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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...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2013
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.
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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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