Cytomegalovirus infection enhances the immune response to influenza

被引:260
作者
Furman, David [1 ]
Jojic, Vladimir [2 ]
Sharma, Shalini [3 ]
Shen-Orr, Shai S. [4 ,5 ]
Angel, Cesar J. L. [1 ]
Onengut-Gumuscu, Suna [6 ]
Kidd, Brian A. [7 ]
Maecker, Holden T. [7 ]
Concannon, Patrick [6 ,8 ]
Dekker, Cornelia L. [9 ]
Thomas, Paul G. [3 ]
Davis, Mark M. [1 ,7 ,10 ]
机构
[1] Stanford Univ, Sch Med, Dept Microbiol & Immunol, Stanford, CA 94305 USA
[2] Univ N Carolina, Dept Comp Sci, Chapel Hill, NC 27599 USA
[3] St Jude Childrens Res Hosp, Dept Immunol, Memphis, TN 38105 USA
[4] Technion Israel Inst Technol, Fac Med, Rappaport Inst Med Res, Dept Immunol, IL-32000 Haifa, Israel
[5] Technion Israel Inst Technol, Fac Biol, IL-32000 Haifa, Israel
[6] Univ Virginia, Ctr Publ Hlth Genom, Charlottesville, VA 22903 USA
[7] Stanford Univ, Sch Med, Inst Immun Transplantat & Infect, Stanford, CA 94305 USA
[8] Univ Virginia, Dept Biochem & Mol Genet, Charlottesville, VA 22903 USA
[9] Stanford Univ, Dept Pediat, Div Infect Dis, Stanford, CA 94305 USA
[10] Howard Hughes Med Inst, Chevy Chase, MD USA
基金
以色列科学基金会;
关键词
EPSTEIN-BARR-VIRUS; C-REACTIVE PROTEIN; GENETIC-VARIANTS; T-CELLS; MEMORY; ASSOCIATION; MORTALITY; CD4(+); CMV; VACCINATION;
D O I
10.1126/scitranslmed.aaa2293
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
Cytomegalovirus (CMV) is a beta-herpesvirus present in a latent form in most people worldwide. In immunosuppressed individuals, CMV can reactivate and cause serious clinical complications, but the effect of the latent state on healthy people remains elusive. We undertook a systems approach to understand the differences between seropositive and negative subjects and measured hundreds of immune system components from blood samples including cytokines and chemokines, immune cell phenotyping, gene expression, ex vivo cell responses to cytokine stimuli, and the antibody response to seasonal influenza vaccination. As expected, we found decreased responses to vaccination and an overall down-regulation of immune components in aged individuals regardless of CMV status. In contrast, CMV-seropositive young adults exhibited enhanced antibody responses to influenza vaccination, increased CD8(+) T cell sensitivity, and elevated levels of circulating interferon-gamma compared to seronegative individuals. Experiments with young mice infected with murine CMV also showed significant protection from an influenza virus challenge compared with uninfected animals, although this effect declined with time. These data show that CMV and its murine equivalent can have a beneficial effect on the immune response of young, healthy individuals, which may explain the ubiquity of CMV infection in humans and many other species.
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页数:10
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