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Immunogenicity of subcutaneous TNF inhibitors and its clinical significance in real-life setting in patients with spondyloarthritis

KEY MESSAGES: Considerable proportion of patients with SpA have been immunized to the subcutaneous anti-TNF drug they are using. Concomitant use of MTX protects from immunization, whereas SASP does not. Patients with SpA using subcutaneous anti-TNF drugs can benefit from monitoring of the drug troug...

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Autores principales: Hiltunen, J., Parmanne, P., Sokka, T., Lamberg, T., Isomäki, P., Kaipiainen-Seppänen, O., Peltomaa, R., Uutela, T., Pirilä, L., Taimen, K., Kauppi, M. J., Yli-Kerttula, T., Tuompo, R., Relas, H., Kortelainen, S., Paalanen, K., Asikainen, J., Ekman, P., Santisteban, A., Vidqvist, K.-L., Tadesse, K., Romu, M., Borodina, J., Elfving, P., Valleala, H., Leirisalo-Repo, M., Rantalaiho, V., Kautiainen, H., Jokiranta, T. S., Eklund, K. K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9124652/
https://www.ncbi.nlm.nih.gov/pubmed/34357455
http://dx.doi.org/10.1007/s00296-021-04955-8
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author Hiltunen, J.
Parmanne, P.
Sokka, T.
Lamberg, T.
Isomäki, P.
Kaipiainen-Seppänen, O.
Peltomaa, R.
Uutela, T.
Pirilä, L.
Taimen, K.
Kauppi, M. J.
Yli-Kerttula, T.
Tuompo, R.
Relas, H.
Kortelainen, S.
Paalanen, K.
Asikainen, J.
Ekman, P.
Santisteban, A.
Vidqvist, K.-L.
Tadesse, K.
Romu, M.
Borodina, J.
Elfving, P.
Valleala, H.
Leirisalo-Repo, M.
Rantalaiho, V.
Kautiainen, H.
Jokiranta, T. S.
Eklund, K. K.
author_facet Hiltunen, J.
Parmanne, P.
Sokka, T.
Lamberg, T.
Isomäki, P.
Kaipiainen-Seppänen, O.
Peltomaa, R.
Uutela, T.
Pirilä, L.
Taimen, K.
Kauppi, M. J.
Yli-Kerttula, T.
Tuompo, R.
Relas, H.
Kortelainen, S.
Paalanen, K.
Asikainen, J.
Ekman, P.
Santisteban, A.
Vidqvist, K.-L.
Tadesse, K.
Romu, M.
Borodina, J.
Elfving, P.
Valleala, H.
Leirisalo-Repo, M.
Rantalaiho, V.
Kautiainen, H.
Jokiranta, T. S.
Eklund, K. K.
author_sort Hiltunen, J.
collection PubMed
description KEY MESSAGES: Considerable proportion of patients with SpA have been immunized to the subcutaneous anti-TNF drug they are using. Concomitant use of MTX protects from immunization, whereas SASP does not. Patients with SpA using subcutaneous anti-TNF drugs can benefit from monitoring of the drug trough levels. ABSTRACT: Immunization to biological drugs can lead to decreased efficacy and increased risk of adverse effects. The objective of this cross-sectional study was to assess the extent and significance of immunization to subcutaneous tumor necrosis factor (TNF) inhibitors in axial spondyloarthritis (axSpA) patients in real-life setting. A serum sample was taken 1–2 days before the next drug injection. Drug trough concentrations, anti-drug antibodies (ADAb) and TNF-blocking capacity were measured in 273 patients with axSpA using subcutaneous anti-TNF drugs. The clinical activity of SpA was assessed using the Bath AS Disease Activity Index (BASDAI) and the Maastricht AS Entheses Score (MASES). ADAb were found in 11% of the 273 patients: in 21/99 (21%) of patients who used adalimumab, in 0/83 (0%) of those who used etanercept, in 2/79 (3%) of those who used golimumab and in 6/12 (50%) of those who used certolizumab pegol. Use of methotrexate reduced the risk of formation of ADAb, whereas sulfasalazine did not. Presence of ADAb resulted in decreased drug concentration and reduced TNF-blocking capacity. However, low levels of ADAb had no effect on TNF-blocking capacity and did not correlate with disease activity. The drug trough levels were below the consensus target level in 36% of the patients. High BMI correlated with low drug trough concentration. Patients with low drug trough levels had higher disease activity. The presence of anti-drug antibodies was associated with reduced drug trough levels, and the patients with low drug trough levels had higher disease activity. The drug trough levels were below target level in significant proportion of patients and, thus, measuring the drug concentration and ADAb could help to optimize the treatment in SpA patients. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00296-021-04955-8.
