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CD164 and FCRL3 are highly expressed on CD4+CD26-T cells in Sézary syndrome patients
Sézary syndrome (SS) cells express cell surface molecules also found on normal activated CD4 T cells. In an effort to find a more specific surface marker for malignant SS cells, a microarray analysis of gene expression was performed. Results showed significantly increased levels of mRNA for CD164, a...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3869886/ https://www.ncbi.nlm.nih.gov/pubmed/23792457 http://dx.doi.org/10.1038/jid.2013.279 |
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author | Wysocka, Maria Kossenkov, Andrew V. Benoit, Bernice M. Troxel, Andrea B. Singer, Elisha Schaffer, Andras Kim, Brian Dentchev, Tzvete Nagata, Satoshi Ise, Tomoko Showe, Louise C. Rook, Alain H. |
author_facet | Wysocka, Maria Kossenkov, Andrew V. Benoit, Bernice M. Troxel, Andrea B. Singer, Elisha Schaffer, Andras Kim, Brian Dentchev, Tzvete Nagata, Satoshi Ise, Tomoko Showe, Louise C. Rook, Alain H. |
author_sort | Wysocka, Maria |
collection | PubMed |
description | Sézary syndrome (SS) cells express cell surface molecules also found on normal activated CD4 T cells. In an effort to find a more specific surface marker for malignant SS cells, a microarray analysis of gene expression was performed. Results showed significantly increased levels of mRNA for CD164, a sialomucin found on human CD34+ hematopoietic stem cells, and FCRL3, a molecule present on a subset of human natural T regulatory cells. Both markers were increased in CD4 T cells from SS patients compared to healthy donors. Flow cytometry studies confirmed the increased expression of CD164 and FCRL3 primarily on CD4+CD26− T cells of SS patients. Importantly, a statistically significant correlation was found between an elevated percentage of CD4+CD164+ T cells and an elevated percentage of CD4+CD26− T cells in all tested SS patients but not in patients with Mycosis Fungoides and atopic dermatitis or healthy donors. FCRL3 expression was significantly increased only in high tumor burden patients. CD4+CD164+ cells displayed cerebriform morphology and their loss correlated with clinical improvement in treated patients. Our results suggest that CD164 can serve as a marker for diagnosis and for monitoring progression of CTCL/SS and that FCRL3 expression correlates with a high circulating tumor burden. |
format | Online Article Text |
id | pubmed-3869886 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
record_format | MEDLINE/PubMed |
spelling | pubmed-38698862014-07-01 CD164 and FCRL3 are highly expressed on CD4+CD26-T cells in Sézary syndrome patients Wysocka, Maria Kossenkov, Andrew V. Benoit, Bernice M. Troxel, Andrea B. Singer, Elisha Schaffer, Andras Kim, Brian Dentchev, Tzvete Nagata, Satoshi Ise, Tomoko Showe, Louise C. Rook, Alain H. J Invest Dermatol Article Sézary syndrome (SS) cells express cell surface molecules also found on normal activated CD4 T cells. In an effort to find a more specific surface marker for malignant SS cells, a microarray analysis of gene expression was performed. Results showed significantly increased levels of mRNA for CD164, a sialomucin found on human CD34+ hematopoietic stem cells, and FCRL3, a molecule present on a subset of human natural T regulatory cells. Both markers were increased in CD4 T cells from SS patients compared to healthy donors. Flow cytometry studies confirmed the increased expression of CD164 and FCRL3 primarily on CD4+CD26− T cells of SS patients. Importantly, a statistically significant correlation was found between an elevated percentage of CD4+CD164+ T cells and an elevated percentage of CD4+CD26− T cells in all tested SS patients but not in patients with Mycosis Fungoides and atopic dermatitis or healthy donors. FCRL3 expression was significantly increased only in high tumor burden patients. CD4+CD164+ cells displayed cerebriform morphology and their loss correlated with clinical improvement in treated patients. Our results suggest that CD164 can serve as a marker for diagnosis and for monitoring progression of CTCL/SS and that FCRL3 expression correlates with a high circulating tumor burden. 2013-06-21 2014-01 /pmc/articles/PMC3869886/ /pubmed/23792457 http://dx.doi.org/10.1038/jid.2013.279 Text en http://www.nature.com/authors/editorial_policies/license.html#terms Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Wysocka, Maria Kossenkov, Andrew V. Benoit, Bernice M. Troxel, Andrea B. Singer, Elisha Schaffer, Andras Kim, Brian Dentchev, Tzvete Nagata, Satoshi Ise, Tomoko Showe, Louise C. Rook, Alain H. CD164 and FCRL3 are highly expressed on CD4+CD26-T cells in Sézary syndrome patients |
title | CD164 and FCRL3 are highly expressed on CD4+CD26-T cells in Sézary syndrome patients |
title_full | CD164 and FCRL3 are highly expressed on CD4+CD26-T cells in Sézary syndrome patients |
title_fullStr | CD164 and FCRL3 are highly expressed on CD4+CD26-T cells in Sézary syndrome patients |
title_full_unstemmed | CD164 and FCRL3 are highly expressed on CD4+CD26-T cells in Sézary syndrome patients |
title_short | CD164 and FCRL3 are highly expressed on CD4+CD26-T cells in Sézary syndrome patients |
title_sort | cd164 and fcrl3 are highly expressed on cd4+cd26-t cells in sézary syndrome patients |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3869886/ https://www.ncbi.nlm.nih.gov/pubmed/23792457 http://dx.doi.org/10.1038/jid.2013.279 |
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