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Peer-reviewed veterinary case report

How long subcutaneous immunotherapy takes to help dogs with atopic

By Tham, Heng L & Olivry, Thierry·Published in Veterinary dermatology·2022·Department of Small Animal Clinical Sciences, United States·View original on PubMed

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Original publication title: Determination of the efficacy rate and time-to-efficacy of subcutaneous immunotherapy in dogs with atopic dermatitis.

Species:
dog

Plain-English summary

A group of dogs with itchy skin due to atopic dermatitis (a common allergic skin condition) was treated with different types of subcutaneous immunotherapy (a treatment that helps reduce allergic reactions). The study found that newer formulations of immunotherapy worked better and faster than traditional ones, with many dogs showing improvement in just three months. In contrast, older treatments could take up to nine months for some dogs to see any benefit. Overall, the newer treatments could provide relief more quickly for dogs suffering from this condition.

People also search for: dog itchy skin treatment · atopic dermatitis in dogs · immunotherapy for dog allergies

Abstract

BACKGROUND: Allergen-specific immunotherapy (ASIT) is reported to have a success rate of 50-70% when given for up to 12 months to dogs with atopic dermatitis (AD). How soon ASIT is clinically effective is unclear. OBJECTIVES: To compare the efficacy rate (ER) and time-to-efficacy (TTE) of various types of subcutaneous immunotherapy (SCIT) administered using conventional dosing regimens using the methodology of a critically appraised topic. METHODS AND MATERIALS: Three databases were searched to extract information on the ER and TTE of SCIT in dogs with AD. Herein, "efficacy" was defined as a ≥50% reduction in pruritus and/or skin lesions, and the TTE as the time needed to achieve such a reduction. RESULTS: We selected 12 publications including 194 dogs. The ER was significantly higher with the polymerised allergoids coupled with nonoxidized mannan than for the "classic" aqueous and alum-precipitated SCIT types. A TTE of three months or shorter was seen in a significantly higher proportion of dogs receiving mannan-couple allergoids, pullulan-conjugated Der f 2 or tyrosine-adjuvanted than aqueous or alum-precipitated SCIT; with the latter two formulations, the TTE might be nine months or longer in ≤20% of atopic dogs. CONCLUSIONS AND CLINICAL RELEVANCE: In spite of the low number of articles available for review and small number of enrolled dogs, novel SCIT regimens appear to have a faster - and possibly higher - efficacy than the currently available aqueous or alum-precipitated formulations. A standardisation of outcome measures for ASIT clearly is needed to allow a more meaningful comparison between SCIT types.

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Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/34883529/