Wang Yongjun, Yang Yuanqing, Li Zhengfeng, Li Wei, Hu Hongbin, Zhao Ding
Department of Blood Transfusion, The Second Xiangya Hospital, Central South University, Changsha, China.
Department of Blood Transfusion, Huazhong University of Science and Technology, Tongji Medical College Affiliated to Wuhan Children's Hospital, Wuhan Women and Children Medical Care Center, Wuhan, China.
Transfus Med Hemother. 2024 Apr 30;51(6):402-413. doi: 10.1159/000538448. eCollection 2024 Dec.
Erythrocyte alloantibodies and autoantibodies complicate transfusion. However, the prevalence of erythrocyte alloimmunization and autoimmunization has not been estimated in the Chinese pediatric population. Therefore, we investigated the prevalence of erythrocyte alloimmunization and autoimmunization in the Chinese pediatric population with the aim of developing a reasonable transfusion management policy in children from China.
This study included 30,603 pediatric inpatients who were admitted to three tertiary hospitals in central China from May 2020 to October 2022. Antibody screening was carried out with a three-cell panel by column agglutination technology, and samples with positive screening were analyzed for antibody specificity with a 16-cell identification panel. Clinical details of the patients were collected to identify associations with antibody formation.
The alloimmunization rate was 0.55% (169/30,603), and the autoimmunization rate was 0.14% (43/30,603). Alloantibodies comprised 80.09% of the antibodies. The most frequent alloantibodies were anti-M (58.77%), anti-E (9.48%), and anti-P1 (4.27%). Autoantibodies comprised 19.91% of antibodies. Age ( = 0.000), sex ( = 0.016), geographical area ( = 0.000), ABO blood group ( = 0.008), and diagnosis ( = 0.000) were independent risk factors for antibody formation. The risk of antibody formation at the ages of 0-28 days and 1-3 months was zero (odds ratio = 0.000). The antibody distribution was significantly different by age ( = 0.000) and diagnosis ( = 0.000).
Repeat pre-transfusion testing for infants less than 4 months of age can be omitted for no risk of antibody formation. MNS system antibodies, especially anti-M, are prominent in younger children, and this decreases with age. Provision of extended phenotype-matched transfusion for Rh system antigens, especially antigen E, is necessary in children to control erythrocyte alloimmunization. The presence of antibodies with high evanescence rates in the pediatric population suggests the pressing need for nationwide shared transfusion records to avoid hemolytic transfusion reactions in children.
红细胞同种抗体和自身抗体使输血变得复杂。然而,中国儿科人群中红细胞同种免疫和自身免疫的发生率尚未得到评估。因此,我们调查了中国儿科人群中红细胞同种免疫和自身免疫的发生率,旨在制定合理的中国儿童输血管理政策。
本研究纳入了2020年5月至2022年10月在中国中部三家三级医院住院的30603名儿科患者。采用柱凝集技术用三细胞面板进行抗体筛查,对筛查阳性的样本用16细胞鉴定面板分析抗体特异性。收集患者的临床细节以确定与抗体形成的关联。
同种免疫率为0.55%(169/30603),自身免疫率为0.14%(43/30603)。同种抗体占抗体的80.09%。最常见的同种抗体是抗-M(58.77%)、抗-E(9.48%)和抗-P1(4.27%)。自身抗体占抗体的19.9l%。年龄(P = 0.000)、性别(P = 0.016)、地理区域(P = 0.000)、ABO血型(P = 0.008)和诊断(P = 0.000)是抗体形成的独立危险因素。0至28天和1至3个月龄时抗体形成的风险为零(比值比 = 0.000)。抗体分布在年龄(P = 0.000)和诊断方面有显著差异(P = 0.000)。
对于4个月龄以下婴儿,由于无抗体形成风险,可省略重复的输血前检测。MNS系统抗体,尤其是抗-M,在年幼儿童中较为突出,且随年龄增长而降低。为控制红细胞同种免疫,有必要为儿童提供针对Rh系统抗原,尤其是抗原E的扩展表型匹配输血。儿科人群中存在高消失率的抗体表明迫切需要全国共享输血记录以避免儿童溶血性输血反应。