Evidence map›Paper›PMID 11396680›Full record

ReviewCritical reviews in immunology2000

Autoimmunity and the immunotherapy of cancer: targeting the "self" to destroy the "other".

W W Overwijk, N P Restifo

Open access · greenAbstract readReview
In one paragraph

Review in Critical reviews in immunology, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

34 citing papers in PubMed, 72 citations in OpenAlex.

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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

2 authors at 1 institution in 1 country.

W W OverwijkSurgery Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892-1502, USA.
N P Restifo
National Institutes of Health · US

Funding

Building on the success of the adoptive immunotherapy of cancerZ01BC010763 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI RESTIFO, NICHOLAS P · 2006 to 2008
$6.4M
Intramural NIH HHS NIH0010139353Intramural NIH HHS Z01 BC010763Intramural NIH HHS Z99 TW999999
6 · The paper itself

Abstract

It is increasingly clear that immunity to "self"-antigens may result in tumor destruction in mouse and man. But which antigens should be targeted with therapeutic cancer vaccines? In the case of melanoma, recognition of melanocyte differentiation antigens (MDA) can be associated with autoimmune depigmentation (vitiligo). We propose that intersection of protein transport to melanosomes and endosomes allows for the loading of MDA-derived peptides on MHC class II molecules, resulting in the activation of MDA-specific CD4+ "helper" T cells that aid the induction of melanoma-specific CD8+ T cells. Thus, the immunogenicity of MDA may be a consequence of their unique cell biology. Studies of MDA-based vaccines can provide new insight into the development of more effective cancer vaccines.

Indexed as

AnimalsAutoimmune DiseasesCancer VaccinesCD4-Positive T-LymphocytesFemalegp100 Melanoma AntigenHumansMaleMelanocytesMelanomaMembrane GlycoproteinsMiceNeoplasm ProteinsVitiligoCancer Vaccinesgp100 Melanoma AntigenMembrane GlycoproteinsNeoplasm ProteinsPMEL protein, humanPmel protein, mouse

Identifiers

PMID11396680
PMCPMC2543120
OpenAlexW2085687864

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.