Patent classifications
C07K16/1232
ERADICATION OF BACTERIAL BIOFILM USING ANTI-AMYLOID MONOCLONAL ANTIBODIES
The present invention features compositions comprising an anti-amyloid antibody and methods of treating microbial infection and treating or preventing microbial biofilms using the composition.
Method for treating infectious diseases using a composition comprising plasma-derived immunoglobulin M (IgM)
Compositions and methods of the present invention prevent, inhibit or reduce the toxic effects of proteins and toxins secreted from microbes. A method for neutralizing microbial protein products in a subject comprises administering a composition to the subject, said composition comprising plasma-derived IgM and optionally one or more excipients in a pharmaceutical carrier, wherein the composition is administered in an amount effective to neutralize the microbial protein products.
ANTI-CfaE ANTIBODIES AND METHODS OF USE
The invention provides anti-CfaE antibodies and methods of using the same.
E. COLI FIMH MUTANTS AND USES THEREOF
This disclosure relates to the design of E. coli mutated FimH polypeptides that result in improved biochemical properties and immunogenicity, compositions comprising such polypeptides, and uses thereof.
COMPOSITIONS AND METHODS FOR THE REMOVAL OF BIOFILMS
This disclosure provides isolated or recombinant polypeptides that are useful to vaccinate individuals suffering from chronic/recurrent biofilm disease or as a therapeutic for those with an existing infection. The individual's immune system will then naturally generate antibodies which prevent or clear these bacteria from the host by interfering with the construction and or maintenance of a functional protective biofilm. Alternatively, antibodies to the polypeptides can be administered to treat or prevent infection. Bacteria that cannot form functional biofilms are more readily cleared by the remainder of the host's immune system and/or traditional antibiotics.
METHODS AND COMPOSITIONS RELATING TO SYNTHETIC BETA-1,6 GLUCOSAMINE OLIGOSACCHARIDES
The invention relates to the compositions of synthetic oligo-γ-(1.fwdarw.6)-2-amino-2-deoxy-D-glu-copyranosides conjugated to carriers, and methods for making and use same.
ESCHERICHIA COLI COMPOSITIONS AND METHODS THEREOF
- Robert G.K. Donald ,
- Annaliesa Sybil Anderson ,
- Laurent Oliver Chorro ,
- Jianxin Gu ,
- Jin-Hwan Kim ,
- Srinivas Kodali ,
- Jason Arnold Lotvin ,
- Justin Keith Moran ,
- Rosalind Pan ,
- Avvari Krishna Prasad ,
- Mark Edward Ruppen ,
- Suddham Singh ,
- Ling Chu ,
- Scott Ellis Lomberk ,
- Karen Kiyoko Takane ,
- Nishith Merchant ,
- Wei Chen
In one aspect, the invention relates to an immunogenic composition comprising modified O-polysaccharide molecules derived from E. coli lipopolysaccharides and conjugates thereof. Multivalent vaccines may be prepared by combining two or more monovalent immunogenic compositions for different E. coli serotypes. In one embodiment, the modified O-polysaccharide molecules are produced by a recombinant bacterium that includes a wzz gene.
Compositions and methods for the treatment of immunodeficiency
The present invention relates to compositions and methods for the treatment of immunodeficiency (e.g., primary immunodeficiency disease). In particular, the invention provides human plasma immunoglobulin compositions containing select antibody titers specific for a plurality of respiratory pathogens, methods of identifying human donors and donor samples for use in the compositions, methods of manufacturing the compositions, and methods of utilizing the compositions (e.g., for prophylactic administration and/or therapeutic treatment (e.g., passive immunization (e.g., immune-prophylaxis))).
Anti-ETEC adhesin protein antibodies and methods of use
The invention provides anti-ETEC adhesin protein antibodies and methods of using the same.
PATHOGEN BINDING PROTEINS
The present invention relates to proteins, compositions and their use, wherein said protein comprises a first peptide having a first binding specificity, a second peptide having a second binding specificity and a linker, wherein said first and said second peptides bind at least one pathogen surface component and/or at least one molecule produced by a pathogen.