Evidence map›Paper›PMID 28363955›Full record

ArticleFASEB journal : official publication of the Federation of American Societies for Experimental Biology2017

Dendritic cells, engineered to overexpress 25-hydroxyvitamin D 1α-hydroxylase and pulsed with a myelin antigen, provide myelin-specific suppression of ongoing experimental allergic encephalomyelitis.

Chih-Huang Li, Jintao Zhang, David J Baylink, Xiaohua Wang, Naga Bharani Goparaju, Yi Xu, Samiksha Wasnik, Yanmei Cheng, Edmundo Carreon Berumen, Xuezhong Qin and 2 more

Open access · hybridAbstract read
In one paragraph

Article in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.8field-weighted citation impact, top 31% 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

13 citing papers in PubMed, 16 citations in OpenAlex.

  1. Talin 1 plays a significant role in the development of tolerogenic dendritic cells, which may contribute to the progression of multiple sclerosis.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2025
    Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Review
  7. Review
  8. Vitamin D as a Potential Therapy for Multiple Sclerosis: Where Are We?International journal of molecular sciences · 2020
    Review
  9. Observational
  10. Towards Clinical Translation of CD8International journal of molecular sciences · 2019
    Review
  11. Article
  12. Review
  13. Article
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

12 authors at 4 institutions in 3 countries.

Chih-Huang LiDivision of Regenerative Medicine, Department of Medicine, Loma Linda University, Loma Linda, California, USA.
Jintao ZhangDivision of Regenerative Medicine, Department of Medicine, Loma Linda University, Loma Linda, California, USA.
David J BaylinkDivision of Regenerative Medicine, Department of Medicine, Loma Linda University, Loma Linda, California, USA.
Xiaohua WangDivision of Regenerative Medicine, Department of Medicine, Loma Linda University, Loma Linda, California, USA.
Naga Bharani GoparajuDivision of Regenerative Medicine, Department of Medicine, Loma Linda University, Loma Linda, California, USA.
Yi XuDivision of Regenerative Medicine, Department of Medicine, Loma Linda University, Loma Linda, California, USA.
Samiksha WasnikDivision of Regenerative Medicine, Department of Medicine, Loma Linda University, Loma Linda, California, USA.
Yanmei ChengDivision of Regenerative Medicine, Department of Medicine, Loma Linda University, Loma Linda, California, USA.
Edmundo Carreon BerumenDivision of Regenerative Medicine, Department of Medicine, Loma Linda University, Loma Linda, California, USA.
Xuezhong QinDivision of Regenerative Medicine, Department of Medicine, Loma Linda University, Loma Linda, California, USA.
Kin-Hing William LauDivision of Regenerative Medicine, Department of Medicine, Loma Linda University, Loma Linda, California, USA.
Xiaolei TangDivision of Regenerative Medicine, Department of Medicine, Loma Linda University, Loma Linda, California, USA; xitang@llu.edu.
Loma Linda University · USChang Gung University · TWJerry L. Pettis Memorial VA Medical Center · USJinan Infectious Disease Hospital · CN

Funding

BLR&D Research Career Scientist AwardIK6BX003782 · VA · VA LOMA LINDA HEALTHCARE SYSTEM · PI LAU, KIN-HING WILLIAM · 2017 to 2021
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BLRD VA IK6 BX003782
6 · The paper itself

Abstract

Multiple sclerosis (MS) is caused by immune-mediated damage of myelin sheath. Current therapies aim to block such immune responses. However, this blocking is not sufficiently specific and hence compromises immunity, leading to severe side effects. In addition, blocking medications usually provide transient effects and require frequent administration, which further increases the chance to compromise immunity. In this regard, myelin-specific therapy may provide the desired specificity and a long-lasting therapeutic effect by inducing myelin-specific regulatory T (T

Indexed as

Myelin Sheath25-Hydroxyvitamin D3 1-alpha-HydroxylaseAnimalsAntigensBone Marrow CellsCell LineCells, CulturedDendritic CellsEncephalomyelitis, Autoimmune, ExperimentalFemaleForkhead Transcription FactorsGene Expression Regulation, EnzymologicLymphoid TissueMiceMice, Inbred C57BLT-Lymphocytes, Regulatory25-Hydroxyvitamin D3 1-alpha-HydroxylaseAntigensForkhead Transcription FactorsFoxp3 protein, mouse1,25(OH)2D, foxp3multiple sclerosisregulatory T cellsTreg

Identifiers

PMID28363955
PMCPMC5471518
OpenAlexW2602487141

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.