Compositions and methods for treatment in broad-spectrum, undifferentiated or mixed clinical applications
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Abstract
The disclosure provides improved compositions and methods for passive immunization. In embodiments, a composition comprising a synergistic combination of specific polyclonal antibodies in a carrier matrix is provided. The disclosure provides effective, economical compositions and methods for the treatment of diarrhea and enteric infections in broad-spectrum, undifferentiated, or mixed clinical applications.
Core Innovation
The invention relates to passive immunization compositions for treatment of diarrhea or enteric infection in a non-neonate human in need thereof. The compositions include a non-neonate human effective amount of at least one specific binding molecule comprising a mixture of IgY antibodies specific for antigens derived from Escherichia coli, rotavirus, and coronavirus pathogens, and pathogen related toxins and/or pathogen related adhesion elements.
The compositions additionally include a carrier matrix comprising a matrix obtained from, isolated from, or derived from non-hyperimmune bovine colostrum. The disclosed composition scope supports use in a non-neonate human effective amount for undifferentiated diarrhea, undifferentiated pediatric diarrhea, traveler's diarrhea, rotavirus diarrhea, toxin-mediated diarrhea, cholera, C. difficile infection, dysentery, typhoid fever, peptic ulcers, and gastrointestinal flora management.
In the disclosed composition scope, the specific binding molecules are configured as a mixture of IgY antibodies that target the listed antigen sources, together with pathogen related toxins and/or pathogen related adhesion elements. The carrier matrix is derived from non-hyperimmune bovine colostrum, and the overall concept supports use in a non-neonate human effective amount for the enumerated diarrhea and enteric infection indications.
Claims Coverage
The document includes two independent claims, directed to a composition for treating diarrhea or enteric infection in a non-neonate human and a method of treating diarrhea or enteric infection in a non-neonate human by administering the composition. The inventive features across the independent claims emphasize a mixture of IgY antibodies with specified antigen targets combined with a non-hyperimmune bovine colostrum carrier matrix for defined diarrhea and enteric infection indications.
Non-neonate effective IgY mixture with pathogen toxin/adhesion targeting
A non-neonate human effective amount of at least one specific binding molecule, wherein the at least one specific binding molecules comprise a mixture of IgY antibodies specific for antigens derived from Escherichia coli, rotavirus, and coronavirus pathogens, pathogen related toxins, and/or pathogen related adhesion elements.
Non-hyperimmune bovine colostrum carrier matrix
A carrier matrix comprising a matrix obtained from, isolated from, or derived from non-hyperimmune bovine colostrum.
Treatment of enumerated diarrhea and enteric infection indications in non-neonate humans
Wherein the human non-neonate effective amount is for the treatment of undifferentiated diarrhea, undifferentiated pediatric diarrhea, traveler's diarrhea, rotavirus diarrhea, toxin-mediated diarrhea, cholera, C. difficile infection, dysentery, typhoid fever, peptic ulcers, or for gastrointestinal flora management.
Administration method for non-neonate diarrhea and enteric infection treatment
The method comprising administration of a composition comprising a non-neonate human effective amount of at least one specific binding molecule comprising a mixture of IgY antibodies specific for antigens derived from Escherichia coli, rotavirus, and coronavirus pathogens, pathogen related toxins, and/or pathogen related adhesion elements; and a carrier matrix comprising a matrix obtained from, isolated from, or derived from non-hyperimmune bovine colostrum, wherein the non-neonate human effective amount is for the treatment of undifferentiated diarrhea, undifferentiated pediatric diarrhea, traveler's diarrhea, rotavirus diarrhea, toxin-mediated diarrhea, cholera, C. difficile infection, dysentery, typhoid fever, peptic ulcers, or for gastrointestinal flora management.
Across the independent claims, coverage centers on administering or providing a composition that combines a non-neonate human effective amount of IgY antibody mixtures, including specificity for Escherichia coli, rotavirus, and coronavirus antigens plus pathogen related toxins and/or adhesion elements, with a carrier matrix derived from non-hyperimmune bovine colostrum, for the explicitly listed diarrhea and enteric infection indications and gastrointestinal flora management.
Stated Advantages
Not explicitly described in patent.
Documented Applications
Not explicitly described in patent.
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