Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

  • Original Article
  • Published:

Retrovirus molecular conjugates: a versatile and efficient gene transfer vector system for primitive human hematopoietic progenitor cells

Abstract

In principle, transient nongenetic modification of a noninfectious gene transfer virus enabling a one time infection and transduction of human cells could eliminate the risk of formation of replication competent virus. Formation of a molecular conjugate vector by conjugation of noninfective ecotropic murine Moloney leukemia virus to polylysine (eMMLV-PL) enabled high-efficiency transduction of human HPC using in vitro and in vivo assays. Xenotransplanted NOD-SCID mice durably expressed the transgene in human leukocytes and human progenitor cells with eMMLV-PL achieving three-fold increased transduction efficiency when directly compared to optimized amphotropic MMLV (aMMLV) transduction. Both aMMLV and eMMLV assembled conjugate vectors showed similar transduction efficiency indicating predominant polylysine-mediated uptake. Integration of retroviral sequences was determined from individual human HPC recovered from eMMLV-PL-xenotransplanted animals. This simple and versatile concept of conjugate gene transfer vectors has the potential to enhance transduction efficiency as well as to improve certain safety aspects of human gene therapy. Moreover, because it permits effective cellular internalization of particles, this concept of molecular conjugates can be used as research tool to investigate the interactions of otherwise noninfectious viruses or modified viral particles at the genomic level.

This is a preview of subscription content, access via your institution

Access options

Buy this article

Prices may be subject to local taxes which are calculated during checkout

Figure 1
Figure 2
Figure 3
Figure 4
Figure 5

Similar content being viewed by others

References

  1. Schuening FG . Gene transfer into hematopoietic stem cells. Curr Top Microbiol Immunol 1992; 177: 237–245.

    CAS  PubMed  Google Scholar 

  2. Reiser J, Harmison G, Kluepfel-Stahl S, Brady RO, Karlsson S, Schubert M . Transduction of nondividing cells using pseudotyped defective high-titer HIV type 1 particles. Proc Natl Acad Sci USA 1996; 93: 15266–15271.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  3. Poeschla E, Corbeau P, Wong-Staal F . Development of HIV vectors for anti-HIV gene therapy. [Review] [50 refs]. Proc Natl Acad Sci USA 1996; 93: 11395–11399.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  4. Wilson CA, Ng TH, Miller AE . Evaluation of recommendations for replication-competent retrovirus testing associated with use of retroviral vectors. Hum Gene Ther 1997; 8: 869–874.

    Article  CAS  PubMed  Google Scholar 

  5. Noguchi P . Risks and benefits of gene therapy. N Engl J Med 2003; 348: 193–194.

    Article  PubMed  Google Scholar 

  6. Hacein-Bey-Abina S, von Kalle C, Schmidt M, Le Deist F, Wulffraat N, McIntyre E et al. A serious adverse event after successful gene therapy for X-linked severe combined immunodeficiency. N Engl J Med 2003; 348: 255–256.

    Article  PubMed  Google Scholar 

  7. Hacein-Bey-Abina S, Le Deist F, Carlier F, Bouneaud C, Hue C, De Villartay JP et al. Sustained correction of X-linked severe combined immunodeficiency by ex vivo gene therapy. N Engl J Med 2002; 346: 1185–1193.

    Article  CAS  PubMed  Google Scholar 

  8. Vile RG, Russell SJ . Retroviruses as vectors. Br Med Bull 1995; 51: 12–30.

    Article  CAS  PubMed  Google Scholar 

  9. Kolls J, Peppel K, Silvia M, Beutler B . Prolonged and effective blockade of tumor necrosis factor activity through adenovirus-mediated gene-transfer. Proc Natl Acad Sci USA 1994; 91: 215–219.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  10. Mulligan RC . The basic science of gene therapy. Sci 1993; 260: 926–932.

    Article  CAS  Google Scholar 

  11. Reiser J, Lai Z, Zhang XY, Brady RO . Development of multigene and regulated lentivirus vectors. J Virol 2000; 74: 10589–10599.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  12. Thoma SJ, Lamping CP, Ziegler BL . Phenotype analysis of hematopoietic CD34+ cell populations derived from human umbilical cord blood using flow cytometry and cDNA-polymerase chain reaction. Blood 1994; 83: 2103–2114.

    CAS  PubMed  Google Scholar 

  13. Crooks GM, Kohn DB . Growth factors increase amphotropic retrovirus binding to human CD34+ bone marrow progenitor cells. Blood 1993; 82: 3290–3297.

    CAS  PubMed  Google Scholar 

  14. Zhong Q, Kolls JK, Schwarzenberger P . Retrovirus molecular conjugates. Cell Mol Life Sci 2002; 59: 2083–2087.

    Article  CAS  PubMed  Google Scholar 

  15. Zhong Q, Kolls JK, Schwarzenberger P . Retrovirus molecular conjugates. A novel, high transduction efficiency, potentially safety-improved, gene transfer system. J Biol Chem 2001; 276: 24601–24607.

    Article  CAS  PubMed  Google Scholar 

  16. Dick JE, Kamel-Reid S, Murdoch B, Doedens M . Gene transfer into normal human hematopoietic cells using in vitro and in vivo assays. Blood 1991; 78: 624–634.

