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Tytuł pozycji:

Risk factors for the development of antibody-mediated rejection in highly sensitized pediatric kidney transplant recipients.

Tytuł:
Risk factors for the development of antibody-mediated rejection in highly sensitized pediatric kidney transplant recipients.
Autorzy:
Kim IK; Comprehensive Transplant Center, Cedars-Sinai Medical Center, Los Angeles, CA, USA.
Choi J; Comprehensive Transplant Center, Cedars-Sinai Medical Center, Los Angeles, CA, USA.
Vo A; Comprehensive Transplant Center, Cedars-Sinai Medical Center, Los Angeles, CA, USA.
Kang A; Comprehensive Transplant Center, Cedars-Sinai Medical Center, Los Angeles, CA, USA.
Steggerda J; Comprehensive Transplant Center, Cedars-Sinai Medical Center, Los Angeles, CA, USA.
Louie S; Comprehensive Transplant Center, Cedars-Sinai Medical Center, Los Angeles, CA, USA.
Haas M; Department of Pathology and Laboratory Medicine, Cedars-Sinai Medical Center, Los Angeles, CA, USA.
Mirocha J; Biostatistics Core, Cedars-Sinai Medical Center, Los Angeles, CA, USA.
Cohen JL; Comprehensive Transplant Center, Cedars-Sinai Medical Center, Los Angeles, CA, USA.
Pizzo H; Comprehensive Transplant Center, Cedars-Sinai Medical Center, Los Angeles, CA, USA.
Kamil ES; Comprehensive Transplant Center, Cedars-Sinai Medical Center, Los Angeles, CA, USA.
Jordan SC; Comprehensive Transplant Center, Cedars-Sinai Medical Center, Los Angeles, CA, USA.
Puliyanda D; Comprehensive Transplant Center, Cedars-Sinai Medical Center, Los Angeles, CA, USA.
Źródło:
Pediatric transplantation [Pediatr Transplant] 2017 Dec; Vol. 21 (8). Date of Electronic Publication: 2017 Sep 19.
Typ publikacji:
Journal Article
Język:
English
Imprint Name(s):
Original Publication: Copenhagen ; Malden, MA : Munksgaard, c1997-
MeSH Terms:
Kidney Transplantation*
Graft Rejection/*immunology
HLA Antigens/*immunology
Isoantibodies/*immunology
Adolescent ; Child ; Child, Preschool ; Desensitization, Immunologic/methods ; Female ; Graft Rejection/prevention & control ; Graft Survival/immunology ; Humans ; Immunosuppressive Agents/therapeutic use ; Kaplan-Meier Estimate ; Male ; Retrospective Studies ; Risk Factors ; Transplantation, Homologous ; Treatment Outcome ; Young Adult
Contributed Indexing:
Keywords: ABMR; DSA; desensitization; high sensitization
Substance Nomenclature:
0 (HLA Antigens)
0 (Immunosuppressive Agents)
0 (Isoantibodies)
Entry Date(s):
Date Created: 20170921 Date Completed: 20180601 Latest Revision: 20180601
Update Code:
20240104
DOI:
10.1111/petr.13042
PMID:
28929636
Czasopismo naukowe
ABMR remains a significant concern for early graft loss, especially for those who are HS against HLA antigens. We sought to determine the risk factors leading to ABMR in HS pediatric kidney transplant recipients. From January 2009 to December 2015, 16 HS pediatric kidney transplant patients at our center (age range 2-21) were retrospectively reviewed for outcomes and risk factors for ABMR. All HS patients received desensitization with high-dose IVIG/rituximab prior to transplant. Two groups were examined: ABMR + (n = 7) and ABMR - (n = 9). Patient survival was 100%; however, one patient in the ABMR + group suffered graft loss from ABMR 16 months post-transplant. ABMR + patients had higher Class I PRA at the time of transplant (Class I: 73.1 ± 19.1 vs 49.1 ± 28.3, P = .075), although not statistically significant. ABMR + patients were more likely to have a history of transplant nephrectomy (P = .013). The characteristic that most strongly correlated with ABMR was the DSA-RIS (P = .045), a scoring system used to quantify cumulative intensity of all DSA. In conclusion, DSA, as quantified by the RIS at the time of transplant, should be considered as part of the initial allocation strategy and patients with high RIS monitored closely for ABMR post-transplant.
(© 2017 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.)

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