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The effects of infliximab therapy on the serum proteome of rheumatoid arthritis patients
INTRODUCTION: Although the clinical effects of infliximab therapy in rheumatoid arthritis have been documented extensively, the biological effects of this intervention continue to be defined. We sought to examine the impact of infliximab therapy on the serum proteome of rheumatoid arthritis patients...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2688177/ https://www.ncbi.nlm.nih.gov/pubmed/19265537 http://dx.doi.org/10.1186/ar2637 |
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author | Dwivedi, Ravi C Dhindsa, Navjot Krokhin, Oleg V Cortens, John Wilkins, John A El-Gabalawy, Hani S |
author_facet | Dwivedi, Ravi C Dhindsa, Navjot Krokhin, Oleg V Cortens, John Wilkins, John A El-Gabalawy, Hani S |
author_sort | Dwivedi, Ravi C |
collection | PubMed |
description | INTRODUCTION: Although the clinical effects of infliximab therapy in rheumatoid arthritis have been documented extensively, the biological effects of this intervention continue to be defined. We sought to examine the impact of infliximab therapy on the serum proteome of rheumatoid arthritis patients by means of a mass spectrometry-based approach. METHODS: Sera from 10 patients with rheumatoid arthritis were obtained prior to and following 12 weeks of infliximab therapy using a standard clinical protocol. The sera were immunodepleted of the 12 highest abundance proteins, labeled by the iTRAQ (isobaric tagging for relative and absolute protein quantification) technique, and analyzed by mass spectrometry to identify proteomic changes associated with treatment. RESULTS: An average of 373 distinct proteins were identified per patient with greater than 95% confidence. In the 3 patients demonstrating the most robust clinical responses, changes of greater than 20% in the serum levels were observed in 39 proteins following treatment. The majority of these proteins were regulated directly or indirectly by tumour necrosis factor-alpha (TNF-α) and nuclear factor-kappa-B, with acute-phase proteins being uniformly down-regulated. A number of proteins, including members of the SERPIN family and S100A8, were down-regulated irrespective of clinical response. CONCLUSIONS: The present study demonstrates that a robust clinical response to infliximab is associated with the down-regulation of a spectrum of serum proteins regulated by TNF-α, and provides a possible basis for defining the broader biological effects of the treatment in vivo. |
format | Text |
id | pubmed-2688177 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-26881772009-05-29 The effects of infliximab therapy on the serum proteome of rheumatoid arthritis patients Dwivedi, Ravi C Dhindsa, Navjot Krokhin, Oleg V Cortens, John Wilkins, John A El-Gabalawy, Hani S Arthritis Res Ther Research Article INTRODUCTION: Although the clinical effects of infliximab therapy in rheumatoid arthritis have been documented extensively, the biological effects of this intervention continue to be defined. We sought to examine the impact of infliximab therapy on the serum proteome of rheumatoid arthritis patients by means of a mass spectrometry-based approach. METHODS: Sera from 10 patients with rheumatoid arthritis were obtained prior to and following 12 weeks of infliximab therapy using a standard clinical protocol. The sera were immunodepleted of the 12 highest abundance proteins, labeled by the iTRAQ (isobaric tagging for relative and absolute protein quantification) technique, and analyzed by mass spectrometry to identify proteomic changes associated with treatment. RESULTS: An average of 373 distinct proteins were identified per patient with greater than 95% confidence. In the 3 patients demonstrating the most robust clinical responses, changes of greater than 20% in the serum levels were observed in 39 proteins following treatment. The majority of these proteins were regulated directly or indirectly by tumour necrosis factor-alpha (TNF-α) and nuclear factor-kappa-B, with acute-phase proteins being uniformly down-regulated. A number of proteins, including members of the SERPIN family and S100A8, were down-regulated irrespective of clinical response. CONCLUSIONS: The present study demonstrates that a robust clinical response to infliximab is associated with the down-regulation of a spectrum of serum proteins regulated by TNF-α, and provides a possible basis for defining the broader biological effects of the treatment in vivo. BioMed Central 2009 2009-03-06 /pmc/articles/PMC2688177/ /pubmed/19265537 http://dx.doi.org/10.1186/ar2637 Text en Copyright © 2009 Dwivedi et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Dwivedi, Ravi C Dhindsa, Navjot Krokhin, Oleg V Cortens, John Wilkins, John A El-Gabalawy, Hani S The effects of infliximab therapy on the serum proteome of rheumatoid arthritis patients |
title | The effects of infliximab therapy on the serum proteome of rheumatoid arthritis patients |
title_full | The effects of infliximab therapy on the serum proteome of rheumatoid arthritis patients |
title_fullStr | The effects of infliximab therapy on the serum proteome of rheumatoid arthritis patients |
title_full_unstemmed | The effects of infliximab therapy on the serum proteome of rheumatoid arthritis patients |
title_short | The effects of infliximab therapy on the serum proteome of rheumatoid arthritis patients |
title_sort | effects of infliximab therapy on the serum proteome of rheumatoid arthritis patients |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2688177/ https://www.ncbi.nlm.nih.gov/pubmed/19265537 http://dx.doi.org/10.1186/ar2637 |
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