The safety and short‐term outcomes of allogeneic hematopoietic stem cell transplantation with donor vaccination for COVID‐19

Dear Editor, Coronavirus disease 2019 (COVID-19), caused by severe acute respiratory syndrome coronavirus-2 (SARS-CoV2), has spread rapidly across the globe, threatening the health and safety of an increasing number of people. It has been shown that the SARS-CoV-2 vaccine is effective in reducing the chance of COVID-19 infection and the severity of the disease.1–3 To control the COVID-19 pandemic, an increasing number of studies are calling for people to receive the SARS-CoV-2 vaccine,4,5 and the Chinese government is also advocating universal vaccination. Patients with malignant hematologic diseases are mostly immunodeficient,6 and recipients are immunosuppressed when undergoing allogeneic hematopoietic stem cell transplantation (allo-HSCT).7 One report on donorderived vaccination indicated that vaccination could induce antigen-specific immune responses in patients after allo-HSCT.8 In addition, most COVID-19 vaccines in China, different from prevailing types in other countries, are inactivated SARS-CoV-2 vaccines. Hitherto, there are no reports on whether the vaccine will induce immune responses impacting immune reconstitution, complications, and outcomes of recipients. Therefore, many clinicians and patients in China hesitate to choose a COVID19-vaccinated person as a donor, which partially inspires us to collect cases of donors who received SARS-CoV-2 vaccination to explore the impact of donor vaccination with SARS-CoV-2 vaccine on recovery and outcomes after transplantation in recipients. From March 2021 to December 2021, we retrospectively collected data on a total of 253 patients who received allo-HSCT at the First Affiliated Hospital of Soochow University, none of them had ever had COVID-19 prior to transplantation, and none of them were vaccinated for COVID-19 before transplantation andduring the posttransplant follow-up period. All donors and patients provided written informed consent for the protocol approved by The

We compared the two groups for posttransplantation complications, such as GVHD and infection, as shown in Figure 1B and C. The cumulative incidences of grade II-IV acute GVHD (aGVHD) were similar between the two groups. The majority of cytomegalovirus (CMV) viremia (95.1%, 137/144) occurred 100 days after transplantation. Therefore, when followed up 100d, the cumulative incidences of CMV viremia were not significantly different between the two groups. Interestingly, the 100-day incidence of Epstein-Barr virus (EBV) viremia was 14.6% in the vaccine group, which had a higher rate of positivity than that in the control group (14.6% vs. 5.8%, p = 0.048).
The median time to onset of EBV viremia was 48d (range 24-220) in the vaccine group and 71d (range 24-214) in the control group (p = 0.046). The incidences of bacterial and fungal infections that were found to have an etiological basis followed a similar pattern.
There are no reports on whether the COVID-19 vaccination of donors affects the safety and efficacy of allo-HSCT. This study preliminarily demonstrated that donors who received the SARS-CoV-2 vaccine did not affect the shortterm outcome of allo-HSCT except for immune reconstitution. We tried to compare the clinical outcome according to the time from vaccination to stem cell collection and whether the full vaccination dosage had been completed, but we did not observe differences because most donors were completely vaccinated. It remains to be explored how the time from inoculation to stem cell collection and whether the full inoculation procedure is completed affects the safety and efficacy of allo-HSCT.
A study of live-attenuated varicella zoster vaccine noted that donor vaccination is safe, but whether it confers significant protection for patients requires further study. 9 Bogeholz et al. 10 indicated in a study of measles, mumps, and rubella antibody titers in allo-HSCT recipients that donor immune status did not appear to have an influence on antibody protection after HSCT. During our observation period, no patients were found with SARS-CoV-2 infection after transplantation, this probably be related to the absence of the COVID-19 epidemic in the area of our center. Notably, in this study, we only analyzed the short-term outcomes with allo-HSCT patients with donor vaccination with the SARS-CoV-2 vaccine, and the long-term outcomes need to be further studied.
In conclusion, pre-HSCT vaccination of the donor with the SARS-CoV-2 vaccine does not affect the shortterm safety and efficacy of allo-HSCT, and well-designed prospective studies are needed to determine whether it influences the long-term clinical outcome and provides protection to the patient.

A U T H O R C O N T R I B U T I O N S
YX and DW designed the study. YD, YS, and YF contributed to the collection of data. YS analyzed the data. YD and JC discussed and interpreted the results. YD wrote the manuscript. All authors contributed to the article and approved the submitted version.

C O N F L I C T S O F I N T E R E S T
The authors declare no conflicts of interest to report.

D ATA AVA I L A B I L I T Y S TAT E M E N T
The datasets generated during and/or analyzed during the current study are available from the corresponding author on reasonable request.

E T H I C S S TAT E M E N T
This study was approved by the ethics committee of the First Affiliated Hospital of Soochow University and was conducted in accordance with the Declaration of Helsinki. Informed consent was obtained from all patients and donors before data collection.