Successful Treatment of TAFRO Syndrome, a Variant of Multicentric Castleman’s Disease, with Cyclosporine A: Possible Pathogenetic Contribution of Interleukin-2
Multicentric Castleman’s disease is a systemic inflammatory disorder characterized by lymphadenopathy and excessive interleukin-6 production. A unique clinicopathologic variant of multicentric Castleman’s disease, TAFRO (i.e., thrombocytopenia, anasarca, fever, renal failure or reticulin fibrosis, a...
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Veröffentlicht in: | The Tohoku Journal of Experimental Medicine 2015, Vol.236(4), pp.289-295 |
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creator | Konishi, Yoshinobu Takahashi, Satoshi Nishi, Katsuyuki Sakamaki, Taro Mitani, Sachiko Kaneko, Hitomi Mizutani, Chisato Ukyo, Naoya Hirata, Hirokazu Tsudo, Mitsuru |
description | Multicentric Castleman’s disease is a systemic inflammatory disorder characterized by lymphadenopathy and excessive interleukin-6 production. A unique clinicopathologic variant of multicentric Castleman’s disease, TAFRO (i.e., thrombocytopenia, anasarca, fever, renal failure or reticulin fibrosis, and organomegaly) syndrome, was recently proposed in Japan. Despite the successful use of anti-interleukin-6 therapy in some patients with TAFRO syndrome, not all patients achieve remission. The pathophysiological etiology of and suitable therapeutic strategies for this variant have not been established. Here, we present our experience of a unique case of TAFRO syndrome in a 78-year-old woman whose symptoms responded differently to several therapies. Tocilizumab, an anti-interleukin-6 receptor antibody, successfully induced remission of fever and lymphadenopathy. However, severe thrombocytopenia persisted and she developed anasarca, ascites, and pleural effusion shortly thereafter. Rituximab, an anti-CD20 antibody, and glucocorticoid therapy provided no symptom relief. In contrast, cyclosporine A, an immunosuppressive agent that blocks T cell function by inhibiting interleukin-2, yielded immediate improvements in systemic fluid retention and a gradual increase in platelet count, with complete resolution of disease symptoms. Excessive serum interleukin-2, when used as an anti-cancer agent, has been reported to cause side effects such as fluid retention, thrombocytopenia, and renal failure. Our case was unique because the anti-interleukin-2 therapy successfully improved symptoms that were not relieved with anti-interleukin-6 therapy. The present report therefore provides insight into the possible role of interleukin-2, in addition to interleukin-6, in TAFRO syndrome. This report will certainly help to clarify the pathogenesis of and optimal treatment strategies for TAFRO syndrome. |
doi_str_mv | 10.1620/tjem.236.289 |
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A unique clinicopathologic variant of multicentric Castleman’s disease, TAFRO (i.e., thrombocytopenia, anasarca, fever, renal failure or reticulin fibrosis, and organomegaly) syndrome, was recently proposed in Japan. Despite the successful use of anti-interleukin-6 therapy in some patients with TAFRO syndrome, not all patients achieve remission. The pathophysiological etiology of and suitable therapeutic strategies for this variant have not been established. Here, we present our experience of a unique case of TAFRO syndrome in a 78-year-old woman whose symptoms responded differently to several therapies. Tocilizumab, an anti-interleukin-6 receptor antibody, successfully induced remission of fever and lymphadenopathy. However, severe thrombocytopenia persisted and she developed anasarca, ascites, and pleural effusion shortly thereafter. Rituximab, an anti-CD20 antibody, and glucocorticoid therapy provided no symptom relief. In contrast, cyclosporine A, an immunosuppressive agent that blocks T cell function by inhibiting interleukin-2, yielded immediate improvements in systemic fluid retention and a gradual increase in platelet count, with complete resolution of disease symptoms. Excessive serum interleukin-2, when used as an anti-cancer agent, has been reported to cause side effects such as fluid retention, thrombocytopenia, and renal failure. Our case was unique because the anti-interleukin-2 therapy successfully improved symptoms that were not relieved with anti-interleukin-6 therapy. The present report therefore provides insight into the possible role of interleukin-2, in addition to interleukin-6, in TAFRO syndrome. This report will certainly help to clarify the pathogenesis of and optimal treatment strategies for TAFRO syndrome.