| Vaccines | |
| Humoral Responses and Chronic GVHD Exacerbation after COVID-19 Vaccination Post Allogeneic Stem Cell Transplantation | |
| Paul Schnitzler1  Carsten Müller-Tidow2  Peter Dreger2  Maria-Luisa Schubert2  Laura Simons2  Caroline Pabst2  Stefan Schönland2  Sascha Dietrich2  Nora Liebers2  Michael Schmitt2  Ute Hegenbart2  Leandra Caille2  Maike Janssen2  Aleksandar Radujkovic2  Lixiazi He2  Thomas Luft2  Claudius Speer3  Louise Benning3  | |
| [1] Department of Infectious Diseases, Virology, University Hospital, 69120 Heidelberg, Germany;Department of Medicine V, University Hospital Heidelberg, 69120 Heidelberg, Germany;Department of Nephrology, University of Heidelberg, 69120 Heidelberg, Germany; | |
| 关键词: allogeneic stem cell transplantation; COVID-19; cGVHD; humoral responses; immunosuppression; | |
| DOI : 10.3390/vaccines10020330 | |
| 来源: DOAJ | |
【 摘 要 】
The COVID-19 pandemic threatens patients with a compromised immune and endothelial system, including patients who underwent allogeneic stem cell transplantation (alloSCT). Thus, there is an unmet need for optimizing vaccination management in this high-risk cohort. Here, we monitored antibodies against SARS-CoV-2 spike protein (anti-S1) in 167 vaccinated alloSCT patients. Humoral immune responses were detectable in 81% of patients after two vaccinations with either mRNA-, vector-based, or heterologous regimens. Age, B-cell counts, time interval from vaccination, and the type of vaccine determined antibody titres in patients without systemic immunosuppression (sIS). Similar to a healthy control cohort, mRNA vaccine-based regimens induced higher titres than vector-based vaccines. Patients on two or more immunosuppressants rarely developed immunity. In contrast, 62% and 45% of patients without or on only one immunosuppressant, respectively, showed a strong humoral vaccination response (titre > 100). Exacerbation of cGVHD upon vaccination was observed in 6% of all patients and in 22% of patients receiving immunosuppression for cGVHD. cGVHD exacerbation and low antibody titres were both associated with higher angiopoietin-2 (ANG2) serum levels. In conclusion, mRNA-based vaccines elicit strong humoral responses in alloSCT patients in the absence of double sIS. Biomarkers such as ANG2 might help with weighing cGVHD risk versus beneficial responses.
【 授权许可】
Unknown