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Going Further: Comprehensive Disease Control of Rheumatoid Arthritis, Targeting Cytokines and Chemokines

OBJECTIVES: Mechanism of action of biological and synthetic disease-modifying antirheumatic drugs (DMARDs) includes the inhibition of specific proinflammatory cytokines. This study aimed to elucidate the cytokines and chemokines inhibited by different treatments (conventional synthetic DMARD [csDMAR...

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Autores principales: Chavarria-Avila, Efrain, Vazquez-Del Mercado, Monica, Pizano-Martínez, Oscar, Roman-Lugo, German, Arrona-Rios, Karla, Perez-Vazquez, Felipe, De-La-Cruz, Jeniffer P., Calderon-Espinoza, Ivette, Aguilar-Vazquez, Andrea, Esesarte-Rodriguez, Marisol, Rubio-Arrellano, Edy D., Duran-Barragan, Sergio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8612915/
https://www.ncbi.nlm.nih.gov/pubmed/32694349
http://dx.doi.org/10.1097/RHU.0000000000001515
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author Chavarria-Avila, Efrain
Vazquez-Del Mercado, Monica
Pizano-Martínez, Oscar
Roman-Lugo, German
Arrona-Rios, Karla
Perez-Vazquez, Felipe
De-La-Cruz, Jeniffer P.
Calderon-Espinoza, Ivette
Aguilar-Vazquez, Andrea
Esesarte-Rodriguez, Marisol
Rubio-Arrellano, Edy D.
Duran-Barragan, Sergio
author_facet Chavarria-Avila, Efrain
Vazquez-Del Mercado, Monica
Pizano-Martínez, Oscar
Roman-Lugo, German
Arrona-Rios, Karla
Perez-Vazquez, Felipe
De-La-Cruz, Jeniffer P.
Calderon-Espinoza, Ivette
Aguilar-Vazquez, Andrea
Esesarte-Rodriguez, Marisol
Rubio-Arrellano, Edy D.
Duran-Barragan, Sergio
author_sort Chavarria-Avila, Efrain
collection PubMed
description OBJECTIVES: Mechanism of action of biological and synthetic disease-modifying antirheumatic drugs (DMARDs) includes the inhibition of specific proinflammatory cytokines. This study aimed to elucidate the cytokines and chemokines inhibited by different treatments (conventional synthetic DMARD [csDMARD], biological and targeted synthetic DMARD) in rheumatoid arthritis (RA). METHODS: Fifty-nine RA patients with low disease activity or remission included in a cross-sectional study were classified by treatment in groups: abatacept, certolizumab, rituximab (RTX), tocilizumab, tofacitinib (TOF), baricitinib (BAR), and csDMARD. Cytokine and chemokine serum levels were measured by LEGENDplex Human Inflammation panel. Quantitative variables were compared using Student t or Mann-Whitney U test as appropriate, whereas qualitative variables were compared using χ(2) or Fisher exact test. p < 0.05 was considered significant. RESULTS: Certolizumab, RTX, tocilizumab, and TOF showed that most cytokine pathways inhibited: tumor necrosis factor α, interferon γ, interleukin 1β (IL-1β), IL-12, IL-18, and IL-23; in addition, csDMARDs showed a similar inhibition patron except for IL-23. Serum level of tumor necrosis factor α pathway was one of the most inhibited being undetectable in RTX, TOF, and BAR groups. Interleukin 6 was shown to be inhibited by abatacept, RTX, and TOF; however, higher levels were observed in 3 patients treated with tocilizumab. Abatacept, certolizumab, RTX, and TOF downregulated IL-10 in this group of patients but remained detectable in almost half of the subjects, with the highest levels in the BAR group. The active pathways that remained the most were CC chemokine ligand 2, IL-8, IL-17, and IL-33. CONCLUSIONS: Understanding the cytokine chemokine pathways inhibition could help rheumatologists to prescribe a tailored therapy using the arsenal of DMARDs for individualized RA treatment in an evidence-based decision manner.
