Evidence map›Paper›PMID 17972902›Full record

ReviewEMBO reports2007

Non-classical major histocompatibility complex proteins as determinants of tumour immunosurveillance.

Anita Q Gomes, Daniel V Correia, Bruno Silva-Santos

Abstract readReview
In one paragraph

Review in EMBO reports, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

20 citing papers in PubMed, 51 citations in OpenAlex.

  1. Review
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  5. Suppression of Non-Random Fertilization by MHC Class I Antigens.International journal of molecular sciences · 2020
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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

3 authors at 2 institutions in 1 country.

Anita Q GomesInstituto de Medicina Molecular, Faculdade de Medicina, Universidade de Lisboa, Av. Prof. Egas Moniz, 1649-028 Lisbon, Portugal.
Daniel V Correia
Bruno Silva-Santos
University of Lisbon · PTInstituto Gulbenkian de Ciência · PT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tumours develop in vertebrate organisms endowed with immune systems that are potentially able to eradicate them. Nevertheless, our ever-increasing understanding of the complex interactions between lymphocytes and tumour cells fuels the long-standing hope of developing efficient immunotherapies against cancer. This review focuses on a versatile family of proteins, the major histocompatibility complex class Ib, which has been recently implicated in both the establishment of anti-tumour immune responses and in tumour immune response evasion. We focus on a subset of class Ib proteins, human leukocyte antigen (HLA)-G, Qa-2, CD1d and NKG2D ligands, which bind to either stimulatory or inhibitory receptors expressed on T, natural killer (NK) and NKT lymphocytes, and thereby modulate their anti-tumour activity.

Indexed as

Major Histocompatibility ComplexMonitoring, ImmunologicAnimalsAntigen PresentationAntigens, CD1Antigens, CD1dHistocompatibility Antigens Class IHLA AntigensHLA-G AntigensHumansKiller Cells, NaturalLipidsNeoplasmsNK Cell Lectin-Like Receptor Subfamily KPeptidesReceptors, ImmunologicAntigens, CD1Antigens, CD1dCD1D protein, humanHistocompatibility Antigens Class IHLA AntigensHLA-G AntigensKLRK1 protein, humanLipidsMHC Ib Qa-2 antigenNK Cell Lectin-Like Receptor Subfamily KPeptidesReceptors, ImmunologicReceptors, Natural Killer Cell

Identifiers

PMID17972902
PMCPMC2247375
OpenAlexW1988941398

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.