Evidence map›Paper›PMID 41975016›Full record

ReviewBioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy2026

Progress in Designing Cytokine Antagonist Antibodies for Cancer Therapy.

Henry McEacheron, Giulia Nisita, Peiying Liu, Jamie B Spangler

Abstract readReview
PubMed Publisher
In one paragraph

Review in BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

4 authors.

Henry McEacheron *Department of Chemical and Biomolecular Engineering, Johns Hopkins University, Baltimore, MD, USA.
Giulia Nisita *Chemistry-Biology Interface Program, Johns Hopkins University, Baltimore, MD, USA.
Peiying Liu *Department of Chemical and Biomolecular Engineering, Johns Hopkins University, Baltimore, MD, USA.
Jamie B SpanglerDepartment of Chemical and Biomolecular Engineering, Johns Hopkins University, Baltimore, MD, USA. jamie.spangler@jhu.edu.ORCID http://orcid.org/0000-0001-8187-3732

Funding

Melanoma Research Alliance 1257538National Institutes of Health (US) T32GM080189
6 · The paper itself

Abstract

Cytokines are a class of secreted proteins that transmit critical signals between cells to maintain homeostatic balance, coordinating processes such as proliferation, migration, polarization, and survival. Cytokines play a particularly important role in regulating the immune system through activation of either proinflammatory or anti-inflammatory pathways on a variety of hematopoietic and nonhematopoietic cell types. As a consequence of their essential roles in dictating cell fate, especially in the context of immune responses, cytokines have become an appealing target for the development of drugs to treat immune-linked diseases. With respect to oncology applications, therapeutic efforts have primarily focused on either promoting the effects of immunostimulatory cytokines or antagonizing the effects of immunosuppressive cytokines, with the goal of stimulating antitumor immunity. Here, we provide an updated overview of preclinical and clinical therapeutic advances in the design of cytokine antagonist antibodies for cancer treatment. We first discuss the structural and functional characteristics of various cytokines, including interleukins, chemokines, and growth factors, as well as their contributions to cancer development and progression. We then highlight successes and failures in generating therapeutic antibodies against each of these cytokines. As the functions of cytokines are complex and multifaceted, we note that complete ablation of cytokine activity may not be therapeutically desirable and that combination strategies are often needed to realize the full potential of anti-cytokine antibodies as therapies. Looking ahead, innovative approaches and novel antagonistic scaffolds promise to continue advancing clinical progress for this important category of oncology drugs.

Indexed as

Antibodies, MonoclonalAntineoplastic AgentsCytokinesNeoplasmsAnimalsDrug DesignHumansAntibodies, MonoclonalAntineoplastic AgentsCytokines

Identifiers

What Socratic 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 Socratic graph.