</description><identifier>ISSN: 0040-8727</identifier><identifier>EISSN: 1349-3329</identifier><identifier>DOI: 10.1620/tjem.236.289</identifier><identifier>PMID: 26250536</identifier><language>eng</language><publisher>Japan: Tohoku University Medical Press</publisher><subject>Aged ; Antibodies, Monoclonal, Humanized - pharmacology ; Antibodies, Monoclonal, Humanized - therapeutic use ; Castleman Disease - drug therapy ; Castleman Disease - pathology ; Cyclosporine - pharmacology ; Cyclosporine - therapeutic use ; cyclosporine A ; Edema - pathology ; Female ; Fever - drug therapy ; Fever - pathology ; Humans ; interleukin-2 ; Interleukin-2 - antagonists & inhibitors ; interleukin-6 ; multicentric Castleman’s disease ; Platelet Count ; Renal Insufficiency - pathology ; Rituximab - pharmacology ; Rituximab - therapeutic use ; Syndrome ; TAFRO syndrome ; Thrombocytopenia - pathology ; Treatment Outcome</subject><ispartof>The Tohoku Journal of Experimental Medicine, 2015, Vol.236(4), pp.289-295</ispartof><rights>2015 Tohoku University Medical Press</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c410t-53f6c3f74594d4fc6c5c963f46e892212c28e86b9d4e0fc740fc7807d24780193</citedby><cites>FETCH-LOGICAL-c410t-53f6c3f74594d4fc6c5c963f46e892212c28e86b9d4e0fc740fc7807d24780193</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,1877,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26250536$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Konishi, Yoshinobu</creatorcontrib><creatorcontrib>Takahashi, Satoshi</creatorcontrib><creatorcontrib>Nishi, Katsuyuki</creatorcontrib><creatorcontrib>Sakamaki, Taro</creatorcontrib><creatorcontrib>Mitani, Sachiko</creatorcontrib><creatorcontrib>Kaneko, Hitomi</creatorcontrib><creatorcontrib>Mizutani, Chisato</creatorcontrib><creatorcontrib>Ukyo, Naoya</creatorcontrib><creatorcontrib>Hirata, Hirokazu</creatorcontrib><creatorcontrib>Tsudo, Mitsuru</creatorcontrib><title>Successful Treatment of TAFRO Syndrome, a Variant of Multicentric Castleman’s Disease, with Cyclosporine A: Possible Pathogenetic Contribution of Interleukin-2</title><title>The Tohoku Journal of Experimental Medicine</title><addtitle>Tohoku J. Exp. Med.</addtitle><description>Multicentric Castleman’s disease is a systemic inflammatory disorder characterized by lymphadenopathy and excessive interleukin-6 production. A unique clinicopathologic variant of multicentric Castleman’s disease, TAFRO (i.e., thrombocytopenia, anasarca, fever, renal failure or reticulin fibrosis, and organomegaly) syndrome, was recently proposed in Japan. Despite the successful use of anti-interleukin-6 therapy in some patients with TAFRO syndrome, not all patients achieve remission. The pathophysiological etiology of and suitable therapeutic strategies for this variant have not been established. Here, we present our experience of a unique case of TAFRO syndrome in a 78-year-old woman whose symptoms responded differently to several therapies. Tocilizumab, an anti-interleukin-6 receptor antibody, successfully induced remission of fever and lymphadenopathy. However, severe thrombocytopenia persisted and she developed anasarca, ascites, and pleural effusion shortly thereafter. Rituximab, an anti-CD20 antibody, and glucocorticoid therapy provided no symptom relief. In contrast, cyclosporine A, an immunosuppressive agent that blocks T cell function by inhibiting interleukin-2, yielded immediate improvements in systemic fluid retention and a gradual increase in platelet count, with complete resolution of disease symptoms. Excessive serum interleukin-2, when used as an anti-cancer agent, has been reported to cause side effects such as fluid retention, thrombocytopenia, and renal failure. Our case was unique because the anti-interleukin-2 therapy successfully improved symptoms that were not relieved with anti-interleukin-6 therapy. The present report therefore provides insight into the possible role of interleukin-2, in addition to interleukin-6, in TAFRO syndrome. This report will certainly help to clarify the pathogenesis of and optimal treatment strategies for TAFRO syndrome.