Genetically defined race, but not sex, is associated with higher humoral and cellular immune responses to measles vaccination

被引:26
作者
Voigt, Emily A. [1 ]
Ovsyannikova, Inna G. [1 ]
Haralambieva, Lana H. [1 ]
Kennedy, Richard B. [1 ]
Larrabee, Beth R. [2 ]
Schaid, Daniel J. [2 ]
Poland, Gregory A. [1 ]
机构
[1] Mayo Clin, Vaccine Res Grp, Rochester, MN 55905 USA
[2] Mayo Clin, Dept Hlth Sci Res, Rochester, MN 55905 USA
基金
美国国家卫生研究院;
关键词
Measles; Measles vaccine; Measles virus; Measles-mumps-rubella vaccine; Continental population groups; Sex factors; Immunity; cellular; humoral; ANTIBODY-RESPONSE; SMALLPOX VACCINE; UNITED-STATES; CYTOKINE RESPONSES; POLYMORPHISMS; SEROPREVALENCE; MUMPS; POPULATION; OUTBREAK; CHILDREN;
D O I
10.1016/j.vaccine.2016.08.060
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
In addition to host genetic and environmental factors, variations in immune responses to vaccination are influenced by demographic variables, such as race and sex. The influence of genetic race and sex on Measles vaccine responses is not well understood, yet important for the development of much-needed improved measles vaccines with lower failure rates. We assessed associations between genetically defined race and sex with measles humoral and cellular immunity after measles vaccination in three independent and geographically distinct cohorts totaling 2872 healthy racially diverse children, older adolescents, and young adults. We found no associations between biological sex and either humoral or cellular immunity to measles vaccine, and no correlation between humoral and cellular immunity in these study subjects. Genetically defined race was, however, significantly associated with both measles vaccine-induced humoral and cellular immune responses, with subjects genetically classified as having African-American ancestry demonstrating significantly higher antibody and cell-mediated immune responses relative to subjects of Caucasian ancestry. This information may be useful in designing novel measles vaccines that are optimally effective across human genetic backgrounds. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:4913 / 4919
页数:7
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