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spelling pubmed-86129152021-11-29 Going Further: Comprehensive Disease Control of Rheumatoid Arthritis, Targeting Cytokines and Chemokines Chavarria-Avila, Efrain Vazquez-Del Mercado, Monica Pizano-Martínez, Oscar Roman-Lugo, German Arrona-Rios, Karla Perez-Vazquez, Felipe De-La-Cruz, Jeniffer P. Calderon-Espinoza, Ivette Aguilar-Vazquez, Andrea Esesarte-Rodriguez, Marisol Rubio-Arrellano, Edy D. Duran-Barragan, Sergio J Clin Rheumatol Original Articles OBJECTIVES: Mechanism of action of biological and synthetic disease-modifying antirheumatic drugs (DMARDs) includes the inhibition of specific proinflammatory cytokines. This study aimed to elucidate the cytokines and chemokines inhibited by different treatments (conventional synthetic DMARD [csDMARD], biological and targeted synthetic DMARD) in rheumatoid arthritis (RA). METHODS: Fifty-nine RA patients with low disease activity or remission included in a cross-sectional study were classified by treatment in groups: abatacept, certolizumab, rituximab (RTX), tocilizumab, tofacitinib (TOF), baricitinib (BAR), and csDMARD. Cytokine and chemokine serum levels were measured by LEGENDplex Human Inflammation panel. Quantitative variables were compared using Student t or Mann-Whitney U test as appropriate, whereas qualitative variables were compared using χ(2) or Fisher exact test. p < 0.05 was considered significant. RESULTS: Certolizumab, RTX, tocilizumab, and TOF showed that most cytokine pathways inhibited: tumor necrosis factor α, interferon γ, interleukin 1β (IL-1β), IL-12, IL-18, and IL-23; in addition, csDMARDs showed a similar inhibition patron except for IL-23. Serum level of tumor necrosis factor α pathway was one of the most inhibited being undetectable in RTX, TOF, and BAR groups. Interleukin 6 was shown to be inhibited by abatacept, RTX, and TOF; however, higher levels were observed in 3 patients treated with tocilizumab. Abatacept, certolizumab, RTX, and TOF downregulated IL-10 in this group of patients but remained detectable in almost half of the subjects, with the highest levels in the BAR group. The active pathways that remained the most were CC chemokine ligand 2, IL-8, IL-17, and IL-33. CONCLUSIONS: Understanding the cytokine chemokine pathways inhibition could help rheumatologists to prescribe a tailored therapy using the arsenal of DMARDs for individualized RA treatment in an evidence-based decision manner. Lippincott Williams & Wilkins 2021-12 2020-07-21 /pmc/articles/PMC8612915/ /pubmed/32694349 http://dx.doi.org/10.1097/RHU.0000000000001515 Text en Copyright © 2020 The Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) , where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal.
spellingShingle Original Articles
Chavarria-Avila, Efrain
Vazquez-Del Mercado, Monica
Pizano-Martínez, Oscar
Roman-Lugo, German
Arrona-Rios, Karla
Perez-Vazquez, Felipe
De-La-Cruz, Jeniffer P.
Calderon-Espinoza, Ivette
Aguilar-Vazquez, Andrea
Esesarte-Rodriguez, Marisol
Rubio-Arrellano, Edy D.
Duran-Barragan, Sergio
Going Further: Comprehensive Disease Control of Rheumatoid Arthritis, Targeting Cytokines and Chemokines
title Going Further: Comprehensive Disease Control of Rheumatoid Arthritis, Targeting Cytokines and Chemokines
title_full Going Further: Comprehensive Disease Control of Rheumatoid Arthritis, Targeting Cytokines and Chemokines
title_fullStr Going Further: Comprehensive Disease Control of Rheumatoid Arthritis, Targeting Cytokines and Chemokines
title_full_unstemmed Going Further: Comprehensive Disease Control of Rheumatoid Arthritis, Targeting Cytokines and Chemokines
title_short Going Further: Comprehensive Disease Control of Rheumatoid Arthritis, Targeting Cytokines and Chemokines
title_sort going further: comprehensive disease control of rheumatoid arthritis, targeting cytokines and chemokines
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8612915/
https://www.ncbi.nlm.nih.gov/pubmed/32694349
http://dx.doi.org/10.1097/RHU.0000000000001515
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