PulseExploreJournal ClubDebatesTrendingResearchersJournals
Instagram
HomeExploreJournal ClubTrending
Synapse
⌘+K
Synapse
April 15, 2026Experimental Dermatology0 citationsOpen Access

Clinical Efficacy and Safety of Intramuscular Injections of Autologous Total IgG in Patients With Chronic Spontaneous Urticaria: An Open‐Label Prospective Pilot Trial

View Full Paper
YYYoung‐Min YeHKHyun Tae KimBKByul Kwon

Key Points

  • The study aims to assess the efficacy and safety of autologous total IgG in treating antihistamine-refractory chronic spontaneous urticaria.
  • Conducted as a prospective open-label pilot trial
  • Involved 15 adults with chronic spontaneous urticaria
  • Administered nine weekly intramuscular injections of 100 mg autologous IgG
  • Measured primary outcome using Urticaria Activity Score over 7 days
  • Evaluated secondary outcomes including Urticaria Control Test and quality of life metrics
  • Median change in Urticaria Activity Score was -13.0 at Week 12 (p < 0.001)
  • Significant improvements in Urticaria Control Test, quality of life, and visual analogue scale (p < 0.05)
  • Improvement in symptoms and quality of life began at Week 4 and persisted to Week 24
  • Serum total IgG increased by a median of +68.0 mg/dL from baseline to Week 12 (p < 0.05)
  • No serious adverse events observed

Abstract

Chronic spontaneous urticaria (CSU) remains challenging to manage in patients who do not respond adequately to antihistamines or currently available immunomodulatory therapies. Intramuscular injection of autologous total IgG (autologous immunoglobulin therapy: AIGT) has demonstrated clinical efficacy, safety and immunomodulatory effects in patients with moderate-to-severe atopic dermatitis in a randomized placebo-controlled clinical trial. However, the clinical usefulness of AIGT in patients with CSU has not been evaluated. We conducted a prospective open-label pilot study to assess the efficacy and safety of AIGT in antihistamine-refractory CSU. Fifteen adults with CSU received nine weekly intramuscular injections of 100 mg autologous IgG from Week 0 through Week 8 (inclusive). The primary outcome was the change in Urticaria Activity Score over 7 days (UAS7) at Week 12 from baseline. Secondary outcomes included the Urticaria Control Test (UCT), chronic urticaria-specific quality of life (CU-QoL) scores and patient-reported disease burden using a visual analogue scale (VAS). The median change in UAS7 at Week 12 from baseline was -13.0 (p < 0.001). Significant improvements in UCT, CU-QoL and VAS were also observed at Week 12 from baseline (p < 0.05). In longitudinal analyses, improvements in symptom burden and quality of life were detectable from Week 4 and were maintained through Week 24. Serum total IgG increased by a median of +68.0 mg/dL from baseline to Week 12 (p < 0.05). No serious adverse events occurred. In conclusion, AIGT improved disease activity, urticaria control, quality of life and patient-reported burden in patients with antihistamine-refractory CSU. Further studies are needed to evaluate the clinical usefulness of AIGT in CSU.

Ask AI
Helpful
Bookmark
Share
View Full Paper

Cite This Study

Ye et al. (2026) studied this question.

synapsesocial.com/papers/69df2a99e4eeef8a2a6afa85https://doi.org/10.1111/exd.70249
Ask AI
Helpful
Bookmark
Share
View Full Paper