Evidence map›Paper›PMID 35975424›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2022

Injectable Nanoparticle-Based Hydrogels Enable the Safe and Effective Deployment of Immunostimulatory CD40 Agonist Antibodies.

Santiago Correa, Emily L Meany, Emily C Gale, John H Klich, Olivia M Saouaf, Aaron T Mayer, Zunyu Xiao, Celine S Liong, Ryanne A Brown, Caitlin L Maikawa and 4 more

Open access · goldAbstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed, 1 pooled it
3.7field-weighted citation impact, top 6% 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

27 citing papers in PubMed, 1 synthesis or guideline pooled it, 46 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Structural immunotherapy: Harnessing chemical design to build powerful next-generation therapeutics.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Review
  19. Review
  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

14 authors at 2 institutions in 1 country.

Santiago CorreaDepartment of Materials Science and Engineering, Stanford University, Stanford, CA, 94305, USA.ORCID 0000-0001-8230-4945
Emily L MeanyDepartment of Bioengineering, Stanford University, Stanford, CA, 94305, USA.
Emily C GaleDepartment of Biochemistry, Stanford University School of Medicine, Stanford, CA, 94305, USA.ORCID 0000-0002-6536-3027
John H KlichDepartment of Bioengineering, Stanford University, Stanford, CA, 94305, USA.
Olivia M SaouafDepartment of Materials Science and Engineering, Stanford University, Stanford, CA, 94305, USA.ORCID 0000-0002-5117-7127
Aaron T MayerDepartment of Bioengineering, Stanford University, Stanford, CA, 94305, USA.
Zunyu XiaoDepartment of Bioengineering, Stanford University, Stanford, CA, 94305, USA.
Celine S LiongDepartment of Bioengineering, Stanford University, Stanford, CA, 94305, USA.
Ryanne A BrownDepartment of Pathology, Stanford University School of Medicine, Stanford, CA, 94305, USA.
Caitlin L MaikawaDepartment of Bioengineering, Stanford University, Stanford, CA, 94305, USA.
Abigail K GrosskopfDepartment of Chemical Engineering, Stanford University, Stanford, CA, 94305, USA.
Joseph L MannDepartment of Materials Science and Engineering, Stanford University, Stanford, CA, 94305, USA.
Juliana IdoyagaDepartment of Microbiology & Immunology, Stanford University School of Medicine, Stanford, CA, 94305, USA.
Eric A AppelDepartment of Materials Science and Engineering, Stanford University, Stanford, CA, 94305, USA.ORCID 0000-0002-2301-7126
Stanford University · USCardiovascular Institute of the South · US

Funding

Translational Oncology Research Program (Project-005)P30CA124435 · NCI · STANFORD UNIVERSITY · PI Vittorio Sebastiano · 2007 to 2026
$71.4M
Supplement to Enhance Wellness and Resiliency in the Graduate EnvironmentT32GM007276 · NIGMS · STANFORD UNIVERSITY · PI MORRISON, ASHBY J. · 1985 to 2023
$32.9M
Graduate Training Program in BiotechnologyT32GM008412 · NIGMS · STANFORD UNIVERSITY · PI COCHRAN, JENNIFER R · 1991 to 2020
$5.5M
Cancer immunotherapy using injectable hydrogels for precise and tunable multidrug deliveryF32CA247352 · NCI · STANFORD UNIVERSITY · PI CORREA, SANTIAGO · 2020 to 2022
$201k
American Cancer Society RSG-18-133-01-CDDGoldman Sachs Foundation 162509National Defense and Science Engineering GraduateNational Science FoundationNCI NIH HHS F32 CA247352NCI NIH HHS P30 CA124435NIGMS NIH HHS T32 GM007276NIGMS NIH HHS T32 GM008412NIH Biotechnology Training Program T32 GM008412NIH Cell and Molecular Biology Training Program T32 GM007276NIH HHS F32CA247352
6 · The paper itself

Abstract

When properly deployed, the immune system can eliminate deadly pathogens, eradicate metastatic cancers, and provide long-lasting protection from diverse diseases. Unfortunately, realizing these remarkable capabilities is inherently risky as disruption to immune homeostasis can elicit dangerous complications or autoimmune disorders. While current research is continuously expanding the arsenal of potent immunotherapeutics, there is a technological gap when it comes to controlling when, where, and how long these drugs act on the body. Here, this study explored the ability of a slow-releasing injectable hydrogel depot to reduce dose-limiting toxicities of immunostimulatory CD40 agonist (CD40a) while maintaining its potent anticancer efficacy. A previously described polymer-nanoparticle (PNP) hydrogel system is leveraged that exhibits shear-thinning and yield-stress properties that are hypothesized to improve locoregional delivery of CD40a immunotherapy. Using positron emission tomography, it is demonstrated that prolonged hydrogel-based delivery redistributes CD40a exposure to the tumor and the tumor draining lymph node (TdLN), thereby reducing weight loss, hepatotoxicity, and cytokine storm associated with standard treatment. Moreover, CD40a-loaded hydrogels mediate improved local cytokine induction in the TdLN and improve treatment efficacy in the B16F10 melanoma model. PNP hydrogels, therefore, represent a facile, drug-agnostic method to ameliorate immune-related adverse effects and explore locoregional delivery of immunostimulatory drugs.

Indexed as

MelanomaNanoparticlesAntibodiesCD40 AntigensCytokinesHumansHydrogelsPolymersTomography, X-Ray ComputedAntibodiesCD40 AntigensCytokinesHydrogelsPolymersbiomaterialscancerdrug deliveryimmunotherapypharmacokinetics

Identifiers

PMID35975424
PMCPMC9534946
OpenAlexW4292080826

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.