The Effect of Age on the Immunogenicity of the Live Attenuated Zoster Vaccine Is Predicted by Baseline Regulatory T Cells and Varicella-Zoster Virus-Specific T Cell Immunity

被引:21
作者
Weinberg, Adriana [1 ]
Pang, Lei [2 ]
Johnson, Michael J. [1 ]
Caldas, Yupanqui [1 ]
Cho, Alice [1 ]
Tovar-Salazar, Adriana [1 ]
Canniff, Jennifer [1 ]
Schmader, Kenneth E. [3 ]
Popmihajlov, Zoran [2 ]
Levin, Myron J. [1 ]
机构
[1] Univ Colorado Denver, Anschutz Med Campus, Aurora, CO 80045 USA
[2] Merck Sharp & Dohme Ltd, Kenilworth, NJ USA
[3] Duke Univ, Durham, NC USA
关键词
cell-mediated immunity; herpes zoster; zoster vaccine live; HERPES-ZOSTER; RESPONSES; TOXICITIES; INFECTION; EFFICACY; BLOOD;
D O I
10.1128/JVI.00305-19
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Older age is associated with increased infectious morbidity and decreased immune responses to vaccines, but the mechanisms that mediate this effect are incompletely understood. The efficacy and immunogenicity of the live attenuated zoster vaccine (ZVL) have a very-well-described negative association with the age of the vaccinee. In a study of 600 ZVL recipients 50 to >80 years of age, we investigated immunological factors that might explain the effect of age on the immunogenicity of ZVL. Using FluoroSpot assays and flow cytometry, we determined that varicella-zoster virus (VZV)-specific peak T helper 1 (VZV-Th1) responses to ZVL were independently predicted by prevaccination VZV-Th1 responses, regulatory T cells (Treg), and PD1-expressing immune checkpoint T cells (Tcheck) but not by the age of the vaccinee. Persistence of VZV-Th1 1 year after vaccination was independently predicted by the factors mentioned above, by peak VZV-Th1 responses to ZVL, and by the age of the vaccinee. We further demonstrated by ex vivo blocking experiments the mechanistic role of PD1 and CTLA4 as modulators of decreased VZV-Th1 responses in the study participants. VZV-specific cytotoxic T cell (VZV-CTL) and T follicular helper responses to ZVL did not correlate with age, but similar to other Th1 responses, VZV-CTL peak and baseline responses were independently correlated. These data expand our understanding of the factors affecting the magnitude and kinetics of T cell responses to ZVL in older adults and show the importance of prevaccination Treg and Tcheck in modulating the immunogenicity of ZVL. This presents new potential interventions to increase vaccine responses in older adults. IMPORTANCE Vaccination is the most effective method to protect older adults against viral infections. However, the immunogenicity of viral vaccines in older adults is notoriously poor. The live attenuated zoster vaccine (ZVL) provides the best example of a gradual decrease of vaccine immunogenicity with every 10-year age increase above 50 years. Here we show that the abundance of regulatory T cells before vaccine administration to older adults has a significant inhibitory effect on immune responses to ZVL and, together with baseline immunity to varicella-zoster virus, explains the effect of age on the immunogenicity of ZVL. Moreover, in vitro blockade of regulatory T cell mechanisms of action with biologic modulators restores immune responses to varicella-zoster virus in vaccinees. Collectively, these observations suggest that immune modulators that block regulatory T cell activity may increase responses to viral attenuated vaccines in older adults.
引用
收藏
页数:17
相关论文
共 29 条
  • [1] Ageing and immunity. Addressing immune senescence to ensure healthy ageing
    Boraschi, Diana
    Del Giudice, Giuseppe
    Dutel, Catherine
    Ivanoff, Bernard
    Rappuoli, Rino
    Grubeck-Loebenstein, Beatrix
    [J]. VACCINE, 2010, 28 (21) : 3627 - 3631
  • [2] The split personality of regulatory T cells in HIV infection
    Chevalier, Mathieu F.
    Weiss, Laurence
    [J]. BLOOD, 2013, 121 (01) : 29 - 37
  • [3] Inflamm-ageing and lifelong antigenic load as major determinants of ageing rate and longevity
    De Martinis, M
    Franceschi, C
    Monti, D
    Ginaldi, L
    [J]. FEBS LETTERS, 2005, 579 (10): : 2035 - 2039
  • [4] Infection with cytomegalovirus but not herpes simplex virus induces the accumulation of late-differentiated CD4+ and CD8+ T-cells in humans
    Derhovanessian, Evelyna
    Maier, Andrea B.
    Hahnel, Karin
    Beck, Robert
    de Craen, Anton J. M.
    Slagboom, Eline P.
    Westendorp, Rudi G. J.
    Pawelec, Graham
    [J]. JOURNAL OF GENERAL VIROLOGY, 2011, 92 : 2746 - 2756
  • [5] Pre-vaccination inflammation and B-cell signalling predict age-related hyporesponse to hepatitis B vaccination
    Fourati, Slim
    Cristescu, Razvan
    Loboda, Andrey
    Talla, Aarthi
    Filali, Ali
    Railkar, Radha
    Schaeffer, Andrea K.
    Favre, David
    Gagnon, Dominic
    Peretz, Yoav
    Wang, I-Ming
    Beals, Chan R.
    Casimiro, Danilo R.
    Carayannopoulos, Leonidas N.
    Sekaly, Rafick-Pierre
    [J]. NATURE COMMUNICATIONS, 2016, 7
  • [6] Franceschi C, 2000, ANN NY ACAD SCI, V908, P244
  • [7] Antibody response to influenza vaccination in the elderly: A quantitative review
    Goodwin, K
    Viboud, C
    Simonsen, L
    [J]. VACCINE, 2006, 24 (08) : 1159 - 1169
  • [8] Foxp3+ Regulatory T Cells in Tuberculosis
    Larson, Ryan P.
    Shafiani, Shahin
    Urdahl, Kevin B.
    [J]. NEW PARADIGM OF IMMUNITY TO TUBERCULOSIS, 2013, 783 : 165 - 180
  • [9] Immunogenicity of Varicella Vaccine and Immunologic Predictors of Response in a Cohort of Elderly Nursing Home Residents
    Lelic, Alina
    Verschoor, Chris P.
    Lau, VivianW. C.
    Parsons, Robin
    Evelegh, Carole
    Bowdish, Dawn M.
    Bramson, Jonathan L.
    Loeb, Mark B.
    [J]. JOURNAL OF INFECTIOUS DISEASES, 2016, 214 (12) : 1905 - 1910
  • [10] Varicella-zoster virus-specific immune responses in elderly recipients of a herpes zoster vaccine
    Levin, M. J.
    Oxman, M. N.
    Zhang, J. H.
    Johnson, G. R.
    Stanley, H.
    Hayward, A. R.
    Caulfield, M. J.
    Irwin, M. R.
    Smith, J. G.
    Clair, J.
    Chan, I. S. F.
    Williams, H.
    Harbecke, R.
    Marchese, R.
    Straus, S. E.
    Gershon, A.
    Weinberg, A.
    [J]. JOURNAL OF INFECTIOUS DISEASES, 2008, 197 (06) : 825 - 835