The impact of sirolimus on hepatocyte proliferation after living donor liver transplantation

Toso C, Patel S, Asthana S, Kawahara T, Girgis S, Kneteman NN, Shapiro AMJ, Bigam DL. The impact of sirolimus on hepatocyte proliferation after living donor liver transplantation.
Clin Transplant 2009 DOI: 10.1111/j.1399‐0012.2009.01159.x
© 2009 John Wiley & Sons A/S. : Background:  There is a l...

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Veröffentlicht in:Clinical transplantation 2010-09, Vol.24 (5), p.695-700
Hauptverfasser: Toso, Christian, Patel, Seema, Asthana, Sonal, Kawahara, Toshiyasu, Girgis, Safwat, Kneteman, Norman N., Shapiro, A.M. James, Bigam, David L.
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container_end_page 700
container_issue 5
container_start_page 695
container_title Clinical transplantation
container_volume 24
creator Toso, Christian
Patel, Seema
Asthana, Sonal
Kawahara, Toshiyasu
Girgis, Safwat
Kneteman, Norman N.
Shapiro, A.M. James
Bigam, David L.
description Toso C, Patel S, Asthana S, Kawahara T, Girgis S, Kneteman NN, Shapiro AMJ, Bigam DL. The impact of sirolimus on hepatocyte proliferation after living donor liver transplantation.
Clin Transplant 2009 DOI: 10.1111/j.1399‐0012.2009.01159.x
© 2009 John Wiley & Sons A/S. : Background:  There is a lack of data on the use of sirolimus after partial liver transplantation, especially regarding its impact on post‐transplant regeneration. Methods:  We reviewed adult living donor transplantations, with de novo sirolimus (n = 7) and without sirolimus (n = 21). Liver biopsies were stained for KI‐67, a proliferation marker. Controls included specimens with normal liver parenchyma (n = 13). Results:  Both groups had similar demographics, graft and patient survival and complication rates. During the first six wk and over the whole first year post‐transplant, the use of sirolimus was associated with lower levels of hepatocyte proliferation compared to sirolimus‐free patients, (overall, 0.3 [0–7.2] vs. 3 [0–49] KI‐67 positive hepatocytes per high power field, p ≤ 0.05). The levels observed in the sirolimus group were similar to those seen in non‐transplanted control patients with normal parenchyma (0.2 [0–1.3], p = NS). Post‐transplant hepatocyte proliferation correlated with the serum levels of sirolimus (p ≤ 0.05), but not with those of tacrolimus or with the dose of mycophenolate mofetil (p = 0.9 and 0.3, respectively). Conclusions:  These data suggest that sirolimus is associated with decreased post‐transplant hepatocyte proliferation. The clinical significance of this observation remains to be fully determined.
doi_str_mv 10.1111/j.1399-0012.2009.01159.x
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Clin Transplant 2009 DOI: 10.1111/j.1399‐0012.2009.01159.x
© 2009 John Wiley &amp; Sons A/S. : Background:  There is a lack of data on the use of sirolimus after partial liver transplantation, especially regarding its impact on post‐transplant regeneration. Methods:  We reviewed adult living donor transplantations, with de novo sirolimus (n = 7) and without sirolimus (n = 21). Liver biopsies were stained for KI‐67, a proliferation marker. Controls included specimens with normal liver parenchyma (n = 13). Results:  Both groups had similar demographics, graft and patient survival and complication rates. During the first six wk and over the whole first year post‐transplant, the use of sirolimus was associated with lower levels of hepatocyte proliferation compared to sirolimus‐free patients, (overall, 0.3 [0–7.2] vs. 3 [0–49] KI‐67 positive hepatocytes per high power field, p ≤ 0.05). The levels observed in the sirolimus group were similar to those seen in non‐transplanted control patients with normal parenchyma (0.2 [0–1.3], p = NS). Post‐transplant hepatocyte proliferation correlated with the serum levels of sirolimus (p ≤ 0.05), but not with those of tacrolimus or with the dose of mycophenolate mofetil (p = 0.9 and 0.3, respectively). Conclusions:  These data suggest that sirolimus is associated with decreased post‐transplant hepatocyte proliferation. The clinical significance of this observation remains to be fully determined.