</description><subject>Aged</subject><subject>Antibodies, Monoclonal, Humanized - pharmacology</subject><subject>Antibodies, Monoclonal, Humanized - therapeutic use</subject><subject>Castleman Disease - drug therapy</subject><subject>Castleman Disease - pathology</subject><subject>Cyclosporine - pharmacology</subject><subject>Cyclosporine - therapeutic use</subject><subject>cyclosporine A</subject><subject>Edema - pathology</subject><subject>Female</subject><subject>Fever - drug therapy</subject><subject>Fever - pathology</subject><subject>Humans</subject><subject>interleukin-2</subject><subject>Interleukin-2 - antagonists & inhibitors</subject><subject>interleukin-6</subject><subject>multicentric Castleman’s disease</subject><subject>Platelet Count</subject><subject>Renal Insufficiency - pathology</subject><subject>Rituximab - pharmacology</subject><subject>Rituximab - therapeutic use</subject><subject>Syndrome</subject><subject>TAFRO syndrome</subject><subject>Thrombocytopenia - pathology</subject><subject>Treatment Outcome</subject><issn>0040-8727</issn><issn>1349-3329</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkcFu0zAYgC0EYt3gxhn5yGEpju04MSeqwmDS0CZWuEau82d1cexiO0K97TU48mo8CY66lYv_w__5k-wPoVclmZeCkrdpC8OcMjGnjXyCZiXjsmCMyqdoRggnRVPT-gSdxrglhHFSi-fohApakYqJGfpzO2oNMfajxasAKg3gEvY9Xi0uvl7j273rgh_gHCv8XQWjDssvo01GZzIYjZcqJguDcn_vf0f8wURQMV_4ZdIGL_fa-rjzwTjAi3f4xsdo1hbwjUobfwcO0mTwk2k9JuPdpL90CYKF8YdxBX2BnvXKRnj5MM_Qt4uPq-Xn4ur60-VycVVoXpJUVKwXmvU1ryTveK-FrrQUrOcCGklpSTVtoBFr2XEgva75dDSk7ijPo5TsDL05eHfB_xwhpnYwUYO1yoEfY1vWhIqqprLM6PkB1SG_J0Df7oIZVNi3JWmnKO0Upc1R2hwl468fzON6gO4IP1bIwPsDsI1J3cERUCH_joX_Nv7oPK70RoUWHPsHAyeiJw</recordid><startdate>20150801</startdate><enddate>20150801</enddate><creator>Konishi, Yoshinobu</creator><creator>Takahashi, Satoshi</creator><creator>Nishi, Katsuyuki</creator><creator>Sakamaki, Taro</creator><creator>Mitani, Sachiko</creator><creator>Kaneko, Hitomi</creator><creator>Mizutani, Chisato</creator><creator>Ukyo, Naoya</creator><creator>Hirata, Hirokazu</creator><creator>Tsudo, Mitsuru</creator><general>Tohoku University Medical Press</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20150801</creationdate><title>Successful Treatment of TAFRO Syndrome, a Variant of Multicentric Castleman’s Disease, with Cyclosporine A: Possible Pathogenetic Contribution of Interleukin-2</title><author>Konishi, Yoshinobu ; Takahashi, Satoshi ; Nishi, Katsuyuki ; Sakamaki, Taro ; Mitani, Sachiko ; Kaneko, Hitomi ; Mizutani, Chisato ; Ukyo, Naoya ; Hirata, Hirokazu ; Tsudo, Mitsuru</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c410t-53f6c3f74594d4fc6c5c963f46e892212c28e86b9d4e0fc740fc7807d24780193</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Aged</topic><topic>Antibodies, Monoclonal, Humanized - pharmacology</topic><topic>Antibodies, Monoclonal, Humanized - therapeutic use</topic><topic>Castleman Disease - drug therapy</topic><topic>Castleman Disease - pathology</topic><topic>Cyclosporine - pharmacology</topic><topic>Cyclosporine - therapeutic use</topic><topic>cyclosporine A</topic><topic>Edema - pathology</topic><topic>Female</topic><topic>Fever - drug therapy</topic><topic>Fever - pathology</topic><topic>Humans</topic><topic>interleukin-2</topic><topic>Interleukin-2 - antagonists & inhibitors</topic><topic>interleukin-6</topic><topic>multicentric Castleman’s disease</topic><topic>Platelet Count</topic><topic>Renal Insufficiency - pathology</topic><topic>Rituximab - pharmacology</topic><topic>Rituximab - therapeutic use</topic><topic>Syndrome</topic><topic>TAFRO syndrome</topic><topic>Thrombocytopenia - pathology</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Konishi, Yoshinobu</creatorcontrib><creatorcontrib>Takahashi, Satoshi</creatorcontrib><creatorcontrib>Nishi, Katsuyuki</creatorcontrib><creatorcontrib>Sakamaki, Taro</creatorcontrib><creatorcontrib>Mitani, Sachiko</creatorcontrib><creatorcontrib>Kaneko, Hitomi</creatorcontrib><creatorcontrib>Mizutani, Chisato</creatorcontrib><creatorcontrib>Ukyo, Naoya</creatorcontrib><creatorcontrib>Hirata, Hirokazu</creatorcontrib><creatorcontrib>Tsudo, Mitsuru</creatorcontrib><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>The Tohoku Journal of Experimental Medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Konishi, Yoshinobu</au><au>Takahashi, Satoshi</au><au>Nishi, Katsuyuki</au><au>Sakamaki, Taro</au><au>Mitani, Sachiko</au><au>Kaneko, Hitomi</au><au>Mizutani, Chisato</au><au>Ukyo, Naoya</au><au>Hirata, Hirokazu</au><au>Tsudo, Mitsuru</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Successful Treatment of TAFRO Syndrome, a Variant of Multicentric Castleman’s Disease, with Cyclosporine A: Possible Pathogenetic Contribution of Interleukin-2</atitle><jtitle>The Tohoku Journal of Experimental Medicine</jtitle><addtitle>Tohoku J. Exp. Med.</addtitle><date>2015-08-01</date><risdate>2015</risdate><volume>236</volume><issue>4</issue><spage>289</spage><epage>295</epage><pages>289-295</pages><issn>0040-8727</issn><eissn>1349-3329</eissn><abstract>Multicentric Castleman’s disease is a systemic inflammatory disorder characterized by lymphadenopathy and excessive interleukin-6 production. A unique clinicopathologic variant of multicentric Castleman’s disease, TAFRO (i.e., thrombocytopenia, anasarca, fever, renal failure or reticulin fibrosis, and organomegaly) syndrome, was recently proposed in Japan. Despite the successful use of anti-interleukin-6 therapy in some patients with TAFRO syndrome, not all patients achieve remission. The pathophysiological etiology of and suitable therapeutic strategies for this variant have not been established. Here, we present our experience of a unique case of TAFRO syndrome in a 78-year-old woman whose symptoms responded differently to several therapies. Tocilizumab, an anti-interleukin-6 receptor antibody, successfully induced remission of fever and lymphadenopathy. However, severe thrombocytopenia persisted and she developed anasarca, ascites, and pleural effusion shortly thereafter. Rituximab, an anti-CD20 antibody, and glucocorticoid therapy provided no symptom relief. In contrast, cyclosporine A, an immunosuppressive agent that blocks T cell function by inhibiting interleukin-2, yielded immediate improvements in systemic fluid retention and a gradual increase in platelet count, with complete resolution of disease symptoms. Excessive serum interleukin-2, when used as an anti-cancer agent, has been reported to cause side effects such as fluid retention, thrombocytopenia, and renal failure. Our case was unique because the anti-interleukin-2 therapy successfully improved symptoms that were not relieved with anti-interleukin-6 therapy. The present report therefore provides insight into the possible role of interleukin-2, in addition to interleukin-6, in TAFRO syndrome. This report will certainly help to clarify the pathogenesis of and optimal treatment strategies for TAFRO syndrome.</abstract><cop>Japan</cop><pub>Tohoku University Medical Press</pub><pmid>26250536</pmid><doi>10.1620/tjem.236.289</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Aged Antibodies, Monoclonal, Humanized - pharmacology Antibodies, Monoclonal, Humanized - therapeutic use Castleman Disease - drug therapy Castleman Disease - pathology Cyclosporine - pharmacology Cyclosporine - therapeutic use cyclosporine A Edema - pathology Female Fever - drug therapy Fever - pathology Humans interleukin-2 Interleukin-2 - antagonists & inhibitors interleukin-6 multicentric Castleman’s disease Platelet Count Renal Insufficiency - pathology Rituximab - pharmacology Rituximab - therapeutic use Syndrome TAFRO syndrome Thrombocytopenia - pathology Treatment Outcome |
title | Successful Treatment of TAFRO Syndrome, a Variant of Multicentric Castleman’s Disease, with Cyclosporine A: Possible Pathogenetic Contribution of Interleukin-2 |
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