Ischemic time of graft liver forces Th1-to-Th2 activity toward Th1 activity in patients who underwent living donor liver transplantation (notice n° 236166)

détails MARC
000 -LEADER
fixed length control field 02504cam a2200313 4500500
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20250112064023.0
041 ## - LANGUAGE CODE
Language code of text/sound track or separate title fre
042 ## - AUTHENTICATION CODE
Authentication code dc
100 10 - MAIN ENTRY--PERSONAL NAME
Personal name Park, Chul Soo
Relator term author
245 00 - TITLE STATEMENT
Title Ischemic time of graft liver forces Th1-to-Th2 activity toward Th1 activity in patients who underwent living donor liver transplantation
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Date of publication, distribution, etc. 2019.<br/>
500 ## - GENERAL NOTE
General note 3
520 ## - SUMMARY, ETC.
Summary, etc. Recipient's immune responses are an important factor in allograft survival in transplantation. Cytokines are reflected with immune responses. In the present study, we aimed to evaluate potential affecting factors of liver allograft survival and their possible correlation with seroum cytokine levels in living donor liver transplantation (LDLT). One hundred and seventy-one adult patients’ data were collected retrospectively. Five cytokines were collected: interferon (IFN)-γ, interleukin (IL)-2, IL-10, IL-6, and IL-17. Ischemic time of liver grafts was divided into two periods: cold and warm ischemic times (CIT and WIT, respectively). CIT had no statically significant correlation, but WIT showed a significant correlation with IFN-γ, IL-2, and IL-17 serum levels ( r = 0.0252, 0.282, 0.178, respectively; P &lt; 0.05). WIT was dichotomized as T1 (&lt;22 min), T2 (22-70 min), and T3 (&gt;70 min). IFN-γ was significantly increased in T2 and T3 as compared to T1. IL-6 was in T3 compared to T1 and T2. IL-17 was in T3 compared to T1. For the Th1-to-Th2 ratio, IFN-γ/IL-10, IFN-γ/IL-6, and IL-2/IL-10 were significantly different in T2 and T3 as compared to T1, and also in T3 as compared to T2. Th1 cell activities were enhanced with increased WIT. In conclusion, the longer WIT (&gt;70 min) in LDLT is more likely to induce immunological reactions of recipients by leading to a deleterious cytokine balances in favor of an reinforced production of Th1 cytokines.
690 ## - LOCAL SUBJECT ADDED ENTRY--TOPICAL TERM (OCLC, RLIN)
Topical term or geographic name as entry element liver transplantation
690 ## - LOCAL SUBJECT ADDED ENTRY--TOPICAL TERM (OCLC, RLIN)
Topical term or geographic name as entry element ischemic time
690 ## - LOCAL SUBJECT ADDED ENTRY--TOPICAL TERM (OCLC, RLIN)
Topical term or geographic name as entry element donor
690 ## - LOCAL SUBJECT ADDED ENTRY--TOPICAL TERM (OCLC, RLIN)
Topical term or geographic name as entry element cytokine
690 ## - LOCAL SUBJECT ADDED ENTRY--TOPICAL TERM (OCLC, RLIN)
Topical term or geographic name as entry element intraoperative
690 ## - LOCAL SUBJECT ADDED ENTRY--TOPICAL TERM (OCLC, RLIN)
Topical term or geographic name as entry element inflammation
700 10 - ADDED ENTRY--PERSONAL NAME
Personal name Moon, Hye Young
Relator term author
700 10 - ADDED ENTRY--PERSONAL NAME
Personal name Han, Sangbin
Relator term author
700 10 - ADDED ENTRY--PERSONAL NAME
Personal name Chon, Jin Young
Relator term author
700 10 - ADDED ENTRY--PERSONAL NAME
Personal name Chae, Min Suk
Relator term author
700 10 - ADDED ENTRY--PERSONAL NAME
Personal name Hong, Sang Hyun
Relator term author
700 10 - ADDED ENTRY--PERSONAL NAME
Personal name Choi, Jong Ho
Relator term author
700 10 - ADDED ENTRY--PERSONAL NAME
Personal name Chung, Hyun Sik
Relator term author
786 0# - DATA SOURCE ENTRY
Note European Cytokine Network | Volume 30 | 1 | 2019-03-01 | p. 23-28 | 1148-5493
856 41 - ELECTRONIC LOCATION AND ACCESS
Uniform Resource Identifier <a href="https://shs.cairn.info/revue-european-cytokine-network-2019-1-page-23?lang=en">https://shs.cairn.info/revue-european-cytokine-network-2019-1-page-23?lang=en</a>

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