Edited by: Hans-Uwe Simon
Early markers for protective mechanisms during rush venom immunotherapy
Article first published online: 29 OCT 2010
© 2010 John Wiley & Sons A/S
Volume 65, Issue 12, pages 1558–1565, December 2010
How to Cite
Bussmann, C., Xia, J., Allam, J.-P., Maintz, L., Bieber, T. and Novak, N. (2010), Early markers for protective mechanisms during rush venom immunotherapy. Allergy, 65: 1558–1565. doi: 10.1111/j.1398-9995.2010.02430.x
- Issue published online: 29 OCT 2010
- Article first published online: 29 OCT 2010
- Accepted for publication 20 May 2010
- allergen-specific immunotherapy;
- insect allergy;
To cite this article: Bussmann C, Xia J, Allam J-P, Maintz L, Bieber T, Novak N. Early markers for protective mechanisms during rush venom immunotherapy. Allergy 2010; 65: 1558–1565.
Background: Allergen-specific venom immunotherapy (VIT) represents the only rational-based option to treat allergic sensitizations against bee and wasp venom. So far, there is not much knowledge about early induction of protective and tolerogenic pathways during VIT.
Objectives: To identify the earliest markers for protective mechanisms against allergic reactions in the peripheral blood during the build-up phase of VIT.
Methods: PBMC and monocytes were isolated, and serum samples were taken before and during a five day build-up phase from 65 hymenoptera venom allergic patients. Expression level of tolerogenic markers was analyzed on mRNA and protein level. Serum levels of different soluble tolerogenic factors were measured.
Results: We observed significantly enhanced tryptophan degradation, elevated ILT4 expression of monocytes as well as IL-10 production of CD3+ T cells only a few hours after the first injection on day 1, followed by increased IL-10 serum levels, monocyte apoptosis and elevated intracellular cAMP levels of monocytes on day 3 combined with a higher ILT3 protein expression and IL-10 secretion of monocytes on day 5.
Conclusion: From these data, we conclude that tryptophan depletion, ILT3/4-mediated inhibition, higher IL-10 production as well as intracellular cAMP might contribute to early induction of protective mechanisms against allergic reactions during the build-up phase of VIT.