The Journal of Allergy and Clinical Immunology
Volume 121, Issue 5 , Pages 1120-1125.e2, May 2008

Grass pollen immunotherapy: IL-10 induction and suppression of late responses precedes IgG4 inhibitory antibody activity

Allergy and Clinical Immunology Section, National Heart and Lung Institute, Imperial College London, London, United Kingdom

Received 31 July 2007; received in revised form 11 January 2008; accepted 21 January 2008. published online 28 March 2008.

Background

Grass pollen immunotherapy is an effective treatment for seasonal allergic rhinitis that provides the opportunity to study the induction and maintenance of allergen-specific immune tolerance.

Objectives

We investigated the relationship between clinical responsiveness, regulatory cytokine production, and antibody responses to allergen during 1 year of immunotherapy.

Methods

Eighteen subjects with severe seasonal allergic rhinitis were randomized double-blind to receive active or placebo injections of an alum-adsorbed grass pollen vaccine (Alutard SQ). Subjects underwent repeated testing of early- and late-phase skin responses to intradermal allergen, and cellular responses to grass pollen allergen were tested. Sera were tested for allergen-specific IgG4, IgA, and inhibitory activity in biologic assays of IgE responses.

Results

Grass pollen immunotherapy was effective in reducing overall symptom scores (P < .05) and conjunctival reactivity (P < .05). In the active group significant IL-10 production occurred early at low allergen doses and at a similar time as inhibition of late skin responses at 2 to 4 weeks. Serum allergen-specific IgG4, IgA, and inhibitory antibody activity for basophil histamine release and IgE-facilitated allergen binding to B cells occurred later, at 6 to 12 weeks, at higher allergen doses and preceded inhibition of early skin responses.

Conclusion

IL-10 responses occur early but at immunotherapy doses that are not clinically effective. Later induction of inhibitory antibodies, including IgG4 and IgA, might be required for efficacy through modulation of IgE-mediated events.

Key words: Immunotherapy, IL-10, late-phase response, IgG4, IgA, early-phase response

 

 Supported by grants from the Immune Tolerance Network, National Institutes of Health; Asthma UK; and GlaxoSmithKline in partnership with Imperial College Trust (academic Drug Discovery Initiative) and ALK-Abelló, Hørsholm, Denmark. S.J.T. is the recipient of a Clinician Scientist Fellowship supported by the Health Foundation.

 Disclosure of potential conflict of interest: M. A. Calderon has consulting arrangements with ALK-Abelló, MSD, and Schering-Plough and has received research support from ALK-Abelló. S. R. Durham has consulting arrangements with ALK-Abelló and GlaxoSmithKline, has received research support from ALK-Abelló and GlaxoSmithKline, and has served as a member of the Immune Tolerance Network and the National Institutes of Health. The rest of the authors have declared that they have no conflict of interest.

PII: S0091-6749(08)00357-6

doi:10.1016/j.jaci.2008.01.072

The Journal of Allergy and Clinical Immunology
Volume 121, Issue 5 , Pages 1120-1125.e2, May 2008