Early and longitudinal response to sublingual immunotherapy across pediatric allergic multimorbidity patterns: A

Victor Gonzalez-Uribe1,2, Jimena Prieto-Gomez1,2, Sebastian Moreno-Castro1,2

  • 1AlergiaMx, Mexico City, Mexico.

Insights

Pediatric sublingual immunotherapy (SLIT) shows varied early responses based on allergic multimorbidity. Asthma plus allergic rhinitis patients responded best, while those with atopic dermatitis showed lower response rates.

Area of Science:

  • Pediatric Allergy and Immunology
  • Immunotherapy Research
  • Clinical Outcomes

Background:

  • Uncertainty exists regarding the timing of clinically significant benefits from pediatric sublingual immunotherapy (SLIT) across diverse allergic multimorbidity patterns.
  • Evaluating early and long-term responses to SLIT in real-world clinical settings is crucial.

Purpose of the Study:

  • To assess the early and longitudinal effectiveness of sublingual immunotherapy (SLIT) in children with allergic multimorbidity.
  • To identify differences in SLIT response based on specific allergic conditions.

Main Methods:

  • Retrospective longitudinal cohort study of 1208 patients aged 3-17 years receiving individualized liquid-drop SLIT.
  • Data collected at baseline and 6, 12, 18, 24, and 36 months.
  • Primary outcome: Pediatric Asthma Quality of Life Questionnaire (PAQLQ) minimal clinically important difference (MCID) at 6 months.

Main Results:

  • 60.8% of patients achieved the PAQLQ MCID at 6 months.
  • Highest response rates observed in patients with asthma plus allergic rhinitis (76.8%), lowest in those with asthma, AR, and atopic dermatitis (28.2%).
  • Significant improvements in PAQLQ, rhinitis quality of life, FeNO, and reduced inhaled corticosteroid use by 36 months.

Conclusions:

  • Early response to pediatric SLIT is influenced by allergic multimorbidity patterns.
  • Outcomes continue to improve up to 36 months in adherent and persistent patients.
  • SLIT demonstrates potential for long-term benefit in pediatric allergic diseases.
Abstract