Successful SARS-CoV-2 mRNA Vaccination Program in Allogeneic Hematopoietic Stem Cell Transplant Recipients—A Retrospective Single-Center Analysis

Author:

Nikoloudis Alexander123,Neumann Ines Julia2,Buxhofer-Ausch Veronika123,Machherndl-Spandl Sigrid123,Binder Michaela13,Kaynak Emine13,Milanov Robert13,Nocker Stefanie13,Stiefel Olga123,Strassl Irene123ORCID,Wipplinger Dagmar13,Moyses Margarete13,Kerschner Heidrun34,Apfalter Petra34,Girschikofsky Michael13,Petzer Andreas123,Weltermann Ansgar123,Clausen Johannes123ORCID

Affiliation:

1. Department of Internal Medicine I: Hematology with Stem Cell Transplantation, Ordensklinikum Linz—Elisabethinen, Hemostaseology and Medical Oncology, 4020 Linz, Austria

2. Medical Faculty, Johannes Kepler University, 4020 Linz, Austria

3. Interdisciplinary Center for Infectious Medicine and Microbiology, Linz, Austria

4. Institute for Hygiene, Microbiology and Tropical Medicine, Ordensklinikum, Linz, Austria

Abstract

(1) Background: mRNA COVID-19 vaccines are effective but show varied efficacy in immunocompromised patients, including allogeneic hematopoietic stem cell transplant (HSCT) recipients. (2) Methods: A retrospective study on 167 HSCT recipients assessed humoral response to two mRNA vaccine doses, using the manufacturer cut-off of ≥7.1 BAU/mL, and examined factors affecting non-response. (3) Results: Twenty-two percent of HSCT recipients failed humoral response. Non-responders received the first vaccine a median of 10.2 (2.5–88.9) months post-HSCT versus 35.3 (3.0–215.0) months for responders (p < 0.001). Higher CD19 (B cell) counts favored vaccination response (adjusted odds ratio (aOR) 3.3 per 100 B-cells/microliters, p < 0.001), while ongoing mycophenolate mofetil (MMF) immunosuppression hindered it (aOR 0.04, p < 0.001). By multivariable analysis, the time from transplant to first vaccine did not remain a significant risk factor. A total of 92% of non-responders received a third mRNA dose, achieving additional 77% seroconversion. Non-converters mostly received a fourth dose, with an additional 50% success. Overall, a cumulative seroconversion rate of 93% was achieved after up to four doses. (4) Conclusion: mRNA vaccines are promising for HSCT recipients as early as 3 months post-HSCT. A majority seroconverted after four doses. MMF usage and low B cell counts are risk factors for non-response.

Publisher

MDPI AG

Subject

Pharmacology (medical),Infectious Diseases,Drug Discovery,Pharmacology,Immunology

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