Cargando…
The role of DMARDs in reducing the immunogenicity of TNF inhibitors in chronic inflammatory diseases
The management of RA, SpA, psoriasis and inflammatory bowel disease has significantly improved over the last decade with the addition of tumour necrosis factor inhibitors (anti-TNFs) to the therapeutic armamentarium. Immunogenicity in response to monoclonal antibody therapies (anti-drug antibodies)...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3894670/ https://www.ncbi.nlm.nih.gov/pubmed/23946436 http://dx.doi.org/10.1093/rheumatology/ket260 |
_version_ | 1782299879284932608 |
---|---|
author | Jani, Meghna Barton, Anne Warren, Richard B. Griffiths, Christopher E. M. Chinoy, Hector |
author_facet | Jani, Meghna Barton, Anne Warren, Richard B. Griffiths, Christopher E. M. Chinoy, Hector |
author_sort | Jani, Meghna |
collection | PubMed |
description | The management of RA, SpA, psoriasis and inflammatory bowel disease has significantly improved over the last decade with the addition of tumour necrosis factor inhibitors (anti-TNFs) to the therapeutic armamentarium. Immunogenicity in response to monoclonal antibody therapies (anti-drug antibodies) may give rise to low serum drug levels, loss of therapeutic response, poor drug survival and/or adverse events such as infusion reactions. To combat these, the use of concomitant MTX may attenuate the frequency of anti-drug antibodies in RA, SpA and Crohn’s disease. Although a similar effect to methotrexate has been observed with AZA usage in the management of Crohn’s disease, there is insufficient evidence to suggest that other DMARDs impact immunogenicity. In this article we review the evidence to date on the effect of immunomodulatory therapy when co-administered with anti-TNFs. We also discuss whether such a strategy should be employed in SpA and psoriasis, and if optimization of the MTX dose could improve biologic drug survival and thereby benefit disease management. |
format | Online Article Text |
id | pubmed-3894670 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-38946702014-01-17 The role of DMARDs in reducing the immunogenicity of TNF inhibitors in chronic inflammatory diseases Jani, Meghna Barton, Anne Warren, Richard B. Griffiths, Christopher E. M. Chinoy, Hector Rheumatology (Oxford) Reviews The management of RA, SpA, psoriasis and inflammatory bowel disease has significantly improved over the last decade with the addition of tumour necrosis factor inhibitors (anti-TNFs) to the therapeutic armamentarium. Immunogenicity in response to monoclonal antibody therapies (anti-drug antibodies) may give rise to low serum drug levels, loss of therapeutic response, poor drug survival and/or adverse events such as infusion reactions. To combat these, the use of concomitant MTX may attenuate the frequency of anti-drug antibodies in RA, SpA and Crohn’s disease. Although a similar effect to methotrexate has been observed with AZA usage in the management of Crohn’s disease, there is insufficient evidence to suggest that other DMARDs impact immunogenicity. In this article we review the evidence to date on the effect of immunomodulatory therapy when co-administered with anti-TNFs. We also discuss whether such a strategy should be employed in SpA and psoriasis, and if optimization of the MTX dose could improve biologic drug survival and thereby benefit disease management. Oxford University Press 2014-02 2013-08-14 /pmc/articles/PMC3894670/ /pubmed/23946436 http://dx.doi.org/10.1093/rheumatology/ket260 Text en © The Author(s) 2013. Published by Oxford University Press on behalf of the British Society to Rheumatology. http://creativecommons.org/licenses/by/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Reviews Jani, Meghna Barton, Anne Warren, Richard B. Griffiths, Christopher E. M. Chinoy, Hector The role of DMARDs in reducing the immunogenicity of TNF inhibitors in chronic inflammatory diseases |
title | The role of DMARDs in reducing the immunogenicity of TNF inhibitors in chronic inflammatory diseases |
title_full | The role of DMARDs in reducing the immunogenicity of TNF inhibitors in chronic inflammatory diseases |
title_fullStr | The role of DMARDs in reducing the immunogenicity of TNF inhibitors in chronic inflammatory diseases |
title_full_unstemmed | The role of DMARDs in reducing the immunogenicity of TNF inhibitors in chronic inflammatory diseases |
title_short | The role of DMARDs in reducing the immunogenicity of TNF inhibitors in chronic inflammatory diseases |
title_sort | role of dmards in reducing the immunogenicity of tnf inhibitors in chronic inflammatory diseases |
topic | Reviews |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3894670/ https://www.ncbi.nlm.nih.gov/pubmed/23946436 http://dx.doi.org/10.1093/rheumatology/ket260 |
work_keys_str_mv | AT janimeghna theroleofdmardsinreducingtheimmunogenicityoftnfinhibitorsinchronicinflammatorydiseases AT bartonanne theroleofdmardsinreducingtheimmunogenicityoftnfinhibitorsinchronicinflammatorydiseases AT warrenrichardb theroleofdmardsinreducingtheimmunogenicityoftnfinhibitorsinchronicinflammatorydiseases AT griffithschristopherem theroleofdmardsinreducingtheimmunogenicityoftnfinhibitorsinchronicinflammatorydiseases AT chinoyhector theroleofdmardsinreducingtheimmunogenicityoftnfinhibitorsinchronicinflammatorydiseases AT janimeghna roleofdmardsinreducingtheimmunogenicityoftnfinhibitorsinchronicinflammatorydiseases AT bartonanne roleofdmardsinreducingtheimmunogenicityoftnfinhibitorsinchronicinflammatorydiseases AT warrenrichardb roleofdmardsinreducingtheimmunogenicityoftnfinhibitorsinchronicinflammatorydiseases AT griffithschristopherem roleofdmardsinreducingtheimmunogenicityoftnfinhibitorsinchronicinflammatorydiseases AT chinoyhector roleofdmardsinreducingtheimmunogenicityoftnfinhibitorsinchronicinflammatorydiseases |