Evidence map›Paper›PMID 28990786›Full record

ArticleNano letters2017

Longitudinal Monitoring of Antibody Responses against Tumor Cells Using Magneto-nanosensors with a Nanoliter of Blood.

Jung-Rok Lee, Carmel T Chan, Daniel Ruderman, Hui-Yen Chuang, Richard S Gaster, Michelle Atallah, Parag Mallick, Scott W Lowe, Sanjiv S Gambhir, Shan X Wang

Open access · greenAbstract read
In one paragraph

Article in Nano letters, 2017. 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
0.9field-weighted citation impact, top 26% 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, 15 citations in OpenAlex.

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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

10 authors at 6 institutions in 2 countries.

Jung-Rok LeeDivision of Mechanical and Biomedical Engineering, Ewha Womans University , Seoul 03760, South Korea.ORCID 0000-0002-3518-3965
Carmel T ChanDepartment of Medicine, Department of Radiology, Stanford University , Stanford, California 94305, United States.
Daniel RudermanEllison Institute of Transformative Medicine of USC, USC Keck School of Medicine , Los Angeles, California 90211, United States.
Hui-Yen ChuangDepartment of Medicine, Department of Radiology, Stanford University , Stanford, California 94305, United States.
Richard S GasterDepartment of Bioengineering, Stanford University , Stanford, California 94305, United States.
Michelle AtallahCancer Biology Program, Stanford School of Medicine , Stanford, California 94305, United States.
Parag MallickDepartment of Medicine, Department of Radiology, Stanford University , Stanford, California 94305, United States.
Scott W LoweCancer Biology and Genetics Program, Memorial Sloan Kettering Cancer Center , New York, New York 10065, United States.
Sanjiv S GambhirDepartment of Medicine, Department of Radiology, Stanford University , Stanford, California 94305, United States.
Shan X WangDepartment of Materials Science and Engineering, Stanford University , Stanford, California 94305, United States.
Stanford University · USEwha Womans University · KRLarry Ellison Foundation · USMemorial Sloan Kettering Cancer Center · USPliant (United States) · USStanford Medicine · US

Funding

TRANS-NETWORK PROJECTSU54CA143907 · NCI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI NOLAN, GARRY P · 2009 to 2013
$15.2M
Pilot ProjectsU54CA151459 · NCI · STANFORD UNIVERSITY · PI GAMBHIR, SANJIV S · 2010 to 2014
$12.6M
Nano Characterization and Nano Fabrication CoreU54CA199075 · NCI · STANFORD UNIVERSITY · PI GAMBHIR, SANJIV S · 2015 to 2019
$9.6M
NCI NIH HHS U54 CA143907NCI NIH HHS U54 CA151459NCI NIH HHS U54 CA199075
6 · The paper itself

Abstract

Each immunoglobulin isotype has unique immune effector functions. The contribution of these functions in the elimination of pathogens and tumors can be determined by monitoring quantitative temporal changes in isotype levels. Here, we developed a novel technique using magneto-nanosensors based on the effect of giant magnetoresistance (GMR) for longitudinal monitoring of total and antigen-specific isotype levels with high precision, using as little as 1 nL of serum. Combining in vitro serologic measurements with in vivo imaging techniques, we investigated the role of the antibody response in the regression of firefly luciferase (FL)-labeled lymphoma cells in spleen, kidney, and lymph nodes in a syngeneic Burkitt's lymphoma mouse model. Regression status was determined by whole body bioluminescent imaging (BLI). The magneto-nanosensors revealed that anti-FL IgG2a and total IgG2a were elevated and sustained in regression mice compared to non-regression mice (p < 0.05). This platform shows promise for monitoring immunotherapy, vaccination, and autoimmunity.

Indexed as

Antibody FormationAnimalsBiosensing TechniquesBurkitt LymphomaEquipment DesignFemaleImmunoglobulin GLuminescent MeasurementsMagneticsMiceMice, Inbred C57BLOptical ImagingSample SizeImmunoglobulin Gbioluminescent imagingcancer immunologyimmunoglobulin isotypeslymphomamagnetic nanoparticlesMagneto-nanosensors

Identifiers

PMID28990786
PMCPMC5851288
OpenAlexW2762166683

What OpenQuestion holds

Textmetadata
LicenceTDM
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.