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spelling pubmed-91246522022-05-24 Immunogenicity of subcutaneous TNF inhibitors and its clinical significance in real-life setting in patients with spondyloarthritis Hiltunen, J. Parmanne, P. Sokka, T. Lamberg, T. Isomäki, P. Kaipiainen-Seppänen, O. Peltomaa, R. Uutela, T. Pirilä, L. Taimen, K. Kauppi, M. J. Yli-Kerttula, T. Tuompo, R. Relas, H. Kortelainen, S. Paalanen, K. Asikainen, J. Ekman, P. Santisteban, A. Vidqvist, K.-L. Tadesse, K. Romu, M. Borodina, J. Elfving, P. Valleala, H. Leirisalo-Repo, M. Rantalaiho, V. Kautiainen, H. Jokiranta, T. S. Eklund, K. K. Rheumatol Int Observational Research KEY MESSAGES: Considerable proportion of patients with SpA have been immunized to the subcutaneous anti-TNF drug they are using. Concomitant use of MTX protects from immunization, whereas SASP does not. Patients with SpA using subcutaneous anti-TNF drugs can benefit from monitoring of the drug trough levels. ABSTRACT: Immunization to biological drugs can lead to decreased efficacy and increased risk of adverse effects. The objective of this cross-sectional study was to assess the extent and significance of immunization to subcutaneous tumor necrosis factor (TNF) inhibitors in axial spondyloarthritis (axSpA) patients in real-life setting. A serum sample was taken 1–2 days before the next drug injection. Drug trough concentrations, anti-drug antibodies (ADAb) and TNF-blocking capacity were measured in 273 patients with axSpA using subcutaneous anti-TNF drugs. The clinical activity of SpA was assessed using the Bath AS Disease Activity Index (BASDAI) and the Maastricht AS Entheses Score (MASES). ADAb were found in 11% of the 273 patients: in 21/99 (21%) of patients who used adalimumab, in 0/83 (0%) of those who used etanercept, in 2/79 (3%) of those who used golimumab and in 6/12 (50%) of those who used certolizumab pegol. Use of methotrexate reduced the risk of formation of ADAb, whereas sulfasalazine did not. Presence of ADAb resulted in decreased drug concentration and reduced TNF-blocking capacity. However, low levels of ADAb had no effect on TNF-blocking capacity and did not correlate with disease activity. The drug trough levels were below the consensus target level in 36% of the patients. High BMI correlated with low drug trough concentration. Patients with low drug trough levels had higher disease activity. The presence of anti-drug antibodies was associated with reduced drug trough levels, and the patients with low drug trough levels had higher disease activity. The drug trough levels were below target level in significant proportion of patients and, thus, measuring the drug concentration and ADAb could help to optimize the treatment in SpA patients. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00296-021-04955-8. Springer Berlin Heidelberg 2021-08-06 2022 /pmc/articles/PMC9124652/ /pubmed/34357455 http://dx.doi.org/10.1007/s00296-021-04955-8 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Observational Research
Hiltunen, J.
Parmanne, P.
Sokka, T.
Lamberg, T.
Isomäki, P.
Kaipiainen-Seppänen, O.
Peltomaa, R.
Uutela, T.
Pirilä, L.
Taimen, K.
Kauppi, M. J.
Yli-Kerttula, T.
Tuompo, R.
Relas, H.
Kortelainen, S.
Paalanen, K.
Asikainen, J.
Ekman, P.
Santisteban, A.
Vidqvist, K.-L.
Tadesse, K.
Romu, M.
Borodina, J.
Elfving, P.
Valleala, H.
Leirisalo-Repo, M.
Rantalaiho, V.
Kautiainen, H.
Jokiranta, T. S.
Eklund, K. K.
Immunogenicity of subcutaneous TNF inhibitors and its clinical significance in real-life setting in patients with spondyloarthritis
title Immunogenicity of subcutaneous TNF inhibitors and its clinical significance in real-life setting in patients with spondyloarthritis
title_full Immunogenicity of subcutaneous TNF inhibitors and its clinical significance in real-life setting in patients with spondyloarthritis
title_fullStr Immunogenicity of subcutaneous TNF inhibitors and its clinical significance in real-life setting in patients with spondyloarthritis
title_full_unstemmed Immunogenicity of subcutaneous TNF inhibitors and its clinical significance in real-life setting in patients with spondyloarthritis
title_short Immunogenicity of subcutaneous TNF inhibitors and its clinical significance in real-life setting in patients with spondyloarthritis
title_sort immunogenicity of subcutaneous tnf inhibitors and its clinical significance in real-life setting in patients with spondyloarthritis
topic Observational Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9124652/
https://www.ncbi.nlm.nih.gov/pubmed/34357455
http://dx.doi.org/10.1007/s00296-021-04955-8
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