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MicroRNA expression profiles in human CD3(+) T cells following stimulation with anti-human CD3 antibodies

BACKGROUND: Anti-CD3 therapy can induce immunosuppression by several non mutually exclusive mechanisms that have been proposed to explain the therapeutic effect the administration anti-CD3 mAb, but its immunoregulatory mechanism is still not completely clear. In T cells, microRNAs (miRNAs) regulate...

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Autores principales: Sousa, Isabel Garcia, do Almo, Manuela Maragno, Simi, Kelly Cristina Rodrigues, Bezerra, Maryani Andressa Gomes, Andrade, Rosângela Vieira, Maranhão, Andréa Queiroz, Brigido, Marcelo Macedo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5351193/
https://www.ncbi.nlm.nih.gov/pubmed/28292330
http://dx.doi.org/10.1186/s13104-017-2442-y
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author Sousa, Isabel Garcia
do Almo, Manuela Maragno
Simi, Kelly Cristina Rodrigues
Bezerra, Maryani Andressa Gomes
Andrade, Rosângela Vieira
Maranhão, Andréa Queiroz
Brigido, Marcelo Macedo
author_facet Sousa, Isabel Garcia
do Almo, Manuela Maragno
Simi, Kelly Cristina Rodrigues
Bezerra, Maryani Andressa Gomes
Andrade, Rosângela Vieira
Maranhão, Andréa Queiroz
Brigido, Marcelo Macedo
author_sort Sousa, Isabel Garcia
collection PubMed
description BACKGROUND: Anti-CD3 therapy can induce immunosuppression by several non mutually exclusive mechanisms that have been proposed to explain the therapeutic effect the administration anti-CD3 mAb, but its immunoregulatory mechanism is still not completely clear. In T cells, microRNAs (miRNAs) regulate several pathways, including those associated with immune tolerance. Here, we report changes in miRNA expression in T cells following treatment with anti-human CD3 antibodies. Peripheral blood mononuclear cells were cultured in the presence of the monoclonal antibody OKT3 or a recombinant fragment of humanized anti-CD3. Following these treatments, the expression profiles of 31 miRNA species were assessed in T cells using TaqMan arrays. RESULTS: Eight of the tested miRNAs (miR-155, miR-21, miR-146a, miR-210, miR-17, miR-590-5p, miR-106b and miR-301a) were statistically significantly up- or down-regulated relative to untreated cells. CONCLUSIONS: Stimulation of T cells with anti-human CD3 antibodies alters miRNA expression patterns, including of miRNA species associated with immune regulatory pathways. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13104-017-2442-y) contains supplementary material, which is available to authorized users.
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spelling pubmed-53511932017-03-17 MicroRNA expression profiles in human CD3(+) T cells following stimulation with anti-human CD3 antibodies Sousa, Isabel Garcia do Almo, Manuela Maragno Simi, Kelly Cristina Rodrigues Bezerra, Maryani Andressa Gomes Andrade, Rosângela Vieira Maranhão, Andréa Queiroz Brigido, Marcelo Macedo BMC Res Notes Short Report BACKGROUND: Anti-CD3 therapy can induce immunosuppression by several non mutually exclusive mechanisms that have been proposed to explain the therapeutic effect the administration anti-CD3 mAb, but its immunoregulatory mechanism is still not completely clear. In T cells, microRNAs (miRNAs) regulate several pathways, including those associated with immune tolerance. Here, we report changes in miRNA expression in T cells following treatment with anti-human CD3 antibodies. Peripheral blood mononuclear cells were cultured in the presence of the monoclonal antibody OKT3 or a recombinant fragment of humanized anti-CD3. Following these treatments, the expression profiles of 31 miRNA species were assessed in T cells using TaqMan arrays. RESULTS: Eight of the tested miRNAs (miR-155, miR-21, miR-146a, miR-210, miR-17, miR-590-5p, miR-106b and miR-301a) were statistically significantly up- or down-regulated relative to untreated cells. CONCLUSIONS: Stimulation of T cells with anti-human CD3 antibodies alters miRNA expression patterns, including of miRNA species associated with immune regulatory pathways. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13104-017-2442-y) contains supplementary material, which is available to authorized users. BioMed Central 2017-03-14 /pmc/articles/PMC5351193/ /pubmed/28292330 http://dx.doi.org/10.1186/s13104-017-2442-y Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Short Report
Sousa, Isabel Garcia
do Almo, Manuela Maragno
Simi, Kelly Cristina Rodrigues
Bezerra, Maryani Andressa Gomes
Andrade, Rosângela Vieira
Maranhão, Andréa Queiroz
Brigido, Marcelo Macedo
MicroRNA expression profiles in human CD3(+) T cells following stimulation with anti-human CD3 antibodies
title MicroRNA expression profiles in human CD3(+) T cells following stimulation with anti-human CD3 antibodies
title_full MicroRNA expression profiles in human CD3(+) T cells following stimulation with anti-human CD3 antibodies
title_fullStr MicroRNA expression profiles in human CD3(+) T cells following stimulation with anti-human CD3 antibodies
title_full_unstemmed MicroRNA expression profiles in human CD3(+) T cells following stimulation with anti-human CD3 antibodies
title_short MicroRNA expression profiles in human CD3(+) T cells following stimulation with anti-human CD3 antibodies
title_sort microrna expression profiles in human cd3(+) t cells following stimulation with anti-human cd3 antibodies
topic Short Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5351193/
https://www.ncbi.nlm.nih.gov/pubmed/28292330
http://dx.doi.org/10.1186/s13104-017-2442-y
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