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Establishment of time‐resolved fluoroimmunoassay of IgG4 based on magnetic microspheres
BACKGROUND: The abnormal increase in serum IgG4 level is an important clinical symptom of IgG4‐related disease (IgG4‐RD), and the detection of serum IgG4 level is a powerful tool for the diagnosis of IgG4‐RD. This study was conducted to establish a simple and rapid immunoassay for the determination...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8373317/ https://www.ncbi.nlm.nih.gov/pubmed/34125973 http://dx.doi.org/10.1002/jcla.23874 |
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author | Wu, Qingqing Hang, Chen Li, Ting Wang, Binrong Qin, Yuan Wang, Yigang Zhou, Xiumei Xia, Pengguo Sheng, Huiming Huang, Pei Huang, Biao |
author_facet | Wu, Qingqing Hang, Chen Li, Ting Wang, Binrong Qin, Yuan Wang, Yigang Zhou, Xiumei Xia, Pengguo Sheng, Huiming Huang, Pei Huang, Biao |
author_sort | Wu, Qingqing |
collection | PubMed |
description | BACKGROUND: The abnormal increase in serum IgG4 level is an important clinical symptom of IgG4‐related disease (IgG4‐RD), and the detection of serum IgG4 level is a powerful tool for the diagnosis of IgG4‐RD. This study was conducted to establish a simple and rapid immunoassay for the determination of human serum IgG4 levels. METHODS: Based on the competition method, a novel immunoassay was established for the determination of human serum IgG4 using a combination of time‐resolved fluoroimmunoassay (TRFIA) and magnetic microspheres. IgG4 was coupled with magnetic microspheres and competed with IgG4 in the samples to bind the Eu(3+)‐labeled anti‐IgG4 antibody. The immunocomplex was separated and washed in a magnetic field, and the fluorescence counts were measured according to the number of dissociated europium ions. RESULTS: The analytical sensitivity of IgG4‐TRFIA based on magnetic microspheres was 0.006 g/L, and the detection range was 0.006–20 g/L under optimal conditions. The precision, recovery, and specificity of this immunoassay were demonstrated to be acceptable. The clinical application of IgG4‐TRFIA based on magnetic microspheres was evaluated and compared with that of immunonephelometry. The results showed that the two detection methods had a good correlation, with a correlation coefficient of .9871. CONCLUSION: IgG4‐TRFIA based on magnetic microspheres has the advantages of high sensitivity, wide detection range, and short analysis time and has the potential to become a useful tool for the diagnosis of IgG4‐RD. |
format | Online Article Text |
id | pubmed-8373317 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-83733172021-08-24 Establishment of time‐resolved fluoroimmunoassay of IgG4 based on magnetic microspheres Wu, Qingqing Hang, Chen Li, Ting Wang, Binrong Qin, Yuan Wang, Yigang Zhou, Xiumei Xia, Pengguo Sheng, Huiming Huang, Pei Huang, Biao J Clin Lab Anal Research Articles BACKGROUND: The abnormal increase in serum IgG4 level is an important clinical symptom of IgG4‐related disease (IgG4‐RD), and the detection of serum IgG4 level is a powerful tool for the diagnosis of IgG4‐RD. This study was conducted to establish a simple and rapid immunoassay for the determination of human serum IgG4 levels. METHODS: Based on the competition method, a novel immunoassay was established for the determination of human serum IgG4 using a combination of time‐resolved fluoroimmunoassay (TRFIA) and magnetic microspheres. IgG4 was coupled with magnetic microspheres and competed with IgG4 in the samples to bind the Eu(3+)‐labeled anti‐IgG4 antibody. The immunocomplex was separated and washed in a magnetic field, and the fluorescence counts were measured according to the number of dissociated europium ions. RESULTS: The analytical sensitivity of IgG4‐TRFIA based on magnetic microspheres was 0.006 g/L, and the detection range was 0.006–20 g/L under optimal conditions. The precision, recovery, and specificity of this immunoassay were demonstrated to be acceptable. The clinical application of IgG4‐TRFIA based on magnetic microspheres was evaluated and compared with that of immunonephelometry. The results showed that the two detection methods had a good correlation, with a correlation coefficient of .9871. CONCLUSION: IgG4‐TRFIA based on magnetic microspheres has the advantages of high sensitivity, wide detection range, and short analysis time and has the potential to become a useful tool for the diagnosis of IgG4‐RD. John Wiley and Sons Inc. 2021-06-14 /pmc/articles/PMC8373317/ /pubmed/34125973 http://dx.doi.org/10.1002/jcla.23874 Text en © 2021 The Authors. Journal of Clinical Laboratory Analysis published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Wu, Qingqing Hang, Chen Li, Ting Wang, Binrong Qin, Yuan Wang, Yigang Zhou, Xiumei Xia, Pengguo Sheng, Huiming Huang, Pei Huang, Biao Establishment of time‐resolved fluoroimmunoassay of IgG4 based on magnetic microspheres |
title | Establishment of time‐resolved fluoroimmunoassay of IgG4 based on magnetic microspheres |
title_full | Establishment of time‐resolved fluoroimmunoassay of IgG4 based on magnetic microspheres |
title_fullStr | Establishment of time‐resolved fluoroimmunoassay of IgG4 based on magnetic microspheres |
title_full_unstemmed | Establishment of time‐resolved fluoroimmunoassay of IgG4 based on magnetic microspheres |
title_short | Establishment of time‐resolved fluoroimmunoassay of IgG4 based on magnetic microspheres |
title_sort | establishment of time‐resolved fluoroimmunoassay of igg4 based on magnetic microspheres |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8373317/ https://www.ncbi.nlm.nih.gov/pubmed/34125973 http://dx.doi.org/10.1002/jcla.23874 |
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