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Flow Cytometry for the Diagnosis of Primary Immunodeficiency Diseases: A Single Center Experience
PURPOSE: While there is an urgent need for diagnosis and therapeutic intervention in patients with primary immunodeficiency diseases (PIDs), current genetic tests have drawbacks. We retrospectively reviewed the usefulness of flow cytometry (FCM) as a quick tool for immunophenotyping and functional a...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Academy of Asthma, Allergy and Clinical Immunology; The Korean Academy of Pediatric Allergy and Respiratory Disease
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6997278/ https://www.ncbi.nlm.nih.gov/pubmed/32009323 http://dx.doi.org/10.4168/aair.2020.12.2.292 |
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author | Kwon, Won Kyung Choi, SooIn Kim, Hee-jin Huh, Hee Jae Kang, Ji-Man Kim, Yae-Jean Yoo, Keon Hee Ahn, Kangmo Cho, Hye Kyung Peck, Kyong Ran Jang, Ja-Hyun Ki, Chang-Seok Kang, Eun-Suk |
author_facet | Kwon, Won Kyung Choi, SooIn Kim, Hee-jin Huh, Hee Jae Kang, Ji-Man Kim, Yae-Jean Yoo, Keon Hee Ahn, Kangmo Cho, Hye Kyung Peck, Kyong Ran Jang, Ja-Hyun Ki, Chang-Seok Kang, Eun-Suk |
author_sort | Kwon, Won Kyung |
collection | PubMed |
description | PURPOSE: While there is an urgent need for diagnosis and therapeutic intervention in patients with primary immunodeficiency diseases (PIDs), current genetic tests have drawbacks. We retrospectively reviewed the usefulness of flow cytometry (FCM) as a quick tool for immunophenotyping and functional assays in patients suspected to have PIDs at a single tertiary care institute. METHODS: Between January 2001 and June 2018, patients suspected of having PIDs were subjected to FCM tests, including lymphocyte subset analysis, detection of surface- or intracellular-target proteins, and functional analysis of immune cells, at Samsung Medical Center, Seoul, Korea. The genetic diagnosis was performed using Sanger or diagnostic exome sequencing. RESULTS: Of 60 patients diagnosed with definite or probable PID according to the European Society of Immune Deficiencies criteria, 24 patients were provided with useful information about immunological dysfunction after initial FCM testing. In 10 patients, the PID diagnosis was based on abnormal findings in FCM testing without genetic tests. The FCM findings provided strong evidence for the diagnosis of severe combined immunodeficiency (n = 6), X-linked chronic granulomatous diseases (CGD) (n = 6), leukocyte adhesion deficiency type 1 (n = 3), X-linked agammaglobulinemia (n = 11), autoimmune lymphoproliferative syndrome-FASLG (n = 1), and familial hemophagocytic lymphohistiocytosis type 2 (n = 1), and probable evidence for autosomal recessive-CGD (n = 2), autosomal dominant-hyper-immunoglobulin E (IgE)-syndrome (n = 1), and STAT1 gain-of-function mutation (n = 1). In PIDs derived from PIK3CD (n = 2), LRBA (n = 2), and CTLA4 mutations (n = 3), the FCM test provided useful evidence of immune abnormalities and a tool for treatment monitoring. CONCLUSIONS: The initial application of FCM, particularly with known protein targets on immune cells, would facilitate the timely diagnosis of PIDs and thus would support clinical decisions and improve the clinical outcome. |
format | Online Article Text |
id | pubmed-6997278 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The Korean Academy of Asthma, Allergy and Clinical Immunology; The Korean Academy of Pediatric Allergy and Respiratory Disease |
record_format | MEDLINE/PubMed |
