Cellular Adjuvants for Viral Infection
US-2024299521-A1 · Sep 12, 2024 · US
US9433673B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9433673-B2 |
| Application number | US-201514611891-A |
| Country | US |
| Kind code | B2 |
| Filing date | Feb 2, 2015 |
| Priority date | Jul 15, 2008 |
| Publication date | Sep 6, 2016 |
| Grant date | Sep 6, 2016 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
The invention relates to ultrasmall, monodisperse nanoparticles comprising silicon dioxide to the surface of which at least one antigen is attached. The nanoparticles can be used for the immunoprophylaxis or immunotherapy of cancer. The invention also relates to a method for the targeting of antigens at antigen-presenting cells and for the activation of the immune system, where the efficiency of targeting and/or immunoactivation are set via the particle characteristics. The invention also relates to a method for the active and passive immunization of a mammal.
Opening claim text (preview).
The invention claimed is: 1. A method for the activation of the immune system of a patient in need thereof and providing an adjuvant immune response, comprising parenterally administering to a patient in need thereof, monodisperse nanoparticles of silicon dioxide, where the nanoparticles have a diameter of 5 to 50 nm and are free of additional adjuvants. 2. The method of claim 1 , wherein the patient is suffering from an infectious disease, septic shock, a tumor, cancer, an autoimmune disease, an allergic or a chronic or acute inflammation process. 3. The method of claim 1 , wherein the nanoparticles have a size between 20 and 30 nm. 4. The method of claim 1 , for activating the complement system of the immune system in a patient in need thereof. 5. The method of claim 1 , wherein the nanoparticles are passively targeted at antigen-presenting cells. 6. The method of claim 1 , additionally comprising administering an antigen, and thereby targeting the antigen at antigen-presenting cells. 7. The method of claim 6 , wherein the antigen is targeted at dendritic cells in lymph nodes. 8. The method of claim 6 , wherein the antigen is attached to a surface functionality on the nanoparticles. 9. The method of claim 6 , wherein the antigen is a cancer antigen. 10. The method of claim 6 , wherein the antigen is survivin. 11. A method for the induction of a T-cell response, antibody response and/or dendritic cell maturation in a mammal, comprising administering an effective amount of a monodispersion of nanoparticles having a diameter of 5 to 50 nm suitable for parenteral administration and a solvent to said mammal, wherein the nanoparticles comprise a) a silicon dioxide matrix, and b) a surface functionality to which an antigen to be targeted is attached, with the proviso that neither said surface functionality nor said antigen is a major histocompatibility (MHC) molecule, and wherein the proliferation of T-cells and/or dendritic cells and/or the formation of neutralizing antibodies is induced. 12. A method for the passive immunization of a mammal, comprising isolating T-cells proliferated by and/or antibodies formed by the method of claim 11 , and administering said T-cells and/or antibodies to a mammal.
Immunosuppressants, e.g. drugs for graft rejection · CPC title
Immunomodulators · CPC title
Drugs for immunological or allergic disorders · CPC title
Antiallergic agents (antiasthmatic agents A61P11/06; ophthalmic antiallergics A61P27/14) · CPC title
Immunostimulants · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.