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Immunosuppressive protocols with tacrolimus after cryopreserved aortal allotransplantation in rats

Identifikátory výsledku

  • Kód výsledku v IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11110%2F18%3A10378504" target="_blank" >RIV/00216208:11110/18:10378504 - isvavai.cz</a>

  • Nalezeny alternativní kódy

    RIV/00179906:_____/18:10378504 RIV/00064165:_____/18:10378504

  • Výsledek na webu

    <a href="https://doi.org/10.1371/journal.pone.0201984" target="_blank" >https://doi.org/10.1371/journal.pone.0201984</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1371/journal.pone.0201984" target="_blank" >10.1371/journal.pone.0201984</a>

Alternativní jazyky

  • Jazyk výsledku

    angličtina

  • Název v původním jazyce

    Immunosuppressive protocols with tacrolimus after cryopreserved aortal allotransplantation in rats

  • Popis výsledku v původním jazyce

    Objectives and design: The aim of our study was to simulate in rats all aspects and techniques used in our new clinical program of cryopreserved alloarterial transplantation and investigate the influence of two immunosuppressive protocols with tacrolimus on acute rejection of these allografts. Materials and methods: Cryopreserved abdominal aortic grafts were transplanted between Brown-Norway and Lewis rats. Tacrolimus (0.2 mg/kg daily) was administered from day 1 to day 30 (TAC1) or from day 7 to day 30 (TAC7), respectively. No immunosuppressed isogeneic (ISO) and allogeneic (ALO) rats combination served as control. Aortal wall infiltration by immunocompetent cells (MHC II+ cells of recipient origin) was studied on day 30 after transplantation. Flow cytometry was used for the analysis of day 30 sera for the presence of donor specific antiMHC class I and II antibodies. Results: The aortal allografts in both immunosuppressed groups showed regular morphology of aortal wall with no depositions of immunoglobulin G on day 30. The adventitial infiltration of non-immunosuppressed aortal allografts by MHC class II positive cells of recipient origin was significantly higher (ALO 20.7 +/- 6.7 cells, P&lt;0.001) compared to both immunosuppressed groups (TAC1 5.9 +/- 5.5 cells, TAC7 6.1 +/- 5.1 cells). Day 30 sera from the allogeneic non-immunosuppressed animals decreased significantly the binding of fluorescence labelled MHC class I (46.9 +/- 19.4%) and class II (65.8 +/- 11.9%) antibody to donors spleen cells compared with day 30 sera from both immunosuppressed groups (TAC1, anti-MHC class 1102.4 +/- 4.2%, p &lt; 0.001, anti-MHC class II 102.6 +/- 6.0%), (TAC7, anti-MHC class I 79.9 +/- 3.3%, p &lt; 0.001, anti-MHC class II 80.9 +/- 2.7%). Conclusion: Both immunosuppressed protocols with tacrolimus (administration from day 1 or from day 7 following transplantation) were able to suppress acute cell- and antibody-mediated rejection of cryopreserved abdominal aortic allografts processed in accordance with our new standardized clinical protocol.

  • Název v anglickém jazyce

    Immunosuppressive protocols with tacrolimus after cryopreserved aortal allotransplantation in rats

  • Popis výsledku anglicky

    Objectives and design: The aim of our study was to simulate in rats all aspects and techniques used in our new clinical program of cryopreserved alloarterial transplantation and investigate the influence of two immunosuppressive protocols with tacrolimus on acute rejection of these allografts. Materials and methods: Cryopreserved abdominal aortic grafts were transplanted between Brown-Norway and Lewis rats. Tacrolimus (0.2 mg/kg daily) was administered from day 1 to day 30 (TAC1) or from day 7 to day 30 (TAC7), respectively. No immunosuppressed isogeneic (ISO) and allogeneic (ALO) rats combination served as control. Aortal wall infiltration by immunocompetent cells (MHC II+ cells of recipient origin) was studied on day 30 after transplantation. Flow cytometry was used for the analysis of day 30 sera for the presence of donor specific antiMHC class I and II antibodies. Results: The aortal allografts in both immunosuppressed groups showed regular morphology of aortal wall with no depositions of immunoglobulin G on day 30. The adventitial infiltration of non-immunosuppressed aortal allografts by MHC class II positive cells of recipient origin was significantly higher (ALO 20.7 +/- 6.7 cells, P&lt;0.001) compared to both immunosuppressed groups (TAC1 5.9 +/- 5.5 cells, TAC7 6.1 +/- 5.1 cells). Day 30 sera from the allogeneic non-immunosuppressed animals decreased significantly the binding of fluorescence labelled MHC class I (46.9 +/- 19.4%) and class II (65.8 +/- 11.9%) antibody to donors spleen cells compared with day 30 sera from both immunosuppressed groups (TAC1, anti-MHC class 1102.4 +/- 4.2%, p &lt; 0.001, anti-MHC class II 102.6 +/- 6.0%), (TAC7, anti-MHC class I 79.9 +/- 3.3%, p &lt; 0.001, anti-MHC class II 80.9 +/- 2.7%). Conclusion: Both immunosuppressed protocols with tacrolimus (administration from day 1 or from day 7 following transplantation) were able to suppress acute cell- and antibody-mediated rejection of cryopreserved abdominal aortic allografts processed in accordance with our new standardized clinical protocol.

Klasifikace

  • Druh

    J<sub>imp</sub> - Článek v periodiku v databázi Web of Science

  • CEP obor

  • OECD FORD obor

    30201 - Cardiac and Cardiovascular systems

Návaznosti výsledku

  • Projekt

  • Návaznosti

    S - Specificky vyzkum na vysokych skolach<br>I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Ostatní

  • Rok uplatnění

    2018

  • Kód důvěrnosti údajů

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Údaje specifické pro druh výsledku

  • Název periodika

    PLoS One

  • ISSN

    1932-6203

  • e-ISSN

  • Svazek periodika

    13

  • Číslo periodika v rámci svazku

    8

  • Stát vydavatele periodika

    US - Spojené státy americké

  • Počet stran výsledku

    17

  • Strana od-do

  • Kód UT WoS článku

    000441232600075

  • EID výsledku v databázi Scopus

    2-s2.0-85052315026