Evidence map›Paper›PMID 27958383›Full record

ArticleScientific reports2016

Mature dendritic cell derived from cryopreserved immature dendritic cell shows impaired homing ability and reduced anti-viral therapeutic effects.

Qianqian Zhou, Yulong Zhang, Man Zhao, Xiaohui Wang, Cong Ma, Xinquan Jiang, Tao Wu, Donggen Wang, Linsheng Zhan

Open access · goldAbstract readComparative Study
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.6field-weighted citation impact, top 29% 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

4 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
  2. Article
  3. Cryomicroneedles for transdermal cell delivery.Nature biomedical engineering · 2021
    Article
  4. 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

9 authors at 3 institutions in 1 country.

Qianqian ZhouBeijing Institute of Transfusion Medicine, Beijing key Laboratory of Blood Safety and Supply Technologies, Beijing 100850, P.R. China.
Yulong ZhangBeijing Institute of Transfusion Medicine, Beijing key Laboratory of Blood Safety and Supply Technologies, Beijing 100850, P.R. China.
Man ZhaoBeijing Institute of Transfusion Medicine, Beijing key Laboratory of Blood Safety and Supply Technologies, Beijing 100850, P.R. China.
Xiaohui WangBeijing Institute of Transfusion Medicine, Beijing key Laboratory of Blood Safety and Supply Technologies, Beijing 100850, P.R. China.
Cong MaSchool of Public Health, Taishan Medical University, Taian, Shandong 271000, China.
Xinquan JiangSchool of Public Health, Taishan Medical University, Taian, Shandong 271000, China.
Tao WuDepartment of Blood Transfusion, PLA Army General Hospital, Beijing 100700, P.R. China.
Donggen WangBeijing Institute of Transfusion Medicine, Beijing key Laboratory of Blood Safety and Supply Technologies, Beijing 100850, P.R. China.
Linsheng ZhanBeijing Institute of Transfusion Medicine, Beijing key Laboratory of Blood Safety and Supply Technologies, Beijing 100850, P.R. China.
Guangzhou Blood Center · CNTaishan Medical University · CNNankai University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cryopreservation is critical in reducing redundant operations and also in quality control in dendritic cell (DC) therapy. Full maturation and efficient homing of DCs to T cell-region constitute a crucial aspect of DC immunotherapy; however, the in vivo migration and distribution pattern, as well as the anti-viral effect of DCs that matured from cryopreserved immature DCs (cryoim-mDCs) remain to be revealed. In the present study, we compared cryoim-mDCs with DCs matured from fresh immature DCs (fmDCs) in the aspects of phenotypes, in vivo homing capacities as well as the anti-viral therapeutic effects to further clarify the effect of cryopreservation on DC-based cytotherapy. The results showed that cryopreservation impaired the homing ability of DCs which was associated with the reduced expression of CCR7 and disturbed cytoskeleton arrangement. Moreover, the antigen-specific CD8+ T cell response induced by cryoim-mDCs was much weaker than that induced by fmDCs in both the spleen and liver draining lymph nodes, which provided reduced protection from viral invasions. In conclusion, cryopreservation is a good method to keep the viability of immature DCs, however, the in vivo homing capacity and anti-viral therapeutic effect of DCs matured from frozen immature DCs were hindered to some extent.

Indexed as

AnimalsAntiviral AgentsCD8-Positive T-LymphocytesCell DifferentiationCell MovementCells, CulturedCell SurvivalCryopreservationDendritic CellsImmunotherapyLiverMicePhenotypeReceptors, CCR7SpleenAntiviral AgentsCcr7 protein, mouseReceptors, CCR7

Identifiers

PMID27958383
PMCPMC5153632
OpenAlexW2566716556

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.