Immunotherapy with a ragweed-toll-like receptor 9 agonist vaccine for allergic rhinitis

被引:440
作者
Creticos, Peter S.
Schroeder, John T.
Hamilton, Robert G.
Balcer-Whaley, Susan L.
Khattignavong, Arouna P.
Lindblad, Robert
Li, Henry
Coffman, Robert
Seyfert, Vicki
Eiden, Joseph J.
Broide, David
机构
[1] Johns Hopkins Univ, Sch Med, Dept Med, Div Clin Immunol & Allergy, Baltimore, MD 21205 USA
[2] Emmes Corp, Rockville, MD USA
[3] Inst Asthma & Allergy, Wheaton, VA USA
[4] Dynavax Technol, Berkeley, CA USA
[5] Immune Tolerance Network, San Francisco, CA USA
[6] Univ Calif San Diego, Dept Med, Sect Allergy & Immunol, San Diego, CA 92103 USA
关键词
D O I
10.1056/NEJMoa052916
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Conjugating immunostimulatory sequences of DNA to specific allergens offers a new approach to allergen immunotherapy that reduces acute allergic responses. Methods: We conducted a randomized, double-blind, placebo-controlled phase 2 trial of a vaccine consisting of Amb a 1, a ragweed-pollen antigen, conjugated to a phosphorothioate oligodeoxyribonucleotide immunostimulatory sequence of DNA (AIC) in 25 adults who were allergic to ragweed. Patients received six weekly injections of the AIC or placebo vaccine before the first ragweed season and were monitored during the next two ragweed seasons. Results: There was no pattern of vaccine-associated systemic reactions or clinically significant laboratory abnormalities. AIC did not alter the primary end point, the vascular permeability response (measured by the albumin level in nasal-lavage fluid) to nasal provocation. During the first ragweed season, the AIC group had better peak-season rhinitis scores on the visual-analogue scale (P=0.006), peak-season daily nasal symptom diary scores (P=0.02), and midseason overall quality-of-life scores (P=0.05) than the placebo group. AIC induced a transient increase in Amb a 1-specific IgG antibody but suppressed the seasonal increase in Amb a 1-specific IgE antibody. A reduction in the number of interleukin-4-positive basophils in AIC-treated patients correlated with lower rhinitis visual-analogue scores (r=0.49, P=0.03). Clinical benefits of AIC were again observed in the subsequent ragweed season, with improvements over placebo in peak-season rhinitis visual-analogue scores (P=0.02) and peak-season daily nasal symptom diary scores (P=0.02). The seasonal specific IgE antibody response was again suppressed, with no significant change in IgE antibody titer during the ragweed season (P=0.19). Conclusions: In this pilot study, a 6-week regimen of the AIC vaccine appeared to offer long-term clinical efficacy in the treatment of ragweed allergic rhinitis. (ClinicalTrials.gov number, NCT00346086.)
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页码:1445 / 1455
页数:11
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