Evidence map›Paper›PMID 18363993›Full record

ArticleImmunological reviews2008

Strategies and challenges in eliciting immunity to melanoma.

Andrew R Ferguson, Lisa A Nichols, Angela L Zarling, Elizabeth D Thompson, C Colin Brinkman, Kristian M Hargadon, Timothy N Bullock, Victor H Engelhard

Abstract read
In one paragraph

Article in Immunological reviews, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
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

9 citing papers in PubMed.

  1. Trial
  2. Article
  3. Article
  4. Review
  5. Regulation of T-cell Tolerance by Lymphatic Endothelial Cells.Journal of clinical & cellular immunology · 2014
    Article
  6. Article
  7. Article
  8. Review
  9. 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

8 authors.

Andrew R FergusonBeirne Carter Center for Immunology Research, Department of Microbiology, University of Virginia School of Medicine, Charlottesville, VA, USA.
Lisa A Nichols
Angela L Zarling
Elizabeth D Thompson
C Colin Brinkman
Kristian M Hargadon
Timothy N Bullock
Victor H Engelhard

Funding

INFECTIOUS DISEASES TRAINING PROGRAMT32AI007046 · NIAID · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI Alison K Criss, William A Petri · 1985 to 2026
$15.3M
MEDICAL SCIENTIST TRAINING PROGRAMT32GM007267 · NIGMS · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI GARCIA-BLANCO, MARIANO A. · 1985 to 2024
$13.4M
INTERDISCIPLINARY TRAINING PROGRAM IN IMMUNOLOGYT32AI007496 · NIAID · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI Michael G. Brown, Coleen A McNamara · 1995 to 2026
$10.2M
Quality and location of presented Ag as determinants of tumor-specific immunityR01CA078400 · NCI · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI ENGELHARD, VICTOR H · 1998 to 2012
$4.4M
Global Biothreats Training ProgramT32AI055432 · NIAID · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI CRISS, ALISON K, PETRI, WILLIAM A · 2003 to 2022
$4.0M
Autoimmune vitiligo and tolerance in the immune response to a melanoma antigenR01AI068836 · NIAID · UNIVERSITY OF VIRGINIA · PI ENGELHARD, VICTOR H · 2007 to 2011
$2.1M
ANTIGENIC DETERMINANTS ON HLA-B7 AND -A2R01AI020963 · NIAID · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI ENGELHARD, VICTOR H · 1985 to 2006
$1.8M
ANTIGENIC DETERMINENTS ON HLA-B7 AND HLA-A2R37AI020963 · NIAID · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI ENGELHARD, VICTOR H. · 1994 to 2001
$653k
Vitiligo in Tyrosinase-specific TCR Transgenic MiceR21AI059996 · NIAID · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI ENGELHARD, VICTOR H. · 2004 to 2005
$457k
The Role of Lymphoid Environments in Guiding T Cell MigrationF32AI072818 · NIAID · UNIVERSITY OF VIRGINIA · PI FERGUSON, ANDREW R. · 2007 to 2009
$130k
NCI NIH HHS CA09109NCI NIH HHS CA78400NCI NIH HHS R01 CA078400NIAID NIH HHS AI059996NIAID NIH HHS AI072818NIAID NIH HHS AI07486NIAID NIH HHS AI07496NIAID NIH HHS AI20963NIAID NIH HHS R01 AI020963NIAID NIH HHS R01 AI068836NIAID NIH HHS T32 AI007046NIAID NIH HHS T32 AI007496NIAID NIH HHS T32 AI055432NIGMS NIH HHS GM007267NIGMS NIH HHS GM08136
6 · The paper itself

Abstract

The ability of CD8+ T cells to recognize melanoma tumors has led to the development of immunotherapeutic approaches that use the antigens CD8+ T cells recognize. However, clinical response rates have been disappointing. Here we summarize our work to understand the mechanisms of self-tolerance that limit responses to currently utilized antigens and our approach to identify new antigens directly tied to malignancy. We also explore several aspects of the anti-tumor immune response induced by peptide-pulsed dendritic cells (DCs). DCs differentially augment the avidity of recall T cells specific for self-antigens and overcome a process of aberrant CD8+ T-cell differentiation that occurs in tumor-draining lymph nodes. DC migration is constrained by injection route, resulting in immune responses in localized lymphoid tissue, and differential control of tumors depending on their location in the body. We demonstrate that CD8+ T-cell differentiation in different lymphoid compartments alters the expression of homing receptor molecules and leads to the presence of systemic central memory cells. Our studies highlight several issues that must be addressed to improve the efficacy of tumor immunotherapy.

Indexed as

AnimalsAntigen PresentationAntigens, NeoplasmCancer VaccinesCD8-Positive T-LymphocytesCell DifferentiationCross-PrimingDendritic CellsHumansImmunologic MemoryImmunotherapyLymphocyte ActivationMelanomaMelanoma, ExperimentalMiceMice, TransgenicAntigens, NeoplasmCancer VaccinesMonophenol MonooxygenasePhosphopeptidesReceptors, Lymphocyte Homing

Identifiers

PMID18363993
PMCPMC2882710

What OpenQuestion holds

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Read underepoch 390

Registered trials

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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.