Anti-Cancer DNA Vaccine Employing Plasmids Encoding Signal Sequence, Mutant Oncoprotein Antigen, and Heat Shock Protein

a plasmid encoding and anti-cancer technology, applied in the field of molecular biology, immunology and medicine, can solve the problems of lack of potency of vaccines, limited administration, and none of these vaccines have been ideally designed for humans use, and achieve enhanced immunogenicity and promote the processing of antigens.

Inactive Publication Date: 2018-05-24
THE JOHN HOPKINS UNIV SCHOOL OF MEDICINE
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

The present invention provides an immunotherapeutic strategy that combines DNA vaccine compositions with a signal peptide for secretion and a second protein, such as HSP70, to enhance the immunogenicity of the vaccine. The invention uses certain polypeptides that target antigen to CD8+ T cells, which are important for immune response. This strategy involves incorporating nucleic acid sequences that encode polypeptides to modify the way the antigen is received and handled by the immune system. Overall, the invention helps to strengthen the vaccine's ability to promote immunity against the antigen.

Problems solved by technology

However, one limitation of these vaccines is their lack of potency, since the DNA vaccine vectors generally do not have the intrinsic ability to be amplified and to spread in vivo as do some replicating viral vaccine vectors.
However, none of these vaccines have been ideally designed use in humans where administration may be limited for practical or other reasons to intramuscular injection.

Method used

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  • Anti-Cancer DNA Vaccine Employing Plasmids Encoding Signal Sequence, Mutant Oncoprotein Antigen, and Heat Shock Protein
  • Anti-Cancer DNA Vaccine Employing Plasmids Encoding Signal Sequence, Mutant Oncoprotein Antigen, and Heat Shock Protein
  • Anti-Cancer DNA Vaccine Employing Plasmids Encoding Signal Sequence, Mutant Oncoprotein Antigen, and Heat Shock Protein

Examples

Experimental program
Comparison scheme
Effect test

example i

Materials and Methods

[0200]Mice: Six- to eight-week-old female C57BL / 6 mice were purchased from the National Cancer Institute (Frederick, Md.) and kept in the oncology animal facility of the Johns Hopkins Hospital (Baltimore, Md.). All animal procedures were performed according to approved protocols and in accordance with the recommendations for the proper use and care of laboratory animals.

[0201]Plasmid DNA Construction: The E7 / 70 gene was cloned into pNGVL4a (National Gene Vector Laboratory) using the EcoRI and KpnI restriction sites. Using site-directed mutagenesis, two point mutations, which had previously been found to reduce Rb binding (Munger, K et al., EMBO J 1989, 8:4099-4105), were introduced into the E7 gene. The primers used to introduce these mutations were as follows:

[0202]mE7 Forward: 5′ ctgatctotacggttatgggcaattaaatgacagetc 3′ [SEQ ID NO: 14] and

[0203]mE7 Reverse: 5′ gagctgtcatttaattgcccataaccgtagagatca 3′ [SEQ ID NO: 15].

[0204]For construction of pNGVL4a-Sig / E7(deto...

example ii

pNGVL4a-Sig / E7(Detox) / FISP70 DNA Vector Administered by Gene Gun Generated Highest Number of E7-Specific CD8+ T Cells in Immunized Mice

[0213]This study compared the ability of the pNGVL4a-Sig / E7(detox) / HSP70 DNA vaccine composition to generate E7-specific CD8+ T cell precursors by evaluation intracellular cytokines in splenocytes from mice vaccinated with the same DNA construct by three different modes of administration: needle i.m., biojector, and gene gun. Splenocytes from nave or immunized vaccinated groups of mice were incubated with or without the MHC class I (H-2 Db)-restricted E7 peptide (aa 49-57) (SEQ ID NO:2) to detect E7-specific CD8+ T cells.

[0214]Results are shown in FIGS. 1A and 1B / Mice vaccinated via gene gun exhibited significantly higher numbers (p+ CD8+ T cell precursors per fixed number of splenocyte (832.5) compared to mice vaccinated via biojector (445.5) and needle i.m. (375.5). These findings suggest that the gene gun approach was somewhat more potent in this ...

example iii

Vaccinated Mice Were Protected In Vivo Against E7-Expressing Tumors

[0215]The next study investigated protection against TC-1 tumor, expressing the same antigen, E7, as the pNGVL4a-Sig / E7(detox) / HSP70 vaccine, administered by the three routes. In vivo tumor protection experiment (vaccination before tumor challenge) used the well-characterized E7-expressing tumor model, TC-1. As shown in FIG. 2, mice receiving pNGVL4a-Sig / E7(detox) / HSP70 via gene gun, biojector, or needle i.m. remained 100% tumor free after TC-1 tumor challenge. Thus, this vaccine vector administered by different routes generated total protection against growth of later-administered tumor cells expressing the E7 antigen.

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Abstract

Novel nucleic acid vectors comprising sequences encoding (a) an antigen, (b) a signal peptide, and (c) a heat shock protein, are disclosed, as are methods for using such vectors to induce antigen-specific immune responses and to treat tumors.

Description

BACKGROUND OF THE INVENTIONField of the Invention[0001]The present invention in the fields of molecular biology, immunology and medicine relates to chimeric nucleic acid molecules that encode an antigen, a signal peptide, and an immunogenicity-potentiating polypeptide (“IPP”) such as the heat shock protein HSP70, and their uses a immunogenic compositions to induce and enhance immune responses, primarily cytotoxic T lymphocyte responses to specific antigens such as tumor or viral antigens.Description of the Background Art[0002]Cytotoxic T lymphocytes (CTL) are critical effectors of anti-viral and antitumor responses (reviewed in Chen, C H et al., J. Biomed Sci. 5: 231-252, 1998; Pardoll, D M. Nat Med. 4: 525-531, 1998; Wang, R F et al., Immunol Rev. 170: 85-100, 1999). Activated CTL are effector cells that mediate antitumor immunity by direct lysis of their target tumor cells or virus-infected cells and by releasing of cytokines that orchestrate immune and inflammatory responses that...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): C07K14/35A61KA61K39/00A61K39/12A61K48/00C12N15/74
CPCC07K14/35A61K2039/585A61K2039/54C12N2710/20022A61K39/12C12N2710/20034C07K2319/02A61K2039/6043A61K2039/55516A61K2039/53A61K39/0011A61P35/00A61K2300/00
Inventor WU, TZYY-CHOOUHUNG, CHIEN-FU
Owner THE JOHN HOPKINS UNIV SCHOOL OF MEDICINE
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