Unique Abnormalities of CD4 + and CD8 + Central Memory Cells Associated with Chronic Graft-versus-Host Disease Improve after Extracorporeal Photopheresis
Chronic graft-versus-host disease (cGVHD) remains a problematic complication of allogeneic hematopoietic stem cell transplantation. Laboratory parameters correlated with cGVHD have not been fully defined, although changes in CD4/CD8 ratios occur and a decrease in CD4 + central memory T cells has bee...
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creator | Yamashita, Kouhei Horwitz, Mitchell E. Kwatemaa, Akua Nomicos, Effie Castro, Kathleen Sokolic, Robert Foster, Susan F. Garofalo, Mary Choi, Uimook Ryherd, Mark Brown, Margaret R. Leitman, Susan F. Wayne, Alan S. Fowler, Daniel H. Bishop, Michael R. Childs, Richard W. Barrett, A. John Pavletic, Steven Z. Malech, Harry L. |
description | Chronic graft-versus-host disease (cGVHD) remains a problematic complication of allogeneic hematopoietic stem cell transplantation. Laboratory parameters correlated with cGVHD have not been fully defined, although changes in CD4/CD8 ratios occur and a decrease in CD4
+ central memory T cells has been noted. Extracorporeal photopheresis (ECP) is an effective therapy for steroid-refractory cGVHD. We have noted changes in lymphocyte subsets after ECP. CD4
+ and CD8
+ T-cell central and effector memory populations were enumerated by flow cytometry in a cohort of 37 patients postallogeneic transplantation with symptomatic cGVHD. Of the patients with symptomatic cGVHD, 7 were treated with ECP over 6 months and prospectively assessed for changes in lymphocyte subsets. There was a highly significant correlation of an increase in CD8
+ central memory cells and a concomitant decrease in CD4
+ central memory cells in patients with symptomatic cGVHD. These changes were not detected in patients without cGVHD posttransplantation. In all, 7 patients with cGVHD followed up prospectively during ECP treatment showed a statistically significant normalization of the pattern of CD4
+ and a trend toward normalization of CD8
+ central memory T cells coincident with improvement of cGVHD. These data indicate a high correlation between disturbances in the balance of central and effector memory populations and cGVHD suggesting use in following up responses to therapy. The normalization of central and effector memory populations in response to ECP coincident with clinical improvement of cGVHD support a correlation between these laboratory parameters and cGVHD. Further studies are needed to demonstrate whether laboratory measurements of the magnitude of changes in central and effector memory populations are useful prognostically or can be used to guide response to therapy. The contrasting change in central memory cells (CD8
+ increased versus CD4
+ decreased) in cGVHD provide support for recent reports suggesting unique differences in the differentiation pathways for CD8
+ versus CD4
+ T cells. |
doi_str_mv | 10.1016/j.bbmt.2005.11.004 |
format | Article |
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+ central memory T cells has been noted. Extracorporeal photopheresis (ECP) is an effective therapy for steroid-refractory cGVHD. We have noted changes in lymphocyte subsets after ECP. CD4
+ and CD8
+ T-cell central and effector memory populations were enumerated by flow cytometry in a cohort of 37 patients postallogeneic transplantation with symptomatic cGVHD. Of the patients with symptomatic cGVHD, 7 were treated with ECP over 6 months and prospectively assessed for changes in lymphocyte subsets. There was a highly significant correlation of an increase in CD8
+ central memory cells and a concomitant decrease in CD4
+ central memory cells in patients with symptomatic cGVHD. These changes were not detected in patients without cGVHD posttransplantation. In all, 7 patients with cGVHD followed up prospectively during ECP treatment showed a statistically significant normalization of the pattern of CD4
+ and a trend toward normalization of CD8
