Predictors of Covid-19 Vaccination Response After In-Vivo T-Cell-Depleted Stem Cell Transplantation

被引:15
作者
Chaekal, Ok-kyong [1 ,2 ]
Gomez-Arteaga, Alexandra [2 ]
Chen, Zhengming [4 ]
Soave, Rosemary [3 ]
Shore, Tsiporah [2 ]
Mayer, Sebastian [2 ]
Phillips, Adrienne [2 ]
Hsu, Jing Mei [2 ]
Drelick, Alexander [3 ]
Kodiyanplakkal, Rosy Priya L. [3 ]
Plate, Markus [3 ]
Satlin, Michael J. [3 ]
van Besien, Koen [1 ,2 ]
机构
[1] New York Presbyterian Hosp, Dept Pathol & Lab Med, Weill Cornell Med, New York, NY USA
[2] New York Presbyterian Hosp, Dept Med, Div Hematol Oncol, Weill Cornell Med,Cell Therapy Program, New York, NY USA
[3] New York Presbyterian Hosp, Div Infect Dis, Weill Cornell Med, Transplantat Oncol Infect Dis Program, New York, NY USA
[4] New York Presbyterian Hosp, Dept Populat Sci, Div Biostat, Weill Cornell Med, New York, NY USA
来源
TRANSPLANTATION AND CELLULAR THERAPY | 2022年 / 28卷 / 09期
关键词
Covid-19; Stem cell transplantation; Vaccination; Umbilical Cord Blood; T-cell Depletion; CORD-BLOOD TRANSPLANTATION; ANTIBODY-RESPONSE; CHRONIC GVHD; ALEMTUZUMAB; SARS-COV-2; FLUDARABINE; RECIPIENTS; MELPHALAN; DISEASE; RISK;
D O I
10.1016/j.jtct.2022.06.012
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Covid-19 vaccination is recommended in allogeneic transplant recipients, but many questions remain regarding its efficacy. Here we studied serologic responses in 145 patients who had undergone allogeneic transplantation using in vivo T cell depletion. Median age was 57 (range 21-79) at transplantation and 61 (range 24-80) at vaccination. Sixty-nine percent were Caucasian. One third each received transplants from HLA-identical related (MRD), adult unrelated (MUD), or haploidentical-cord blood donors. Graft-versus-host disease (GVHD) prophylaxis involved in-vivo T-cell depletion using alemtuzumab for MRD or MUD transplants and anti-thymocyte globulin for haplo-cord transplants. Patients were vaccinated between January 2021 and January 2022, an average of 31 months (range 3-111 months) after transplantation. Sixty-one percent received the BNT162b2 (bioNtech/Pfizer) vaccine, 34% received mRNA-1273 (Modema), and 5% received JNJ-78436735 (Johnson & Johnson). After the initial vaccinations (2 doses for BNT162b2 and mRNA-1273, 1 dose for JNJ-7843673), 124 of the 145 (85%) patients had a detectable SARS-CoV-2 spike protein (5) antibody, and 21 (15%) did not respond. Ninety-nine (68%) had high-level responses (>= 100 binding antibody units [BAUI/mL)m and 25 (17%) had a low-level response (<100 BAU/mL). In multivariable analysis, lymphocyte count less than 1 x 10(9)/ mL, having chronic GVHD, and being vaccinated in the first year after transplantation emerged as independent predictors for poor response. Neither donor source nor prior exposure to rituximab was predictive of antibody response. SARS-CoV-2 vaccination induced generally high response rates in recipients of allogeneic transplants including recipients of umbilical cord blood transplants and after in-vivo T cell depletion. Responses are less robust in those vaccinated in the first year after transplantation, those with low lymphocyte counts, and those with chronic GVHD. (C) 2022 The American Society for Transplantation and Cellular Therapy. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:618.e1 / 618.e10
页数:10
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