Immunogenicity of dupilumab in adult and pediatric patients with atopic dermatitis

Front Immunol. 2024 Nov 11:15:1466372. doi: 10.3389/fimmu.2024.1466372. eCollection 2024.

Abstract

Background: Development of anti-drug antibodies (ADAs) and neutralizing antibodies (NAbs) to monoclonal antibodies may adversely impact pharmacokinetics, efficacy, and/or safety.

Objective: To describe incidence, titer, and persistence of dupilumab ADAs and NAbs, and their effects on pharmacokinetics, efficacy, and safety in patients with atopic dermatitis (AD).

Methods: This analysis included seven phase 3 randomized, placebo-controlled (N=2,992) and two long-term open-label extension (N=2,287) trials of subcutaneous dupilumab in adults and pediatric patients with moderate-to-severe AD. ADA, NAb, and dupilumab concentration in serum were assessed using validated immunoassays. ADA impacts on efficacy (EASI) and safety were assessed.

Results: Treatment-emergent ADAs were observed in up to 8.6% (aged ≥18 years), 16.0% (12-17 years), 5.3% (6-11 years), and 2.0% (6 months to 5 years) dupilumab-treated patients. Among dupilumab-treated patients, ≤3.7% had persistent responses, <1% had high titers (≥10,000), and ≤5.1% were NAb-positive. NAbs were more common in patients with moderate- and high-titer ADA responses. High-titer ADAs, while infrequent, were the variable most associated with lower dupilumab concentrations in serum and loss of efficacy, independent of NAb status. Efficacy was generally similar in ADA-positive and -negative patients. For most patients with high- or moderate-titer ADAs, titers decreased and efficacy improved over time with continued dupilumab treatment. ADA-positive and -negative patients had similar incidences of treatment-emergent and serious treatment-emergent adverse events. One patient with high-titer ADAs developed serum sickness.

Conclusion: In patients with AD, ADAs and NAbs had minimal impact on dupilumab concentration, efficacy, and safety, except for high-titer ADAs in a small number of patients.

Clinical trial registration: ClinicalTrials.gov, identifiers (NCT02277743, NCT02277769, NCT02260986, NCT02395133, NCT01949311, NCT03054428, NCT03345914, NCT02612454, and NCT03346434).

Keywords: ADA; NAb; anti-drug antibody; atopic dermatitis; dupilumab; immunogenicity; neutralizing antibody.

Publication types

  • Clinical Trial, Phase III
  • Randomized Controlled Trial

MeSH terms

  • Adolescent
  • Adult
  • Antibodies, Monoclonal, Humanized* / adverse effects
  • Antibodies, Monoclonal, Humanized* / pharmacokinetics
  • Antibodies, Monoclonal, Humanized* / therapeutic use
  • Antibodies, Neutralizing / blood
  • Antibodies, Neutralizing / immunology
  • Child
  • Child, Preschool
  • Dermatitis, Atopic* / blood
  • Dermatitis, Atopic* / drug therapy
  • Dermatitis, Atopic* / immunology
  • Female
  • Humans
  • Male
  • Middle Aged
  • Treatment Outcome
  • Young Adult

Substances

  • Antibodies, Monoclonal, Humanized
  • Antibodies, Neutralizing
  • dupilumab

Associated data

  • ClinicalTrials.gov/NCT02260986
  • ClinicalTrials.gov/NCT03345914
  • ClinicalTrials.gov/NCT02395133
  • ClinicalTrials.gov/NCT02277769
  • ClinicalTrials.gov/NCT03346434
  • ClinicalTrials.gov/NCT03054428
  • ClinicalTrials.gov/NCT01949311
  • ClinicalTrials.gov/NCT02612454
  • ClinicalTrials.gov/NCT02277743