Evidence map›Paper›PMID 34838057›Full record

ArticleJournal of nanobiotechnology2021

Intracellular signaling pathway in dendritic cells and antigen transport pathway in vivo mediated by an OVA@DDAB/PLGA nano-vaccine.

Shulan Han, Wenyan Ma, Dawei Jiang, Logan Sutherlin, Jing Zhang, Yu Lu, Nan Huo, Zhao Chen, Jonathan W Engle, Yanping Wang and 4 more

Open access · goldAbstract read
In one paragraph

Article in Journal of nanobiotechnology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.7field-weighted citation impact, top 9% 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

20 citing papers in PubMed, 41 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Review
  6. Synthetic Polymers for Drug, Gene, and Vaccine Delivery.Polymer science & technology (Washington, D.C.) · 2025
    Review
  7. Article
  8. Journal of pharmaceutical analysis · 2024
    Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Multimodality imaging of nanoparticle-based vaccines: Shedding light on immunology.Wiley interdisciplinary reviews. Nanomedicine and nanobiotechnology · 2022
    Review
  16. Self-adjuvanting cancer nanovaccines.Journal of nanobiotechnology · 2022
    Review
  17. Article
  18. Article
  19. Article
  20. 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

14 authors at 8 institutions in 2 countries.

Shulan Han *Key Laboratory of Green Process and Engineering, State Key Laboratory of Biochemical Engineering, Institute of Process Engineering, Chinese Academy of Sciences, Beijing, 100190, People's Republic of China.
Wenyan Ma *Key Laboratory of Green Process and Engineering, State Key Laboratory of Biochemical Engineering, Institute of Process Engineering, Chinese Academy of Sciences, Beijing, 100190, People's Republic of China.
Dawei Jiang *Department of Nuclear Medicine, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430022, People's Republic of China.
Logan SutherlinDepartments of Radiology and Medical Physics, University of Wisconsin - Madison, Madison, WI, 53705, USA.
Jing ZhangKey Laboratory of Green Process and Engineering, State Key Laboratory of Biochemical Engineering, Institute of Process Engineering, Chinese Academy of Sciences, Beijing, 100190, People's Republic of China.
Yu LuInstitute of Veterinary Immunology &Engineering, Jiangsu Academy of Agricultural Sciences, Nanjing, 210014, People's Republic of China.
Nan HuoDepartment of Genetic Engineering Laboratory, Beijing Institute of Biotechnology, Beijing, 100850, People's Republic of China.
Zhao ChenDepartment of Nuclear Medicine, Peking University First Hospital, Beijing, 100034, People's Republic of China.
Jonathan W EngleDepartments of Radiology and Medical Physics, University of Wisconsin - Madison, Madison, WI, 53705, USA.
Yanping WangTianjin University of Science and Technology, Tianjin, 300222, People's Republic of China. ypwang@tust.edu.cn.
Xiaojie XuDepartment of Genetic Engineering Laboratory, Beijing Institute of Biotechnology, Beijing, 100850, People's Republic of China. miraclexxj@126.com.
Lei KangDepartment of Nuclear Medicine, Peking University First Hospital, Beijing, 100034, People's Republic of China. kanglei@bjmu.edu.cn.
Weibo CaiDepartments of Radiology and Medical Physics, University of Wisconsin - Madison, Madison, WI, 53705, USA. wcai@uwhealth.org.
Lianyan WangKey Laboratory of Green Process and Engineering, State Key Laboratory of Biochemical Engineering, Institute of Process Engineering, Chinese Academy of Sciences, Beijing, 100190, People's Republic of China. wanglianyan@ipe.ac.cn.
University of Chinese Academy of Sciences · CNUniversity of Wisconsin–Madison · USInstitute of Process Engineering · CNJiangsu Academy of Agricultural Sciences · CNPeking University · CNPeking University First Hospital · CNTianjin University of Science and Technology · CNUnion Hospital · CN

Funding

UW COMPREHENSIVE CANCER CENTER SUPPORTP30CA014520 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI Justine Yang Bruce · 1985 to 2026
$142.6M
NCI NIH HHS P30 CA014520NIH HHS P30CA014520
6 · The paper itself

Abstract

backgroundPoly(D, L-lactic-co-glycolic acid) (PLGA) nanoparticles have potential applications as a vaccine adjuvant and delivery system due to its unique advantages as biodegradability and biocompatibility. EXPERIMENTAL: We fabricated cationic solid lipid nanoparticles using PLGA and dimethyl-dioctadecyl-ammonium bromide (DDAB), followed by loading of model antigen OVA (antigen ovalbumin, OVA

resultsIn vitro experiments revealed that the antigen uptake of BMDCs after nanovaccine incubation was two times higher than pure OVA or OVA@Al at 12 h. The BMDCs were well activated by p38 MAPK signaling pathway. Furthermore, the nano-vaccine induced antigen escape from lysosome into cytoplasm with 10 times increased cross-presentation activity than those of OVA or OVA@Al. Regarding the transport of antigen into draining lymph nodes (LNs), the nano-vaccine could rapidly transfer antigen to LNs by passive lymphatic drainage and active DC transport. The antigen

conclusionThese results indicated that DDAB/PLGA NP was a potent platform to improve vaccine immunogenicity by p38 signaling pathway in BMDCs, enhancing transport of antigens to LNs, and higher immunity response.

Indexed as

Antigen PresentationDendritic CellsSignal TransductionVaccinesAdjuvants, VaccineAnimalsFemaleMiceMice, Inbred BALB CNanostructuresOvalbuminPolylactic Acid-Polyglycolic Acid CopolymerQuaternary Ammonium CompoundsAdjuvants, VaccinedidodecyldimethylammoniumOvalbuminPolylactic Acid-Polyglycolic Acid CopolymerQuaternary Ammonium CompoundsVaccinesAntigen transportDCs activationDDAB/PLGANano-vaccinep38 signaling pathway

Identifiers

PMID34838057
PMCPMC8626881
OpenAlexW3216673535

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.