Peripheral immune cell markers in children with recurrent respiratory infections in the absence of primary immunodeficiency.

double-negative T cells memory B cells recurrent respiratory infections

Journal

Experimental and therapeutic medicine
ISSN: 1792-0981
Titre abrégé: Exp Ther Med
Pays: Greece
ID NLM: 101531947

Informations de publication

Date de publication:
Sep 2019
Historique:
received: 21 05 2019
accepted: 24 06 2019
entrez: 15 8 2019
pubmed: 15 8 2019
medline: 15 8 2019
Statut: ppublish

Résumé

The immune system of a child has a degree of immaturity that is maintained until 6-7 years of age. Immaturity may be due to age-related functional disorders in the immune response. A healthy child can contract a series of infections which contribute to the maturation of the immune system during the pre-pubertal period. If repeated infections with prolonged or severe complications occur during childhood, the presence of an immunodeficiency should then be considered. Much more frequent than primary immunodeficiency are recurrent infections (frequently involving the upper respiratory tract), which are less severe and occur under the conditions of an immune system with no apparent major defects. A child can present with 4 to 8 episodes of respiratory infections within a year, during the first 5 years of its life. The average duration of infection is 8 days and up to 2 weeks; if the child presents with 3 episodes of acute infections over a period of 6 months, the respiratory infections are then considered recurrent. The aim of this study was to identify the immunological changes or deviations that cause this clinical syndrome in children. For this purpose, 30 children with recurrent respiratory infections and 10 healthy children were included. Immunoglobulin levels were examined and immunophenotyping was performed. We found that the serum immunoglobulin levels were in the normal range in 70% of the children. On the contrary, our data revealed changes in peripheral cell populations, the most important being the decrease in the T-cluster of differentiation (CD)8

Identifiants

pubmed: 31410127
doi: 10.3892/etm.2019.7714
pii: ETM-0-0-7714
pmc: PMC6676098
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1693-1700

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Auteurs

Adriana Narcisa Munteanu (AN)

Immunobiology Laboratory, 'Victor Babes' National Institute of Pathology, 050096 Bucharest, Romania.
Doctoral School of Biology, Faculty of Biology, University of Bucharest, 050095 Bucharest, Romania.

Mihaela Surcel (M)

Immunobiology Laboratory, 'Victor Babes' National Institute of Pathology, 050096 Bucharest, Romania.
Doctoral School of Biology, Faculty of Biology, University of Bucharest, 050095 Bucharest, Romania.

Radu-Ionuț Huică (RI)

Division of Cellular and Molecular Biology and Histology, 'Carol Davila' University of Pharmacy and Medicine, 050474 Bucharest, Romania.

Gheorghița Isvoranu (G)

Animal Husbandry, 'Victor Babes' National Institute of Pathology, 050096 Bucharest, Romania.

Carolina Constantin (C)

Immunobiology Laboratory, 'Victor Babes' National Institute of Pathology, 050096 Bucharest, Romania.
Department of Pathology, Colentina University Hospital, 020125 Bucharest, Romania.

Ioana Ruxandra Pîrvu (IR)

Immunobiology Laboratory, 'Victor Babes' National Institute of Pathology, 050096 Bucharest, Romania.

Carmen Chifiriuc (C)

Doctoral School of Biology, Faculty of Biology, University of Bucharest, 050095 Bucharest, Romania.

Coriolan Ulmeanu (C)

Department of Toxicology, 'Grigore Alexandrescu' Children's Emergency Clinical Hospital, 011743 Bucharest, Romania.

Cornel Ursaciuc (C)

Immunobiology Laboratory, 'Victor Babes' National Institute of Pathology, 050096 Bucharest, Romania.

Monica Neagu (M)

Immunobiology Laboratory, 'Victor Babes' National Institute of Pathology, 050096 Bucharest, Romania.
Doctoral School of Biology, Faculty of Biology, University of Bucharest, 050095 Bucharest, Romania.
Department of Pathology, Colentina University Hospital, 020125 Bucharest, Romania.

Classifications MeSH