Evidence map›Paper›PMID 40854817›Full record

ReviewJournal for immunotherapy of cancer2025

Constructing the cure: engineering the next wave of antibody and cellular immune therapies.

Stefanie R Bailey, Eric Bartee, Kyle G Daniels, Christopher R Heery, Pravin Kaumaya, Gregory B Lesinski, Timothy B Lowinger, Michelle H Nelson, Mark P Rubinstein, Megen C Wittling and 2 more

Abstract readReview
In one paragraph

Review in Journal for immunotherapy of cancer, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Review
  3. Adoptive T-cell therapies in the clinic.Bioengineering & translational medicine · 2026
    Review
  4. 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

12 authors.

Stefanie R BaileyDepartment of Pediatrics, University of Virginia, Charlottesville, Virginia, USA.
Eric BarteeDepartment of Internal Medicine, Health Sciences Center, University of New Mexico, Albuquerque, New Mexico, USA.ORCID http://orcid.org/0000-0003-1793-446X
Kyle G DanielsDepartment of Genetics, Stanford School of Medicine, Stanford, California, USA.
Christopher R HeeryArcellx, Redwood City, California, USA.
Pravin KaumayaDepartment of Microbiology and Immunology, Indiana University School of Medicine, Indianapolis, Indiana, USA.ORCID http://orcid.org/0000-0002-8647-3911
Gregory B LesinskiDepartment of Hematology and Oncology, Emory University Winship Cancer Institute, Atlanta, Georgia, USA.ORCID http://orcid.org/0000-0002-8787-7678
Timothy B LowingerMersana Therapeutics, Cambridge, Massachusetts, USA.
Michelle H NelsonAptevo Therapeutics, Seattle, Washington, USA.
Mark P RubinsteinDivision of Medical Oncology, The Ohio State University, Columbus, Ohio, USA.
Megen C WittlingDepartment of Surgery, Emory University, Atlanta, Georgia, USA.ORCID http://orcid.org/0000-0002-3631-4955
Chrystal M PaulosDepartment of Surgery, Emory University, Atlanta, Georgia, USA aposey@pennmedicine.upenn.edu chrystal.mary.paulos@emory.edu.
Avery D PoseyDepartment of Systems Pharmacology and Translational Therapeutics, University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania, USA aposey@pennmedicine.upenn.edu chrystal.mary.paulos@emory.edu.ORCID http://orcid.org/0000-0001-8711-629X

Funding

Impact of TNF on Oncolytic VirotherapyR01CA276134 · NCI · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI Eric Carter Bartee · 2023 to 2026
$1.7M
NCI NIH HHS R01 CA276134
6 · The paper itself

Abstract

Immuno-oncology has revolutionized cancer treatment by mobilizing the immune system to eliminate tumors. Although immune checkpoint inhibitors and T cell therapies have mediated durable responses in hematologic malignancies and select solid tumors, most patients still relapse or fail to respond. To overcome these limitations, novel, next-generation immune constructs, including bispecific-cell therapy combinations, armored cells, tethered cytokines, immune-stimulatory antibody conjugates, and in vivo gene editing, are being developed to enhance specificity, persistence, and immune activation. This Society for Immunotherapy of Cancer roadmap highlights emerging technologies that integrate, redirect, or potentiate immune response. We examine advances in construct design, strategies for clinical translation, and opportunities for combinatorial approaches. By addressing translational barriers and real-world challenges, we outline how innovative engineering can unlock a new era of safe, durable, and accessible immunotherapies. Realizing this potential will require coordinated efforts from researchers, clinicians, industry leaders, and policymakers to deliver curative outcomes to patients worldwide.

Indexed as

Cell- and Tissue-Based TherapyImmunotherapyNeoplasmsHumansCombination therapyCytokineImmune Checkpoint InhibitorMonoclonal antibodyOncolytic virus

Identifiers

PMID40854817
PMCPMC12382549

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.