Author: Monger, Wendy; Alamillo, Josefa M.; Sola, Isabel; Perrin, Yolande; Bestagno, Marco; Burrone, Oscar R.; Sabella, Patricia; Planaâ€Duran, Joan; Enjuanes, Luis; Garcia, Juan A.; Lomonossoff, George P.
Title: An antibody derivative expressed from viral vectors passively immunizes pigs against transmissible gastroenteritis virus infection when supplied orally in crude plant extracts Cord-id: p2h6nysu Document date: 2006_6_29
ID: p2h6nysu
Snippet: To investigate the potential of antibody derivatives to provide passive protection against enteric infections when supplied orally in crude plant extracts, we have expressed a small immune protein (SIP) in plants using two different plant virus vectors based on potato virus X (PVX) and cowpea mosaic virus (CPMV). The É›SIP molecule consisted of a singleâ€chain antibody (scFv) specific for the porcine coronavirus transmissible gastroenteritis virus (TGEV) linked to the É›â€CH4 domain from human
Document: To investigate the potential of antibody derivatives to provide passive protection against enteric infections when supplied orally in crude plant extracts, we have expressed a small immune protein (SIP) in plants using two different plant virus vectors based on potato virus X (PVX) and cowpea mosaic virus (CPMV). The É›SIP molecule consisted of a singleâ€chain antibody (scFv) specific for the porcine coronavirus transmissible gastroenteritis virus (TGEV) linked to the É›â€CH4 domain from human immunoglobulin E (IgE). In some constructs, the sequence encoding the É›SIP molecule was flanked by the leader peptide from the original murine antibody at its Nâ€terminus and an endoplasmic reticulum retention signal (HDEL) at its Câ€terminus to allow the expressed protein to be directed to, and retained within, the endoplasmic reticulum. Western blot analysis of samples from Nicotiana clevelandii or cowpea tissue infected with constructs revealed the presence of SIP molecules which retained their ability to dimerize. The analysis of crude plant extracts revealed that the plantâ€expressed É›SIP molecules could bind to and neutralize TGEV in tissue culture, the levels of binding and neutralization reflecting the level of expression. Oral administration of crude extracts from SIPâ€expressing plant tissue to 2â€dayâ€old piglets demonstrated that the extracts which showed the highest levels of in vitro neutralization could also provide in vivo protection against challenge with TGEV.
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