Evidence map›Paper›PMID 20087680›Full record

ReviewImmunologic research2010

Overview of a HLA-Ig based "Lego-like system" for T cell monitoring, modulation and expansion.

Mathias Oelke, Jonathan P Schneck

Abstract readReview
In one paragraph

Review in Immunologic research, 2010. 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
0.8field-weighted citation impact, top 28% 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, 34 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Review
  7. Engineering Platforms for T Cell Modulation.International review of cell and molecular biology · 2018
    Review
  8. Article
  9. Surface engineering for lymphocyte programming.Advanced drug delivery reviews · 2017
    Review
  10. Article
  11. Article
  12. Review
  13. CD47 Enhances In Vivo Functionality of Artificial Antigen-Presenting Cells.Clinical cancer research : an official journal of the American Association for Cancer Research · 2015
    Article
  14. Review
  15. Review
  16. Article
  17. Article
  18. Nanoscale artificial antigen presenting cells for T cell immunotherapy.Nanomedicine : nanotechnology, biology, and medicine · 2014
    Article
  19. Article
  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

2 authors at 1 institution in 1 country.

Mathias OelkeDepartment of Pathology, Johns Hopkins University, School of Medicine, Ross Research Bldg Room 644 B, Baltimore, MD 21205-2196, USA.
Jonathan P Schneck
Johns Hopkins University · US

Funding

The influence of TCR spatial organization on the T cell responsesP01AI072677 · NIAID · JOHNS HOPKINS UNIVERSITY · PI SCHNECK, JONATHAN P · 2008 to 2012
$10.3M
Use of aAPC for Melanoma Adoptive ImmunotherapyR01CA108835 · NCI · JOHNS HOPKINS UNIVERSITY · PI SCHNECK, JONATHAN P · 2004 to 2015
$3.3M
ANTIGEN SPECIFIC MODULATION OF T CELL RESPONSESR01AI044129 · NIAID · JOHNS HOPKINS UNIVERSITY · PI SCHNECK, JONATHAN P · 1999 to 2009
$3.0M
IMMUNOREGULATORY FUNCTIONS OF TCR AND MHC COMPLEXESR01AI029575 · NIAID · JOHNS HOPKINS UNIVERSITY · PI SCHNECK, JONATHAN P · 1991 to 2007
$2.1M
NCI NIH HHS R01 CA108835NIAID NIH HHS P01 AI072677NIAID NIH HHS R01 AI029575NIAID NIH HHS R01 AI044129
6 · The paper itself

Abstract

Recent advances in molecular medicine have shown that soluble MHC-multimers can be valuable tools for both analysis and modulation of antigen-specific immune responses in vitro and in vivo. In this review, we describe the use of dimeric human and mouse major histocompatibility complexes, MHC-Ig, as part of an artificial Antigen-Presenting Cell (aAPC). MHC-Ig-based aAPC and its derivatives represent an exciting new platform technology for measuring and manipulating immune responses in vitro as well as in vivo. This new technology has the potential to help overcome many of the obstacles associated with limitations in current antigen-specific approaches of immunotherapy for the treatment of cancer, infectious diseases and autoimmunity.

Indexed as

AnimalsAntigen PresentationAntigen-Presenting CellsCommunicable DiseasesDimerizationHLA AntigensHumansImmunoglobulinsImmunotherapy, AdoptiveLymphocyte ActivationMiceNeoplasmsT-Lymphocytes, CytotoxicHLA AntigensImmunoglobulins

Identifiers

PMID20087680
PMCPMC2891436
OpenAlexW2029035669

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.