Evidence map›Paper›PMID 30091313›Full record

ReviewYonsei medical journal2018

Generation, Characteristics and Clinical Trials of Ex Vivo Generated Tolerogenic Dendritic Cells.

Sang Hyun Kim, Ho Hyun Jung, Chong Kil Lee

Abstract readReview
In one paragraph

Review in Yonsei medical journal, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing 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

27 citing papers in PubMed.

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  9. 1,25(OH)International journal of molecular sciences · 2023
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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

3 authors.

Sang Hyun KimCollege of Pharmacy, Chungbuk National University, Cheongju, Korea.
Ho Hyun JungCollege of Pharmacy, Chungbuk National University, Cheongju, Korea.
Chong Kil LeeCollege of Pharmacy, Chungbuk National University, Cheongju, Korea. cklee@chungbuk.ac.kr.ORCID https://orcid.org/0000-0001-9070-341X

Funding

National Research Foundation of Korea NRF-2017R1A2B4006828
6 · The paper itself

Abstract

Dendritic cells (DCs) play a key role not only in the initiation of primary immune responses, but also in the development and maintenance of immune tolerance. Numerous protocols have been developed to generate tolerogenic DCs (tolDCs) ex vivo, and the therapeutic efficacy of ex vivo-generated tolDCs has been demonstrated in autoimmune disease animal models. Based on successes in small animal models, several clinical trials have been completed or are on-going in patients with autoimmune diseases such as rheumatoid arthritis, type 1 diabetes, multiple sclerosis, and Crohn's disease. Here we describe the methods used to generate tolDCs ex vivo, and the common features shared by tolDCs. In addition, we overview five completed clinical trials with reported outcomes and summarize the tolDC-based clinical trials that are currently registered with the U.S. National Institutes of Health. Although the number of tolDC-based clinical trials is much smaller than the hundreds of clinical trials using immunogenic DCs, tolDC-based treatment of autoimmune diseases is becoming a reality, and could serve as an innovative cellular therapy in the future.

Indexed as

Clinical Trials as TopicImmune ToleranceAnimalsArthritis, RheumatoidAutoimmune DiseasesCell Culture TechniquesCrohn DiseaseDendritic CellsDiabetes Mellitus, Type 1HumansIchthyosiform Erythroderma, CongenitalLipid Metabolism, Inborn ErrorsMuscular Diseasesautoimmune diseasecellular therapyclinical trialDendritic cellimmune tolerance

Identifiers

PMID30091313
PMCPMC6082979

What OpenQuestion holds

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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.