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Expression of NK (CD16+56+) and B cells (CD19) Receptor Molecules as a Reliable Clinical Response Biomarkers of SLE and RA Patients Under the Rituximab Treatment
INTRODUCTION: Lately, the use of biological therapy in various autoimmune diseases is increasing. The ideal marker for monitoring the effects of modern therapy is still non-existent. AIM: To investigate early response biomarkers of SLE and RA patients under the rituximab treatment are in research ph...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Academy of Medical Sciences of Bosnia and Herzegovina
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7007611/ https://www.ncbi.nlm.nih.gov/pubmed/32082002 http://dx.doi.org/10.5455/medarh.2019.73.374-377 |
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author | Zecevic, Lamija Mekic, Mevludin Subasic, Djemo Hadziabulic, Majda Isak, Edmira Subasic, Emina Selmanovic, Kenan |
author_facet | Zecevic, Lamija Mekic, Mevludin Subasic, Djemo Hadziabulic, Majda Isak, Edmira Subasic, Emina Selmanovic, Kenan |
author_sort | Zecevic, Lamija |
collection | PubMed |
description | INTRODUCTION: Lately, the use of biological therapy in various autoimmune diseases is increasing. The ideal marker for monitoring the effects of modern therapy is still non-existent. AIM: To investigate early response biomarkers of SLE and RA patients under the rituximab treatment are in research phase and each new investigations offer new and original useful data. MATERIAL AND METHODS: Immunophenotyping of cells was carried out by a standard method of sample preparation. We investigated by flow cytometric analyses expression of NK and CD19+ cells at ten SLE and five RA patients before and after treatment with rituximab, in laboratory of Department of Clinical immunology in the Clinical Centre University of Sarajevo. RESULTS: In both cases, SLE and RA patients, reduced number of CD16+ parameter indicates lower cytotoxic activity of NK cells. Increased number of B cells indicates higher pathological activity leading to severe autoimmune disease allegation. CONCLUSION: Determining the proportion of NK and B will be useful diagnostic tool in therapeutic strategy, and also in monitoring of effect of biological therapy. |
format | Online Article Text |
id | pubmed-7007611 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Academy of Medical Sciences of Bosnia and Herzegovina |
record_format | MEDLINE/PubMed |
spelling | pubmed-70076112020-02-20 Expression of NK (CD16+56+) and B cells (CD19) Receptor Molecules as a Reliable Clinical Response Biomarkers of SLE and RA Patients Under the Rituximab Treatment Zecevic, Lamija Mekic, Mevludin Subasic, Djemo Hadziabulic, Majda Isak, Edmira Subasic, Emina Selmanovic, Kenan Med Arch Original Paper INTRODUCTION: Lately, the use of biological therapy in various autoimmune diseases is increasing. The ideal marker for monitoring the effects of modern therapy is still non-existent. AIM: To investigate early response biomarkers of SLE and RA patients under the rituximab treatment are in research phase and each new investigations offer new and original useful data. MATERIAL AND METHODS: Immunophenotyping of cells was carried out by a standard method of sample preparation. We investigated by flow cytometric analyses expression of NK and CD19+ cells at ten SLE and five RA patients before and after treatment with rituximab, in laboratory of Department of Clinical immunology in the Clinical Centre University of Sarajevo. RESULTS: In both cases, SLE and RA patients, reduced number of CD16+ parameter indicates lower cytotoxic activity of NK cells. Increased number of B cells indicates higher pathological activity leading to severe autoimmune disease allegation. CONCLUSION: Determining the proportion of NK and B will be useful diagnostic tool in therapeutic strategy, and also in monitoring of effect of biological therapy. Academy of Medical Sciences of Bosnia and Herzegovina 2019-12 /pmc/articles/PMC7007611/ /pubmed/32082002 http://dx.doi.org/10.5455/medarh.2019.73.374-377 Text en © 2019 Lamija Zecevic, Mevludin Mekic, Djemo Subasic, Majda Hadzibulic, Edmira Isak, Emina, Kenan Selmanovic http://creativecommons.org/licenses/by-nc/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Paper Zecevic, Lamija Mekic, Mevludin Subasic, Djemo Hadziabulic, Majda Isak, Edmira Subasic, Emina Selmanovic, Kenan Expression of NK (CD16+56+) and B cells (CD19) Receptor Molecules as a Reliable Clinical Response Biomarkers of SLE and RA Patients Under the Rituximab Treatment |
title | Expression of NK (CD16+56+) and B cells (CD19) Receptor Molecules as a Reliable Clinical Response Biomarkers of SLE and RA Patients Under the Rituximab Treatment |
title_full | Expression of NK (CD16+56+) and B cells (CD19) Receptor Molecules as a Reliable Clinical Response Biomarkers of SLE and RA Patients Under the Rituximab Treatment |
title_fullStr | Expression of NK (CD16+56+) and B cells (CD19) Receptor Molecules as a Reliable Clinical Response Biomarkers of SLE and RA Patients Under the Rituximab Treatment |
title_full_unstemmed | Expression of NK (CD16+56+) and B cells (CD19) Receptor Molecules as a Reliable Clinical Response Biomarkers of SLE and RA Patients Under the Rituximab Treatment |
title_short | Expression of NK (CD16+56+) and B cells (CD19) Receptor Molecules as a Reliable Clinical Response Biomarkers of SLE and RA Patients Under the Rituximab Treatment |
title_sort | expression of nk (cd16+56+) and b cells (cd19) receptor molecules as a reliable clinical response biomarkers of sle and ra patients under the rituximab treatment |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7007611/ https://www.ncbi.nlm.nih.gov/pubmed/32082002 http://dx.doi.org/10.5455/medarh.2019.73.374-377 |
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