The present disclosure provides methods and composition including vaccines, monoclonal antibodies, polyclonal antibodies, chimeric molecule of an extracellular fibrinogen binding protein (Efb) and targeted agent delivery pharmaceutical composition comprising at least a portion of a modified N-terminus region, at least a portion of a modified C-terminus region, or both, wherein the modified extracellular fibrinogen binding protein results in inhibiting the fibrinogen binding, C3 binding, or both or administering to a subject a pharmacologically effective amount of a vaccine in a pharmaceutically acceptable excipient, comprising a modified extracellular fibrinogen binding protein comprising at least a portion of a modified N-terminus region, at least a portion of a modified C-terminus region, or both, wherein the modified extracellular fibrinogen binding protein results in not shielding the staphylococcus bacterium from recognition by a phagocytic receptor.

Compositions and the use of a fibrinogn binding motif presence in efb and coa for vaccine against staphylococcus aureus and drug delivery

VISAI LIVIA
;
BERTOGLIO FEDERICO;
2020-01-01

Abstract

The present disclosure provides methods and composition including vaccines, monoclonal antibodies, polyclonal antibodies, chimeric molecule of an extracellular fibrinogen binding protein (Efb) and targeted agent delivery pharmaceutical composition comprising at least a portion of a modified N-terminus region, at least a portion of a modified C-terminus region, or both, wherein the modified extracellular fibrinogen binding protein results in inhibiting the fibrinogen binding, C3 binding, or both or administering to a subject a pharmacologically effective amount of a vaccine in a pharmaceutically acceptable excipient, comprising a modified extracellular fibrinogen binding protein comprising at least a portion of a modified N-terminus region, at least a portion of a modified C-terminus region, or both, wherein the modified extracellular fibrinogen binding protein results in not shielding the staphylococcus bacterium from recognition by a phagocytic receptor.
2020
20-mag-2020
Immunology incorporates cellular and molecular studies in immunology, as well as clinical research in immunopathology, infectious disease, autoimmunity, and allergy. Host-pathogen interactions in infectious disease, as well as experimental therapeutic applications of immunomodulating agents are also considered. Resources dealing primarily with the biology of microbial, viral, or parasitic pathogens are excluded and are covered in the Microbiology category.
US20200283508A1
TECHNISCHE UNIVERSITAET BRAUNSCHWEIG, TEXAS A & M UNIVERSITY UMC UTRECHT HOLDING, UNIVERSITA DEGLI STUDI DI PAVIA, UNIVERSITY MEDICAL CENTER UTRECHT THE NETHERLANDS
Inglese
Internazionale
fibrinogn binding motif , Efb, CoA, vaccine, Stap.aureus, drug delivery
https://patents.google.com/patent/US20160235832A1/en
6 Brevetti::6.1 Brevetto
none
KO YA-PING, (US); HOOK MAGNUS, (US); ROOIJAKKERS SUZAN HM, (NL); Visai, Livia; Bertoglio, Federico; HUST MICHAEL, (DE); MEIER DORIS, (DE)
info:eu-repo/semantics/patent
285
7
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11571/1464044
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