Evidence map›Paper›PMID 38166251›Full record

ReviewJournal of immunology (Baltimore, Md. : 1950)2024

Engineering Challenges and Opportunities in Autologous Cellular Cancer Immunotherapy.

Colleen R Foley, Sheridan L Swan, Melody A Swartz

Open access · greenAbstract readReview
In one paragraph

Review in Journal of immunology (Baltimore, Md. : 1950), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

6 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
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  6. 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

3 authors at 1 institution in 1 country.

Colleen R FoleyPritzker School of Molecular Engineering, University of Chicago, Chicago, IL.ORCID 0009-0002-1636-7205
Sheridan L SwanPritzker School of Molecular Engineering, University of Chicago, Chicago, IL.ORCID 0000-0002-0668-2386
Melody A SwartzPritzker School of Molecular Engineering, University of Chicago, Chicago, IL.
University of Chicago · US

Funding

Probing cellular, molecular and biomechanical barriers to immunotherapy in the tumor microenvironment with organotypic in vitro models of the tumor-lympho-immune interfaceR01CA253248 · NCI · UNIVERSITY OF CHICAGO · PI SWARTZ, MELODY ANN · 2021 to 2025
$2.8M
Immunoengineering Postdoctoral Training Program - Resubmission - 1T32AI153020 · NIAID · UNIVERSITY OF CHICAGO · PI ALEGRE, MARIA-LUISA, SWARTZ, MELODY ANN · 2021 to 2025
$2.1M
Paradoxical roles of tumor lymphangiogenesis on tumor immunity and implications for immunotherapy - Resubmission 01R01CA219304 · NCI · UNIVERSITY OF CHICAGO · PI SWARTZ, MELODY ANN · 2018 to 2022
$1.8M
HHS | NIH | National Cancer Institute (NCI) R01-CA219304HHS | NIH | National Cancer Institute (NCI) R01-CA253248HHS | NIH | National Institute of Allergy and Infectious Diseases (NIAID) T32-AI153020NCI NIH HHS R01 CA219304NCI NIH HHS R01 CA253248NIAID NIH HHS T32 AI153020
6 · The paper itself

Abstract

The use of a patient's own immune or tumor cells, manipulated ex vivo, enables Ag- or patient-specific immunotherapy. Despite some clinical successes, there remain significant barriers to efficacy, broad patient population applicability, and safety. Immunotherapies that target specific tumor Ags, such as chimeric Ag receptor T cells and some dendritic cell vaccines, can mount robust immune responses against immunodominant Ags, but evolving tumor heterogeneity and antigenic downregulation can drive resistance. In contrast, whole tumor cell vaccines and tumor lysate-loaded dendritic cell vaccines target the patient's unique tumor antigenic repertoire without prior neoantigen selection; however, efficacy can be weak when lower-affinity clones dominate the T cell pool. Chimeric Ag receptor T cell and tumor-infiltrating lymphocyte therapies additionally face challenges related to genetic modification, T cell exhaustion, and immunotoxicity. In this review, we highlight some engineering approaches and opportunities to these challenges among four classes of autologous cell therapies.

Indexed as

Cancer VaccinesNeoplasmsVaccinesAntigens, NeoplasmDendritic CellsHumansImmunotherapyImmunotherapy, AdoptiveT-LymphocytesAntigens, NeoplasmCancer VaccinesVaccines

Identifiers

PMID38166251
PMCPMC11155266
OpenAlexW4390493337

What OpenQuestion holds

Textmetadata
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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.