Evidence map›Paper›PMID 26372309›Full record

ArticleNature communications2015

dNP2 is a blood-brain barrier-permeable peptide enabling ctCTLA-4 protein delivery to ameliorate experimental autoimmune encephalomyelitis.

Sangho Lim, Won-Ju Kim, Yeon-Ho Kim, Sohee Lee, Ja-Hyun Koo, Jung-Ah Lee, Heeseok Yoon, Do-Hyun Kim, Hong-Jai Park, Hye-Mi Kim and 11 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed, 1 pooled it
5.0field-weighted citation impact, top 4% 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

56 citing papers in PubMed, 1 synthesis or guideline pooled it, 117 citations in OpenAlex.

  1. Pooled it
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  6. Review
  7. A SynB1-conjugated antibody cocktail crosses the blood-brain barrier to produce a therapeutic effect on rabies.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  8. Article
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  10. Article
  11. Article
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  13. Article
  14. The Application of Nanovaccines in Autoimmune Diseases.International journal of nanomedicine · 2024
    Review
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  16. Article
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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

21 authors at 5 institutions in 2 countries.

Sangho LimDepartment of Life Science, College of Natural Sciences, Hanyang University, Seoul 133-791, Republic of Korea.
Won-Ju KimDepartment of Life Science, College of Natural Sciences, Hanyang University, Seoul 133-791, Republic of Korea.
Yeon-Ho KimDepartment of Life Science, College of Natural Sciences, Hanyang University, Seoul 133-791, Republic of Korea.
Sohee LeeCenter for Neuroscience Imaging Research (CNIR), Institute for Basic Science (IBS), Suwon 440-746, Republic of Korea.
Ja-Hyun KooDepartment of Life Science, College of Natural Sciences, Hanyang University, Seoul 133-791, Republic of Korea.
Jung-Ah LeeDepartment of Life Science, College of Natural Sciences, Hanyang University, Seoul 133-791, Republic of Korea.
Heeseok YoonDepartment of Life Science, College of Natural Sciences, Hanyang University, Seoul 133-791, Republic of Korea.
Do-Hyun KimDepartment of Life Science, College of Natural Sciences, Hanyang University, Seoul 133-791, Republic of Korea.
Hong-Jai ParkDepartment of Life Science, College of Natural Sciences, Hanyang University, Seoul 133-791, Republic of Korea.
Hye-Mi KimDivision of Integrative Bioscience and Biotechnology, Pohang University of Science and Technology, Pohang 790-784, Republic of Korea.
Hong-Gyun LeeDepartment of Life Science, College of Natural Sciences, Hanyang University, Seoul 133-791, Republic of Korea.
Ji Yun KimDepartment of Life Science, College of Natural Sciences, Hanyang University, Seoul 133-791, Republic of Korea.
Jae-Ung LeeDepartment of Life Science, College of Natural Sciences, Hanyang University, Seoul 133-791, Republic of Korea.
Jae Hun ShinDepartment of Immunobiology, Yale University School of Medicine, New Haven, Connecticut 06520, USA.
Lark Kyun KimDepartment of Immunobiology, Yale University School of Medicine, New Haven, Connecticut 06520, USA.
Junsang DohDepartment of Mechanical Engineering, School of Interdisciplinary Bioscience and Bioengineering, Pohang University of Science and Technology, Pohang 790-784, Republic of Korea.
Hongtae KimCenter for Neuroscience Imaging Research (CNIR), Institute for Basic Science (IBS), Suwon 440-746, Republic of Korea.
Sang-Kyou LeeDepartment of Biotechnology, Yonsei University, Seoul 120-749, Republic of Korea.
Alfred L M BothwellDepartment of Immunobiology, Yale University School of Medicine, New Haven, Connecticut 06520, USA.
Minah SuhCenter for Neuroscience Imaging Research (CNIR), Institute for Basic Science (IBS), Suwon 440-746, Republic of Korea.
Je-Min ChoiDepartment of Life Science, College of Natural Sciences, Hanyang University, Seoul 133-791, Republic of Korea.
Hanyang University · KRInstitute for Basic Science · KRPohang University of Science and Technology · KRYale University · USYonsei University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Central nervous system (CNS)-infiltrating effector T cells play critical roles in the development and progression of multiple sclerosis (MS). However, current drugs for MS are very limited due to the difficulty of delivering drugs into the CNS. Here we identify a cell-permeable peptide, dNP2, which efficiently delivers proteins into mouse and human T cells, as well as various tissues. Moreover, it enters the brain tissue and resident cells through blood vessels by penetrating the tightly organized blood-brain barrier. The dNP2-conjugated cytoplasmic domain of cytotoxic T-lymphocyte antigen 4 (dNP2-ctCTLA-4) negatively regulates activated T cells and shows inhibitory effects on experimental autoimmune encephalomyelitis in both preventive and therapeutic mouse models, resulting in the reduction of demyelination and CNS-infiltrating T helper 1 and T helper 17 cells. Thus, this study demonstrates that dNP2 is a blood-brain barrier-permeable peptide and dNP2-ctCTLA-4 could be an effective agent for treating CNS inflammatory diseases such as MS.

Indexed as

AnimalsBlood-Brain BarrierCarrier ProteinsCell-Penetrating PeptidesCTLA-4 AntigenDisease Models, AnimalEncephalomyelitis, Autoimmune, ExperimentalHeLa CellsHumansIn Vitro TechniquesJurkat CellsMiceMice, Inbred C57BLPeptide FragmentsTh17 CellsT-LymphocytesCarrier ProteinsCell-Penetrating PeptidesCTLA-4 AntigendNP2 peptidePeptide FragmentsUbiquitin-Protein LigasesUFL1 protein, human

Identifiers

PMID26372309
PMCPMC4579786
OpenAlexW2255772379

What OpenQuestion holds

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LicenceCC BY
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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.