2005
DOI: 10.1016/j.ijpara.2005.03.005
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Efficacy of a DNA vaccine delivered in attenuated Salmonella typhimurium against Eimeria tenella infection in chickens

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Cited by 64 publications
(32 citation statements)
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“…Several genes coding microneme proteins of E. tenella have been identified and cloned (Ryan et al 2000). The microneme proteins from E.tenella, Etmic2 and Etmic4 have shown protective effect (Du and Wang 2005) and in ovo vaccination with Etmic2 gene reportedly stimulated intestinal protective immunity against E. tenella and E. acervulina . Administration of short oligodeoxy nucleotide containing unmethylated CpG motifs (CpG ODNs), which are known to enhance both innate and adaptative immune responses (Krieg 1995), along with the MIC2 antigen in ovo has shown promising results .…”
Section: Recombinant Vaccinementioning
confidence: 99%
“…Several genes coding microneme proteins of E. tenella have been identified and cloned (Ryan et al 2000). The microneme proteins from E.tenella, Etmic2 and Etmic4 have shown protective effect (Du and Wang 2005) and in ovo vaccination with Etmic2 gene reportedly stimulated intestinal protective immunity against E. tenella and E. acervulina . Administration of short oligodeoxy nucleotide containing unmethylated CpG motifs (CpG ODNs), which are known to enhance both innate and adaptative immune responses (Krieg 1995), along with the MIC2 antigen in ovo has shown promising results .…”
Section: Recombinant Vaccinementioning
confidence: 99%
“…In recent years, several studies have demonstrated the feasibility of using attenuated Gram-positive and Gram-negative intracellular bacteria as live vectors for the oral delivery of recombinant vaccine antigens [20], [21]. Several Salmonella enterica Typhimurium strains submitted to attenuation procedures lost their pathogenicity but remained invasive and are used as live vectors for delivery of foreign antigens.…”
Section: Introductionmentioning
confidence: 99%
“…There are some data in the literature to suggest that complete immunity to Eimeria infections requires prior exposure to viable oocysts with sporozites capable of invading epithelial cells and carrying out some intracellular metabolism (Jenkins, Seferian, Augustine, & Danforth, 1993) and possibly schizony (Rose & Hesketh, 1976). However, potential vaccines based on Eimeria antigens have been demonstrated to provide partial protection to infection (Crane et al, 1991;Du & Wang, 2005). A vaccine derived from the whole oocyst and lacking pathogenicity upon primary infection without fecal shedding would be desirable.…”
Section: Discussionmentioning
confidence: 99%