Tetanus-diphtheria-pertussis vaccine may suppress the immune response to subsequent immunization with pneumococcal CRM197-conjugate vaccine (coadministered with quadrivalent meningococcal TT-conjugate vaccine): a randomized, controlled triala⟨†

被引:13
作者
Tashani, Mohamed [1 ,2 ]
Heron, Leon [1 ,3 ]
Wong, Melanie [4 ]
Rashid, Harunor [1 ,2 ,5 ,6 ]
Booy, Robert [1 ,2 ,5 ,6 ,7 ]
机构
[1] Childrens Hosp, NCIRS, Westmead, NSW, Australia
[2] Univ Sydney, Discipline Paediat & Child Hlth, Sydney Med Sch, Sydney, NSW, Australia
[3] Childrens Hosp, Kids Res Inst, Westmead, NSW, Australia
[4] Childrens Hosp, Dept Immunol, Westmead, NSW, Australia
[5] Univ Sydney, Marie Bashir Inst Infect Dis & Biosecur, Sch Biol Sci, Sydney, NSW, Australia
[6] Univ Sydney, Sydney Med Sch, Sydney, NSW, Australia
[7] Flinders Univ S Australia, WHO Collaborating Ctr Mass Gatherings & High Cons, Adelaide, SA, Australia
关键词
Pneumococcal conjugate vaccine; Hajj; carrier priming; carrier interference; pneumococcal opsonophagocytic assay; GLYCOCONJUGATE VACCINES; ANTIBODY-RESPONSE; INFLUENZA VACCINE; CARRIER PROTEIN; IMMUNOGENICITY; INFANTS; SAFETY;
D O I
10.1093/jtm/tax006
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Background: Due to their antigenic similarities, there is a potential for immunological interaction between tetanus/diphtheria-containing vaccines and carrier proteins presented on conjugate vaccines. The interaction could, unpredictably, result in either enhancement or suppression of the immune response to conjugate vaccines if they are injected soon after or concurrently with diphtheria or tetanus toxoid. We examined this interaction among adult Australian travellers before attending the Hajj pilgrimage of 2015. Methods: We randomly assigned each participant to one of three vaccination schedules. Group A received tetanus, diphtheria and acellular pertussis vaccine (Tdap) 3-4 weeks before receiving CRM197-conjugated 13-valent pneumococcal vaccine (PCV13) coadministered with TT-conjugated quadrivalent meningococcal vaccine (MCV4). Group B received all three vaccines concurrently. Group C received PCV13 and MCV4 3-4 weeks before Tdap. Blood samples collected at baseline, at each vaccination visit and 3-4 weeks after vaccination were tested for the pneumococcal opsonophagocytic assay (OPA). Results: A total of 166 participants aged 18-64 (median 42) years were recruited, 159 completed the study. Compared with the other groups, Group A had significantly (P < 0.05) lower geometric mean titres (GMTs) post-vaccination in seven serotypes of PCV13 (1, 3, 4, 5, 14, 18C and 9V). Additionally, Group A had lower frequency of serorises (a parts per thousand<yen> 4-fold rise in OPA titres) in serotype5 (79%, p= 0.01) and 18C (73.5%, p= 0.06); whereas Groups B and C had significantly lower frequencies of serorises in Serotype 4 (82%) and 6A (73.5%), respectively. No statistically significant difference was detected across the three groups in frequencies achieving OPA titre a parts per thousand<yen> 1:8 post-vaccination. Conclusions: Tdap vaccination 3-4 weeks before administration of PCV13 and MCV4 significantly reduced the GMTs to seven of the 13 pneumococcal serotypes in adults. If multiple vaccination is required before travel, deferring tetanus/diphtheria until after administering the conjugate vaccine is recommended to avoid immune interference.
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页数:7
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