Evidence map›Paper›PMID 32902245›Full record

ArticleACS nano2020

Efficient Lymph Node-Targeted Delivery of Personalized Cancer Vaccines with Reactive Oxygen Species-Inducing Reduced Graphene Oxide Nanosheets.

Cheng Xu, Hao Hong, Yonghyun Lee, Kyung Soo Park, Mingjiao Sun, Tianrui Wang, Marisa E Aikins, Yao Xu, James J Moon

Open access · greenAbstract read
In one paragraph

Article in ACS nano, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
5.6field-weighted citation impact, top 3% 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

48 citing papers in PubMed, 102 citations in OpenAlex.

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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

9 authors at 3 institutions in 3 countries.

Cheng XuDepartment of Pharmaceutical Sciences, University of Michigan, Ann Arbor, Michigan 48109, United States.ORCID 0000-0003-1000-733X
Hao HongMedical School of Nanjing University, 22 Hankou Road, Nanjing, Jiangsu 210093, China.ORCID 0000-0002-9730-9367
Yonghyun LeeDepartment of Pharmaceutical Sciences, University of Michigan, Ann Arbor, Michigan 48109, United States.
Kyung Soo ParkBiointerfaces Institute, University of Michigan, Ann Arbor, Michigan 48109, United States.
Mingjiao SunDepartment of Pharmaceutical Sciences, University of Michigan, Ann Arbor, Michigan 48109, United States.
Tianrui WangDepartment of Pharmaceutical Sciences, University of Michigan, Ann Arbor, Michigan 48109, United States.
Marisa E AikinsDepartment of Pharmaceutical Sciences, University of Michigan, Ann Arbor, Michigan 48109, United States.
Yao XuDepartment of Pharmaceutical Sciences, University of Michigan, Ann Arbor, Michigan 48109, United States.ORCID 0000-0001-7528-6646
James J MoonDepartment of Pharmaceutical Sciences, University of Michigan, Ann Arbor, Michigan 48109, United States.ORCID 0000-0003-2238-2372
University of Michigan · USEwha Womans University · KRHankou University · CN

Funding

Tissue Engineering and RegenerationT32DE007057 · NIDCR · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI DAVID H. KOHN · 1985 to 2026
$17.3M
Environmental Regulation of Cancer Stem Cell Plasticity in MetastasisU01CA210152 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LAHANN, JOERG, LUKER, GARY D · 2017 to 2021
$3.6M
Novel biomaterials for IBD treatmentR01DK125087 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI KAMADA, NOBUHIKO, MOON, JAMES J. · 2020 to 2023
$2.5M
Elicitation of mucosal immune responses against HIVR01AI127070 · NIAID · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MOON, JAMES J. · 2016 to 2020
$2.3M
Nanomaterials for eliciting anti-tumor T-cells-Diversity SupplementR01CA210273 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MOON, JAMES J. · 2017 to 2021
$2.2M
Tuning Biomaterials-immune cell interactions for treatment of glioblastoma multiformeR01EB022563 · NIBIB · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MOON, JAMES J. · 2016 to 2019
$1.7M
NCI NIH HHS R01 CA210273NCI NIH HHS U01 CA210152NIAID NIH HHS HHSN272201300006CNIAID NIH HHS R01 AI127070NIBIB NIH HHS R01 EB022563NIDCR NIH HHS T32 DE007057NIDDK NIH HHS R01 DK125087
6 · The paper itself

Abstract

Therapeutic cancer vaccines require robust cellular immunity for the efficient killing of tumor cells, and recent advances in neoantigen discovery may provide safe and promising targets for cancer vaccines. However, elicitation of T cells with strong antitumor efficacy requires intricate multistep processes that have been difficult to attain with traditional vaccination approaches. Here, a multifunctional nanovaccine platform has been developed for direct delivery of neoantigens and adjuvants to lymph nodes (LNs) and highly efficient induction of neoantigen-specific T cell responses. A PEGylated reduced graphene oxide nanosheet (RGO-PEG, 20-30 nm in diameter) is a highly modular and biodegradable platform for facile preparation of neoantigen vaccines within 2 h. RGO-PEG exhibits rapid, efficient (15-20% ID/g), and sustained (up to 72 h) accumulation in LNs, achieving >100-fold improvement in LN-targeted delivery, compared with soluble vaccines. Moreover, RGO-PEG induces intracellular reactive oxygen species in dendritic cells, guiding antigen processing and presentation to T cells. Importantly, a single injection of RGO-PEG vaccine elicits potent neoantigen-specific T cell responses lasting up to 30 days and eradicates established MC-38 colon carcinoma. Further combination with anti-PD-1 therapy achieved great therapeutic improvements against B16F10 melanoma. RGO-PEG may serve a powerful delivery platform for personalized cancer vaccination.

Indexed as

Cancer VaccinesGraphiteNeoplasmsLymph NodesReactive Oxygen SpeciesCancer Vaccinesgraphene oxideGraphiteReactive Oxygen Speciescancer immunotherapycancer vaccinenanosheetpositron emission tomographyreduced graphene oxide

Identifiers

PMID32902245
PMCPMC7606610
OpenAlexW3084181050

What OpenQuestion holds

Textmetadata
LicenceTDM
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.