Evidence map›Paper›PMID 26846666›Full record

ArticleJournal of nanobiotechnology2016

Immunotoxicity assessment of CdSe/ZnS quantum dots in macrophages, lymphocytes and BALB/c mice.

Xiaomei Wang, Jinglin Tian, Ken-Tye Yong, Xuedan Zhu, Marie Chia-Mi Lin, Wenxiao Jiang, Jiefeng Li, Qijun Huang, Guimiao Lin

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Journal of nanobiotechnology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
5.1field-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

32 citing papers in PubMed, 89 citations in OpenAlex.

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  12. Green synthesis of glyco-CuInSJournal of nanobiotechnology · 2023
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  20. Immunotoxicity Considerations for Next Generation Cancer Nanomedicines.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2019
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 2 institutions in 2 countries.

Xiaomei WangCollege of Life Science and Oceanography, Shenzhen University, Shenzhen, 518060, People's Republic of China. xmwang@szu.edu.cn.
Jinglin TianCollege of Life Science and Oceanography, Shenzhen University, Shenzhen, 518060, People's Republic of China. tianshilinzi@sina.com.
Ken-Tye YongSchool of Electrical and Electronic Engineering, Nanyang Technological University, Singapore, 639798, Singapore. ktyong@ntu.edu.sg.
Xuedan ZhuKey Lab of Biomedical Engineering, School of Medicine, Shenzhen University, Shenzhen, 518060, People's Republic of China. zhuxuedan0612@hotmail.com.
Marie Chia-Mi LinKey Lab of Biomedical Engineering, School of Medicine, Shenzhen University, Shenzhen, 518060, People's Republic of China. mcmlin@163.com.
Wenxiao JiangKey Lab of Biomedical Engineering, School of Medicine, Shenzhen University, Shenzhen, 518060, People's Republic of China. jiangwenxiao@szu.edu.cn.
Jiefeng LiKey Lab of Biomedical Engineering, School of Medicine, Shenzhen University, Shenzhen, 518060, People's Republic of China. 395717640@qq.com.
Qijun HuangKey Lab of Biomedical Engineering, School of Medicine, Shenzhen University, Shenzhen, 518060, People's Republic of China. xiaobai.qj@163.com.
Guimiao LinKey Lab of Biomedical Engineering, School of Medicine, Shenzhen University, Shenzhen, 518060, People's Republic of China. gmlin@szu.edu.cn.
Shenzhen University · CNNanyang Technological University · SG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe toxicity of CdSe/ZnS quantum dots (QDs) in the environment and biological systems has become a major concern for the nanoparticle community. However, the potential toxicity of QDs on immune cells and its corresponding immune functions remains poorly understood. In this study, we investigated the immunotoxicity of CdSe/ZnS QDs using the in vitro in macrophages and lymphocytes and in vivo in BALB/c mice.

resultsOur results indicated that macrophages treated with 1.25 or 2.5 nM QDs exhibited decreased cell viability, increased levels of reactive oxygen species (ROS), elevated apoptotic events, altered phagocytic ability, and decreased release of TNF-α and IL-6 by upon subsequent stimulation with Lipopolysaccharide (LPS). In contrast, lymphocytes exposed to QDs exhibited enhanced cell viability, increased release of TNF-α and IL-6 following exposure with CpG-ODN, and decreased transformation ability treatment in response to LPS. To study the in vivo effects in mice, we showed that QDs injection did not cause significant changes to body weight, hematology, organ histology, and phagocytic function of peritoneal macrophages in QDs-treated mice. In addition, the QDs formulation accumulated in major immune organs for more than 42 days. Lymphocytes from QDs-treated mice showed reduced cell viability, changed subtype proportions, increased TNF-α and IL-6 release, and reduced transformation ability in response to LPS.

conclusionsTaken together, these results suggested that exposures to CdSe/ZnS QDs could suppress immune-defense against foreign stimuli, which in turn could result in increased susceptibility of hosts to diseases.

Indexed as

AnimalsCadmium CompoundsCell LineCell SurvivalInterleukin-6LymphocytesMacrophagesMaleMiceMice, Inbred BALB CNanoparticlesOligodeoxyribonucleotidesQuantum DotsReactive Oxygen SpeciesSulfidesTumor Necrosis Factor-alphaCadmium CompoundsCPG-oligonucleotideInterleukin-6OligodeoxyribonucleotidesReactive Oxygen SpeciesSulfidesTumor Necrosis Factor-alpha

Identifiers

PMID26846666
PMCPMC4743154
OpenAlexW2261214326

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.