</description><identifier>ISSN: 0902-0063</identifier><identifier>EISSN: 1399-0012</identifier><identifier>DOI: 10.1111/j.1399-0012.2009.01159.x</identifier><identifier>PMID: 20002466</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Adolescent ; Adult ; Aged ; Antibacterial agents ; Antibiotics. Antiinfectious agents. Antiparasitic agents ; Biological and medical sciences ; Cells, Cultured ; donor ; Female ; Fundamental and applied biological sciences. Psychology ; Fundamental immunology ; Graft Rejection - drug therapy ; hepatocyte ; Hepatocytes - cytology ; Hepatocytes - drug effects ; Humans ; Immunosuppressive Agents - therapeutic use ; live ; liver ; Liver Regeneration - drug effects ; Liver Transplantation ; Liver, biliary tract, pancreas, portal circulation, spleen ; Living Donors ; Male ; Medical sciences ; Middle Aged ; Pharmacology. Drug treatments ; proliferation ; Prospective Studies ; regeneration ; Retrospective Studies ; sirolimus ; Sirolimus - therapeutic use ; Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases ; Surgery of the digestive system ; Tissue, organ and graft immunology ; Treatment Outcome ; Young Adult</subject><ispartof>Clinical transplantation, 2010-09, Vol.24 (5), p.695-700</ispartof><rights>2009 John Wiley &amp; Sons A/S.</rights><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5029-580c93d86396968a5055a1abddfd1cc30c7b428989ac0dc1f48d6636774cb9da3</citedby><cites>FETCH-LOGICAL-c5029-580c93d86396968a5055a1abddfd1cc30c7b428989ac0dc1f48d6636774cb9da3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1399-0012.2009.01159.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1399-0012.2009.01159.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=23336659$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20002466$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Toso, Christian</creatorcontrib><creatorcontrib>Patel, Seema</creatorcontrib><creatorcontrib>Asthana, Sonal</creatorcontrib><creatorcontrib>Kawahara, Toshiyasu</creatorcontrib><creatorcontrib>Girgis, Safwat</creatorcontrib><creatorcontrib>Kneteman, Norman N.</creatorcontrib><creatorcontrib>Shapiro, A.M. James</creatorcontrib><creatorcontrib>Bigam, David L.</creatorcontrib><title>The impact of sirolimus on hepatocyte proliferation after living donor liver transplantation</title><title>Clinical transplantation</title><addtitle>Clin Transplant</addtitle><description>Toso C, Patel S, Asthana S, Kawahara T, Girgis S, Kneteman NN, Shapiro AMJ, Bigam DL. The impact of sirolimus on hepatocyte proliferation after living donor liver transplantation.
Clin Transplant 2009 DOI: 10.1111/j.1399‐0012.2009.01159.x
© 2009 John Wiley &amp; Sons A/S. : Background:  There is a lack of data on the use of sirolimus after partial liver transplantation, especially regarding its impact on post‐transplant regeneration. Methods:  We reviewed adult living donor transplantations, with de novo sirolimus (n = 7) and without sirolimus (n = 21). Liver biopsies were stained for KI‐67, a proliferation marker. Controls included specimens with normal liver parenchyma (n = 13). Results:  Both groups had similar demographics, graft and patient survival and complication rates. During the first six wk and over the whole first year post‐transplant, the use of sirolimus was associated with lower levels of hepatocyte proliferation compared to sirolimus‐free patients, (overall, 0.3 [0–7.2] vs. 3 [0–49] KI‐67 positive hepatocytes per high power field, p ≤ 0.05). The levels observed in the sirolimus group were similar to those seen in non‐transplanted control patients with normal parenchyma (0.2 [0–1.3], p = NS). Post‐transplant hepatocyte proliferation correlated with the serum levels of sirolimus (p ≤ 0.05), but not with those of tacrolimus or with the dose of mycophenolate mofetil (p = 0.9 and 0.3, respectively). Conclusions:  These data suggest that sirolimus is associated with decreased post‐transplant hepatocyte proliferation. The clinical significance of this observation remains to be fully determined.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Antibacterial agents</subject><subject>Antibiotics. Antiinfectious agents. Antiparasitic agents</subject><subject>Biological and medical sciences</subject><subject>Cells, Cultured</subject><subject>donor</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Fundamental immunology</subject><subject>Graft Rejection - drug therapy</subject><subject>hepatocyte</subject><subject>Hepatocytes - cytology</subject><subject>Hepatocytes - drug effects</subject><subject>Humans</subject><subject>Immunosuppressive Agents - therapeutic use</subject><subject>live</subject><subject>liver</subject><subject>Liver Regeneration - drug effects</subject><subject>Liver Transplantation</subject><subject>Liver, biliary tract, pancreas, portal circulation, spleen</subject><subject>Living Donors</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Pharmacology. Drug treatments</subject><subject>proliferation</subject><subject>Prospective Studies</subject><subject>regeneration</subject><subject>Retrospective