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Clostridium difficile toxin peptide acts as mucosal adjuvant.

Vaccine Weekly

| July 07, 2004 | COPYRIGHT 2004 NewsRX. This material is published under license from the publisher through the Gale Group, Farmington Hills, Michigan.  All inquiries regarding rights should be directed to the Gale Group. (Hide copyright information)Copyright

2004 JUL 7 - (NewsRx.com & NewsRx.net) -- Clostridium difficile toxin A carboxyl-terminus peptide lacking ADP-ribosyltransferase activity acts as a mucosal adjuvant.

"The receptor binding domains of the most potent mucosal adjuvants, bacterial toxins and plant lectins, are organized in repeat units to recognize specific sugar residues. The lectin-like structure of the C-terminal region of Clostridium difficile toxin A prompted us to investigate the mucosal adjuvant properties of a nontoxigenic peptide corresponding to amino acids 2394 to 2706 (TxA[subscript]C314). We compared TxA[subscript]C314 adjuvant activity to those of cholera toxin (CT) and Escherichia coli heat-labile enterotoxin subunit B (EtxB) co-administered orally or nasotracheally with poor peptide antigens (keyhole limpet hemocyanin [KLH] and hen egg lysozyme [HEL])," investigators in Italy report.

"Levels of anti-KLH-specific serum immunoglobulin G (IgG) and IgA as well as that of mucosal IgA were significantly higher in animals immunized orally with TxA[subscript]C314 plus KLH than with KLH alone, CT plus KLH, or EtxB plus KLH," said Ignazio Castagliuolo and colleagues at the University of Padua. "Following intranasal immunization with TxA[subscript]C314 plus HEL, levels of serum- and mucosa-specific antibodies were comparable to those induced by co-administering HEL with CT or EtxB. The TxA[subscript]C314 adjuvant effect following oral, but not intranasal, immunization was dose dependent."

"The analysis of the subclasses of anti-KLH-specific IgG ...

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