Single-Shot Vaccines against Bovine Respiratory Syncytial Virus (BRSV): Comparative Evaluation of Long-Term Protection after Immunization in the Presence of BRSV-Specific Maternal Antibodies

被引:9
作者
Valarcher, Jean Francois [1 ]
Hagglund, Sara [1 ]
Naslund, Katarina [1 ]
Jouneau, Luc [2 ]
Malmstrom, Ester [1 ]
Boulesteix, Olivier [3 ]
Pinard, Anne [3 ]
Leguere, Dany [3 ]
Deslis, Alain [3 ]
Gauthier, David [3 ]
Dubuquoy, Catherine [2 ]
Pietralunga, Vincent [2 ]
Remot, Aude [4 ]
Falk, Alexander [5 ]
Shevchenko, Ganna [5 ]
Bergstrom Lind, Sara [5 ]
Von Bromssen, Claudia [6 ]
Vargmar, Karin [7 ]
Zhang, Baoshan [8 ]
Kwong, Peter D. [8 ]
Rodriguez, Maria Jose [9 ]
Garcia Duran, Marga [9 ]
Schwartz-Cornil, Isabelle [2 ]
Taylor, Geraldine [10 ]
Riffault, Sabine [2 ]
机构
[1] Swedish Univ Agr Sci, Dept Clin Sci, S-75007 Uppsala, Sweden
[2] Univ Paris Saclay, INRAE, UVSQ, VIM, F-78350 Jouy En Josas, France
[3] INRAE, PFIE, F-37380 Nouzilly, France
[4] Univ Tours, INRAE, ISP, F-37380 Nouzilly, France
[5] Uppsala Univ, Dept Chem BMC, S-75237 Uppsala, Sweden
[6] Swedish Univ Agr Sci, Dept Energy & Technol, S-75007 Uppsala, Sweden
[7] Swedish Univ Agr Sci, Dept Biomed & Vet Publ Hlth, S-75007 Uppsala, Sweden
[8] NIAID, Vaccine Res Ctr, NIH, 9000 Rockville Pike, Bethesda, MD 20892 USA
[9] Inmunol & Genet Aplicada SA INGENASA, Madrid 28037, Spain
[10] Pirbright Inst, Woking GU24 0NF, Surrey, England
基金
美国国家卫生研究院;
关键词
respiratory syncytial virus; bovine; neonatal; subunit vaccine; pre-fusion; live-attenuated vaccine; deleted SHrBRSV; one-shot; duration of protection; correlate of protection;
D O I
10.3390/vaccines9030236
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The induction of long-lasting clinical and virological protection is needed for a successful vaccination program against the bovine respiratory syncytial virus (BRSV). In this study, calves with BRSV-specific maternally derived antibodies were vaccinated once, either with (i) a BRSV pre-fusion protein (PreF) and Montanide(TM) ISA61 VG (ISA61, n = 6), (ii) BRSV lacking the SH gene (Delta SHrBRSV, n = 6), (iii) a commercial vaccine (CV, n = 6), or were injected with ISA61 alone (n = 6). All calves were challenged with BRSV 92 days later and were euthanized 13 days post-infection. Based on clinical, pathological, and proteomic data, all vaccines appeared safe. Compared to the controls, PreF induced the most significant clinical and virological protection post-challenge, followed by Delta SHrBRSV and CV, whereas the protection of PreF-vaccinated calves was correlated with BRSV-specific serum immunoglobulin (Ig)G antibody responses 84 days post-vaccination, and the IgG antibody titers of Delta SHrBRSV- and CV-vaccinated calves did not differ from the controls on this day. Nevertheless, strong anamnestic BRSV- and PreF-specific IgG responses occurred in calves vaccinated with either of the vaccines, following a BRSV challenge. In conclusion, PreF and Delta SHrBRSV are two efficient one-shot candidate vaccines. By inducing a protection for at least three months, they could potentially improve the control of BRSV in calves.
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页码:1 / 27
页数:27
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