Instituto de Biomedicina de Sevilla (IBIS), University Hospital Virgen del Rocío, CSIC, University of Seville, Seville, Spain.
Department of Medicine, University of Seville, Seville, Spain.
Front Immunol. 2020 Oct 6;11:1917. doi: 10.3389/fimmu.2020.01917. eCollection 2020.
Our goal was to study whether influenza vaccination induced antibody mediated rejection in a large cohort of solid organ transplant recipients (SOTR).
Serum anti-Human Leukocyte Antigen (HLA) antibodies were determined using class I and class II antibody-coated latex beads (FlowPRA Screening Test) by flow cytometry. Anti-HLA antibody specificity was determined using the single-antigen bead flow cytometry (SAFC) assay and assignation of donor specific antibodies (DSA) was performed by virtual-crossmatch.
We studied a cohort of 490 SOTR that received an influenza vaccination from 2009 to 2013: 110 (22.4%) received the pandemic adjuvanted vaccine, 59 (12%) within the first 6 months post-transplantation, 185 (37.7%) more than 6 months after transplantation and 136 (27.7%) received two vaccination doses. Overall, no differences of anti-HLA antibodies were found after immunization in patients that received the adjuvanted vaccine, within the first 6 months post-transplantation, or based on the type of organ transplanted. However, the second immunization dose increased the percentage of patients positive for anti-HLA class I significantly compared with patients with one dose (14.6% vs. 3.8%; = 0.003). Patients with pre-existing antibodies before vaccination (15.7% for anti-HLA class I and 15.9% for class II) did not increase reactivity after immunization. A group of 75 (14.4%) patients developed anti-HLA antibodies, however, only 5 (1.02%) of them were DSA, and none experienced allograft rejection. Only two (0.4%) patients were diagnosed with graft rejection with favorable outcomes and neither of them developed DSA.
Our results suggest that influenza vaccination is not associated with graft rejection in this cohort of SOTR.
我们的目的是研究流感疫苗接种是否会在一大群实体器官移植受者(SOTR)中引起抗体介导的排斥反应。
使用类 I 和类 II 抗体包被乳胶珠(FlowPRA 筛查试验)通过流式细胞术测定血清抗人类白细胞抗原(HLA)抗体。使用单抗原珠流式细胞术(SAFC)测定抗 HLA 抗体特异性,并通过虚拟交叉配型分配供体特异性抗体(DSA)。
我们研究了一组在 2009 年至 2013 年期间接种流感疫苗的 490 名 SOTR:110 名(22.4%)接种了大流行性佐剂疫苗,59 名(12%)在移植后 6 个月内,185 名(37.7%)在移植后 6 个月以上,136 名(27.7%)接种了两剂疫苗。总体而言,在接种疫苗后,接受佐剂疫苗、移植后 6 个月内或根据移植器官类型的患者中,未发现抗 HLA 抗体有差异。然而,与接受一剂疫苗的患者相比,第二剂免疫接种显著增加了 HLA 类 I 抗体阳性患者的百分比(14.6%比 3.8%; = 0.003)。接种疫苗前存在抗体的患者(HLA 类 I 为 15.7%,类 II 为 15.9%)接种疫苗后反应性并未增加。一组 75 名(14.4%)患者产生了抗 HLA 抗体,但只有 5 名(1.02%)为 DSA,且均未发生移植物排斥反应。只有两名(0.4%)患者被诊断为移植排斥反应,且结果良好,且均未产生 DSA。
我们的结果表明,在这组 SOTR 中,流感疫苗接种与移植物排斥无关。