+ central memory T cells coincident with improvement of cGVHD. These data indicate a high correlation between disturbances in the balance of central and effector memory populations and cGVHD suggesting use in following up responses to therapy. The normalization of central and effector memory populations in response to ECP coincident with clinical improvement of cGVHD support a correlation between these laboratory parameters and cGVHD. Further studies are needed to demonstrate whether laboratory measurements of the magnitude of changes in central and effector memory populations are useful prognostically or can be used to guide response to therapy. The contrasting change in central memory cells (CD8
+ increased versus CD4
+ decreased) in cGVHD provide support for recent reports suggesting unique differences in the differentiation pathways for CD8
+ versus CD4
+ T cells.</description><identifier>ISSN: 1083-8791</identifier><identifier>EISSN: 1523-6536</identifier><identifier>DOI: 10.1016/j.bbmt.2005.11.004</identifier><identifier>PMID: 16399598</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Adult ; Alloimmune ; Bone marrow transplantation ; CD4-CD8 Ratio - methods ; CD4-Positive T-Lymphocytes - immunology ; CD4-Positive T-Lymphocytes - pathology ; CD8-Positive T-Lymphocytes - immunology ; CD8-Positive T-Lymphocytes - pathology ; Cell Differentiation - drug effects ; Cell Differentiation - immunology ; Central memory T cell ; Chronic Disease ; Chronic GVHD ; Cohort Studies ; Extracorporeal photopheresis ; Female ; Graft vs Host Disease - blood ; Graft vs Host Disease - immunology ; Graft vs Host Disease - pathology ; Hematologic Neoplasms - blood ; Hematologic Neoplasms - immunology ; Hematologic Neoplasms - pathology ; Hematologic Neoplasms - therapy ; Hematopoietic Stem Cell Transplantation ; Humans ; Immunologic Memory - drug effects ; Immunologic Memory - immunology ; Male ; Middle Aged ; PUVA Therapy - methods ; Transplantation, Homologous</subject><ispartof>Biology of blood and marrow transplantation, 2006, Vol.12 (1), p.22-30</ispartof><rights>2006 American Society for Blood and Marrow Transplantation</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c398t-9e7a8992e5677681f72d0dd5f24f02e6e5eadbbb8702db14f94d2dc9878f31193</citedby><cites>FETCH-LOGICAL-c398t-9e7a8992e5677681f72d0dd5f24f02e6e5eadbbb8702db14f94d2dc9878f31193</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1083879105007755$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>314,776,780,3537,4010,27900,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16399598$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yamashita, Kouhei</creatorcontrib><creatorcontrib>Horwitz, Mitchell E.</creatorcontrib><creatorcontrib>Kwatemaa, Akua</creatorcontrib><creatorcontrib>Nomicos, Effie</creatorcontrib><creatorcontrib>Castro, Kathleen</creatorcontrib><creatorcontrib>Sokolic, Robert</creatorcontrib><creatorcontrib>Foster, Susan F.</creatorcontrib><creatorcontrib>Garofalo, Mary</creatorcontrib><creatorcontrib>Choi, Uimook</creatorcontrib><creatorcontrib>Ryherd, Mark</creatorcontrib><creatorcontrib>Brown, Margaret R.</creatorcontrib><creatorcontrib>Leitman, Susan F.</creatorcontrib><creatorcontrib>Wayne, Alan S.</creatorcontrib><creatorcontrib>Fowler, Daniel H.</creatorcontrib><creatorcontrib>Bishop, Michael R.</creatorcontrib><creatorcontrib>Childs, Richard W.</creatorcontrib><creatorcontrib>Barrett, A. John</creatorcontrib><creatorcontrib>Pavletic, Steven Z.</creatorcontrib><creatorcontrib>Malech, Harry L.</creatorcontrib><title>Unique Abnormalities of CD4 + and CD8 + Central Memory Cells Associated with Chronic Graft-versus-Host Disease Improve after Extracorporeal Photopheresis</title><title>Biology of blood and marrow transplantation</title><addtitle>Biol Blood Marrow Transplant</addtitle><description>Chronic graft-versus-host disease (cGVHD) remains a problematic complication of allogeneic hematopoietic stem cell transplantation. Laboratory parameters correlated with cGVHD have not been fully defined, although changes in CD4/CD8 ratios occur and a decrease in CD4
+ central memory T cells has been noted. Extracorporeal photopheresis (ECP) is an effective therapy for steroid-refractory cGVHD. We have noted changes in lymphocyte subsets after ECP. CD4
+ and CD8
+ T-cell central and effector memory populations were enumerated by flow cytometry in a cohort of 37 patients postallogeneic transplantation with symptomatic cGVHD. Of the patients with symptomatic cGVHD, 7 were treated with ECP over 6 months and prospectively assessed for changes in lymphocyte subsets. There was a highly significant correlation of an increase in CD8
