4.8 Review

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

Journal

FRONTIERS IN IMMUNOLOGY
Volume 13, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fimmu.2022.923362

Keywords

atopic dermatitis; interleukin-13 inhibitor; efficacy; safety; meta-analysis

Categories

Funding

  1. Natural Science Foundation of China
  2. National Key Research and Development Program of China
  3. National Science Foundation for Post-doctoral Scientists of China
  4. Hunan Outstanding Postdoctoral Innovative Talents Program
  5. Natural Science Foundation of Hunan Province for outstanding Young Scholars
  6. Youth Foundation of Xiangya Hospital
  7. [82100037]
  8. [82022060]
  9. [2019YFA0111600]
  10. [2019YFE0120800]
  11. [2021TQ0375]
  12. [2022M713538]
  13. [2021RC2018]
  14. [2019JJ30040]
  15. [2020Q06]

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IL-13 inhibitors lebrikizumab and tralokinumab have demonstrated good efficacy and safety in the treatment of moderate to severe AD. Compared to placebo treatment, these IL-13 inhibitors can significantly improve skin symptoms and quality of life in patients with AD, albeit with a higher risk of conjunctivitis.
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 9(th), 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.

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