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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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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. |
format | Online Article Text |
id | pubmed-5351193 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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