The efficacy and safety of IL-13 inhibitors in atopic dermatitis: A systematic review and meta-analysis

Front Immunol. 2022 Jul 27:13:923362. doi: 10.3389/fimmu.2022.923362. eCollection 2022.

Abstract

Background: Several clinical trials have evaluated the efficacy and safety of interleukin-13 (IL-13) with lebrikizumab and tralokinumab in patients with moderate to severe atopic dermatitis (AD). However, the safety and efficacy of IL-13 inhibitors as a potent biologic for AD remain elusive.

Objective: To assess the efficacy and safety of IL-13 inhibitors in moderate to severe AD.

Method: Randomized clinical trials (RCTs), comparing IL-13 inhibitors vs placebo treatment in patients with moderate to severe AD, were identified from public database from its inception to November 9th, 2021. The study was registered in PROSPERO (CRD42021254920).

Results: Six studies reporting 7 RCTs involving 2946 patients with moderate-to-severe AD were included for the pooled analysis. Compared with placebo, antagonizing IL-13 with lebrikizumab and tralokinumab showed a greater improvement in percentage change of EASI (MD -20.37, 95%CI -32.28, -8.47), and a larger proportion of patients achieving numerical rating scale (NRS) with more than 4-points improvement (RR 1.59, 95%CI 1.23, 2.05). Additionally, IL-13 inhibitors also improved impaired dermatology life quality index (DLQI) (MD -14.49, 95%CI -19.23, -9.75). In terms of safety, both lebrikizumab and tralokinumab were well tolerated, with the except that they were linked to an increased risk of conjunctivitis compared to placebo treatment.

Conclusion: Antagonizing IL-13 with lebrikizumab and tralokinumab have demonstrated encouraging clinical efficacy against moderate-to-severe AD with excellent safety profile, albeit they did come with a higher risk of conjunctivitis than placebo treatment.

Systematic review registration: https://www.crd.york.ac.uk/prospero/, identifier ID=CRD42021254920.

Keywords: atopic dermatitis; efficacy; interleukin-13 inhibitor; meta-analysis; safety.

Publication types

  • Meta-Analysis
  • Systematic Review
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Conjunctivitis*
  • Dermatitis, Atopic* / drug therapy
  • Humans
  • Interleukin Inhibitors
  • Interleukin-13
  • Treatment Outcome

Substances

  • Interleukin Inhibitors
  • Interleukin-13