+ central memory cells and a concomitant decrease in CD4
+ central memory cells in patients with symptomatic cGVHD. These changes were not detected in patients without cGVHD posttransplantation. In all, 7 patients with cGVHD followed up prospectively during ECP treatment showed a statistically significant normalization of the pattern of CD4
+ and a trend toward normalization of CD8
+ central memory T cells coincident with improvement of cGVHD. These data indicate a high correlation between disturbances in the balance of central and effector memory populations and cGVHD suggesting use in following up responses to therapy. The normalization of central and effector memory populations in response to ECP coincident with clinical improvement of cGVHD support a correlation between these laboratory parameters and cGVHD. Further studies are needed to demonstrate whether laboratory measurements of the magnitude of changes in central and effector memory populations are useful prognostically or can be used to guide response to therapy. The contrasting change in central memory cells (CD8
+ increased versus CD4
+ decreased) in cGVHD provide support for recent reports suggesting unique differences in the differentiation pathways for CD8
+ versus CD4
+ T cells.</description><subject>Adult</subject><subject>Alloimmune</subject><subject>Bone marrow transplantation</subject><subject>CD4-CD8 Ratio - methods</subject><subject>CD4-Positive T-Lymphocytes - immunology</subject><subject>CD4-Positive T-Lymphocytes - pathology</subject><subject>CD8-Positive T-Lymphocytes - immunology</subject><subject>CD8-Positive T-Lymphocytes - pathology</subject><subject>Cell Differentiation - drug effects</subject><subject>Cell Differentiation - immunology</subject><subject>Central memory T cell</subject><subject>Chronic Disease</subject><subject>Chronic GVHD</subject><subject>Cohort Studies</subject><subject>Extracorporeal photopheresis</subject><subject>Female</subject><subject>Graft vs Host Disease - blood</subject><subject>Graft vs Host Disease - immunology</subject><subject>Graft vs Host Disease - pathology</subject><subject>Hematologic Neoplasms - blood</subject><subject>Hematologic Neoplasms - immunology</subject><subject>Hematologic Neoplasms - pathology</subject><subject>Hematologic Neoplasms - therapy</subject><subject>Hematopoietic Stem Cell Transplantation</subject><subject>Humans</subject><subject>Immunologic Memory - drug effects</subject><subject>Immunologic Memory - immunology</subject><subject>Male</subject><subject>Middle Aged</subject><subject>PUVA Therapy - methods</subject><subject>Transplantation, Homologous</subject><issn>1083-8791</issn><issn>1523-6536</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kU1v1DAQhiMEoqXtH-CAfOKCEux8-EPiskpLW6lVOdCz5dgTrVdJvHi8W_pT-Ld4tStx4zTvyO88mvFbFB8ZrRhl_OumGoY5VTWlXcVYRWn7pjhnXd2UvGv426ypbEopFDsrPiBuKKWilep9ccZ4o1Sn5Hnx53nxv3ZAVsMS4mwmnzwgCSPpr1vyhZjFZSWz6mFJ0UzkEeYQX3M7TUhWiMF6k8CRF5_WpF_HsHhLbqMZU7mHiDss7wImcu0RDAK5n7cx7IHkd4jk5ndm2hC3IUJm_1iHFLZriIAeL4t3o5kQrk71onj-fvOzvysfnm7v-9VDaRslU6lAGKlUDR0Xgks2itpR57qxbkdaA4cOjBuGQQpau4G1o2pd7aySQo4NY6q5KD4fuXmx_BOY9OzR5vPMAmGHmgvOuOJNNtZHo40BMcKot9HPJr5qRvUhEL3Rh0D0IRDNmM6B5KFPJ_pumMH9GzklkA3fjgbIN-49RI3Ww2LB-Qg2aRf8__h_Ac8-ngE</recordid><startdate>2006</startdate><enddate>2006</enddate><creator>Yamashita, Kouhei</creator><creator>Horwitz, Mitchell E.</creator><creator>Kwatemaa, Akua</creator><creator>Nomicos, Effie</creator><creator>Castro, Kathleen</creator><creator>Sokolic, Robert</creator><creator>Foster, Susan F.</creator><creator>Garofalo, Mary</creator><creator>Choi, Uimook</creator><creator>Ryherd, Mark</creator><creator>Brown, Margaret R.</creator><creator>Leitman, Susan F.</creator><creator>Wayne, Alan S.</creator><creator>Fowler, Daniel H.</creator><creator>Bishop, Michael R.</creator><creator>Childs, Richard W.</creator><creator>Barrett, A. 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John</creatorcontrib><creatorcontrib>Pavletic, Steven Z.</creatorcontrib><creatorcontrib>Malech, Harry L.</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Biology of blood and marrow transplantation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yamashita, Kouhei</au><au>Horwitz, Mitchell E.