Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Carbon nanotube compositions and methods of use thereof

a technology of carbon nanotubes and compositions, applied in the field of carbon nanotube compositions, can solve the problems of limited malaria and hiv, and many other infectious diseases involving intracellular pathogens, and achieve the limitation of the development of deadly diseases vaccines, and the development of many other infectious diseases

Inactive Publication Date: 2016-07-28
YALE UNIV
View PDF3 Cites 4 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

This patent describes a new type of vaccine that uses a unique carbon structure called CNT to activate T cells. CNTs help deliver antigens to natural immune cells and activate them. The vaccine is made by attaching anti-CD3 antibodies onto CNT bundles, which are better at stimulating T cells than other materials. The CNTs provide a superior scaffold for the immune cells and help make the vaccine more effective. Overall, this new vaccine is a more efficient and effective way to activate T cells and has potential applications in immunotherapy.

Problems solved by technology

By contrast vaccines for many other infectious diseases, such as malaria and HIV, which involve intracellular pathogens, are poorly developed or simply unavailable.
The lack of such vaccines will result in two million unnecessary deaths each year in many parts of the world.
Although economic factors play a role, there are a number of significant scientific challenges that have limited the development of vaccines for deadly diseases.
First, few if any approaches are available that efficiently prime cell-mediated immunity by direct intracellular delivery of an antigen.
Second, ‘tunable’ adjuvants, that is, adjuvants that can be engineered to optimize the magnitude and direction of an immune response, have not been developed.
Third, the general requirement for parenteral (i.e. subcutaneous or intramuscular injection) administration of vaccines, a situation that has made it difficult to deploy vaccines in underdeveloped countries where medical support systems, resources, and even refrigeration are limited.
Finally, there is a lack of a general approach to designing oral vaccines targeted to both systemic and mucosal immunity; oral vaccines are significantly less expensive to administer and transport.
Despite the successes of these studies, adoptive T cell transfer by clonal expansion is not clinically viable since it does not consistently generate therapeutic numbers of T cells.

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Carbon nanotube compositions and methods of use thereof
  • Carbon nanotube compositions and methods of use thereof
  • Carbon nanotube compositions and methods of use thereof

Examples

Experimental program
Comparison scheme
Effect test

example 1

Effect of Chemical Treatments on Surface Area of SWNTs and Protein Adsorption

Materials and Methods

[0242]Materials

[0243]Biotin Anti-CD3 was purchased from BD Biosciences—Pharminogen (San Jose, Calif.). Treated and raw SWNT were obtained from the Department of Chemical Engineering at Yale University.

[0244]Raw SWNT Chemical Treatment

[0245]SWNT bundles were stirred in a 3M HNO3 at 70° C. for 1 hour. The sample was then filtered through a 5 μm pore size PTFE membrane and dried at 45° C. overnight in an oven. Reduced samples entailed the addition of LiBH4 solution in THF (200 mg SWNT+125 ml THF+400 mg LiBH4), then sonication for 1.5 hour. This chemical procedure gives the (3M HNO3 / LiBH4) SWNT group. If the procedure was stopped after the oxidation step (without LiBH4 treatment), the SWNT group is simply called (3M HNO3).

[0246]Determination of Dry SWNT Surface Area

[0247]Dry SWNT (or A.C.) surface area was determined by physisorption of nitrogen using the Brunauer-Emmett-Teller method (B.E....

example 2

Cytocompatibility of SWNTs

[0261]Materials and methods were as described above with respect to Example 1, except as noted below.

[0262]Materials and Methods:

[0263]Cytotoxicity Study

[0264]A metabolic assay, Cell Titer Blue (CTB) assay, was used to assess cell viability exposed to SWNT. Each group was cultured in triplicates. A measured amount of sterile SWNT at 2.5 mg / ml was serially diluted in a sterile 96 well U-bottom cell culture plate with RPMI 1640 containing 10% fetal bovine serum (FBS) and 2% penicillin streptomycin (PS). Sodium azide was included as a negative control at an initial volume of 2.5% and was diluted analogously. Hybridoma T cells (B3Z) at a concentration of 4×105 cells / ml were then added uniformly to the assay. The plate was incubated for 24 hours at 37° C. and 5% CO2. Forty microliters of CTB proliferation reagent was added to each well, including the control (no SWNT) then incubation was allowed for 4 more hours at 37° C. and 5% CO2. Cell proliferation was monit...

example 3

Stimulation of T Cells Using SWNTs

[0267]Materials and methods were as described above with respect to Examples 1 and 2, except as noted below.

[0268]Materials and Methods:

[0269]T-Cell Stimulation Using Anti CD3 Loaded SWNT

[0270]The stimulation of T-cells (B3z) was quantified using a mouse IL-2 ELISA. Anti-CD3 and SWNT bundles were mixed overnight at 4° C. on a rotary mixer to allow for physical adsorption of anti-CD3, followed by a washing step to remove unbound anti-CD3. The washed sample was then re-suspended in sterile PBS at the same initial volume. SWNT antibody solution was serially diluted in a microplate followed by the addition of 100 μl of T-Cells (B3z) at 4×105 cells / ml. The cell culture plate was incubated for 24 hrs. at 37° C. and 5% CO2. An identical protocol was used for all SWNT groups. For control, soluble and plated anti-CD3, the stimulus was used in similar amounts to anti CD3 loaded SWNT before the wash step. After incubation an ELISA was then performed on IL-2 ex...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

PropertyMeasurementUnit
concentrationaaaaaaaaaa
pHaaaaaaaaaa
pHaaaaaaaaaa
Login to View More

Abstract

Carbon nanotube (CNT)-based compositions for activating cellular immune responses are provided. The CNTs function as high surface area scaffolds for the attachment of T cell ligands and / or antigens. The CNT compositions function as artificial antigen-presenting cells (aAPCs) or as modular vaccines. The disclosed CNT aAPCs are efficient at activating T cells and may be used to activate T cells ex vivo or in vivo for adoptive or active immunotherapy.

Description

CROSS REFERENCE TO RELATED APPLICATIONS[0001]This application is a continuation of pending application Ser. No. 13 / 842,782, filed Mar. 15, 2013, which is a continuation in part of U.S. Ser. No. 12 / 933,223, now U.S. Pat. No. 8,658,174, filed Sep. 17, 2010, which is the National Stage of International Application No. PCT / US09 / 37727 filed Mar. 19, 2009, which claims priority to and benefit of U.S. Provisional Patent Application No. 61 / 037,798, filed on Mar. 19, 2008, the contents of which are incorporated by reference in their entirety.STATEMENT REGARDING FEDERALLY SPONSORED RESEARCH OR DEVELOPMENT[0002]This invention was made with government support awarded by the National Science Foundation under Career Award Number 0747577 to Tarek M. Fahmy. The United States government has certain rights in this invention.FIELD OF THE INVENTION[0003]The present disclosure generally relates to the field of carbon nanotube compositions and methods for making and using these compositions.BACKGROUND OF...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
Patent Type & Authority Applications(United States)
IPC IPC(8): A61K39/00A61K35/17
CPCA61K35/17A61K39/00A61K39/385A61K2039/55555A61K2039/6093A61K39/39A61K38/2013Y10S977/746Y10S977/75Y10S977/847Y10S977/918A61K39/4611A61K2239/57A61K39/4644A61K39/0011A61K2039/5158Y02A50/30A61K9/20A61K2035/124B82Y5/00B82Y40/00
Inventor FAHMY, TAREK M.PFEFFERLE, LISA D.HALLER, GARY L.
Owner YALE UNIV
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com