Interacting, Nonspecific, Immunological Effects of Bacille Calmette-Guerin and Tetanus-diphtheria-pertussis Inactivated Polio Vaccinations: An Explorative, Randomized Trial

被引:50
作者
Blok, Bastiaan A. [1 ,2 ,3 ,4 ]
de Bree, L. Charlotte J. [1 ,2 ,3 ,4 ]
Diavatopoulos, Dimitri A. [5 ,6 ]
Langereis, Jeroen D. [5 ,6 ]
Joosten, Leo A. B. [1 ,2 ]
Aaby, Peter [3 ]
van Crevel, Reinout [1 ,2 ]
Benn, Christine S. [3 ,4 ]
Netea, Mihai G. [1 ,2 ]
机构
[1] Radboud Univ Nijmegen, Med Ctr, Dept Internal Med, NL-6526 GA Nijmegen, Netherlands
[2] Radboud Univ Nijmegen, Med Ctr, Radboud Ctr Infect Dis, NL-6526 GA Nijmegen, Netherlands
[3] Statens Serum Inst, Bandim Hlth Project, Res Ctr Vitamins & Vaccines, Copenhagen, Denmark
[4] Univ Southern Denmark, Odense Univ Hosp, Odense Patient Data Explorat Network, Odense, Denmark
[5] Radboud Univ Nijmegen, Med Ctr, Radboud Inst Mol Life Sci, Lab Med Immunol,Sect Pediat Infect Dis, Nijmegen, Netherlands
[6] Radboud Univ Nijmegen, Med Ctr, Radboud Inst Mol Life Sci, Radboud Ctr Infect Dis,Lab Med Immunol, Nijmegen, Netherlands
基金
欧洲研究理事会; 新加坡国家研究基金会;
关键词
BCG; Tdap; heterologous immunity; trained immunity; BCG VACCINATION; ROUTINE VACCINATIONS; COMMUNITY COHORT; MORTALITY; VACCINES; IMMUNOGENICITY; RESPONSES; INFANTS; BIRTH;
D O I
10.1093/cid/ciz246
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. Certain vaccines, such as Bacille Calmette-Guerin (BCG), have nonspecific effects, which modulate innate immune responses and lead to protection against mortality from unrelated infections (trained immunity). In contrast, in spite of the disease-specific effects, an enhanced overall mortality has been described after diphtheria-tetanus-pertussis (DTP) vaccination in females. This randomized trial aimed to investigate the nonspecific immunological effects of BCG and DTP-containing vaccines on the immune response to unrelated pathogens. Methods. We randomized 75 healthy, female, adult volunteers to receive either BCG, followed by a booster dose of tetanus-diphtheria-pertussis inactivated polio vaccine (Tdap) 3 months later; BCG and Tdap combined; or Tdap followed by BCG 3 months later. Blood was collected before vaccination, as well as at 1 day, 4 days, 2 weeks, and 3 months after the first vaccination(s), plus 2 weeks after the second vaccination. Ex vivo leukocyte responses to unrelated stimuli and pathogens were assessed. Results. Tdap vaccination led to short-term potentiation and long-term repression of monocyte-derived cytokine responses, and short-term as well as long-term repression of T-cell reactivity to unrelated pathogens. BCG led to short-term and long-term potentiation of monocyte-derived cytokine responses. When given together with Tdap or after Tdap, BCG abrogated the immunosuppressive effects of Tdap vaccination. Conclusions. Tdap induces immunotolerance to unrelated antigens, which is partially restored by concurrent or subsequent BCG vaccination. These data indicate that the modulation of heterologous immune responses is induced by vaccination with Tdap and BCG, and more studies are warranted to investigate whether this is involved in the nonspecific effects of vaccines on mortality.
引用
收藏
页码:455 / 463
页数:9
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