Adenovirus targeting to HLA-A1/MAGE-A1-positive tumor cells by fusing a single-chain T-cell receptor with minor capsid protein IX

Gene Therapy

Volumn 15, Issue 13, 2008, Pages 978-989

  de Vrij, J ^a   Uil, T G ^a   van den Hengel, S K ^a   Cramer, S J ^a   Koppers Lalic, D ^a   Verweij, M C ^a   Wiertz, E J H J ^a   Vellinga, J ^a   Willemsen, R A ^b   Hoeben, R C ^a  

^a LEIDEN UNIVERSITY MEDICAL CENTER   (Netherlands)

^b ERASMUS MEDICAL CENTER   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

ADENOVIRUS VECTOR; CAPSID PROTEIN; HLA A1 ANTIGEN; HYBRID PROTEIN; LENTIVIRUS VECTOR; MELANOMA ANTIGEN; MELANOMA ASSOCIATED ANTIGEN A1; PROTEIN IX; RETROVIRUS VECTOR; T LYMPHOCYTE RECEPTOR;

ANTIGEN EXPRESSION; ARTICLE; CANCER CELL CULTURE; CARBOXY TERMINAL SEQUENCE; CONTROLLED STUDY; FLOW CYTOMETRY; GENE DELETION; HAPLOTYPE; HUMAN; HUMAN CELL; IMMUNOBLOTTING; IMMUNOHISTOCHEMISTRY; MELANOMA CELL; NONHUMAN; PRIORITY JOURNAL; VIRAL GENE DELIVERY SYSTEM; VIRUS PARTICLE;

ADENOVIRIDAE; ANTIGEN PRESENTATION; ANTIGENS, NEOPLASM; CAPSID PROTEINS; CELL LINE, TUMOR; CYTOTOXICITY, IMMUNOLOGIC; FLOW CYTOMETRY; GENE TARGETING; GENE THERAPY; GENETIC ENGINEERING; GENETIC VECTORS; HLA-A1 ANTIGEN; HUMANS; MALE; MELANOMA; NEOPLASM PROTEINS; RECEPTORS, ANTIGEN, T-CELL; TRANSDUCTION, GENETIC;

ADENOVIRIDAE; HUMAN ADENOVIRUS TYPE 5; MIRIDAE;

EID: 45749089745     PISSN: 09697128     EISSN: 14765462     Source Type: Journal    
DOI: 10.1038/gt.2008.26     Document Type: Article

References (55)

