ORIGINAL PAPER: Hev b 6.01 and Hev b 5 induce pro-inflammatory cytokines and chemokines from peripheral blood mononuclear cells in latex allergy

Background: Hev b 6.01 (prohevein) and Hev b 5 [acidic natural rubber latex (NRL) protein] are major IgE-binding allergens in NRL allergy. Objective: To examine allergen-specific cytokine and chemokine responses in NRL-allergic patients. Methods: Fourteen NRL-allergic patients and 10 healthy control...

Full description

Saved in:
Bibliographic Details
Published in:Clinical and experimental allergy Vol. 37; no. 1; pp. 133 - 140
Main Authors: Lehto, M, Kotovuori, A, Palosuo, K, Varjonen, E, Lehtimaeki, S, Kalkkinen, N, Palosuo, T, Reunala, T, Alenius, H
Format: Journal Article
Language:English
Published: 01-01-2007
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:Background: Hev b 6.01 (prohevein) and Hev b 5 [acidic natural rubber latex (NRL) protein] are major IgE-binding allergens in NRL allergy. Objective: To examine allergen-specific cytokine and chemokine responses in NRL-allergic patients. Methods: Fourteen NRL-allergic patients and 10 healthy controls participated in the study. Hev b 6.01 and Hev b 5 were purified under non-denaturating conditions by chromatographic methods. Specific IgE antibodies were measured by ELISA and proliferation of peripheral blood mononuclear cells (PBMC) by super(3)H-thymidine incorporation assay. Allergen-specific induction of cytokine and chemokine mRNA in PBMC was measured by real-time PCR and protein levels by ELISA. Surface expression of chemokine receptors was analysed by flow cytometry. Results: Twelve (86%) NRL-allergic patients had positive skin prick test reactions and IgE antibodies against Hev b 6.01, but less than 30% responded to Hev b 5. Cell proliferation against Hev b 6.01, but not against Hev b 5, was significantly increased. Both allergens elicited significantly higher expression of pro-inflammatory and T-helper type 2 cytokines (TNF, IL-12p40, IL-13) and chemokines (CCL3, CCL4, CCL20) in the NRL-allergic patients than in controls. Interestingly, mRNA expression of the regulatory cytokine TGF- beta 1 was reduced, whereas IL-10 expression was enhanced after allergen stimulations in patients with NRL allergy. Finally, the NRL-allergic patients showed increased CCR4 expression on CD3 super(+)CD8 super(-) T cells and decreased CXCR3 expression on CD3 super(+)CD8 super(+) T cells. Conclusion: Allergen-specific induction of cytokines and chemokines in PBMC and chemokine receptor expression on circulating T cells may contribute to the pathogenesis of NRL allergy.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
content type line 23
ObjectType-Feature-2
ISSN:0954-7894
1365-2222
DOI:10.1111/j.1365-2222.2006.02622.x