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Cord blood versus age 5 mononuclear cell proliferation on IgE and asthma

BACKGROUND: Fetal immune responses following exposure of mothers to allergens during pregnancy may influence the subsequent risk of childhood asthma. However, the association of allergen-induced cord blood mononuclear cell (CBMC) proliferation and cytokine production with later allergic immune respo...

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Autores principales: Chang, Carolyn, Gauvey-Kern, Kevin, Johnson, Alina, Kelvin, Elizabeth A, Chew, Ginger L, Perera, Frederica, Miller, Rachel L
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2922078/
https://www.ncbi.nlm.nih.gov/pubmed/20684781
http://dx.doi.org/10.1186/1476-7961-8-11
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author Chang, Carolyn
Gauvey-Kern, Kevin
Johnson, Alina
Kelvin, Elizabeth A
Chew, Ginger L
Perera, Frederica
Miller, Rachel L
author_facet Chang, Carolyn
Gauvey-Kern, Kevin
Johnson, Alina
Kelvin, Elizabeth A
Chew, Ginger L
Perera, Frederica
Miller, Rachel L
author_sort Chang, Carolyn
collection PubMed
description BACKGROUND: Fetal immune responses following exposure of mothers to allergens during pregnancy may influence the subsequent risk of childhood asthma. However, the association of allergen-induced cord blood mononuclear cell (CBMC) proliferation and cytokine production with later allergic immune responses and asthma has been controversial. Our objective was to compare indoor allergen-induced CBMC with age 5 peripheral blood mononuclear cell (PBMC) proliferation and determine which may be associated with age 5 allergic immune responses and asthma in an inner city cohort. METHODS: As part of an ongoing cohort study of the Columbia Center for Children's Environmental Health (CCCEH), CBMCs and age 5 PBMCs were cultured with cockroach, mouse, and dust mite protein extracts. CBMC proliferation and cytokine (IL-5 and IFN-γ) responses, and age 5 PBMC proliferation responses, were compared to anti-cockroach, anti-mouse, and anti-dust mite IgE levels, wheeze, cough, eczema and asthma. RESULTS: Correlations between CBMC and age 5 PBMC proliferation in response to cockroach, mouse, and dust mite antigens were nonsignificant. Cockroach-, mouse-, and dust mite-induced CBMC proliferation and cytokine responses were not associated with allergen-specific IgE at ages 2, 3, and 5, or with asthma and eczema at age 5. However, after adjusting for potential confounders, age 5 cockroach-induced PBMC proliferation was associated with anti-cockroach IgE, total IgE, and asthma (p < 0.05). CONCLUSION: In contrast to allergen-induced CBMC proliferation, age 5 cockroach-induced PBMC proliferation was associated with age 5 specific and total IgE, and asthma, in an inner-city cohort where cockroach allergens are prevalent and exposure can be high.
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spelling pubmed-29220782010-08-17 Cord blood versus age 5 mononuclear cell proliferation on IgE and asthma Chang, Carolyn Gauvey-Kern, Kevin Johnson, Alina Kelvin, Elizabeth A Chew, Ginger L Perera, Frederica Miller, Rachel L Clin Mol Allergy Research BACKGROUND: Fetal immune responses following exposure of mothers to allergens during pregnancy may influence the subsequent risk of childhood asthma. However, the association of allergen-induced cord blood mononuclear cell (CBMC) proliferation and cytokine production with later allergic immune responses and asthma has been controversial. Our objective was to compare indoor allergen-induced CBMC with age 5 peripheral blood mononuclear cell (PBMC) proliferation and determine which may be associated with age 5 allergic immune responses and asthma in an inner city cohort. METHODS: As part of an ongoing cohort study of the Columbia Center for Children's Environmental Health (CCCEH), CBMCs and age 5 PBMCs were cultured with cockroach, mouse, and dust mite protein extracts. CBMC proliferation and cytokine (IL-5 and IFN-γ) responses, and age 5 PBMC proliferation responses, were compared to anti-cockroach, anti-mouse, and anti-dust mite IgE levels, wheeze, cough, eczema and asthma. RESULTS: Correlations between CBMC and age 5 PBMC proliferation in response to cockroach, mouse, and dust mite antigens were nonsignificant. Cockroach-, mouse-, and dust mite-induced CBMC proliferation and cytokine responses were not associated with allergen-specific IgE at ages 2, 3, and 5, or with asthma and eczema at age 5. However, after adjusting for potential confounders, age 5 cockroach-induced PBMC proliferation was associated with anti-cockroach IgE, total IgE, and asthma (p < 0.05). CONCLUSION: In contrast to allergen-induced CBMC proliferation, age 5 cockroach-induced PBMC proliferation was associated with age 5 specific and total IgE, and asthma, in an inner-city cohort where cockroach allergens are prevalent and exposure can be high. BioMed Central 2010-08-04 /pmc/articles/PMC2922078/ /pubmed/20684781 http://dx.doi.org/10.1186/1476-7961-8-11 Text en Copyright ©2010 Chang et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Chang, Carolyn
Gauvey-Kern, Kevin
Johnson, Alina
Kelvin, Elizabeth A
Chew, Ginger L
Perera, Frederica
Miller, Rachel L
Cord blood versus age 5 mononuclear cell proliferation on IgE and asthma
title Cord blood versus age 5 mononuclear cell proliferation on IgE and asthma
title_full Cord blood versus age 5 mononuclear cell proliferation on IgE and asthma
title_fullStr Cord blood versus age 5 mononuclear cell proliferation on IgE and asthma
title_full_unstemmed Cord blood versus age 5 mononuclear cell proliferation on IgE and asthma
title_short Cord blood versus age 5 mononuclear cell proliferation on IgE and asthma
title_sort cord blood versus age 5 mononuclear cell proliferation on ige and asthma
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2922078/
https://www.ncbi.nlm.nih.gov/pubmed/20684781
http://dx.doi.org/10.1186/1476-7961-8-11
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