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Clinical and Diagnostic Laboratory Immunology, 03 1997, 147-155, Vol 4, No. 2
NL Tout and JS Lam
Immunotherapy with antibodies (Abs) against the lipopolysaccharide (LPS) of
Pseudomonas aeruginosa remains an alternative to serotype- specific
LPS-based vaccines due to their limited use and to antibiotics due to the
intrinsic resistance to antimicrobials observed in P. aeruginosa. We have
chosen a monoclonal Ab (MAb), MF23-1, that binds to the O antigen of the
most clinically relevant serotype, IATS O6, for producing a recombinant
antibody. Heavy (H) and light (L) chain genes were isolated from MF23-1 to
form a functional Fab molecule in the periplasm of Escherichia coli and on
the surface of phage by using phagemid vector pComb3. The entire kappa L
chain gene was used, but the H chain gene was amplified to 2 amino acids
past cysteine 128 which is involved in interchain disulfide bond formation
with the L chain. The truncated H chain associated with the L chain in the
periplasm of E. coli to form a functional Fab molecule that bound in both
enzyme-linked immunosorbent assay (ELISA) and immunofluorescence assay to
O6 LPS. Therefore, the remainder of the CH1 past cysteine 128 is not
essential for stable formation of the Fab portion of MF23-1. This
recombinant Fab (r-Fab) was shown to be specific for the LPS of the most
predominant clinical isolate, serotype O6, while no cross-reactivity was
detected to the LPS of the other 19 remaining serotypes. This r-Fab was
also expressed on the surface of filamentous phage upon addition of helper
phage to recombinant E. coli containing phagemid. Recombinant phage from
clones MT13 and MT24 bound specifically to O6 LPS in ELISA. These results
represent an important step toward the design of therapeutic Abs to be used
against P. aeruginosa infections.
Copyright © 1997 by the American Society for Microbiology. All rights reserved.
Phage display and bacterial expression of a recombinant Fab specific for Pseudomonas aeruginosa serotype O6 lipopolysaccharide
Department of Microbiology, University of Guelph, Ontario, Canada.
| Antimicrob. Agents Chemother. | Clin. Microbiol. Rev. | Infect. Immun. |
|---|---|---|
| J. Clin. Microbiol. | J. Virol. | ALL ASM JOURNALS |