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Clinical and Immunological Features of Common Variable Immunodeficiency in China
BACKGROUND: Common variable immunodeficiency (CVID) is one of the most common symptomatic primary immunodeficiency syndromes. The purpose of this article was to broaden our knowledge about CVID for better diagnosis and treatment. METHODS: Clinical and immunological features of 40 Chinese patients wi...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2015
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4837860/ https://www.ncbi.nlm.nih.gov/pubmed/25635425 http://dx.doi.org/10.4103/0366-6999.150092 |
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author | Lin, Lian-Jun Wang, Yu-Chuan Liu, Xin-Min |
author_facet | Lin, Lian-Jun Wang, Yu-Chuan Liu, Xin-Min |
author_sort | Lin, Lian-Jun |
collection | PubMed |
description | BACKGROUND: Common variable immunodeficiency (CVID) is one of the most common symptomatic primary immunodeficiency syndromes. The purpose of this article was to broaden our knowledge about CVID for better diagnosis and treatment. METHODS: Clinical and immunological features of 40 Chinese patients with CVID were analyzed retrospectively. RESULTS: The median age at onset was 11-year-old (range 4–51 years). The median age at diagnosis was 14.5-year-old (range 5–66 years). The average time of delay in diagnosis was 5.3 years (range 1–41 years). The most common main complaint was fever due to infections (35 cases, 87.5%). Pneumonia (28 cases, 70%) was the most common type of infections. Bronchiectasis was present in 6 patients (15%). Autoimmune disease was detected in 6 cases of CVID, and malignancy in 2 cases. The median total serum levels of IgG, IgA, and IgM at diagnosis were 1.07 g/L, 0.07 g/L, and 0.28 g/L, respectively. The percentages of CD3(−)/CD10(+) B-cells were 1%–3.14%. CONCLUSIONS: Infection is the most frequent presentation of CVID. Patients with unexplainable infections should receive further examination including serum immunoglobulin (Ig) and lymphocyte subset analysis. Regular and sufficient substitution with Ig is recommended. |
format | Online Article Text |
id | pubmed-4837860 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-48378602016-05-02 Clinical and Immunological Features of Common Variable Immunodeficiency in China Lin, Lian-Jun Wang, Yu-Chuan Liu, Xin-Min Chin Med J (Engl) Original Article BACKGROUND: Common variable immunodeficiency (CVID) is one of the most common symptomatic primary immunodeficiency syndromes. The purpose of this article was to broaden our knowledge about CVID for better diagnosis and treatment. METHODS: Clinical and immunological features of 40 Chinese patients with CVID were analyzed retrospectively. RESULTS: The median age at onset was 11-year-old (range 4–51 years). The median age at diagnosis was 14.5-year-old (range 5–66 years). The average time of delay in diagnosis was 5.3 years (range 1–41 years). The most common main complaint was fever due to infections (35 cases, 87.5%). Pneumonia (28 cases, 70%) was the most common type of infections. Bronchiectasis was present in 6 patients (15%). Autoimmune disease was detected in 6 cases of CVID, and malignancy in 2 cases. The median total serum levels of IgG, IgA, and IgM at diagnosis were 1.07 g/L, 0.07 g/L, and 0.28 g/L, respectively. The percentages of CD3(−)/CD10(+) B-cells were 1%–3.14%. CONCLUSIONS: Infection is the most frequent presentation of CVID. Patients with unexplainable infections should receive further examination including serum immunoglobulin (Ig) and lymphocyte subset analysis. Regular and sufficient substitution with Ig is recommended. Medknow Publications & Media Pvt Ltd 2015-02-05 /pmc/articles/PMC4837860/ /pubmed/25635425 http://dx.doi.org/10.4103/0366-6999.150092 Text en Copyright: © 2015 Chinese Medical Journal http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms. |
spellingShingle | Original Article Lin, Lian-Jun Wang, Yu-Chuan Liu, Xin-Min Clinical and Immunological Features of Common Variable Immunodeficiency in China |
title | Clinical and Immunological Features of Common Variable Immunodeficiency in China |
title_full | Clinical and Immunological Features of Common Variable Immunodeficiency in China |
title_fullStr | Clinical and Immunological Features of Common Variable Immunodeficiency in China |
title_full_unstemmed | Clinical and Immunological Features of Common Variable Immunodeficiency in China |
title_short | Clinical and Immunological Features of Common Variable Immunodeficiency in China |
title_sort | clinical and immunological features of common variable immunodeficiency in china |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4837860/ https://www.ncbi.nlm.nih.gov/pubmed/25635425 http://dx.doi.org/10.4103/0366-6999.150092 |
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