Evidence map›Paper›PMID 32047498›Full record

ArticleFrontiers in immunology2019

Enhanced Delivery of Rituximab Into Brain and Lymph Nodes Using Timed-Release Nanocapsules in Non-Human Primates.

Meng Qin, Lan Wang, Di Wu, Christopher K Williams, Duo Xu, Emiko Kranz, Qi Guo, Jiaoqiong Guan, Harry V Vinters, YooJin Lee and 9 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2019. 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
1.9field-weighted citation impact, top 12% 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, 26 citations in OpenAlex.

  1. A proimmunotoxin nanodrug targeting AIDS-associated non-Hodgkin lymphoma.Journal of controlled release : official journal of the Controlled Release Society · 2026
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  8. Synthetic Polymers for Drug, Gene, and Vaccine Delivery.Polymer science & technology (Washington, D.C.) · 2025
    Review
  9. Review
  10. [Ocular mucous membrane pemphigoid].Die Ophthalmologie · 2023
    Article
  11. Article
  12. Article
  13. Recent progress of nanomedicine in the treatment of Alzheimer's disease.Frontiers in cell and developmental biology · 2023
    Review
  14. Article
  15. Article
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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

19 authors at 3 institutions in 2 countries.

Meng QinDepartment of Microbiology, Immunology and Molecular Genetics, David Geffen School of Medicine at University of California, Los Angeles, Los Angeles, CA, United States.
Lan WangDepartment of Microbiology, Immunology and Molecular Genetics, David Geffen School of Medicine at University of California, Los Angeles, Los Angeles, CA, United States.
Di WuDepartment of Chemical and Biomolecular Engineering, School of Engineering, UCLA, Los Angeles, CA, United States.
Christopher K WilliamsDepartments of Pathology & Laboratory Medicine (Neuropathology) and Neurology, David Geffen School of Medicine at UCLA, Los Angeles, CA, United States.
Duo XuDepartment of Chemical and Biomolecular Engineering, School of Engineering, UCLA, Los Angeles, CA, United States.
Emiko KranzUCLA AIDS Institute, Los Angeles, CA, United States.
Qi GuoUCLA AIDS Institute, Los Angeles, CA, United States.
Jiaoqiong GuanInstitute of Medical Biology, Peking Union Medical College, Chinese Academy of Medical Sciences, Kunming, China.
Harry V VintersDepartments of Pathology & Laboratory Medicine (Neuropathology) and Neurology, David Geffen School of Medicine at UCLA, Los Angeles, CA, United States.
YooJin LeeDepartment of Microbiology, Immunology and Molecular Genetics, David Geffen School of Medicine at University of California, Los Angeles, Los Angeles, CA, United States.
Yiming XieDepartment of Microbiology, Immunology and Molecular Genetics, David Geffen School of Medicine at University of California, Los Angeles, Los Angeles, CA, United States.
Yun LuoInstitute of Medicinal Plant Development, Peking Union Medical College, Chinese Academy of Medical Sciences, Beijing, China.
Guibo SunInstitute of Medicinal Plant Development, Peking Union Medical College, Chinese Academy of Medical Sciences, Beijing, China.
Xiaobo SunInstitute of Medicinal Plant Development, Peking Union Medical College, Chinese Academy of Medical Sciences, Beijing, China.
Zhanlong HeInstitute of Medical Biology, Peking Union Medical College, Chinese Academy of Medical Sciences, Kunming, China.
Yunfeng LuDepartment of Chemical and Biomolecular Engineering, School of Engineering, UCLA, Los Angeles, CA, United States.
Masakazu KamataUCLA AIDS Institute, Los Angeles, CA, United States.
Jing WenDepartment of Microbiology, Immunology and Molecular Genetics, David Geffen School of Medicine at University of California, Los Angeles, Los Angeles, CA, United States.
Irvin S Y ChenDepartment of Microbiology, Immunology and Molecular Genetics, David Geffen School of Medicine at University of California, Los Angeles, Los Angeles, CA, United States.
University of California, Los Angeles · USChinese Academy of Medical Sciences & Peking Union Medical College · CNBlack AIDS Institute · US

