Evidence map›Paper›PMID 29121461›Full record

ArticleACS nano2017

Nanomagnetic System for Rapid Diagnosis of Acute Infection.

Ki Soo Park, Hoyoung Kim, Soojin Kim, Kyungheon Lee, Sohyeon Park, Jun Song, Changwook Min, Farhana Khanam, Rasheduzzaman Rashu, Taufiqur Rahman Bhuiyan and 6 more

Open access · greenAbstract read
In one paragraph

Article in ACS nano, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

4 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. 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

16 authors at 3 institutions in 3 countries.

Ki Soo ParkCenter for Systems Biology, Massachusetts General Hospital and Harvard Medical School , Boston, Massachusetts 02114, United States.ORCID 0000-0002-0545-0970
Hoyoung KimCenter for NanoMedicine, Institute for Basic Science (IBS) , Seoul 03722, Republic of Korea.
Soojin KimCenter for NanoMedicine, Institute for Basic Science (IBS) , Seoul 03722, Republic of Korea.
Kyungheon LeeCenter for Systems Biology, Massachusetts General Hospital and Harvard Medical School , Boston, Massachusetts 02114, United States.
Sohyeon ParkCenter for NanoMedicine, Institute for Basic Science (IBS) , Seoul 03722, Republic of Korea.
Jun SongCenter for Systems Biology, Massachusetts General Hospital and Harvard Medical School , Boston, Massachusetts 02114, United States.
Changwook MinCenter for Systems Biology, Massachusetts General Hospital and Harvard Medical School , Boston, Massachusetts 02114, United States.
Farhana KhanamInternational Centre for Diarrhoeal Disease Research, Bangladesh (icddr,b) , Dhaka, Bangladesh.
Rasheduzzaman RashuInternational Centre for Diarrhoeal Disease Research, Bangladesh (icddr,b) , Dhaka, Bangladesh.
Taufiqur Rahman BhuiyanInternational Centre for Diarrhoeal Disease Research, Bangladesh (icddr,b) , Dhaka, Bangladesh.
Edward T RyanDepartment of Medicine, Harvard Medical School , Boston, Massachusetts 02114, United States.
Firdausi QadriInternational Centre for Diarrhoeal Disease Research, Bangladesh (icddr,b) , Dhaka, Bangladesh.
Ralph WeisslederCenter for Systems Biology, Massachusetts General Hospital and Harvard Medical School , Boston, Massachusetts 02114, United States.ORCID 0000-0003-0828-4143
Jinwoo CheonCenter for NanoMedicine, Institute for Basic Science (IBS) , Seoul 03722, Republic of Korea.ORCID 0000-0001-8948-5929
Richelle C CharlesDepartment of Medicine, Harvard Medical School , Boston, Massachusetts 02114, United States.
Hakho LeeCenter for Systems Biology, Massachusetts General Hospital and Harvard Medical School , Boston, Massachusetts 02114, United States.ORCID 0000-0002-0087-0909
Harvard University · USInternational Centre for Diarrhoeal Disease Research · BDYonsei University · KR

Funding

Training program in vaccine development and public healthD43TW005572 · FIC · MASSACHUSETTS GENERAL HOSPITAL · PI QADRI, FIRDAUSI, RYAN, EDWARD T. · 2000 to 2025
$5.4M
Magnetic nanoswitches for sensing biomoleculesR01EB004626 · NIBIB · MASSACHUSETTS GENERAL HOSPITAL · PI WEISSLEDER, MD, PHD, RALPH · 2004 to 2012
$3.2M
Novel Clickdyes for Biomedical SensingR01EB010011 · NIBIB · MASSACHUSETTS GENERAL HOSPITAL · PI WEISSLEDER, MD, PHD, RALPH · 2010 to 2017
$3.1M
MAGNETIC NANOSENSORS FOR BIOMEDICAL ANALYSES OF MICROVESICLESR01HL113156 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI LEE, HAKHO · 2012 to 2016
$2.1M
Analysis of scant cancer cells in fine needle aspiratesR33CA202064 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI WEISSLEDER, MD, PHD, RALPH · 2016 to 2018
$1.3M
Improving diagnostic capabilities for typhoid feverR33AI100023 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI RYAN, EDWARD T. · 2014 to 2016
$987k
Multiplexed exosome analyses with DNA barcodingR21CA205322 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI LEE, HAKHO · 2016 to 2017
$440k
Humoral and adaptive immune responses study in Vibrio cholerae infectionK43TW010362 · FIC · INTERNATIONAL CTR/DIARRHOEAL DIS RES · PI BHUIYAN, MD TAUFIQUR RAHMAN · 2016 to 2020
$359k
FIC NIH HHS D43 TW005572FIC NIH HHS K43 TW010362NCI NIH HHS R21 CA205322NCI NIH HHS R33 CA202064NHLBI NIH HHS R01 HL113156NIAID NIH HHS R33 AI100023NIBIB NIH HHS R01 EB004626NIBIB NIH HHS R01 EB010011
6 · The paper itself

Abstract

Pathogen-activated antibody-secreting cells (ASCs) produce and secrete antigen-specific antibodies. ASCs are detectable in the peripheral blood as early as 3 days after antigen exposure, which makes ASCs a potential biomarker for early disease detection. Here, we present a magnetic capture and detection (MCD) assay for sensitive, on-site detection of ASCs. In this approach, ASCs are enriched through magnetic capture, and secreted antibodies are magnetically detected by a miniaturized nuclear magnetic resonance (μNMR) system. This approach is based entirely on magnetics, which supports high contrast against biological background and simplifies assay procedures. We advanced the MCD system by (i) synthesizing magnetic nanoparticles with high magnetic moments for both cell capture and antibody detection, (ii) developing a miniaturized magnetic device for high-yield cell capture, and (iii) optimizing the μNMR assay for antibody detection. Antibody responses targeting hemolysin E (HlyE) can accurately identify individuals with acute enteric fever. As a proof-of-concept, we applied MCD to detect antibodies produced by HlyE-specific hybridoma cells. The MCD achieved high sensitivity in detecting antibodies secreted from as few as 5 hybridoma cells (50 cells/mL). Importantly, the assay could be performed with whole blood with minimal sample processing.

Indexed as

Acute DiseaseAntibodies, BacterialAntibody-Producing CellsAntigens, BacterialBacterial InfectionsBiosensing TechniquesCell SeparationHemolysin ProteinsHumansHybridomasIronLab-On-A-Chip DevicesMagnetite NanoparticlesOxidesProof of Concept StudySalmonella paratyphi AAntibodies, BacterialAntigens, BacterialHemolysin ProteinsIronMagnetite NanoparticlesOxidesZincacute infectionsbiosensorsenteric feverhost responsemagnetic nanoparticlesnuclear magnetic resonance

Identifiers

PMID29121461
PMCPMC6296367
OpenAlexW2767706956

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.