Publications

Publications, Books, Book Chapters and Reviews by Prof. Marcus Maurer, MD

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Evaluation of the Immunogenicity of the Synthetic α-Melanocyte-Stimulating Hormone (α-MSH) Analogue Afamelanotide ([Nle 4 - D -Phe 7 ]-α-MSH, Scenesse ® ) in Erythropoietic Protoporphyria Patients by ELISA Detecting Both Anti-Afamelanotide and Anti-α-MSH Antibodies

Filename 203. Lengweiler et al., Eval.of Immunogen. alpha-Melanoc,SkinPharmPhys.2015.pdf
Filesize 635.69 KB
Version o.203
Date added July 28, 2020
Downloaded 0 times
Category Original Work
Tags Afamelanotide, Anti-drug antibodies, Biological, ELISA, Erythropoietic protoporphyria, Immunogenicity, Photodermatoses, α-Melanocyte-stimulating hormone analogues
Authors Lengweiler, S. , Kreim, S. , Barman-Aksozen, J., Maurer, M. and Minder, E.
Citation Lengweiler, S. , Kreim, S. , Barman-Aksozen, J., Maurer, M. and Minder, E.: Evaluation of the immunogenicity of the α-melanocyte-stimulating hormone (α-MSH) analogue afamelanotide ([Nle 4-D-Phe 7] - α-MSH, scenesse®) in erythropoietic protoporphyria patients by ELISA detecting both anti-afamelanotide and anti-α-MSH antibodies. Skin Pharmacol. Physiol. 2015: 28; 103-113.
Corresponding authors Minder, E.
DocNum o.203
DocType PDF
Edition; Page 28; 103-113
IF 2.48
Publisher Skin Pharmacol. Physiol.
ReleaseDate 2015

Afamelanotide is an α-melanocyte-stimulating hormone (α-MSH) agonist with proven efficacy in photodermatoses such as erythropoietic protoporphyria (EPP). This peptide drug, repeatedly administered over prolonged time, may in-duce anti-drug antibodies (ADA). Here, we describe a new ELISA method developed to monitor the occurrence of ADA against afamelanotide as well as against α-MSH. Covalent binding instead of absorption of antigen onto the microtitre wells prevented antigen leakage and enabled extensive washings followed by lower background. The cut-off be-tween antibody-negative and -positive sera was determined. Inhibition of the antigen-antibody reaction by excess solu-ble antigen tested for specificity. The sensitivity of the ELISA was 608 and 1,390 ng/ml of specific ADA against afamela-notide and α-MSH, respectively. This ELISA method enabled us to investigate the occurrence of ADA during long-term administration of afamelanotide. No immunoreactivity was found in 23 of the 26 EPP patients exposed to the drug for up to 6 years. Pre-existing immunoreactivity against afamel-anotide as well as α-MSH was found in 3 patients, whose ti-tres did not change during afamelanotide administration.

Conclusion: The new ELISA is suitable to determine ADA against afamelanotide and α-MSH. Afamelanotide did not elicit ADA during long-term administration in patients with EPP.

 

(Last update: 07.2025)

Number of original publications in peer-reviewed journals:650
Number of reviews in peer-reviewed journals:229
Number of publications (original work and reviews) in peer-reviewed journals:879
Cumulative IF for original publications in peer-reviewed journals:4648.29
Cumulative IF for reviews in peer-reviewed journals:1689.22
Cumulative IF of publications (original work & reviews) in peer-reviewed journals:6761.91
Total number of citations: 45,522 h-index: 109 (Web of Science July 2025)45,522

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