Evidence map›Paper›PMID 26761780›Full record

ArticleBiomaterials2016

Cell source determines the immunological impact of biomimetic nanoparticles.

Michael Evangelopoulos, Alessandro Parodi, Jonathan O Martinez, Iman K Yazdi, Armando Cevenini, Anne L van de Ven, Nicoletta Quattrocchi, Christian Boada, Nima Taghipour, Claudia Corbo and 5 more

Open access · hybridAbstract readComparative StudyEvaluation Study
In one paragraph

Article in Biomaterials, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
2.8field-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

33 citing papers in PubMed, 56 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Nanoparticle-Based Interventions for Liver Transplantation.International journal of molecular sciences · 2023
    Review
  8. Review
  9. Review
  10. Review
  11. Research update on cell membrane camouflaged nanoparticles for cancer therapy.Frontiers in bioengineering and biotechnology · 2022
    Review
  12. Review
  13. Review
  14. Review
  15. Biomimetic Nanocarriers for Cancer Target Therapy.Bioengineering (Basel, Switzerland) · 2020
    Review
  16. Article
  17. Article
  18. Article
  19. Review
  20. 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

15 authors at 1 institution in 3 countries.

Michael EvangelopoulosDepartment of Nanomedicine, Houston Methodist Research Institute, Houston, TX 77030, USA.
Alessandro ParodiDepartment of Nanomedicine, Houston Methodist Research Institute, Houston, TX 77030, USA; Department of Experimental Oncology and Molecular Medicine, Fondazione IRCCS Istituto Nazionale Tumori, Milan 20133, Italy.
Jonathan O MartinezDepartment of Nanomedicine, Houston Methodist Research Institute, Houston, TX 77030, USA.
Iman K YazdiDepartment of Nanomedicine, Houston Methodist Research Institute, Houston, TX 77030, USA.
Armando CeveniniDepartment of Nanomedicine, Houston Methodist Research Institute, Houston, TX 77030, USA; Department of Molecular Medicine and Medical Biotechnology, University of Naples "Federico II", Via Pansini 5, 80131 Naples, Italy; CEINGE-Biotecnologie Avanzate s.c.a.r.l., Via Gaetano Salvatore 486, 80145 Naples, Italy.
Anne L van de VenDepartment of Nanomedicine, Houston Methodist Research Institute, Houston, TX 77030, USA.
Nicoletta QuattrocchiDepartment of Nanomedicine, Houston Methodist Research Institute, Houston, TX 77030, USA.
Christian BoadaDepartment of Nanomedicine, Houston Methodist Research Institute, Houston, TX 77030, USA; Escuela de Medicina y Ciencias de la Salud, Tecnologico de Monterrey, Monterrey, Nuevo Leon, Mexico.
Nima TaghipourDepartment of Nanomedicine, Houston Methodist Research Institute, Houston, TX 77030, USA.
Claudia CorboDepartment of Nanomedicine, Houston Methodist Research Institute, Houston, TX 77030, USA.
Brandon S BrownDepartment of Nanomedicine, Houston Methodist Research Institute, Houston, TX 77030, USA.
Shilpa ScariaDepartment of Nanomedicine, Houston Methodist Research Institute, Houston, TX 77030, USA.
Xuewu LiuDepartment of Nanomedicine, Houston Methodist Research Institute, Houston, TX 77030, USA.
Mauro FerrariDepartment of Nanomedicine, Houston Methodist Research Institute, Houston, TX 77030, USA.
Ennio TasciottiDepartment of Nanomedicine, Houston Methodist Research Institute, Houston, TX 77030, USA. Electronic address: etasciotti@tmhs.org.
Houston Methodist · US

Funding

TRANS-NETWORK PROJECTSU54CA143837 · NCI · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI FERRARI, MAURO · 2009 to 2014
$10.8M
Leukocyte Membrane Cloaked Carriers to Target and Overcome Tumor VasculatureR21CA173579 · NCI · METHODIST HOSPITAL RESEARCH INSTITUTE · PI TASCIOTTI, ENNIO · 2013 to 2014
$371k
NCI NIH HHS 1R21CA173579-01A1NCI NIH HHS 5U54CA143837NCI NIH HHS R21 CA173579NCI NIH HHS U54 CA143837
6 · The paper itself

Abstract

Recently, engineering the surface of nanotherapeutics with biologics to provide them with superior biocompatibility and targeting towards pathological tissues has gained significant popularity. Although the functionalization of drug delivery vectors with cellular materials has been shown to provide synthetic particles with unique biological properties, these approaches may have undesirable immunological repercussions upon systemic administration. Herein, we comparatively analyzed unmodified multistage nanovectors and particles functionalized with murine and human leukocyte cellular membrane, dubbed Leukolike Vectors (LLV), and the immunological effects that may arise in vitro and in vivo. Previously, LLV demonstrated an avoidance of opsonization and phagocytosis, in addition to superior targeting of inflammation and prolonged circulation. In this work, we performed a comprehensive evaluation of the importance of the source of cellular membrane in increasing their systemic tolerance and minimizing an inflammatory response. Time-lapse microscopy revealed LLV developed using a cellular coating derived from a murine (i.e., syngeneic) source resulted in an active avoidance of uptake by macrophage cells. Additionally, LLV composed of a murine membrane were found to have decreased uptake in the liver with no significant effect on hepatic function. As biomimicry continues to develop, this work demonstrates the necessity to consider the source of biological material in the development of future drug delivery carriers.

Indexed as

AnimalsBiocompatible MaterialsBiomimetic MaterialsCells, CulturedImmunity, InnateLeukocytesMiceMice, Inbred BALB CNanocapsulesBiocompatible MaterialsNanocapsulesBiomimicryDrug deliveryImmunobiologyLeukolike VectorMultistage nanovectorNanoparticles

Identifiers

PMID26761780
PMCPMC4916497
OpenAlexW2182921456

What OpenQuestion holds

Textmetadata
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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.