Literature DB >> 12532112

A double-blind, placebo-controlled immunotherapy dose-response study with standardized cat extract.

Penelope A Ewbank1, Jacquelyn Murray, Karrie Sanders, Douglas Curran-Everett, Stephen Dreskin, Harold S Nelson.   

Abstract

BACKGROUND: Allergen immunotherapy with doses of cat extract containing approximately 15 microg of the major allergen, Fel d 1, have been proved clinically effective in several double-blind, placebo-controlled studies. However, the maintenance doses used in allergy practice in the United States are often considerably less than this proven dose.
OBJECTIVE: The purpose of this investigation was to determine whether maintenance immunotherapy with cat dander extract containing 0.6 microg or 3.0 microg of Fel d 1 was more effective than placebo and similar in efficacy to treatment with extracts containing 15.0 microg Fel d 1, immunologic parameters being used as the outcome.
METHODS: Twenty-eight cat-allergic patients were randomly entered, 7 in each group, into a double-blind, placebo-controlled comparison of the immunologic response to treatment with placebo or cat dander extract containing 0.6 microg, 3.0 microg, or 15.0 microg of Fel d 1. Maintenance doses were achieved in 8 visits over a period of 4 weeks through use of a cluster regimen; each subject then received 1 weekly maintenance injection before posttreatment measurements were made. The response to immunotherapy was assessed before immunotherapy and after the first weekly maintenance injection. Studies included responses to titrated skin prick tests to cat extract and an unrelated allergen and serum allergen-specific IgE and IgG4. Titrated nasal challenges were performed with cat extract; measurement of mRNA and secreted cytokines (IL-4, IL-5, and IFN-gamma) was done at 6 hours. Serum cytokines (IL-4, IL-5, IFN-gamma) were measured, and flow cytometric analysis of intracellular cytokines (IL-4, IL-5, IFN-gamma) was performed. Cat allergen-stimulated lymphocyte proliferation was performed with measurement of cytokines in the supernatant (IL-4, IL-5, IFN-gamma).
RESULTS: All 28 subjects completed the study. Significant and dose-dependent differences were encountered in the titrated skin prick tests (P =.008), the cat-specific IgG(4) (P =.01), and the reduction in CD4+/IL-4+ PBMCs on flow cytometry (P =.03). There were no significant differences between placebo and cat dander extract containing Fel d 1 0.6 microg. Both extracts containing 3.0 microg and 15.0 microg produced significant decreases in skin prick test sensitivity (P =.02 and P =.002, respectively). The extracts containing 3.0 microg and 15.0 microg produced significant increases in cat-specific IgG4 (P =.01 and P =.006, respectively). Only the 15.0-microg-per-dose extract produced a significant reduction in the percent of CD4+/IL-4+ PBMCs (P =.003).
CONCLUSION: In this double-blind, placebo-controlled study, a maintenance dose of cat dander extract containing 15.0 microg Fel d 1 produced the most consistent immunologic response. A dose of 3.0 microg reduced skin prick test sensitivity and increased cat-specific IgG4 but did not reduce the circulating CD4+/IL-4+ PBMCs, a change that is likely related to the clinically significant response to allergen immunotherapy. These findings suggest that a maintenance dose of 15.0 microg of Fel d 1 is most apt to be clinically effective for allergen immunotherapy.

Entities:  

Mesh:

Substances:

Year:  2003        PMID: 12532112     DOI: 10.1067/mai.2003.41

Source DB:  PubMed          Journal:  J Allergy Clin Immunol        ISSN: 0091-6749            Impact factor:   10.793


  13 in total

1.  High-dose allergen exposure leads to tolerance.

Authors:  Judith A Woodfolk
Journal:  Clin Rev Allergy Immunol       Date:  2005-02       Impact factor: 8.667

Review 2.  [Allergen-specific immunotherapy in pet allergy - an update].

Authors:  U Raap; M Wagenmann; O Pfaar
Journal:  Hautarzt       Date:  2011-09       Impact factor: 0.751

3.  Diagnostic utility of concentrated Mus m 1 allergen extract in humans.

Authors:  Allison Norton; Keegan Smith; Kristina James; Aimee Hoskins; Theresa A Scott; Greg Plunkett; John Fahrenholz; Ryszard Dworski
Journal:  Ann Allergy Asthma Immunol       Date:  2014-02-28       Impact factor: 6.347

Review 4.  Sublingual immunotherapy in pediatric allergic rhinitis and asthma: efficacy, safety, and practical considerations.

Authors:  Linda Cox
Journal:  Curr Allergy Asthma Rep       Date:  2007-11       Impact factor: 4.806

5.  Tracking antigen-specific T-cells during clinical tolerance induction in humans.

Authors:  Aamir Aslam; Hsien Chan; David A Warrell; Siraj Misbah; Graham S Ogg
Journal:  PLoS One       Date:  2010-06-09       Impact factor: 3.240

Review 6.  Accelerated immunotherapy schedules.

Authors:  Christopher W Calabria
Journal:  Curr Allergy Asthma Rep       Date:  2013-08       Impact factor: 4.806

7.  In vitro evaluation of allergen potencies of commercial house dust mite sublingual immunotherapy reagents.

Authors:  Kyung Hee Park; Mina Son; Soo-Young Choi; Hey Jung Park; Jae-Hyun Lee; Kyoung Yong Jeong; Joo-Shil Lee; Jung-Won Park
Journal:  Allergy Asthma Immunol Res       Date:  2014-12-18       Impact factor: 5.764

8.  The efficacy assessment of a self-administered immunotherapy protocol.

Authors:  Frederick M Schaffer; Larry M Garner; Myla Ebeling; Jeffrey M Adelglass; Thomas C Hulsey; Andrew R Naples
Journal:  Int Forum Allergy Rhinol       Date:  2015-10-14       Impact factor: 3.858

9.  Glutaraldehyde-Modified Recombinant Fel d 1: A Hypoallergen With Negligible Biological Activity But Retained Immunogenicity.

Authors:  Serge A Versteeg; Ingrid Bulder; Martin Himly; Toni M van Capel; R van den Hout; Stef J Koppelman; Esther C de Jong; Fatima Ferreira; Ronald van Ree
Journal:  World Allergy Organ J       Date:  2011-07-14       Impact factor: 4.084

10.  Local and systemic effects of cat allergen nasal provocation.

Authors:  G W Scadding; A Eifan; M Penagos; A Dumitru; A Switzer; O McMahon; D Phippard; A Togias; S R Durham; M H Shamji
Journal:  Clin Exp Allergy       Date:  2015-03       Impact factor: 5.018

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.