Vaccination against tick-borne encephalitis (TBE) after autologous and allogeneic stem cell transplantation

•Tick-borne encephalitis (TBE) can result in severe disease in immunocompromised patients.•Four vaccine doses induced seropositivity in a majority (77%) of patients.•We found no safety issues using FSME-immun® after stem cell transplant.•Graft-versus host disease (GVHD) was associated with lower ant...

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Veröffentlicht in:Vaccine 2021-02, Vol.39 (7), p.1035-1038
Hauptverfasser: Einarsdottir, Sigrun, Nicklasson, Malin, Veje, Malin, Bergström, Tomas, Studahl, Marie, Lisak, Mikael, Olsson, Mikael, Johansson, Berit, Andreasson, Björn, Piauger, Bénédicte, Roth, Anette, Friman, Vanda, Ljungman, Per, Brune, Mats
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Sprache:eng
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Zusammenfassung:•Tick-borne encephalitis (TBE) can result in severe disease in immunocompromised patients.•Four vaccine doses induced seropositivity in a majority (77%) of patients.•We found no safety issues using FSME-immun® after stem cell transplant.•Graft-versus host disease (GVHD) was associated with lower antibody levels.•It seems important to prime patients with four vaccine doses. Our aim was to assess response and side effects of 4 doses of TBE vaccine to patients (pts) after allo- and autologous stem cell transplantation (SCT). PATIENTS: Included were 104 pts with leukaemia, myeloma and lymphoma, median age 61 yrs. METHODS: Vaccine (FSME-Immun®) was given at 9, 10, 12, and 21 months post-transplant. Serum samples were obtained before and after vaccinations. Healthy controls (n = 27) received 3 vaccinations. Assessments of TBE specific IgG antibodies were performed by Enzygnost anti-TBE ELISA test (Siemens, Sweden). Antibody levels (>12 U/mL; “seropositivity”) were seen in 77% and 80% of pts after allo- and autoSCT; IgG levels; 89 vs 94 U/mL. Ongoing chronic GvHD and immunosuppression (n = 29) was associated with sero-negativity in the last sample (p = 0.007). All controls (n = 27) developed protective antibody levels. TBE vaccination was safe, and 4 doses starting 9 months post-SCT, induced seropositivity in a vast majority of pts.
ISSN:0264-410X
1873-2518
DOI:10.1016/j.vaccine.2020.12.073