Studies</subject><subject>sirolimus</subject><subject>Sirolimus - therapeutic use</subject><subject>Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases</subject><subject>Surgery of the digestive system</subject><subject>Tissue, organ and graft immunology</subject><subject>Treatment Outcome</subject><subject>Young Adult</subject><issn>0902-0063</issn><issn>1399-0012</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkEtPGzEUhS1UBCnlL1TeoK5m6sfYM16waCMKrYCKKlUlhGQ5tqc4nRe2A8m_rycJ6bbe-Pre7_geHQAgRjlO5-Mix1SIDCFMcoKQyBHGTOSrAzDZD96ACRKIpJrTY_A2hEXqcszZEThOGkQKzifgYfZooWsHpSPsaxic7xvXLgPsO_hoBxV7vY4WDmO7tl5FlwaqjtbDxj277jc0fddvHqkVverC0KgubsB34LBWTbCnu_sE_PxyMZteZdffL79OP11nmiEiMlYhLaipOBVc8EoxxJjCam5MbbDWFOlyXpBKVEJpZDSui8pwTnlZFnoujKIn4MP232TzaWlDlK0L2jbJiO2XQZackKogFCWy2pLa9yF4W8vBu1b5tcRIjtHKhRwTlGOCcoxWbqKVqyR9v1uynLfW7IWvWSbgbAeooFVTpyy0C_84SinnTCTufMu9uMau_9uAnM5-jFXSZ1u9C9Gu9nrl_0he0pLJX7eX8v7-293N3eertPYv2cSk7g</recordid><startdate>201009</startdate><enddate>201009</enddate><creator>Toso, Christian</creator><creator>Patel, Seema</creator><creator>Asthana, Sonal</creator><creator>Kawahara, Toshiyasu</creator><creator>Girgis, Safwat</creator><creator>Kneteman, Norman N.</creator><creator>Shapiro, A.M. 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James</au><au>Bigam, David L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The impact of sirolimus on hepatocyte proliferation after living donor liver transplantation</atitle><jtitle>Clinical transplantation</jtitle><addtitle>Clin Transplant</addtitle><date>2010-09</date><risdate>2010</risdate><volume>24</volume><issue>5</issue><spage>695</spage><epage>700</epage><pages>695-700</pages><issn>0902-0063</issn><eissn>1399-0012</eissn><abstract>Toso C, Patel S, Asthana S, Kawahara T, Girgis S, Kneteman NN, Shapiro AMJ, Bigam DL. The impact of sirolimus on hepatocyte proliferation after living donor liver transplantation.
Clin Transplant 2009 DOI: 10.1111/j.1399‐0012.2009.01159.x
© 2009 John Wiley &amp; Sons A/S. : Background:  There is a lack of data on the use of sirolimus after partial liver transplantation, especially regarding its impact on post‐transplant regeneration. Methods:  We reviewed adult living donor transplantations, with de novo sirolimus (n = 7) and without sirolimus (n = 21). Liver biopsies were stained for KI‐67, a proliferation marker. Controls included specimens with normal liver parenchyma (n = 13). Results:  Both groups had similar demographics, graft and patient survival and complication rates. During the first six wk and over the whole first year post‐transplant, the use of sirolimus was associated with lower levels of hepatocyte proliferation compared to sirolimus‐free patients, (overall, 0.3 [0–7.2] vs. 3 [0–49] KI‐67 positive hepatocytes per high power field, p ≤ 0.05). The levels observed in the sirolimus group were similar to those seen in non‐transplanted control patients with normal parenchyma (0.2 [0–1.3], p = NS). Post‐transplant hepatocyte proliferation correlated with the serum levels of sirolimus (p ≤ 0.05), but not with those of tacrolimus or with the dose of mycophenolate mofetil (p = 0.9 and 0.3, respectively). Conclusions:  These data suggest that sirolimus is associated with decreased post‐transplant hepatocyte proliferation. The clinical significance of this observation remains to be fully determined.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>20002466</pmid><doi>10.1111/j.1399-0012.2009.01159.x</doi><tpages>6</tpages></addata></record>
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source MEDLINE; Access via Wiley Online Library
subjects Adolescent
Adult
Aged
Antibacterial agents
Antibiotics. Antiinfectious agents. Antiparasitic agents
Biological and medical sciences
Cells, Cultured
donor
Female
Fundamental and applied biological sciences. Psychology
Fundamental immunology
Graft Rejection - drug therapy
hepatocyte
Hepatocytes - cytology
Hepatocytes - drug effects
Humans
Immunosuppressive Agents - therapeutic use
live
liver
Liver Regeneration - drug effects
Liver Transplantation
Liver, biliary tract, pancreas, portal circulation, spleen
Living Donors
Male
Medical sciences
Middle Aged
Pharmacology. Drug treatments
proliferation
Prospective Studies
regeneration
Retrospective Studies
sirolimus
Sirolimus - therapeutic use
Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases
Surgery of the digestive system
Tissue, organ and graft immunology
Treatment Outcome
Young Adult
title The impact of sirolimus on hepatocyte proliferation after living donor liver transplantation
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