Provided herein are self-assembling pharmaceutical compositions comprising a heat shock protein fused to a biotin-binding protein, wherein the biotin-binding protein is non-covalently bound to four biotinylated components, and further wherein at least two of the four biotinylated components are not identical.

Provided herein are self-assembling pharmaceutical compositions comprising a heat shock protein fused to a biotin-binding protein, wherein the biotin-binding protein is non-covalently bound to four biotinylated components, and further wherein at least two of the four biotinylated components are not identical.

The present disclosure provides fusion proteins comprising Mycobacterium tuberculosis (Mtb) antigens, nucleic acid molecules encoding the same, vectors comprising nucleic acid molecules, compositions comprising the same, and methods of eliciting an immune response against tuberculosis.

The present disclosure provides fusion proteins comprising Mycobacterium tuberculosis (Mtb) antigens, nucleic acid molecules encoding the same, vectors comprising nucleic acid molecules, compositions comprising the same, and methods of eliciting an immune response against tuberculosis.

The present disclosure relates to chimeric small molecules, which find utility as modifiers of target substrates according to the formula A-L.sub.1-E-B or A-L.sub.1-E-L.sub.2-B, wherein A is a kinase binding moiety; B is a target binding moiety; L.sub.1 and L.sub.2 are each a linker; and E is an electrophilic reactive group. Molecules according to the present invention find use making substrate modifications such as post-translational modifications to targets that are not the natural substrate of the kinase; accordingly, diseases or disorders may be treated or prevented with molecules of the present disclosure.

The invention features combination therapies using an IL-15-based superagonist complex and an antibody to effectively treat subjects with cancer and infectious diseases.

The invention features combination therapies using an IL-15-based superagonist complex and an antibody to effectively treat subjects with cancer and infectious diseases.

The present invention provides a fusion protein comprising an HPV cancer-causing protein segment, a coding sequence thereof and an application thereof in preparing drugs for detecting or treating HPV-related diseases. The fusion protein can simultaneously induce the humoral immunity and the cellular immunity for a high-risk HPV cancer protein and has anti-cancer activity in vivo.

The present invention provides a fusion protein comprising an HPV cancer-causing protein segment, a coding sequence thereof and an application thereof in preparing drugs for detecting or treating HPV-related diseases. The fusion protein can simultaneously induce the humoral immunity and the cellular immunity for a high-risk HPV cancer protein and has anti-cancer activity in vivo.

The present invention refers to the use of gene sequences or portions thereof characterized in that the same belong to the classes of in vitro and ex vivo induced, repressed or conserved genes in Mycobacterium tuberculosis currently infected human macrophages and to corresponding peptides or consensus peptides or proteins for the preparation of specific bio-markers for the diagnosis and prevention of active or latent disease.