Immunogenic compositions, antigen screening methods, and methods of generating immune responses
An immunogenic composition is provided herein. The immunogenic compositions are used to identify and select immunogenic antigens that elicit immune responses in a subject and may be subsequently used in multi-antigen vaccine compositions against one or more diseases or conditions. According to some embodiments, the immunogenic composition may include a plurality of nucleic acid fragments or minigenes derived from a nucleic acid library, wherein each nucleic acid fragment encodes a different antigen or functional portion thereof, and wherein the different antigens or functional portions thereof are associated with one or more disease or condition. The immunogenic composition may also include a delivery medium loaded with the plurality of nucleic acid fragments and in some embodiments, the delivery medium is loaded with nucleic acid fragments in such a way that individual antigen presenting cells receive only a subset of the nucleic acids within a vaccine in order to minimize antigenic competition.
1. An immunogenic composition comprising:
two or more plasmid pools, including a first plasmid pool and a second plasmid pool;
where at least the first plasmid pool is loaded onto a first delivery medium and where at least the second plasmid pool is loaded onto a second delivery medium;
where the first and the second delivery media are loaded into a dosing container;
where the first plasmid pool comprises a first plurality of plasmids and where the second plasmid pool comprises a second plurality of plasmids different from the first plurality of plasmids;
where each plasmid in the two or more plasmid pools contains one or more nucleic-acid sequences encoding a protein, or proteins, or a protein fragment;
where the first and the second delivery media comprise particles, each smaller than the size of the cell receiving the particle, or micro-needles; and
where at least the first and the second plasmid pools in the dosing container together contain more than one of the nucleic-acid sequences.
2. The immunogenic composition of claim 1 where the particles or micro-needles are gold.
3. The immunogenic composition of claim 1 where the number of plasmid pools is three or more.
4. The immunogenic composition of claim 1 where each of the plasmid pools encodes for a different set of proteins or protein fragments.
5. An immunogenic composition comprising:
two or more nucleic-acid pools, including a first nucleic-acid pool and a second nucleic-acid pool;
where at least the first nucleic-acid pool is loaded onto a first delivery medium and where at least the second nucleic-acid pool is loaded onto a second delivery medium;
where the first and the second delivery media are loaded into a dosing container;
where the first nucleic-acid pool comprises a first plurality of nucleic-acid fragments and where the second nucleic-acid pool comprises a second plurality of nucleic-acid fragments different from the first plurality of nucleic-acid fragments;
where each nucleic-acid fragment in the two or more nucleic-acid pools contains one or more nucleic-acid sequences encoding a protein, or proteins, or a protein fragment;
where the first and the second delivery media comprise particles, each smaller than the size of the cell receiving the particle, or micro-needles;
where at least the first and the second nucleic-acid pools in the dosing container together contain more than one of the nucleic-acid sequences.
6. The immunogenic composition of claim 5 where the particles or micro-needles are gold.
7. The immunogenic composition of claim 5 where the number of nucleic-acid pools is three or more.
8. The immunogenic composition of claim 5 where each of the nucleic-acid pools encodes for a different set of proteins or protein fragments.
9. A method of eliciting an immune response in a subject comprising administering the immunogenic composition of claim 1 to the subject to treat a disease or condition, wherein the disease or condition is caused by one or more of an infectious pathogen, by a malignancy, by an autoimmune disease, or by transplantation.
10. The method of claim 9 , wherein the disease or condition is malaria.
11. A method of eliciting an immune response in a subject comprising administering the immunogenic composition of claim 5 to the subject to treat disease or condition, wherein the disease or condition is caused by one or more of an infectious pathogen, by a malignancy, by an autoimmune disease, or by transplantation.
12. The method of claim 11 , wherein the disease or condition is malaria.
13. A method of screening candidate antigens or epitopes associated with a disease or condition comprising:
exposing one or more subjects to the immunogenic composition of claim 1 ;
analyzing one or more biological samples obtained from the one or more subjects using an assay to measure the response to the immunogenic composition; and
identifying a nucleic acid fragment that is part of the immunogenic composition as encoding a candidate antigen or epitope when the nucleic acid fragment elicits a response measured by the assay in the one or more biological samples.
14. A method of screening candidate antigens or epitopes associated with a disease or condition comprising:
exposing one or more subjects to the immunogenic composition of claim 5 ;
analyzing one or more biological samples obtained from the one or more subjects using an assay to measure the response to the immunogenic composition; and
identifying a nucleic acid fragment that is part of the immunogenic composition as encoding a candidate antigen or epitope when the nucleic acid fragment elicits a response measured by the assay in the one or more biological samples.