1. Van den Eynde BJ, Mandruzzato S, Gueguen M, van der Bruggen P, Marchand M, Coulie PG et al. Tumor antigens recognized by cytolytic T lymphocytes. Cancer Gene Ther 1997; 4: 308.
2. Scanlan MJ, Simpson AJ, Old LJ. The cancer/testis genes: Review, standardization, and commentary. Cancer Immun 2004; 4: 1.
3. Yang B, O'Herrin SM, Wu J, Reagan-Shaw S, Ma Y, Bhat KMR et al. MAGE-A, mMage-b, and MAGE-C proteins form complexes with KAP1 and suppress p53-dependent apoptosis in MAGE-positive cell lines. Cancer Res 2007; 67: 9954-9962.
4. Willemsen RA, Debets R, Chames P, Bolhuis RLH. Genetic engineering of T cell specificity for immunotherapy of cancer. Hum Immunol 2003; 64: 56-68.
5. Peng KW, Holler PD, Orr BA, Kranz DM, Russell SJ. Targeting virus entry and membrane fusion through specific peptide/MHC complexes using a high-affinity T-cell receptor. Gene Therapy 2004; 11: 1234-1239.
6. Sebestyen Z, de Vrij J, Magnusson M, Debets R, Willemsen R. An oncolytic adenovirus redirected with a tumor-specific T-cell receptor. Cancer Res 2007; 67: 11309-11316.
7. Glasgow JN, Everts M, Curiel DT. Transductional targeting of adenovirus vectors for gene therapy. Cancer Gene Ther 2006; 13: 830-844.
8. Wickham TJ, Mathias P, Cheresh DA, Nemerow GR. Integrin-alpha-V-beta-3 and integrin-alpha-V-beta-5 promote adenovirus internalization but not virus attachment. Cell 1993; 73: 309-319.
9. Cohen CJ, Shieh JT, Pickles RJ, Okegawa T, Hsieh JT, Bergelson JM. The coxsackievirus and adenovirus, receptor is a transmembrane component of the tight junction. Proc Natl Acad Sci USA 2001; 98: 15191-15196.
10. Vigne E, Mahfouz I, Dedieu. JF, Brie A, Perricaudet M, Yeh P. RGD inclusion in the hexon monomer provides adenovirus type 5-based vectors with a fiber knob-independent pathway for infection. J Virol 1999; 73: 5156-5161.
11. Wu HJ, Han T, Belousova N, Krasnykh V, Kashentseva, E, Dmitriev I et al. Identification of sites in adenovirus hexon for foreign peptide incorporation. J Virol 2005; 79: 3382-3390.
12. Einfeld DA, Brough DE, Roelvink PW, Kovesdi I, Wickham TJ. Construction of a pseudoreceptor that mediates transduction by adenoviruses expressing a ligand in fiber or penton base. J Virol 1999; 73 9130-9136.
13. Dmitriev IP, Kashentseva EA, Curiel DT. Engineering of adenovirus vectors containing heterologous peptide sequences in the C terminus of capsid protein IX. J Virol 2002; 76: 6893-6899.
14. Le LP, Everts M, Dmitriev IP, Davydova JG, Yamamoto M, Curiel DT. Fluorescently labeled adenovirus with pIX-EGFP for vector detection. Mol Imaging 2004; 3: 105-116.
15. Meulenbroek RA, Sargent KL, Lunde J, Jasmin BJ, Parks RJ. Use of adenovirus protein IX (pIX) to display large polypeptides on the virion-generation of fluorescent virus through the incorporation of pIX-GFP. Mol Ther 2004; 9: 617-624.
16. Campos SK, Parrott MB, Barry MA. Avidin-based targeting and purification of a protein IX-modified, metabolically biotinylated adenoviral vector. Mol Ther 2004; 9: 942-954.
17. Vellinga J, Rabelink MJWE, Cramer SJ, van den Wollenberg DJM, Van der Meulen H, Leppard KN et al. Spacers increase the accessibility of peptide ligands linked to the carboxyl terminus of adenovirus minor capsid protein IX. J Virol 2004; 78: 1-10.
18. Vellinga J, de Vrij J, Myhre S, Uil T, Martineau P, Lindholm L et al. Efficient incorporation of a functional hyper-stable single-chain antibody fragment protein-IX fusion in the adenovirus capsid. Gene Therapy 2007; 14: 664-670.
19. Glasgow JN, Kashentseva, E, Dmitriev IP, Curiel DT. Adenovirus polypeptide IIIa as a novel locale for incorporation of heterologous peptides. Mol Ther 2005; 11: S338.
