Wenyuan Shi - Los Angeles CA, US Sherie Morrison - Los Angeles CA, US Kham Trinh - Alhambra CA, US Letitia Wims - Culver City CA, US Li Chen - Los Angeles CA, US Maxwell Anderson - Seattle WA, US
International Classification:
A61K039/09
US Classification:
424/185100, 424/244100
Abstract:
Dental caries in man may be prevented or treated by oral ingestion of human or humanized murine monoclonal IgG and IgM antibodies that bind to surface antigens of cariogenic organisms, such as . The genetically engineered monoclonal antibodies engage the effector apparatus of the human immune system when they bind to cariogenic organisms, resulting in their destruction. In a preferred embodiment, monoclonal antibodies to cariogenic organisms are produced by edible plants, including fruits and vegetables, transformed by DNA sequences that code on expression for the desired antibodies. The antibodies are applied by eating the plants.
Wenyuan Shi - Los Angeles CA, US Sherie Morrison - Los Angeles CA, US Kham Trinh - Alhambra CA, US Letitia Wims - Culver City CA, US Li Chen - Los Angeles CA, US Maxwell Anderson - Seattle WA, US Fengxia Qi - Harbor City CA, US
International Classification:
A61K039/40 C07K016/46
US Classification:
424/178100, 530/391100
Abstract:
The present invention is based on the discovery of a composition that provides targeted anti-microbial effect. Specifically the composition contains a targeting moiety which recognizes a target microbial organism and an anti-microbial peptide moiety which has anti-microbial activity. In addition, the present invention provides methods of treating a microbial infection, e.g., on mucosal surfaces by using the compositions provided by the present invention.
Fusion Proteins For Targeted Delivery Of Antimicrobial Peptides
Wenyuan Shi - Los Angeles CA, US Sherie Morrison - Los Angeles CA, US Kham Trinh - Alhambra CA, US Letitia Wims - Culver City CA, US Li Chen - Los Angeles CA, US Maxwell Anderson - Seattle WA, US
Microbial infection may be treated by administration of a fusion protein comprising one or more recognition sequences and at least one antimicrobial peptide. In preferred embodiments, a linker peptide connects the recognition sequence and one or more antimicrobial peptides. The recognition sequence may be an immunoglobulin molecule, or fragment thereof, that specifically binds to a target antigen present on a pathogen. The recognition sequence may also be a non-immunological polypeptide, providing that the polypeptide binds specifically to a particular ligand. In presently preferred embodiments the recognition sequence is monoclonal antibody that binds specifically to and the antimicrobial peptides are derivatives of histatin.
Method For Targeted And Sustained Antiviral Therapy
Arash Shahangian - Los Angeles CA, US Genhong Cheng - Calabassas CA, US Lucy S. Cheng - Calabassas CA, US Kham Moc Trinh - Alhambra CA, US Paul W. Dempsey - Studio City CA, US Beichu Guo - Arcadia CA, US Sherie L. Morrison - Los Angeles CA, US
Assignee:
The Regents of the University of California - Oakland CA
Compounds compositions and methods of modulating the immune response are provided. The method uses fusion proteins of a cytokine and an antibody to potentiate the action of the cytokine.
Modified Immunoglobin Molecules And Methods For Use Thereof
Sherie L. Morrison - Los Angeles CA Koteswara R. Chintalacharuvu - Los Angeles CA Esther Mikyung Yoo - Thousand Oaks CA Kham M. Trinh - Monterey Park CA M. Josefina Coloma - Santa Monica CA
Assignee:
The Regents of the University of California - Oakland CA
International Classification:
C12N 506 C12Q 170 G01N 3353 A61K 39395 C12P 2108
US Classification:
435328
Abstract:
Disclosed are modified immunoglobulin (Ig) molecules, a method of producing modified Ig molecules, and methods for treatment and prevention of infectious diseases using modified Ig molecules. In one embodiment, the modified Ig molecule comprises a C. sub. H 3 domain of an IgA molecule (. alpha. C. sub. H 3). The combination of an. alpha. C. sub. H 3 with other domains selected from one or more nonIgA Ig molecules provides an Ig molecule that has the capacity to bind J chain and/or secretory component (SC) together with features of a nonIgA molecule. In another embodiment, the modified Ig molecule comprises a C. sub. H 1 and/or a C. sub. H 2 domain of an IgA molecule. The combination of an. alpha. C. sub. H 1 and/or C. sub. H 2 domain with other domains selected from one or more nonIgA Ig molecules provides an Ig molecule that has the capacity to form higher polymers (trimers, tetramers, pentamers, etc.
Antibody-Interferon Fusion Proteins For Enhancing Adoptive T Cell Therapies For The Treatment Of Cancer
- Oakland CA, US Reiko King - Los Angeles CA, US Patricia Young - Los Angeles CA, US Alex Vasuthasawat - Los Angeles CA, US Kham M. Trinh - Alhambra CA, US Sherie Leaver Morrison - Los Angeles CA, US
In various embodiments methods are provided that involve the use of antibody-interferon (Ab-IFN) fusion proteins to boost the cancer-fighting capacity of adoptive T cell therapies (ACT), including any T cells that are manipulated and grown outside the body, then returned to the patient with the goal of having the infused T cells home to sites of tumor and destroy the cancer in an immunologic attack. Illustrative, but non-limiting, adoptive T cell therapies include chimeric antigen receptor (CAR) T cells, tumor-infiltrating lymphocytes (TILs), virus-specific T cells, and T cell receptor transgenic T cells.
Fusion Protein Composition(S) Comprising Masked Type I Interferons (Ifna And Ifnb) For Use In The Treatment Of Cancer And Methods Thereof
- Los Angeles CA, US Sherie MORRISON - Los Angeles CA, US Alex VASUTHASAWAT - Los Angeles CA, US Kham TRINH - Porter Ranch CA, US George AYOUB - Los Angeles CA, US
Assignee:
Qwixel Therapeutics - Los Angeles CA
International Classification:
C07K 7/08 A61K 47/65 A61P 35/00
Abstract:
Fusion Protein compositions comprising masked IFNs and methods of making masked IFNs are disclosed herein. Consequently, the masked IFNs can be fused to a Mab or binding fragment thereof and be administered to patients as a therapeutic modality and provide a method of treating cancer, immunological disorders and other disease.
Anti-Cspg4 Fusions With Interferon For The Treatment Of Malignancy
In various embodiments chimeric moieties (constructs) are provided that show significant efficacy against cancers. In certain embodiments the constructs comprise a targeting moiety that specifically binds CSPG4 attached to an interferon or to a mutant interferon. In certain embodiments, the constructs comprise anti-CSPG4 antibody attached to an interferon alpha (IFN-α) or to a mutant interferon alpha or to an interferon beta (IFN-β) or to a mutant interferon beta, or to an interferon gamma (IFN-γ) or to a mutant interferon gamma.
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