</au><au>Kwatemaa, Akua</au><au>Nomicos, Effie</au><au>Castro, Kathleen</au><au>Sokolic, Robert</au><au>Foster, Susan F.</au><au>Garofalo, Mary</au><au>Choi, Uimook</au><au>Ryherd, Mark</au><au>Brown, Margaret R.</au><au>Leitman, Susan F.</au><au>Wayne, Alan S.</au><au>Fowler, Daniel H.</au><au>Bishop, Michael R.</au><au>Childs, Richard W.</au><au>Barrett, A. John</au><au>Pavletic, Steven Z.</au><au>Malech, Harry L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Unique Abnormalities of CD4 + and CD8 + Central Memory Cells Associated with Chronic Graft-versus-Host Disease Improve after Extracorporeal Photopheresis</atitle><jtitle>Biology of blood and marrow transplantation</jtitle><addtitle>Biol Blood Marrow Transplant</addtitle><date>2006</date><risdate>2006</risdate><volume>12</volume><issue>1</issue><spage>22</spage><epage>30</epage><pages>22-30</pages><issn>1083-8791</issn><eissn>1523-6536</eissn><abstract>Chronic graft-versus-host disease (cGVHD) remains a problematic complication of allogeneic hematopoietic stem cell transplantation. Laboratory parameters correlated with cGVHD have not been fully defined, although changes in CD4/CD8 ratios occur and a decrease in CD4
+ central memory T cells has been noted. Extracorporeal photopheresis (ECP) is an effective therapy for steroid-refractory cGVHD. We have noted changes in lymphocyte subsets after ECP. CD4
+ and CD8
+ T-cell central and effector memory populations were enumerated by flow cytometry in a cohort of 37 patients postallogeneic transplantation with symptomatic cGVHD. Of the patients with symptomatic cGVHD, 7 were treated with ECP over 6 months and prospectively assessed for changes in lymphocyte subsets. There was a highly significant correlation of an increase in CD8
+ central memory cells and a concomitant decrease in CD4
+ central memory cells in patients with symptomatic cGVHD. These changes were not detected in patients without cGVHD posttransplantation. In all, 7 patients with cGVHD followed up prospectively during ECP treatment showed a statistically significant normalization of the pattern of CD4
+ and a trend toward normalization of CD8
+ central memory T cells coincident with improvement of cGVHD. These data indicate a high correlation between disturbances in the balance of central and effector memory populations and cGVHD suggesting use in following up responses to therapy. The normalization of central and effector memory populations in response to ECP coincident with clinical improvement of cGVHD support a correlation between these laboratory parameters and cGVHD. Further studies are needed to demonstrate whether laboratory measurements of the magnitude of changes in central and effector memory populations are useful prognostically or can be used to guide response to therapy. The contrasting change in central memory cells (CD8
+ increased versus CD4
+ decreased) in cGVHD provide support for recent reports suggesting unique differences in the differentiation pathways for CD8
+ versus CD4
+ T cells.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>16399598</pmid><doi>10.1016/j.bbmt.2005.11.004</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adult Alloimmune Bone marrow transplantation CD4-CD8 Ratio - methods CD4-Positive T-Lymphocytes - immunology CD4-Positive T-Lymphocytes - pathology CD8-Positive T-Lymphocytes - immunology CD8-Positive T-Lymphocytes - pathology Cell Differentiation - drug effects Cell Differentiation - immunology Central memory T cell Chronic Disease Chronic GVHD Cohort Studies Extracorporeal photopheresis Female Graft vs Host Disease - blood Graft vs Host Disease - immunology Graft vs Host Disease - pathology Hematologic Neoplasms - blood Hematologic Neoplasms - immunology Hematologic Neoplasms - pathology Hematologic Neoplasms - therapy Hematopoietic Stem Cell Transplantation Humans Immunologic Memory - drug effects Immunologic Memory - immunology Male Middle Aged PUVA Therapy - methods Transplantation, Homologous |
title | Unique Abnormalities of CD4 + and CD8 + Central Memory Cells Associated with Chronic Graft-versus-Host Disease Improve after Extracorporeal Photopheresis |
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