Th1 versus Th2 T cell polarization by whole-cell and acellular childhood pertussis vaccines persists upon re-immunization in adolescence and adulthood

被引:72
作者
Bancroft, Tara [1 ]
Dillon, Myles B. C. [1 ]
Antunes, Ricardo da Silva [1 ]
Paul, Sinu [1 ]
Peters, Bjoern [1 ]
Crotty, Shane [1 ]
Arlehamn, Cecilia S. Lindestam [1 ]
Sette, Alessandro [1 ]
机构
[1] La Jolla Inst Allergy & Immunol, 9420 Athena Circle, La Jolla, CA 92037 USA
基金
美国国家卫生研究院;
关键词
Epitope; Pertussis; Re-immunization; T cell polarization; Vaccine; CHEMOKINE RECEPTOR EXPRESSION; ANTIBODY-RESPONSE; IMMUNE-RESPONSES; UNITED-STATES; VACCINATION; INFANTS; KINETICS; CHILDREN; PROTEINS; MEMORY;
D O I
10.1016/j.cellimm.2016.05.002
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The recent increase in cases of whooping cough among teenagers in the US suggests that the acellular Bordetella pertussis vaccine (aP) that became standard in the mid 1990s might be relatively less effective than the whole-bacteria formulation (wP) previously used since the 1950s. To understand this effect, we compared antibody and T cell responses to a booster immunization in subjects who received either the wP or aP vaccine as their initial priming dose in childhood. Antibody responses in wP- and aP-primed donors were similar. Magnitude of T cell responses was higher in aP-primed individuals. Epitope mapping revealed the T cell immunodominance patterns were similar for both vaccines. Further comparison of the ratios of IFN gamma and IL-5 revealed that IFN gamma strongly dominates the T cell response in wP-primed donors, while IL-5 is dominant in aP primed individuals. Surprisingly, this differential pattern is maintained after booster vaccination, at times from eighteen years to several decades after the original aP/wP priming. These findings suggest that childhood aP versus wP vaccination induces functionally different T cell responses to pertussis that become fixed and are unchanged even upon boosting. (C) 2016 Elsevier Inc. All rights reserved.
引用
收藏
页码:35 / 43
页数:9
相关论文
共 38 条
[1]   Anti-pertussis antibody kinetics following DTaP-IPV booster vaccination in Norwegian children 7-8 years of age [J].
Aase, Audun ;
Herstad, Tove Karin ;
Jorgensen, Silje Bakken ;
Leegaard, Truls Michael ;
Berbers, Guy ;
Steinbakk, Martin ;
Aaberge, Ingeborg .
VACCINE, 2014, 32 (45) :5931-5936
[2]  
[Anonymous], 1992, MMWR Recomm Rep, V41, P1
[3]  
[Anonymous], 2015, PERT CAS YEAR
[4]   Memory T Cells in Latent Mycobacterium tuberculosis Infection Are Directed against Three Antigenic Islands and Largely Contained in a CXCR3+CCR6+ Th1 Subset [J].
Arlehamn, Cecilia S. Lindestam ;
Gerasimova, Anna ;
Mele, Federico ;
Henderson, Ryan ;
Swann, Justine ;
Greenbaum, Jason A. ;
Kim, Yohan ;
Sidney, John ;
James, Eddie A. ;
Taplitz, Randy ;
McKinney, Denise M. ;
Kwok, William W. ;
Grey, Howard ;
Sallusto, Federica ;
Peters, Bjoern ;
Sette, Alessandro .
PLOS PATHOGENS, 2013, 9 (01)
[5]   Vaccine- and antigen-dependent type 1 and type 2 cytokine induction after primary vaccination of infants with whole-cell or acellular pertussis vaccines [J].
Ausiello, CM ;
Urbani, F ;
laSala, A ;
Lande, R ;
Cassone, A .
INFECTION AND IMMUNITY, 1997, 65 (06) :2168-2174
[6]   Th1/Th2 cell dichotomy in acquired immunity to Bordetella pertussis: Variables in the in vivo priming and in vitro cytokine detection techniques affect the classification of T-cell subsets as Th1, Th2 or Th0 [J].
Barnard, A ;
Mahon, BP ;
Watkins, J ;
Redhead, K ;
Mills, KHG .
IMMUNOLOGY, 1996, 87 (03) :372-380
[7]   Pertussis vaccine effectiveness among children 6 to 59 months of age in the United States, 1998-2001 [J].
Bisgard, KM ;
Rhodes, P ;
Connelly, BL ;
Bi, DL ;
Hahn, C ;
Patrick, S ;
Glodé, MP ;
Ehresmann, KR .
PEDIATRICS, 2005, 116 (02) :E285-E294
[8]  
CDC, 2015, PERT OUTBR TRENDS
[9]   Pertussis re-emergence in the post-vaccination era [J].
Chiappini, Elena ;
Stival, Alessia ;
Galli, Luisa ;
de Martino, Maurizio .
BMC INFECTIOUS DISEASES, 2013, 13
[10]  
CODY CL, 1981, PEDIATRICS, V68, P650