Evidence map›Paper›PMID 25120362›Full record

ArticleInternational journal of nanomedicine2014

Tolerance-like innate immunity and spleen injury: a novel discovery via the weekly administrations and consecutive injections of PEGylated emulsions.

Long Wang, Chunling Wang, Jiao Jiao, Yuqing Su, Xiaobo Cheng, Zhenjun Huang, Xinrong Liu, Yihui Deng

Open access · goldAbstract read
In one paragraph

Article in International journal of nanomedicine, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.8field-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

9 citing papers in PubMed, 16 citations in OpenAlex.

  1. Review
  2. Article
  3. Immunomodulatory Effects of theMolecules (Basel, Switzerland) · 2019
    Article
  4. Article
  5. Article
  6. Liposome-induced immunosuppression and tumor growth is mediated by macrophages and mitigated by liposome-encapsulated alendronate.Journal of controlled release : official journal of the Controlled Release Society · 2018
    Article
  7. Article
  8. Article
  9. The janus facet of nanomaterials.BioMed research international · 2015
    Review
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

8 authors at 1 institution in 1 country.

Long WangCollege of Pharmacy, Shenyang Pharmaceutical University, Shenyang, People's Republic of China.
Chunling WangCollege of Pharmacy, Shenyang Pharmaceutical University, Shenyang, People's Republic of China.
Jiao JiaoCollege of Pharmacy, Shenyang Pharmaceutical University, Shenyang, People's Republic of China.
Yuqing SuCollege of Pharmacy, Shenyang Pharmaceutical University, Shenyang, People's Republic of China.
Xiaobo ChengCollege of Pharmacy, Shenyang Pharmaceutical University, Shenyang, People's Republic of China.
Zhenjun HuangCollege of Pharmacy, Shenyang Pharmaceutical University, Shenyang, People's Republic of China.
Xinrong LiuCollege of Pharmacy, Shenyang Pharmaceutical University, Shenyang, People's Republic of China.
Yihui DengCollege of Pharmacy, Shenyang Pharmaceutical University, Shenyang, People's Republic of China.
Shenyang Pharmaceutical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

There has been an increasing interest in the study of the innate immune system in recent years. However, few studies have focused on whether innate immunity can acquire tolerance. Therefore, in this study, we investigated tolerance in the innate immune system via the consecutive weekly and daily injections of emulsions modified with polyethylene glycol (PEG), referred to as PEGylated emulsions (PE). The effects of these injections of PE on pharmacokinetics and biodistribution were studied in normal and macrophage-depleted rats. Additionally, we evaluated the antigenic specificity of immunologic tolerance. Immunologic tolerance against PE developed after 21 days of consecutive daily injections or the fourth week of PE administration. Compared with a single administration, it was observed that the tolerant rats had a lower rate of PE clearance from the blood, which was independent of the stress response. In addition, weekly PE injections caused injury to the spleen. Furthermore, the rats tolerant to PEs with the methoxy group (-OCH3) of PEG, failed to respond to the PEs with a different terminal group of PEG or to non-PEG emulsions. Innate immunity tolerance was induced by PE, regardless of the mode of administration. Further study of this mechanism suggested that monocytes play an essential role in the suppression of innate immunity. These findings provide novel insights into the understanding of the innate immune system.

Indexed as

AnimalsEmulsionsImmune ToleranceImmunity, InnateInjections, IntravenousMacrophagesMaleOrgan SizePolyethylene GlycolsRatsRats, WistarSpleenEmulsionsPolyethylene Glycolsantigenic specificitybiodistributionimmunologic toleranceinnate immune systempharmacokinetics

Identifiers

PMID25120362
PMCPMC4128795
OpenAlexW2040506012

What OpenQuestion holds

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LicenceCC BY-NC
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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.