Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Observational Study
. 2015 Nov 13;10(11):e0142930.
doi: 10.1371/journal.pone.0142930. eCollection 2015.

The Association between Clinical Response to Ustekinumab and Immunogenicity to Ustekinumab and Prior Adalimumab

Affiliations
Observational Study

The Association between Clinical Response to Ustekinumab and Immunogenicity to Ustekinumab and Prior Adalimumab

Hsien-Yi Chiu et al. PLoS One. .

Abstract

Background: Immunogenicity due to antidrug antibodies (ADA) to tumor necrosis factor (TNF)-α antagonists is known to decrease treatment response. However, few studies have investigated ADA in ustekinumab, an interleukin-12 and -23 antagonist, in a clinical setting. This study aimed to investigate the immunogenicity of ustekinumab and its clinical consequences in psoriasis.

Methods: This prospective observational study enrolled 76 patients with plaque psoriasis who were treated with ustekinumab for a minimum of 7 months. Blood samples were drawn just prior to scheduled ustekinumab injection during clinic visits. Levels of anti-ustekinumab antibody (AUA) and serum ustekinumab concentration were measured respectively by radioimmunoassays and enzyme-linked immunoassays respectively, and correlated to clinical data and Psoriasis Area and Severity Index (PASI).

Results: AUA was detected in 6.5% of patients after a mean of 13 months of treatment. Patients with positive AUA had significantly lower serum ustekinumab concentrations (0.01 vs. 0.2 mg/L, p<0.001) and lower PASI 50 response than patients without AUA (0% vs. 69%, p = 0.004).The percentage of AUA formation was comparable between patients who had failed previous adalimumab with or without anti-adalimumab antibodies (AAA) (14.3% vs. 12.5%, p = 1.00). However, a higher proportion of switchers without AAA obtaining PASI50 (71.4% vs. 37.5%) and PASI75 response (42.9% vs.12.5%) within 7 months of ustekinumab treatment than with AAA though this difference did not reach statistical significance.

Conclusions: Our results suggest that presence of AUA was significantly associated with treatment failure for ustekinumab, though limited by a small sample size. Also, determining the presence of ADA to antecedent TNF-α antagonists may assist in choosing an optimized subsequent treatment modality achieving treatment success.

PubMed Disclaimer

Conflict of interest statement

Competing Interests: The authors of this manuscript have the following competing interests: Dr. Tsen-Fang Tsai has conducted clinical trials or received honoraria for serving as a consultant for Pfizer Pharmaceuticals, Serono International SA (now Merck Serono International), UniPharma/Biogen Idec, Galderma, Celgene, Novartis Pharmaceuticals and Janssen-Cilag Pharmaceutical, and has received speaking fees from AbbVie. Dr. Chiu has received speaking fees from AbbVie, Janssen-Cilag Pharmaceutical and Pfizer. Drs. Chu, and Cheng have no conflicts of interest to declare. This does not alter the authors' adherence to PLOS ONE policies on sharing data and materials.

Figures

Fig 1
Fig 1. Ustekinumab trough concentration are shown by responder status and anti-ustekinumab antibody (A) Patients with negative anti-ustekinumab antibody had significantly higher drug trough levels compared with those with positive anti-ustekinumab antibody. (B) Nonresponders attained significantly lower ustekinumab trough levels than responders.
Responders were defined as 50% reduction in psoriasis area and severity index (PASI 50) compared to baseline within 7 months of treatment.

References

    1. Nestle FO, Kaplan DH, Barker J. (2009) Psoriasis. N Engl J Med 361: 496–509. 10.1056/NEJMra0804595 - DOI - PubMed
    1. Mitra A, Fallen RS, Lima HC. (2013) Cytokine-based therapy in psoriasis. Clin Rev Allergy Immunol 44: 173–182. 10.1007/s12016-012-8306-2 - DOI - PubMed
    1. Chiu H-Y, Cheng Y-P, Tsai T-F. (2012) T helper type 17 in psoriasis: From basic immunology to clinical practice. Dermatologica Sinica 30: 136–141.
    1. Sandoval LF, Pierce A, Feldman SR. (2014) Systemic therapies for psoriasis: an evidence-based update. Am J Clin Dermatol 15: 165–180. 10.1007/s40257-014-0064-x - DOI - PubMed
    1. Bartelds GM, Krieckaert CL, Nurmohamed MT, van Schouwenburg PA, Lems WF, Twisk JW, et al. (2011) Development of antidrug antibodies against adalimumab and association with disease activity and treatment failure during long-term follow-up. JAMA 305: 1460–1468. 10.1001/jama.2011.406 - DOI - PubMed

Publication types

MeSH terms