4.7 Article

Response to Measles, Mumps and Rubella (MMR) Vaccine in Transfusion-Dependent Patients

期刊

VACCINES
卷 9, 期 6, 页码 -

出版社

MDPI
DOI: 10.3390/vaccines9060561

关键词

transfusion; red blood cells; measles; mumps; rubella; live attenuated vaccine

资金

  1. University of Campania Luigi Vanvitelli (VALERE Project)
  2. American Society of Hematology (ASH Global Research Award 2019)

向作者/读者索取更多资源

This study investigated the impact of blood transfusions on the immunogenicity of the MMR vaccine, finding no significant difference in immune responses to measles, mumps, and rubella between transfusion-dependent and non-transfusion-dependent patients. Further larger studies are needed to assess the impact of chronic transfusions on vaccine response.
Measles, mumps and rubella (MMR) still determine significant morbidity and mortality, although a highly effective vaccine is available. Postponing the MMR vaccination until 6 months after the last red blood cell (RBC) transfusion is recommended, but this delay is incompatible with chronic transfusions. The present study aimed at investigating the impact of blood transfusions on the immunogenicity of the MMR vaccine. In this observational study, a group of 45 transfusion- dependent (TD) patients was compared to 24 non-transfusion-dependent (NTD) patients. Immunity to measles was achieved in 35 (78%) TD and 21 (88%) NTD subjects (p = 0.7), to mumps in 36 (80%) TD and 21 (88%) NTD subjects (p = 0.99), and to rubella in 40 (89%) TD and 23 (96%) NTD subjects (p = 0.99). No significant difference was observed in the number of non-immune individuals or those with doubtful protection between the two groups (p > 0.05). The mean IgG value, assayed in 50 pre-storage leukoreduced RBC units, was 0.075 +/- 0.064 mg/mL, ten times lower than the level assumed in blood units and considered detrimental to the immune response in TD patients. This work shows a favorable response to MMR vaccination in TD and NTDT patients and paves the way for further larger studies assessing the impact of chronic transfusions on vaccine response.

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