Influence of Acute and Chronic Graft-Versus-Host Disease on Persistence of Antibodies against Measles, Mumps, Rubella and Varicella in the First Year after Autologous or Allogeneic Hematopoietic Stem Cell Transplantation.
Nicole HarrisonHeinz BurgmannWerner RabitschClaudia HonsigOliver RobakPublished in: Vaccines (2023)
Patients after hematopoietic stem cell transplantation (HSCT) are vulnerable to infections due to severe immunosuppression. Live-attenuated vaccines are contraindicated for two years after HSCT. The aim of this study was to assess the persistence of antibodies against measles, mumps, rubella and varicella in the first year after HSCT. Forty patients undergoing autologous ( n = 12) or allogeneic ( n = 28) HSCT were included in this study. Specific IgG antibodies to measles, mumps, rubella and varicella virus in serum samples were assessed by the LIAISON XL, a fully automated chemiluminescence analyzer, at seven different time points starting one week before HSCT and up to 12 months after HSCT. At baseline, before HSCT, most patients showed antibodies against measles (100%), mumps (80%), rubella (97.5%) and varicella (92.5%). Although titers declined over time, most patients retained antibodies against measles (92.5%), mumps (62.5%), rubella (87.5%) and varicella (85%) up to 12 months after HSCT. There was no significant difference between patients with and without GvHD concerning persistence of antibody titers. Significantly higher varicella titers were detected in autologous patients compared to patients with chronic GvHD. Considering that live-attenuated vaccines should not be administered during the first year after HSCT, the persistence of antibodies against these diseases is relevant.
Keyphrases
- end stage renal disease
- ejection fraction
- hematopoietic stem cell
- newly diagnosed
- prognostic factors
- patients undergoing
- allogeneic hematopoietic stem cell transplantation
- chronic kidney disease
- bone marrow
- peritoneal dialysis
- low dose
- intensive care unit
- randomized controlled trial
- liver failure
- machine learning
- mesenchymal stem cells
- deep learning
- high throughput
- patient reported outcomes
- study protocol
- patient reported
- stem cells
- acute respiratory distress syndrome