spelling | pubmed-69972782020-03-01 Flow Cytometry for the Diagnosis of Primary Immunodeficiency Diseases: A Single Center Experience Kwon, Won Kyung Choi, SooIn Kim, Hee-jin Huh, Hee Jae Kang, Ji-Man Kim, Yae-Jean Yoo, Keon Hee Ahn, Kangmo Cho, Hye Kyung Peck, Kyong Ran Jang, Ja-Hyun Ki, Chang-Seok Kang, Eun-Suk Allergy Asthma Immunol Res Original Article PURPOSE: While there is an urgent need for diagnosis and therapeutic intervention in patients with primary immunodeficiency diseases (PIDs), current genetic tests have drawbacks. We retrospectively reviewed the usefulness of flow cytometry (FCM) as a quick tool for immunophenotyping and functional assays in patients suspected to have PIDs at a single tertiary care institute. METHODS: Between January 2001 and June 2018, patients suspected of having PIDs were subjected to FCM tests, including lymphocyte subset analysis, detection of surface- or intracellular-target proteins, and functional analysis of immune cells, at Samsung Medical Center, Seoul, Korea. The genetic diagnosis was performed using Sanger or diagnostic exome sequencing. RESULTS: Of 60 patients diagnosed with definite or probable PID according to the European Society of Immune Deficiencies criteria, 24 patients were provided with useful information about immunological dysfunction after initial FCM testing. In 10 patients, the PID diagnosis was based on abnormal findings in FCM testing without genetic tests. The FCM findings provided strong evidence for the diagnosis of severe combined immunodeficiency (n = 6), X-linked chronic granulomatous diseases (CGD) (n = 6), leukocyte adhesion deficiency type 1 (n = 3), X-linked agammaglobulinemia (n = 11), autoimmune lymphoproliferative syndrome-FASLG (n = 1), and familial hemophagocytic lymphohistiocytosis type 2 (n = 1), and probable evidence for autosomal recessive-CGD (n = 2), autosomal dominant-hyper-immunoglobulin E (IgE)-syndrome (n = 1), and STAT1 gain-of-function mutation (n = 1). In PIDs derived from PIK3CD (n = 2), LRBA (n = 2), and CTLA4 mutations (n = 3), the FCM test provided useful evidence of immune abnormalities and a tool for treatment monitoring. CONCLUSIONS: The initial application of FCM, particularly with known protein targets on immune cells, would facilitate the timely diagnosis of PIDs and thus would support clinical decisions and improve the clinical outcome. The Korean Academy of Asthma, Allergy and Clinical Immunology; The Korean Academy of Pediatric Allergy and Respiratory Disease 2020-01-20 /pmc/articles/PMC6997278/ /pubmed/32009323 http://dx.doi.org/10.4168/aair.2020.12.2.292 Text en Copyright © 2020 The Korean Academy of Asthma, Allergy and Clinical Immunology • The Korean Academy of Pediatric Allergy and Respiratory Disease https://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Kwon, Won Kyung Choi, SooIn Kim, Hee-jin Huh, Hee Jae Kang, Ji-Man Kim, Yae-Jean Yoo, Keon Hee Ahn, Kangmo Cho, Hye Kyung Peck, Kyong Ran Jang, Ja-Hyun Ki, Chang-Seok Kang, Eun-Suk Flow Cytometry for the Diagnosis of Primary Immunodeficiency Diseases: A Single Center Experience |
title | Flow Cytometry for the Diagnosis of Primary Immunodeficiency Diseases: A Single Center Experience |
title_full | Flow Cytometry for the Diagnosis of Primary Immunodeficiency Diseases: A Single Center Experience |
title_fullStr | Flow Cytometry for the Diagnosis of Primary Immunodeficiency Diseases: A Single Center Experience |
title_full_unstemmed | Flow Cytometry for the Diagnosis of Primary Immunodeficiency Diseases: A Single Center Experience |
title_short | Flow Cytometry for the Diagnosis of Primary Immunodeficiency Diseases: A Single Center Experience |
title_sort | flow cytometry for the diagnosis of primary immunodeficiency diseases: a single center experience |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6997278/ https://www.ncbi.nlm.nih.gov/pubmed/32009323 http://dx.doi.org/10.4168/aair.2020.12.2.292 |
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