Funding

Women's CancersP30CA016042 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Samuel Wheeler French · 1985 to 2026
$134.5M
Virology CoreP30AI028697 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI ANTON, PETER A · 1991 to 2018
$39.9M
Nanodelivery platform for antibody drugs targeting NHLR01CA232015 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI KAMATA, MASAKAZU · 2018 to 2022
$2.5M
Hematopoietic stem/progenitor cell reservoirsR01AI110297 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI CHEN, IRVIN S.Y. · 2014 to 2018
$1.9M
Gene-Engineered Stem Cell Memory T-Cells With Anti-HIV Chimeric Antigen ReceptorsR01AI110200 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI KAMATA, MASAKAZU · 2016 to 2019
$1.5M
Survival of the fittest HSPC repopulating clones by anti-HIV-1 gene-modificationR01HL125030 · NHLBI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI CHEN, IRVIN S.Y. · 2014 to 2017
$1.5M
Gene engineering using CRISPR/Cas9 mutagenesis to eliminate latent HIV-1R21AI114433 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI CHEN, IRVIN S.Y. · 2014 to 2015
$424k
NCI NIH HHS P30 CA016042NCI NIH HHS R01 CA232015NHLBI NIH HHS R01 HL125030NIAID NIH HHS P30 AI028697NIAID NIH HHS R01 AI110200NIAID NIH HHS R01 AI110297NIAID NIH HHS R21 AI114433
6 · The paper itself

Abstract

Tumor metastasis into the central nervous system (CNS) and lymph nodes (LNs) is a major obstacle for effective therapies. Therapeutic monoclonal antibodies (mAb) have revolutionized tumor treatment; however, their efficacy for treating metastatic tumors-particularly, CNS and LN metastases-is poor due to inefficient penetration into the CNS and LNs following intravenous injection. We recently reported an effective delivery of mAb to the CNS by encapsulating the anti-CD20 mAb rituximab (RTX) within a thin shell of polymer that contains the analogs of choline and acetylcholine receptors. This encapsulated RTX, denoted as n-RTX, eliminated lymphoma cells systemically in a xenografted humanized mouse model using an immunodeficient mouse as a recipient of human hematopoietic stem/progenitor cells and fetal thymus more effectively than native RTX; importantly, n-RTX showed notable anti-tumor effect on CNS metastases which is unable to show by native RTX. As an important step toward future clinical translation of this technology, we further analyzed the properties of n-RTX in immunocompetent animals, rats, and non-human primates (NHPs). Our results show that a single intravenous injection of n-RTX resulted in 10-fold greater levels in the CNS and 2-3-fold greater levels in the LNs of RTX, respectively, than the injection of native RTX in both rats and NHPs. In addition, we demonstrate the enhanced delivery and efficient B-cell depletion in lymphoid organs of NHPs with n-RTX. Moreover, detailed hematological analysis and liver enzyme activity tests indicate n-RTX treatment is safe in NHPs. As this nanocapsule platform can be universally applied to other therapeutic mAbs, it holds great promise for extending mAb therapy to poorly accessible body compartments.

Indexed as

BrainLymph NodesNanocapsulesAnimalsAntineoplastic Agents, ImmunologicalDelayed-Action PreparationsMacaca mulattaMaleRatsRats, Sprague-DawleyRituximabAntineoplastic Agents, ImmunologicalDelayed-Action PreparationsNanocapsulesRituximabcentral nervous system deliveryLNs deliverymonoclonal antibodynanocapsulesnon-human primate

Identifiers

PMID32047498
PMCPMC6996053
OpenAlexW3003104679

What OpenQuestion holds

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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.