Contribution of Fc fragment of monoclonal antibodies to tetanus toxin neutralization
Neurotoxicity Research, 2020•Springer
Abstract Background Monoclonal antibodies (MAbs) against neurotoxin of Clostridium tetani
are considered as a novel source of immunoglobulins for passive immunotherapy of tetanus.
Toxin neutralization is classically attributed to the Fab and F (ab′) 2 fragments of
antibodies. Herein, we generated Fab and F (ab′) 2 fragments of three toxin neutralizing
mouse MAbs and compared their neutralizing activities to those of their intact molecules.
Methods Fab and F (ab′) 2 fragments of the antibodies were generated by papain and …
are considered as a novel source of immunoglobulins for passive immunotherapy of tetanus.
Toxin neutralization is classically attributed to the Fab and F (ab′) 2 fragments of
antibodies. Herein, we generated Fab and F (ab′) 2 fragments of three toxin neutralizing
mouse MAbs and compared their neutralizing activities to those of their intact molecules.
Methods Fab and F (ab′) 2 fragments of the antibodies were generated by papain and …
Background
Monoclonal antibodies (MAbs) against neurotoxin of Clostridium tetani are considered as a novel source of immunoglobulins for passive immunotherapy of tetanus. Toxin neutralization is classically attributed to the Fab and F(ab′)2 fragments of antibodies. Herein, we generated Fab and F(ab′)2 fragments of three toxin neutralizing mouse MAbs and compared their neutralizing activities to those of their intact molecules.
Methods
Fab and F (ab′)2 fragments of the antibodies were generated by papain and pepsin digestions, respectively, and their toxin neutralizing activities were compared with those of the intact antibodies in an in vivo toxin neutralization assay.
Results
While low doses of the intact MAbs were able to fully protect the mice against tetanus toxin, none of the mice which received Fab or F(ab′)2 fragments survived until day 14, even at the highest administered dose. All mice receiving human polyclonal anti-tetanus immunoglobulin or their fragments were fully protected.
Conclusion
Reduction in toxin neutralization activities of Fab and F(ab′)2 fragments of our MAbs seems to be influenced by their Fc regions. Steric hindrance of the Fc region on the receptor-binding site of the toxin may explain the stronger neutralization of the toxin by the intact MAbs in comparison to their fragments.
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