Methods for treating HPV-associated diseases
OwnerScott Loughhead, LeeAnn Talarico +7inventors
InventorsScott Loughhead, LeeAnn Talarico, Alfonso Vicente-Suarez, Matt Booty, Howard Bernstein, Katarina Blagovic, Armon R. Sharei, Kelan Hlavaty, Melissa Myint
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Abstract
The present application provides immune cells comprising an HPV antigen and an adjuvant, methods of manufacturing such modified immune cells, and methods of using such modified immune cells for treating an HPV-associated disease, preventing an HPV-associated disease and/or for modulating an immune response in an individual with an HPV-associated disease.
Claims9
A composition comprising modified immune cells, wherein the immune cells are modified to comprise intracellularly a CpG ODN and an HPV antigen with at least 90% similarity to any one of SEQ ID NOs:18-25.
A composition comprising modified immune cells, wherein the immune cells are modified to comprise an HPV antigen, wherein the HPV antigen comprises an amino acid sequence with at least 90% similarity to any one of SEQ ID NOs:18-25.
A composition comprising an antigen, wherein the antigen comprises an amino acid sequence with at least 90% similarity to SEQ ID NO:23.
A plurality of modified peripheral blood mononuclear cells (PBMCs), wherein the PBMCs are modified to comprise an antigen and an increased expression of one or more of IFN-γ, IL-6, MCP-1, MIP-1β, IP-10, or TNF-α compared to a plurality of unmodified PBMCs, wherein the expression of one or more of IFN-γ, IL-6, MCP-1, MIP-1β, IP-10 or TNF-α is increased upon incubation of the plurality of modified PBMCs with an adjuvant, and wherein the antigen is exogenous to the modified PBMCs.
A plurality of modified PBMCs, wherein the PBMCs are modified to comprise an antigen and an adjuvant and an increased expression of one or more of IFN-γ, IL-6, MCP-1, MIP-1β, IP-10, or TNF-α compared to a plurality of unmodified PBMCs, wherein the expression of one or more of IFN-γ, IL-6, MCP-1, MIP-1β, IP-10, or TNF-α is increased upon incubation of the plurality of modified PBMCs with a second adjuvant, and wherein the antigen is exogenous to the modified PBMCs.
A plurality of modified PBMCs, wherein the PBMCs are modified to comprise an antigen and an increased expression of one or more of IFN-γ, IL-6, MCP-1, MIP-1β, IP-10, or TNF-α compared to a plurality of unmodified PBMCs, prepared by a process comprising the steps of:
- a) passing a cell suspension comprising a plurality of input PBMCs through a cell-deforming constriction, wherein a diameter of the constriction is a function of a diameter of the input PBMCs in the suspension, thereby causing perturbations of the input PBMCs large enough for the antigen to pass through to form a plurality of perturbed input PBMCs;
- b) incubating the plurality of perturbed input PBMCs with the antigen for a sufficient time to allow the antigen to enter the perturbed input PBMCs, thereby generating a plurality of modified PBMCs comprising the antigen;
- and
- c) incubating the plurality of modified PBMCs comprising the antigen with an adjuvant for a sufficient time to generate the modified PBMCs comprising the antigen with increased expression of one or more of IFN-γ, IL-6, MCP-1, MIP-1β, IP-10, or TNF-α.
A plurality of modified PBMCs, wherein the PBMCs are modified to comprise an antigen and an increased expression of one or more of IFN-γ, IL-6, MCP-1, MIP-1β, IP-10, or TNF-α compared to a plurality of unmodified PBMCs, prepared by a process comprising the steps of;
- a) incubating a plurality of input PBMCs with an adjuvant for a sufficient time to generate PBMCs with increased expression of one or more of IFN-γ, IL-6, MCP-1, MIP-1β, IP-10, or TNF-α;
- b) passing a cell suspension comprising the plurality of input PBMCs through a cell-deforming constriction, wherein a diameter of the constriction is a function of a diameter of the input PBMCs in the suspension, thereby causing perturbations of the input PBMCs large enough for the antigen to pass through to form a plurality of perturbed input PBMCs;
- and
- c) incubating the plurality of perturbed input PBMCs with the antigen for a sufficient time to allow the antigen to enter the perturbed input PBMCs, thereby generating the plurality of modified PBMCs comprising the antigen.
Dependencies are inferred from the claim text.