantly impaired the in vivo growth of other tumorigenic cell lines, such as melanoma, renal carcinoma, and breast tumors, which were not engineered to express HMW-MAA. One hypothesis is that the vaccine could be targeting pericytes, which are important for tumor angiogenesis. In a breast tumor model, immunization with Lm-LLO-HMW-MAA-C caused CD8(+) T-cell infiltration in the tumor stroma and a significant decrease in the number of pericytes in the tumor blood vessels. In conclusion, a Lm-based vaccine against HMW-MAA can trigger cell-mediated immune responses to this antigen that can target not only tumor cells but also pericytes in the tumor vasculature.

Indexed as

ImmunotherapyAnimalsAntigens, NeoplasmCancer VaccinesCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesChondroitin Sulfate Proteoglycan 4FemaleImmunity, CellularListeria monocytogenesMelanoma, ExperimentalMiceMice, Inbred BALB CMice, Inbred C57BLMice, TransgenicNeovascularization, PathologicAntigens, NeoplasmCancer VaccinesChondroitin Sulfate Proteoglycan 4Recombinant Proteins

Identifiers

PMID18829565
PMCPMC3004011
OpenAlexW1975053700

What OpenQuestion holds

Textmetadata
LicenceTDM
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.