Vaccine compositions and method for induction of mucosal immune response via systemic vaccination
AssigneeUniversity of Utah Research Foundation
InventorsRaymond A. Daynes, Barbara A. Araneo
Life of this patent
Estimating the term…
Loading patent…
AssigneeUniversity of Utah Research Foundation
InventorsRaymond A. Daynes, Barbara A. Araneo
Estimating the term…
The invention relates to a vaccine which comprises an antigen and a lymphoid organ modifying agent. Suitable lymphoid organ modifying agents include 1,25-dihydroxy Vitamin D.sub.3, biologically active Vitamin D.sub.3 derivatives which are capable of activating the intracellular Vitamin D.sub.3 receptor, all trans-retinoic acid, retinoic acid derivatives, retinol, retinol derivatives and glucocorticoid. The vaccine composition may further comprise an immune response augmenting agent which enhances T cell lymphokine production. Suitable immune response augmenting agents include dehydroepiandrosterone (DHEA) and DHEA-derivatives. Examples of DHEA derivatives include DHEA-sulfate (DHEA-S), 16-.alpha.-bromo-DHEA, 7-oxo-DHEA, 16-.alpha.-Br-DHEA-S and 7-oxo-DHEA-S. The invention also relates to a method for inducing an antigen-specific mucosal immune response in a vertebrate animal which comprises administering a vaccine which comprises an antigen and a lymphoid organ modifying agent with or without an immune response augmenting agent to a site which drains into a peripheral lymphoid compartment.
A method for inducing an antigen-specific mucosal immune response in a vertebrate animal, which comprises administering an effective amount of at least one lymphoid organ modifying agent to the vertebrate animal at a peripheral, non-mucosal site which drains into a peripheral lymphoid organ or compartment, and administering an effective amount of a specific antigen to the vertebrate animal at a peripheral, non-mucosal site which drains into said peripheral lymphoid organ or compartment, said lymphoid organ modifying agent selected from the group consisting of all trans-retinoic acid and 1,25(OH).sub.2 D.sub.3.
A vaccine composition comprising an effective amount of at least one lymphoid organ modifying agent and an effective amount of a specific antigen in a pharmaceutically acceptable carrier to induce an antigen-specific mucosal immune response, said lymphoid organ modifying agent is selected from the group consisting of all trans-retinoic acid and 1,25(OH).sub.2 D.sub.3.
Dependencies are inferred from the claim text.