Evidence map›Paper›PMID 35876221›Full record

ArticleACS nano2022

Multivalent, Bispecific αB7-H3-αCD3 Chemically Self-Assembled Nanorings Direct Potent T Cell Responses against Medulloblastoma.

Ellie A Mews, Pauline Beckmann, Mahathi Patchava, Yiao Wang, David A Largaespada, Carston R Wagner

Abstract read
In one paragraph

Article in ACS nano, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. T-cell Receptor (TCR) Targeting with Multivalent T-cell Engagers.bioRxiv : the preprint server for biology · 2026
    Article
  2. Article
  3. Review
  4. Review
  5. Review
  6. Article
  7. Review
  8. Medulloblastoma: biology and immunotherapy.Frontiers in immunology · 2025
    Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. B7-H3 in Brain Malignancies: Immunology and Immunotherapy.International journal of biological sciences · 2023
    Review
  14. 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

6 authors.

Ellie A MewsDepartment of Medicinal Chemistry, University of Minnesota, Cancer and Cardiovascular Research Building, 2231 Sixth Street SE, Minneapolis, Minnesota 55455 United States.ORCID 0000-0002-4073-7096
Pauline BeckmannDepartment of Pediatrics, Center for Genome Engineering, Masonic Cancer Center, University of Minnesota, Malcolm Moos Tower, 515 Delaware Street SE, Minneapolis, Minnesota 55455 United States.
Mahathi PatchavaDepartment of Pediatrics, Center for Genome Engineering, Masonic Cancer Center, University of Minnesota, Malcolm Moos Tower, 515 Delaware Street SE, Minneapolis, Minnesota 55455 United States.
Yiao WangDepartment of Medicinal Chemistry, University of Minnesota, Cancer and Cardiovascular Research Building, 2231 Sixth Street SE, Minneapolis, Minnesota 55455 United States.
David A LargaespadaDepartment of Pediatrics, Center for Genome Engineering, Masonic Cancer Center, University of Minnesota, Malcolm Moos Tower, 515 Delaware Street SE, Minneapolis, Minnesota 55455 United States.
Carston R WagnerDepartment of Medicinal Chemistry, University of Minnesota, Cancer and Cardiovascular Research Building, 2231 Sixth Street SE, Minneapolis, Minnesota 55455 United States.ORCID 0000-0001-7927-719X

Funding

Targeting Effector Immune cells to Cancer with Chemically Self-Assembled Nanorings (CSANs)R01CA247681 · NCI · UNIVERSITY OF MINNESOTA · PI WAGNER, CARSTON R. · 2020 to 2024
$2.8M
NCI NIH HHS R01 CA247681
6 · The paper itself

Abstract

Few therapeutic options have been made available for treating central nervous system tumors, especially upon recurrence. Recurrent medulloblastoma is uniformly lethal with no approved therapies. Recent preclinical studies have shown promising results for eradicating various solid tumors by targeting the overexpressed immune checkpoint molecule, B7-H3. However, due to several therapy-related toxicities and reports of tumor escape, the full potential of targeting this pan-cancer antigen has yet to be realized. Here, we designed and characterized bispecific chemically self-assembling nanorings (CSANs) that target the T cell receptor, CD3ε, and tumor associated antigen, B7-H3, derived from the humanized 8H9 single chain variable fragment. We show that the αB7-H3-αCD3 CSANs increase T cell infiltration and facilitate selective cytotoxicity of B7-H3

Indexed as

Brain NeoplasmsCerebellar NeoplasmsMedulloblastomaAntigens, NeoplasmCell Line, TumorHumansLymphocyte ActivationT-LymphocytesAntigens, NeoplasmB7-H3bispecificCD3CSANsmedulloblastoma

Identifiers

PMID35876221
PMCPMC9885520

What OpenQuestion holds

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Registered trials

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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.