(2024) Noninfectious Complications in B-Lymphopenic Common Variable Immunodeficiency. Journal of Investigational Allergology and Clinical Immunology. pp. 233-245. ISSN 1018-9068
Full text not available from this repository.
Abstract
Background: Common variable immunodeficiency (CVID) is considered the most symptomatic type of inborn errors of immunity in humans. Along with infectious complications, which have numerous consequences, noninfectious complications are a major challenge among CVID patients. Methods: All CVID patients registered in the national database were included in this retrospective cohort study. Patients were divided into 2 groups based on the presence of B-cell lymphopenia. Demographic characteristics, laboratory findings, noninfectious organ involvement, autoimmunity, and lymphoproliferative diseases were evaluated. Results: Among 387 enrolled patients, 66.4 were diagnosed with noninfectious complications and 33.6 with isolated infectious presentations. Enteropathy, autoimmunity, and lymphoproliferative disorders were reported in 35.1, 24.3, and 21.4 of patients, respectively. Some complications, including autoimmunity and hepatosplenomegaly, were reported to be significantly more frequent among patients with B-cell lymphopenia. As for organ involvement, the dermatologic, endocrine, and musculoskeletal systems were predominantly affected in CVID patients with B-cell lymphopenia. Among autoimmune manifestations, the frequency of rheumatologic, hematologic, and gastrointestinal autoimmunity was reported to be higher than that of other types of autoimmunity not associated with B cell-lymphopenia. Furthermore, hematological cancers, particularly lymphoma, were the most common type of malignancy. The mortality rate was 24.5, and respiratory failure and malignancies were the most common causes of death, with no significant differences between the 2 groups. Conclusion: Considering that some of the noninfectious complications might be associated with B-cell lymphopenia, regular patient monitoring and follow-up with proper medication (in addition to immunoglobulin replacement therapy) are highly recommended to prevent sequelae and increase patient quality of life.
Item Type: | Article |
---|---|
Keywords: | Primary immunodeficiency Inborn errors of immunity Common variable immunodeficiency.Autoimmunity immunodeficiency.Autoimmunity Malignancy Immune dysregulation regulatory t-cells iga deficiency autoimmunity disorders subsets cohort lymphocytes phenotype children criteria Allergy Immunology |
Page Range: | pp. 233-245 |
Journal or Publication Title: | Journal of Investigational Allergology and Clinical Immunology |
Journal Index: | ISI |
Volume: | 34 |
Number: | 4 |
Identification Number: | https://doi.org/10.18176/jiaci.0902 |
ISSN: | 1018-9068 |
Depositing User: | خانم ناهید ضیائی |
URI: | http://eprints.mui.ac.ir/id/eprint/30048 |
Actions (login required)
![]() |
View Item |