Literature DB >> 7590827

Idiotypic DNA vaccines against B-cell lymphoma.

F K Stevenson1, D Zhu, C A King, L J Ashworth, S Kumar, R E Hawkins.   

Abstract

Idiotypic antigens are clearly defined tumor-associated protein antigens, which can induce protective immunity against lymphoma. Because each patient requires an individual vaccine, idiotypic antigens also provide ideal candidates for exploring the feasibility of replacing protein antigens by DNA vaccines. Component idiotypic variable region genes can be identified in patients' tumor biopsies and rapidly assembled as scFv sequences. These can be used to produce recombinant scFv protein in bacteria, or as direct naked DNA vaccines. A preliminary small trial of DNA vaccines for chemotherapy-resistant patients with lymphoma has begun. Intramuscular idiotypic DNA vaccination in a mouse model induces low levels of anti-idiotypic antibody in serum. Levels can be increased dramatically by coinjection of DNA plasmids encoding either IL-2 or GM-CSF, and specific proliferative anti-idiotypic T cells are induced. However protective immunity remains to be demonstrated, and a possible reason for this may lie in the continued secretion of idiotypic scFv antigen which blocks antibody activity by formation of immune complexes. Methods for regulating secretion of antigen are required before this category of tumor antigen can be fully exploited as a vaccine. The power of DNA technology should allow analysis and manipulation of pathways of antigen presentation to induce maximal therapeutic attack on neoplastic B cells. In addition, lymphoma presents a model for application of DNA technology to the wide range of human tumors known to harbor potential tumor antigens.

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Year:  1995        PMID: 7590827     DOI: 10.1111/j.1600-065x.1995.tb00083.x

Source DB:  PubMed          Journal:  Immunol Rev        ISSN: 0105-2896            Impact factor:   12.988


  8 in total

Review 1.  Stem cell transplantation.

Authors:  A L Lennard; G H Jackson
Journal:  BMJ       Date:  2000-08-12

Review 2.  Vaccination strategies for lymphomas.

Authors:  Mohammed M Dar; Larry W Kwak
Journal:  Curr Oncol Rep       Date:  2003-09       Impact factor: 5.075

3.  Comparison of adenoviruses as oncolytics and cancer vaccines in an immunocompetent B cell lymphoma model.

Authors:  Eric A Weaver; Christopher Y Chen; Shannon M May; Mary E Barry; Michael A Barry
Journal:  Hum Gene Ther       Date:  2011-09-06       Impact factor: 5.695

4.  Inhibition of a vaccine-induced anti-tumor B cell response by soluble protein antigen in the absence of continuing T cell help.

Authors:  Natalia Savelyeva; Catherine A King; Ellen S Vitetta; Freda K Stevenson
Journal:  Proc Natl Acad Sci U S A       Date:  2005-07-21       Impact factor: 11.205

5.  Vaccination with syngeneic, lymphoma-derived immunoglobulin idiotype combined with granulocyte/macrophage colony-stimulating factor primes mice for a protective T-cell response.

Authors:  L W Kwak; H A Young; R W Pennington; S D Weeks
Journal:  Proc Natl Acad Sci U S A       Date:  1996-10-01       Impact factor: 11.205

6.  Tumor-associated embryonic antigen-expressing vaccines that target CCR6 elicit potent CD8+ T cell-mediated protective and therapeutic antitumor immunity.

Authors:  Arya Biragyn; Roberta Schiavo; Purevdorj Olkhanud; Kenya Sumitomo; Alan King; Megan McCain; Fred E Indig; Giovanni Almanzar; Dolgor Baatar
Journal:  J Immunol       Date:  2007-07-15       Impact factor: 5.422

7.  Enhancement of DNA vaccine potency through linkage of antigen to filamentous bacteriophage coat protein III domain I.

Authors:  Angel M Cuesta; Eduardo Suárez; Martin Larsen; Kim Bak Jensen; Laura Sanz; Marta Compte; Peter Kristensen; Luis Alvarez-Vallina
Journal:  Immunology       Date:  2006-04       Impact factor: 7.397

8.  Targeted DNA vaccines for enhanced induction of idiotype-specific B and T cells.

Authors:  Agnete B Fredriksen; Inger Sandlie; Bjarne Bogen
Journal:  Front Oncol       Date:  2012-10-30       Impact factor: 6.244

  8 in total

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