Association between anti-Anisakis simplex antibodies and interleukin-7 levels.


Journal

International immunopharmacology
ISSN: 1878-1705
Titre abrégé: Int Immunopharmacol
Pays: Netherlands
ID NLM: 100965259

Informations de publication

Date de publication:
Oct 2022
Historique:
received: 26 05 2022
revised: 27 07 2022
accepted: 03 08 2022
pubmed: 15 8 2022
medline: 15 9 2022
entrez: 14 8 2022
Statut: ppublish

Résumé

IL-7 is a crucial factor for the development of lymphocytes, and it is absolutely necessary for γδ T cells. Mice deficient in L-7 have a deficit of B and αβ T lymphocytes, and an absence of mature γδ TCR cells. IL-7 is essential for the survival, development and maturation of Schistosoma sp., although its production is associated with protection against intestinal helminths. The presence of anti-Anisakis simplex antibodies, especially IgA, is related to a lower frequency in CD3 + CD56 + αβ + lymphocytes and all subpopulations of γδ T cells. In this work, the relationship of IL-7 with humoral and cellular responses against A. simplex in 100 healthy subjects was studied. We have found significantly higher IL-7 levels in anti-A. simplex IgA-positive subjects (p < 0.001). The positivity of anti-A. simplex IgA was associated with a significant reduction in the frequency of CD3 + αβ+ (p < 0.01), CD3 + CD4 + αβ+, CD3 + CD8 + αβ+, CD3 + CD56 + αβ+, CD3 + γδ+, CD3 + CD4-CD8-γδ+ and CD3 + CD56 + γδ+ (p < 0.05) cells. In the case of NKT cells, this same phenomenon was also associated with IgE positivity. There was a weak inverse correlation (Spearman) of IL-7 levels with the frequencies of CD3 + CD4 + αβ+ (-0.125, p = 0.047), CD3 + CD8 + αβ+ (-0.204, p = 0.032), CD3 + CD56 + αβ+ (-0.247, p = 0.007), CD3 + γδ+ (-0.267, p = 0.007), CD3 + CD4-CD8-γδ+ (-0.266, p = 0.003), and CD3 + CD8 + γδ + (-0.302, p = 0.002) cells. The role of NKT cells in the anti-A. simplex response was confirmed and an association between IL and 7 levels and specific antibodies, especially IgA, was demonstrated. The higher production of IL-7 would represent a compensatory mechanism in response to the reduction in lymphocyte populations associated with the response against this parasite.

Identifiants

pubmed: 35964412
pii: S1567-5769(22)00618-X
doi: 10.1016/j.intimp.2022.109134
pii:
doi:

Substances chimiques

Immunoglobulin A 0
Interleukin-7 0
Receptors, Antigen, T-Cell, alpha-beta 0
Receptors, Antigen, T-Cell, gamma-delta 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

109134

Informations de copyright

Copyright © 2022 Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Carmen Cuéllar (C)

Departamento de Microbiología y Parasitología, Facultad de Farmacia, Universidad Complutense, 28040 Madrid, Spain. Electronic address: cuellarh@ucm.es.

Marta Rodero (M)

Departamento de Microbiología y Parasitología, Facultad de Farmacia, Universidad Complutense, 28040 Madrid, Spain.

Jaime Pérez-Griera (J)

Departamento de Biopatología, Hospital Clínico Universitario, 46010 Valencia, Spain.

Lorena Galindo-Regal (L)

Laboratorio de Biología Molecular, Hospital Arnau de Vilanova, 46015 Valencia, Spain.

Francisca Lopez-Chulia (F)

Departamento de Hematología, Hospital Arnau de Vilanova, 46015 Valencia, Spain.

Carlos García-Ballesteros (C)

Laboratorio de Biología Molecular, Hospital Arnau de Vilanova, 46015 Valencia, Spain.

Juan Carlos Andreu-Ballester (J)

Departamento de Investigación, Hospital Arnau de Vilanova, 46015 Valencia, Spain.

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Classifications MeSH