Methods and Compositions for Preventing a Condition

a technology of compositions and methods, applied in the field of methods and compositions for preventing a condition, can solve the problems of few effective vaccines available, reduce one or more symptoms, and prevent or reduce the likelihood of the subject developing cancer

Inactive Publication Date: 2014-01-09
CYVAX
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

The composition elicits a synergistic and enhanced immune response, potentially equivalent to or greater than that achieved by irradiated sporozoites, effectively preventing or reducing the likelihood of malaria, cancer, or Alzheimer's disease, by targeting specific immune cells and enhancing antigen presentation.

Problems solved by technology

For some conditions, e.g., malaria, few effective vaccines are available.

Method used

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  • Methods and Compositions for Preventing a Condition
  • Methods and Compositions for Preventing a Condition
  • Methods and Compositions for Preventing a Condition

Examples

Experimental program
Comparison scheme
Effect test

example 1

[0274]C57BL / 6 mice were immunized with 2 μg of the constructs (FIG. 1), and were delivered as single injection in 100 μl of PBS or PBS formulated with Vaxfectin. Mice received three immunizations at bi-weekly intervals (i.e. over 6 weeks). For the control group, 105 (initial immunization) and 5×104 (booster immunizations) irradiated P. yoelii sporozoites (17XN) were inoculated by tail-vein injection at the same time-points. All challenges were accomplished by injecting 5×103 sporozoites in the tail vein two weeks after last immunization. Results for antibody responses are illustrated in FIG. 2; results for protective efficacy against sporozoites challenge are illustrated in FIG. 3; and results for antibody neutralization activity are illustrated in FIG. 4.

example 2

[0275]C57BL / 6 mice were immunized with 2 μg of pCSP or pMCSP constructs (see FIG. 1) and were delivered as single injection in 100 μl of PBS formulated with Vaxfectin. Mice received three immunizations at bi-weekly intervals (i.e. over 6 weeks). To deplete the CD4+, CD8+, or both T cell subsets, immunized mice were injected (intraperitoneal; i.p) with anti-CD4, anti-CD8, or both mAbs two weeks after last immunization. Twenty four hours later, the efficacy of the depletion was estimated by two-color flow cytometry analysis of peripheral blood lymphocytes using FITC-conjugated anti-CD4 or APC-conjugated anti-CD8 mAbs (FIG. 5). Data show the CD4 and CD8 expression on combined peripheral lymphocytes of three mice in each group. Sporozoites challenge was performed by injecting 2500 sporozoites in mice tail vein. FIG. 6 illustrates protection mediated by immunization with Vaxfectin-formulated CSP or MCSP. Antibody response is illustrated in FIG. 7 and antibody neutralization activity is i...

example 3

[0276]C57BL / 6 mice were immunized with 100 μl PBS or 2 μg of Vaxfectin formulated plasmids DNA (100 μl) (see FIG. 1). 24 or 48 hours later, injected muscles are harvested and total RNA is isolated. Indicated cytokine or chemokine levels were analyzed by real-time PCR.

[0277]FIG. 9 illustrates real-time PCR evaluation of expression levels of cytokines (24 h after immunization). FIG. 10 illustrates real-time PCR evaluation of expression levels of cytokines (48 h after immunization).

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Abstract

Provided herein are methods, compositions, and kits for preventing, inhibiting, reducing the severity of, or treating a disease or condition. A pharmaceutical composition provided herein can comprise a nucleic acid sequence encoding an antigen fused to an immune cell product, e.g., MIP-3α, and an adjuvant. The antigen can be from a bacteria, virus, fungus, parasite, or cancer. The antigen can be an Alzheimer's disease antigen.

Description

CROSS-REFERENCE TO RELATED APPLICATIONS[0001]This application is a continuation of U.S. application Ser. No. 13 / 206,471, filed on Aug. 9, 2011, which claims the benefit of U.S. Provisional Applications Nos. 61 / 371,923, filed Aug. 9, 2010, and 61 / 466,175, filed Mar. 22, 2011, all of which are incorporated herein by reference in their entireties.STATEMENT AS TO FEDERALLY SPONSORED RESEARCH[0002]This invention was made with the support of the United States government under Grant number R21AI073619 by National Institutes of Health. The government has certain rights in the invention.BACKGROUND OF THE INVENTION[0003]Vaccines play a role in the prevention and treatment of diseases, including cancer and infections. For some conditions, e.g., malaria, few effective vaccines are available. Vaccine studies using irradiated sporozoites have demonstrated the theoretical feasibility of an effective vaccine to protect against the pre-erythrocytic stages of malaria infection. Subsequent studies hav...

Claims

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Application Information

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Patent Type & AuthorityApplications(United States)
IPC IPC(8): A61K39/39A61K39/015
CPCA61K2039/53A61K39/39A61K39/015A61K2039/55522A61K31/713A61K2039/6031A61K31/7105A61K39/0011A61P25/00A61P25/28A61P31/04A61P31/10A61P31/12A61P33/00A61P33/06A61P35/00A61P37/02A61P37/04Y02A50/30A61K39/295C12N15/62
InventorMARKHAM, RICHARD
OwnerCYVAX