TY - JOUR
T1 - Nanomagnetic System for Rapid Diagnosis of Acute Infection
AU - Park, Ki Soo
AU - Kim, Hoyoung
AU - Kim, Soojin
AU - Lee, Kyungheon
AU - Park, Sohyeon
AU - Song, Jun
AU - Min, Changwook
AU - Khanam, Farhana
AU - Rashu, Rasheduzzaman
AU - Bhuiyan, Taufiqur Rahman
AU - Ryan, Edward T.
AU - Qadri, Firdausi
AU - Weissleder, Ralph
AU - Cheon, Jinwoo
AU - Charles, Richelle C.
AU - Lee, Hakho
N1 - The authors were supported in part by NIH Grants R33CA202064 (R.W., H.L.), R01HL113156 (H.L.), R21CA205322 (H.L.), R01EB004626 (R.W.), R01EB010011 (R.W.), R33AI100023 (E.T.R., F.Q.), D43 TW005572 (F.K., R.R., T.R.B.), 43TW010362 (T.R.B.); the Massachusetts General Hospital Research Scholar Fund (H.L.); the Massachusetts General Hospital Department of Medicine Transformative Scholars Award (R.C.C.); the Robert Wood Johnson Foundation Harold Amos Medical Faculty Development Program (R.C.C.); the Harvard Medical School DCIP Faculty Fellowship (R.C.C.); the National Research Foundation (NRF) awards by the Ministry of Science, ICT & Future Planning (MSIP) of Korea, 2014R1A6A3A0305972 (K.S.P.) and 2017R1C1B5017724 (K.S.P.); the Massachusetts General Hospital Tosteson Award (K.S.P.); the Institute for Basic Science, IBS-R026-D1 (J.C., H.L.); the IBS Global Postdoctoral Fellowship Award (IBS GPF) (K.S.P.); and the Korea Healthcare Technology R&D Project, Ministry for Health & Welfare Affairs, HI08C2149 (J.C.). The authors thank Prof. Dongwon Yoo for coordinating the IBS GPF, and Dr. Tae-Hyun Shin for helpful comments and discussions.
PY - 2017/11/28
Y1 - 2017/11/28
N2 - 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.
AB - 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.
KW - acute infections
KW - biosensors
KW - enteric fever
KW - host response
KW - magnetic nanoparticles
KW - nuclear magnetic resonance
UR - http://www.scopus.com/inward/record.url?scp=85035771488&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85035771488&partnerID=8YFLogxK
U2 - 10.1021/acsnano.7b06074
DO - 10.1021/acsnano.7b06074
M3 - Article
C2 - 29121461
AN - SCOPUS:85035771488
SN - 1936-0851
VL - 11
SP - 11425
EP - 11432
JO - ACS Nano
JF - ACS Nano
IS - 11
ER -