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    • 域名年龄:28年1个月18天  注册日期:1996年04月04日  到期时间:
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    jci.org

    域名年龄: 28年1个月18天
    注册时间: 1996-04-04
    注 册 商: GoDaddy.com, LLC
    注册邮箱: sysadmin
    联系电话: +1.17342226050

    获取时间: 2016年02月23日 22:16:58
    Domain Name: JCI.ORG
    Domain ID: D2795739-LROR
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    Referral URL: http://www.godaddy.com
    Updated Date: 2013-12-10T15:32:02Z
    Creation Date: 1996-04-04T05:00:00Z
    Registry Expiry Date: 2017-04-05T05:00:00Z
    Sponsoring Registrar: GoDaddy.com, LLC
    Sponsoring Registrar IANA ID: 146
    Domain Status: clientDeleteProhibited https://www.icann.org/epp#clientDeleteProhibited
    Domain Status: clientRenewProhibited https://www.icann.org/epp#clientRenewProhibited
    Domain Status: clientTransferProhibited https://www.icann.org/epp#clientTransferProhibited
    Domain Status: clientUpdateProhibited https://www.icann.org/epp#clientUpdateProhibited
    Registrant ID: CR34517954
    Registrant Name: John Hawley
    Registrant Organization: American Society for Clinical Investigation
    Registrant Street: 2015 Manchester Road
    Registrant City: Ann Arbor
    Registrant State/Province: Michigan
    Registrant Postal Code: 48104
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    Admin Name: John Hawley
    Admin Organization: American Society for Clinical Investigation
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    Tech ID: CR34517956
    Tech Name: Shawn Pyle
    Tech Organization: American Society for Clinical Investigation
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    Name Server: NS-799.AWSDNS-35.NET
    Name Server: NS-480.AWSDNS-60.COM
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    抓取时间:2017年01月10日 08:02:37
    网址:http://jci.org/
    标题:JCI - Welcome
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    Go toJCI InsightAboutEditorsConsulting EditorsFor authorsAlertsAdvertiseSubscribeContactCurrent IssuePast IssuesBy specialtyCardiologyGastroenterologyImmunologyMetabolismNephrologyNeuroscienceOncologyPulmonologyVascular biologyAll...VideosConversations with Giants in MedicineAuthor's TakesReviewsReviewsView all reviews...Review SeriesMetabolism and Inflammation (Jan 2017)Hypoxia and Inflammation (Oct 2016)Extracellular Vesicles (Apr 2016)HIV (Feb 2016)Cancer Immunotherapy (Sep 2015)Autoimmunity (Jun 2015)Enteric Nervous System (Mar 2015)View all review series...CollectionsRecently publishedCommentariesEditorialsOpinionScientific Show StoppersTop read articlesClinical MedicineJCI This MonthCurrent issuePast issuesThe Journal of Clinical InvestigationAboutEditorsConsulting EditorsFor authorsCurrent issuePast issuesBy specialtySubscribeAlertsAdvertiseContactVideosConversations with Giants in MedicineAuthor's TakesCollectionsRecently publishedBrief ReportsTechnical AdvancesCommentariesEditorialsHindsightReview seriesReviewsThe Attending PhysicianFirst Author PerspectivesScientific Show StoppersTop read articlesRecently published- MoreSelective graft-versus-leukemia depends on magnitude and diversity of the alloreactive T cell responsePatients with leukemia who receive a T cell–depleted allogeneic stem cell graft followed by postponed donor lymphocyte infusion (DLI) can experience graft-versus-leukemia (GVL) reactivity, with a...Published January  9, 2017Categories:Research ArticleHematologyTransplantationSelective graft-versus-leukemia depends on magnitude and diversity of the alloreactive T cell responseTextPDFAbstractPatients with leukemia who receive a T cell–depleted allogeneic stem cell graft followed by postponed donor lymphocyte infusion (DLI) can experience graft-versus-leukemia (GVL) reactivity, with a lower risk of graft-versus-host disease (GVHD). Here, we have investigated the magnitude, diversity, and specificity of alloreactive CD8 T cells in patients who developed GVL reactivity after DLI in the absence or presence of GVHD. We observed a lower magnitude and diversity of CD8 T cells for minor histocompatibility antigens (MiHAs) in patients with selective GVL reactivity without GVHD. Furthermore, we demonstrated that MiHA-specific T cell clones from patients with selective GVL reactivity showed lower reactivity against nonhematopoietic cells, even when pretreated with inflammatory cytokines. Expression analysis of MiHA-encoding genes showed that similar types of antigens were recognized in both patient groups, but in patients who developed GVHD, T cell reactivity was skewed to target broadly expressed MiHAs. As an inflammatory environment can render nonhematopoietic cells susceptible to T cell recognition, prevention of such circumstances favors induction of selective GVL reactivity without development of GVHD.AuthorsCornelis A.M. van Bergen, Simone A.P. van Luxemburg-Heijs, Liesbeth C. de Wreede, Matthijs Eefting, Peter A. von d

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