20. Vellinga J, Van der Heijdt S, Hoeben RC. The adenovirus capsid: Major progress in minor proteins. J Gen Virol 2005; 86: 1581-1588.
21. Furcinitti PS, Van Oostrum, J, Burnett RM, Adenovirus polypeptide-IX revealed as capsid cement by difference images from electron-microscopy and crystallography. EMBO J 1989; 8: 3563-3570.
22. Van Oostrum J, Burnett RM. Molecular composition of the adenovirus type-2 virion. J Virol 1985; 56: 439-448.
23. Saban SD, Nepomuceno RR, Gritton LD, Nemerow GR, Stewart PL. CryoEM structure at 9 Angstrom resolution of an adenovirus vector targeted to hematopoietic cells. J Mol Biol 2005; 349: 526-537.
24. Marsh MP, Campos SK, Baker ML, Chen CY, Chiu W, Barry MA. Cryoelectron microscopy of protein IX-modified adenoviruses suggests a new position for the C terminus of protein IX. J Virol 2006; 80: 11881-11886.
25. Fabry CMS, Rosa-Calatrava K Conway JF, Zubieta C, Cusack S, Ruigrok RWH et al. A quasi-atomic model of human adenovirus type 5 capsid. EMBO J 2005; 24: 1645-1654.
26. Saban SD, Silvestry M, Nemerow GR, Stewart PL. Visualization of alpha-helices in a 6-Angstrom resolution cryoelectron microscopy structure of adenovirus allows refinement of capsid protein assignments. J Virol 2006; 80: 12049-12059.
27. Zufferey R, Dull T, Mandel RJ, Bukovsky A, Quiroz D, Naldini L et al. Self-inactivating lentivirus vector for safe and efficient in vivo gene delivery. J Virol 1998; 72: 9873-9880.
28. Mautino MR, Ramsey WJ, Reiser J, Morgan RA. Modified human immunodeficiency virus-based lentiviral vectors display decreased sensitivity to trans-dominant rev. Hum Gene Ther 2000; 11: 895-908.
29. Barry SC, Harder B, Brzezinski M, Flint LY, Seppen J, Osborne WRA. Lentivirus vectors encoding both central polypurine tract and posttranscriptional regulatory element provide enchanced transduction and transgene expression. Hum Gene Ther 2001; 12: 1103-1108
30. Sirven A, Pflumio F, Zennou V, Titeux M, Vainchenker W, Coulumbel L et al. The human immunodeficiency virus type-1 central DNA flap is a crucial determinant for lentiviral vector nuclear import and gene transduction of human hematopoietic stem cells. Blood 2000; 96 4103-4110.
31. Follenzi A, Ailles LE, Bakovic S, Geuna M, Naldini L. Gene transfer by lentiviral vectors is limited by nuclear translocation and rescued by HIV-1 pol sequences. Nat Genet 2000; 25: 217-222.
32. Swick AG, Janicot M, Chenevalkastelic T, Mclenithan JC, Lane MD. Promoter cDNA-directed heterologous protein expression in Xenopus-laevis oocytes. Proc Natl Acad Sci USA 1992; 89: 1812-1816.
33. Vellinga J, van den Wollenberg DJM, Van der Heijdt S, Rabelink MJWE, Hoeben RC. The coiled-coil domain of the adenovirus type 5 protein IX is dispensable for capsid incorporation and thermostability. J Virol 2005; 79: 3206-3210.
34. Wiertz EJHJ, Jones TR, Sun L, Bogyo M, Geuze HJ, Ploegh HL. The human cytomegalovirus US11 gene product dislocates MHC class I heavy chains from the endoplasmic reticulum. to the cytosol. Cell 1996; 84 769-779.
35. Magnusson MK, Hong SS, Henning P, Boulanger P, Lindholm L. Genetic retargeting of adenovirus vectors: Functionality of targeting ligands and their influence on virus viability. J Gene Med 2002; 4: 356-370.
36. Matthews QL, Sibley DA, Wu HJ, Li J, Stoff-Khahli MA, Waehler R et al. Genetic incorporation of a herpes simplex virus type 1 thymidine kinase and firefly luciferase fusion into the adenovirus protein IX for functional display on the virion. Mol Imaging 2006; 5: 510-519.
37. Vellinga J, Uil TG, de Vrij J, Rabelink MJWE, Lindholm L, Hoeben RC. A system for efficient generation of adenovirus protein IX-producing helper cell lines. J Gene Med 2006; 8: 147-154.
