Monitoring of molecular profiling of allergen-antibody responses in HDM-immunotherapy patients

Hum Vaccin Immunother. 2022 Dec 30;18(7):2148815. doi: 10.1080/21645515.2022.2148815. Epub 2022 Nov 29.

Abstract

Among the potential hazards of HDM immunotherapy (AIT) with HDM allergenic extracts is the possible initiation of de novosensitizations caused by a lack of complementarity between a given HDM vaccine's content and a patient's molecular sensitization profile. To investigate whether immunotherapy with HDM extracts affects changes in the profile of sensitizations to allergens contained in the extract and whether neosensitizations occur. Serum samples from patients with HDM allergies (N=63) who received 1 year of treatment with subcutaneous AIT were tested for allergen-specific IgE (sIgE) reactivity to 7 microarrayed HDM allergen molecules (Der p 1, 2,10,11,23; D far 1 and 2) with ImmunoCAP. The HDM non-AIT patients (N=22) who did not receive immunotherapy constituted the study's control group. The obtained data were analysed at baseline and after 6 and 12 months. In the HDM-AIT group, no neosensitizations after 6 and 12 months of immunotherapy were reported. Conversely, in the HDM non-AIT group, only neosensitizations to Der p 10 were observed. In the study group, sIgE levels against the HDM extract of D. pteronyssinus, D. farinae, rDer p 1, rDer p 2 and Der f 2 decreased after 12 months of AIT (p< .05). SIgE levels against Der f 1, Der p 10, 11 and 23 remained unchanged in the course of 12 months of immunotherapy. In patients with allergic rhinitis with or without concomitant HDM-induced asthma treated with HDM AIT for 12 months, no neosensitizations related to the examined HDM molecules were observed.

Keywords: Mite allergy; allergen-specific immunotherapy; allergic rhinitis; molecular reactivity profile; neosensitization.

MeSH terms

  • Allergens*
  • Animals
  • Antibody Formation
  • Antigens, Dermatophagoides
  • Dermatophagoides pteronyssinus
  • Humans
  • Immunotherapy
  • Pyroglyphidae
  • Rhinitis, Allergic* / therapy

Substances

  • Allergens
  • Antigens, Dermatophagoides

Grants and funding

The author(s) reported there is no funding associated with the work featured in this article.