研究动态
Articles below are published ahead of final publication in an issue. Please cite articles in the following format: authors, (year), title, journal, DOI.

红细胞抗原的异体免疫不会影响肝移植接受者的生存率。

Alloimmunization Against RBC Antigens Is Not Associated With Decreased Survival in Liver Transplant Recipients.

发表日期:2023 Jan 10
作者: Yevgen Chornenkyy, Alcino Pires Gama, Christopher Felicelli, Nigar Khurram, Adam L Booth, Joseph R Leventhal, Glenn Eugene Ramsey, Guang-Yu Yang
来源: AMERICAN JOURNAL OF CLINICAL PATHOLOGY

摘要:

肝移植(LT)效果的改善需要更好地了解影响存活的因素。本研究评估了RBC抗体(RBCAs)对LT受体存活的影响。本研究是一项单中心、回顾性队列研究,回顾了2002年至2021年之间的输血记录和全因死亡情况。在2002年至2021年期间,完成了2079例LT,其中1396例符合纳入标准(1305例RBCA阴性;91例RBCA阳性[6.5%])。两组在年龄(平均[范围],分别为55.8 [17-79]岁和56.8 [25-73]岁;P = .41)或性别(RBCA阴性,男性859例[65%]和女性446例[35%],RBCA阳性,男性51例[56%]和女性40例[44%];P = .0684)方面相似。检测到的132种RBCA中,最常见的10种分别为E(27.27%)、Jka(15.91%)、K(9.09%)、C(8.33%)、M(6.06%)、D(5.3%)、Fya(4.55%)、e(2.27%)、c(2.27%)和Jkb(2.27%)。27名患者(29.7%)有两种以上的RBCA,最常见的组合是C和Jka(7.4%)以及E和Dia(7.4%)。总死亡率在男性(男性,14.45年 vs 女性,17.27年;P = .0266)和65岁及以上的患者(≥65岁,10.21年 vs <64岁,17.22年;P < .0001)中增加。RBCA(≥1)的存在并不影响全因死亡率(RBCA阴性,14.17年 vs RBCA阳性,15.29年;P = .4367)。死亡的前5种原因是感染(11.9%)、恶性肿瘤(实体性)(10.8%)、复发性肿瘤(10.5%)、心血管停搏(7.1%)和肺功能不全/呼吸衰竭(5.7%)。RBCA阳性的LT受体的存活与RBCA阴性的LT受体的存活没有区别。 ©作者(们)2023。由牛津大学出版社代表美国临床病理学会出版。保留所有权利。如需授权,请发送电子邮件至journals.permissions@oup.com。
Improvement of liver transplantation (LT) outcomes requires better understanding of factors affecting survival. The presence of RBC alloantibodies (RBCAs) on survival in LT recipients was evaluated.This study was a single-center, retrospective cohort study reviewing transfusion records and all-cause mortality between 2002 and 2021.Between 2002 and 2021, 2079 LTs were completed, 1,396 of which met inclusion criteria (1,305 RBCA negative; 91 RBCA positive [6.5%]). The cohorts were similar in age (mean [range], 55.8 [17-79] years vs 56.8 [25-73] years; P = .41, respectively) or sex (RBCA negative, 859 [65%] men and 446 [35%] women vs RBCA positive, 51 [56%] men and 40 [44%] women; P = .0684). Of 132 RBCAs detected, 10 were most common were to E (27.27%), Jka (15.91%), K (9.09%), C (8.33%), M (6.06%), D (5.3%), Fya (4.55%), e (2.27%), c (2.27%), and Jkb (2.27%). Twenty-seven patients (29.7%) had more than 1 RBCA; the most common combinations were C with Jka (7.4%) and E with Dia (7.4%). All-cause mortality was increased in men (men, 14.45 years vs women, 17.27 years; P = .0266) and patients 65 years of age and older (≥65 years of age, 10.21 years vs <64 years of age, 17.22 years; P < .0001). The presence of RBCA (≥1) did not affect all-cause mortality (RBCA negative, 14.17 years vs RBCA positive, 15.29 years; P = .4367). The top 5 causes of death were infection (11.9%), primary malignancy (solid) (10.8%), recurrent malignancy (10.5%), cardiovascular arrest (7.1%), and pulmonary insufficiency/respiratory failure (5.7%).Survival in RBCA-positive LT recipients is no different from that in RBCA-negative LT recipients.© The Author(s) 2023. Published by Oxford University Press on behalf of American Society for Clinical Pathology. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.