38. Rosa-Calatrava M, Grave L, Puvion-Dutilleul F, Chatton B, Kedinger C. Functional analysis of adenovirus protein IX identifies domains involved in capsid stability transcriptional activity and nuclear reorganization. J Virol 2001; 75: 7131-7141.
39. Davis MM, Boniface JJ, Reich Z, Lyons D, Hampl J, Arden B et al. Ligand recognition by, alpha beta T cell receptors. Annu Rev Immunol 1998; 16: 523-544.
40. Norkin LC. Simian virus 40 infection via MHC class I molecules and caveolae. Immunol Rev 1999; 168: 13-22.
41. Hong SS, Karayan L, Tournier J, Curiel DT, Boulanger PA. Adenovirus type 5 fiber knob binds to MHC class I alpha 2 domain at the surface of human epithelial and B lymphoblastoid, cells. EMBO J 1997; 16: 2294-2306.
42. Cattaneo A, Biocca S. The selection of intracellular antibodies. Trends Biotechnol 1999; 17: 115-121.
43. Magnusson MK, Hong SS, Henning P, Boulanger P, Lindholm L. Genetic retargeting of adenovirus vectors: Functionality of targeting ligands and their influence on virus viability. J Gene Med 2002; 4: 356-370.
44. Magnusson MK, Henning P, Myhre S, Wikman M, Uil TG, Friedman M et al. Adenovirus 5 vector genetically re-targeted by an Affibody molecule with specificity for tumor antigen HER2/neu. Cancer Gene Ther 2007; 14: 468-479.
45. Witlox MA, van Beusechem VW, Grill J, Haisma HJ, Schaap G, Bras J et al. Epidermal growth factor receptor targeting enhances adenoviral vector based suicide gene therapy of osteosarcoma. J Gene Med 2002; 4: 510-516.
46. Willemsen RA, Weijtens MEM, Ronteltap C, Eshhar Z, Gratama JW, Chames P et al. Grafting primary human T lymphocytes with cancer-specific chimeric single chain and two chain TCR. Gene Therapy 2000; 7 1369-1377.
47. van der Bruggen P, Traversari C, Chomez P, Lurquin C, De Plaen E, Van den Eynde BJ et al. A gene encoding an antigen recognized by cytolytic T lymphocytes on a human melanoma. Science 1991; 254 1643-1647.
48. Fallaux FJ, Kranenburg O, Cramer SJ, Houweling A, VanOrmondt H, Hoeben RC et al. Characterization of 911: A new helper cell line for the titration and propagation of early region 1-deleted adenoviral vectors. Hum Gene Ther 1996; 7: 215-222.
49. Carlotti F, Bazuine M, Kekarainen T, Seppen J, Pognonec P, Maassen JA et al. Lentiviral vectors efficiently transduce quiescent mature 3T3-L1 adipocytes. Mol Ther 2004; 9: 209-217.
50. Barel MT, Pizzato N, van Leeuwen D, Le Bouteiller P, Wiertz EJHJ, Lenfant F. Amino add composition of alpha 1/alpha 2 domains and cytoplasmic tad of MHC class I molecules determine their susceptibility to human cytomegalovirus US11-mediated down-regulation. Eur J Immunol 2003; 33: 1707-1716.
51. Mittereder N, March KL, Trapnell BC. Evaluation of the concentration and bioactivity of adenovirus vectors for gene therapy. J Virol 1996; 70: 7498-7509.
52. Caravokyri C, Leppard KN. Constitutive episomal expression of polypeptide-IX (pIX) in a 293-based cell-line complements the deficiency of pIX mutant Adenovirus type-5. J Virol 1995; 69: 6627-6633.
53. Douglas JT, Rogers BE, Rosenfeld ME, Michael SI, Feng MZ, Curiel DT. Targeted gene delivery by tropism-modified adenoviral vectors. Nat Biotechnol 1996; 14: 1574-1578.
54. Willemsen RA, Debets R, Hart E, Hoogenboom HR, Bolhuis RLH Chames P. A phage display selected Fab fragment with MHC class I-restricted specificity for MAGE-A1 allows for retargeting of primary human T lymphocytes. Gene Therapy 2001; 8: 1601-1608.
55. Hsu KHL, Lonbergholm K, Alstein B, Crowell RL. A monoclonal-antibody specific for the cellular receptor for the group-B coxsackie-viruses. J Virol 1988; 62: 1647-1652.