Primary immunodeficiency in infection-prone children in southern Sweden: occurrence, clinical characteristics and immunological findings

被引:13
作者
Brodszki, Nicholas [1 ]
Jonsson, Goran [2 ]
Skattum, Lillemor [3 ]
Truedsson, Lennart [3 ]
机构
[1] Skane Univ Hosp, Childrens Hosp, SE-22185 Lund, Sweden
[2] Lund Univ, Skane Univ Hosp, Dept Infect Dis, SE-22185 Lund, Sweden
[3] Lund Univ, Sect Microbiol Immunol & Glycobiol, Dept Lab Med, SE-22185 Lund, Sweden
关键词
Children; Complement; Immunodeficiency; Immunoglobulin; Immunoglobulin subclass; Lymphocyte; COMMON VARIABLE IMMUNODEFICIENCY; HEREDITARY C2 DEFICIENCY; CYSTIC-FIBROSIS; LECTIN-PATHWAY; BIRTH COHORT; COMPLEMENT; DISEASES; UPDATE; DIAGNOSIS; PATIENT;
D O I
10.1186/s12865-014-0031-6
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background: Primary immunodeficiency diseases (PIDs) comprise a heterogeneous group of disorders mainly characterized by increased susceptibility to infections. The aims of this study were to estimate the occurrence rate of PID in the paediatric (age <= 18 years) population of southern Sweden (approx. 265,000 children) and to describe their demographic, clinical and immunological characteristics. During a period of 4 years, in four paediatric speciality clinics in Sk ne County in southern Sweden, children being seen for infections and fulfilling specific criteria were evaluated according to a predefined examination schedule. The initial analysis consisted of complete blood counts with analysis of lymphocyte subpopulations (T, B, NK cells), measurement of immunoglobulins (IgG, IgA, IgM, IgE and IgG subclasses), and assessment of the complement system (classical, alternative and lectin pathways). In addition, results of these immunological analyses in other children from the same area and time period were evaluated. Results: In total, 259 children (53.6% males) met the criteria and were included. The most common infection was recurrent otitis media. Immunological analyses results for about two thirds of the patients were outside age-related reference intervals. Further examination in this latter group identified 15 children with PID (9 males); 7 (2.7%) had genetically defined PID, representing 4 different diagnoses, and another 8 (3.1%) had a clinically defined PID common variable immunodeficiency. No additional PID patient was identified from the evaluation of laboratory results in children not included in the study. The median age at diagnosis was 3.5 years (range 1-12 years). Conclusions: The occurrence rate of PID was about 4 new cases per year in this population. Several different PID diagnoses were found, and the application of specified criteria to identify PID patients was useful. In children who are prone to infection, the use of a predefined set of immunological laboratory analyses at their first examination was beneficial for early identification of patients with PID.
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