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Follow-up of pediatric patients with recurrent infection and mild serologic immune abnormalities.

作者信息

Herrod H G

机构信息

Crippled Children's Foundation Research Center, LeBonheur Children's Medical Center, Department of Pediatrics, University of Tennessee, Memphis, USA.

出版信息

Ann Allergy Asthma Immunol. 1997 Nov;79(5):460-4. doi: 10.1016/S1081-1206(10)63044-X.

DOI:10.1016/S1081-1206(10)63044-X
PMID:9396982
Abstract

BACKGROUND

Children with recurrent infections significant enough to warrant referral to an immunologist frequently have mild abnormalities of the humoral immune system. Parents of these children are generally reassured that their child will outgrow the clinical problems that prompted their referral.

OBJECTIVE

This is a retrospective study with the objective being to evaluate changes in immune measurements and clinical status of children with recurrent infections followed in an immunology clinic.

METHODS

Forty-two patients (mean age 60 months) previously evaluated for recurrent infections were re-evaluated after at least 12 months (mean 37 months). Initial evaluation studies included quantitative immunoglobulins in all patients and IgG subclass determinations and pre- and postvaccination pneumococcal polysaccharide antibody titers in a subpopulation of patients.

RESULTS

Patients were assigned to one of two categories: those with initial laboratory abnormalities (27 patients) and those with normal initial studies (15 patients). Among the patients with initial abnormalities, partial IgA deficiency was most commonly seen (20/27). It persisted in 15. Only 6/27 patients had studies that were completely normal on follow-up. Among patients with no initial abnormality, 9/15 developed a partial deficiency of at least one immunoglobulin isotype or IgG subclass. Eighty-six percent of the patients were clinically improved at the time of their last follow-up visit regardless of their laboratory values.

CONCLUSIONS

A high proportion of children with recurrent infection have persistent, partial immunoglobulin deficiencies lasting in some cases for years. Despite this finding almost all patients demonstrate clinical improvement with time.

摘要

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