    CAS  PubMed  Google Scholar 

  17. Bahnson AB, Dunigan JT, Baysal BE, Mohney T, Atchison RW, Nimgaonkar MT et al. Centrifugal enhancement of retroviral mediated gene transfer. J Virol Methods 1995; 54: 131–143.

    Article  CAS  PubMed  Google Scholar 

  18. Brandt JE, Srour EF, van Besien K, Briddell RA, Hoffman R . Cytokine dependent long-term culture of highly enriched precursors of hematopoietic progenitor cells from human bone marrow. J Clin Invest 1990; 86: 932–941.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  19. Shultz LD, Schweitzer PA, Christianson SW, Gott B, Schweitzer IB, Tennent B et al. Multiple defects in innate and adaptive immunologic function in NOD/LtSz-scid mice. J Immunol 1995; 154: 180–191.

    CAS  PubMed  Google Scholar 

  20. Schwarzenberger P, Spence S, Lohrey N, Kmiecik T, Longo DL, Murphy WJ et al. Gene transfer of multidrug resistance into a factor-dependent human hematopoietic progenitor cell line: in vivo model for genetically transferred chemoprotection. Blood 1996; 87: 2723–2731.

    CAS  PubMed  Google Scholar 

  21. Zhang XY, La Russa VF, Bao L, Kolls J, Schwarzenberger P, Reiser J . Lentiviral vectors for sustained transgene expression in human bone marrow-derived stromal cells. Mol Ther 2002; 5(5 Part 1): 555–565.

    Article  CAS  PubMed  Google Scholar 

  22. Nolta JA, Dao MA, Wells S, Smogorzewska EM, Kohn DB . Transduction of pluripotent human hematopoietic stem cells demonstrated by clonal analysis after engraftment in immune-deficient mice. Proc Natl Acad Sci USA 1996; 93: 2414–2419.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  23. Rill DR, Santana VM, Roberts WM, Nilson T, Bowman LC, Krance RA et al. Direct demonstration that autologous bone marrow transplantation for solid tumors can return a multiplicity of tumorigenic cells. Blood 1994; 84: 380–383.

    CAS  PubMed  Google Scholar 

  24. Byrne P, Huang W, Wallace VM, Shean MK, Zhang Z, Zhong Q et al. Chimerism analysis in sex-mismatched murine transplantation using quantitative real-time PCR. Biotechniques 2002; 32: 279–280, 282–284, 286.

    Article  CAS  PubMed  Google Scholar 

  25. Cornetta K, Anderson WF . Protamine sulfate as an effective alternative to polybrene in retroviral-mediated gene-transfer: implications for human gene therapy. J Virol Methods 1989; 23: 187–194.

    Article  CAS  PubMed  Google Scholar 

  26. Cornetta K, Nguyen N, Morgan RA, Blaese M, Anderson WF . Infection of human cells with murine amphotropic replication competent retroviruses. Hum Gene Ther 1993; 4: 579–588.

    Article  CAS  PubMed  Google Scholar 

  27. MacNeill EC, Hanenberg H, Pollok KE, van der Loo JC, Bierhuizen MF, Wagemaker G et al. Simultaneous infection with retroviruses pseudotyped with different envelope proteins bypasses viral receptor interference associated with colocalization of gp70 and target cells on fibronectin CH-296. J Virol 1999; 73: 3960–3967.

    CAS  PubMed  PubMed Central  Google Scholar 

  28. Saunders S, Bernfield M . Cell surface proteoglycan binds mouse mammary epithelial cells to fibronectin and behaves as a receptor for interstitial matrix. J Cell Biol 1988; 106: 423–430.

    Article  CAS  PubMed  Google Scholar 

  29. Moritz T, Dutt P, Xiao X, Carstanjen D, Vik T, Hanenberg H et al. Fibronectin improves transduction of reconstituting hematopoietic stem cells by retroviral vectors: evidence of direct viral binding to chymotryptic carboxy-terminal fragments. Blood 1996; 88: 855–862.

    CAS  PubMed  Google Scholar 

  30. Asada K, Uemori T, Ueno T, Hashino K, Koyama N, Kawamura A et al. Enhancement of retroviral gene transduction on a dish coated with a cocktail of two different polypeptides: one exhibiting binding activity toward target cells, and the other toward retroviral vectors. J Biochem (Tokyo) 1998; 123: 1041–1047.

    Article  CAS  Google Scholar 

  31. Skutelsky E, Danon D . Redistribution of surface anionic sites on the luminal front of blood vessel endothelium after interaction with polycationic ligand. J Cell Biol 1976; 71: 232–241.

    Article  CAS  PubMed  Google Scholar 

  32. Wickham TJ, Roelvink PW, Brough DE, Kovesdi I . Adenovirus targeted to heparin-containing receptors increases its gene delivery efficiency to multiple cell types. Nat Biotechnol 1996; 14: 1570–1573.

    Article  CAS  PubMed  Google Scholar 

  33. Wickham TJ, Tzeng E, Shears LL, Roelvink PW, Li Y, Lee GM et al. Increased in vitro and in vivo gene transfer by adenovirus vectors containing chimeric fiber proteins. J Virol 1997; 71: 8221–8229.

    CAS  PubMed  PubMed Central  Google Scholar 

  34. Chiou HC, Tangco MV, Levine SM, Robertson D, Kormis K, Wu CH et al. Enhanced resistance to nuclease degradation of nucleic acids complexed to asialoglycoprotein-polylysine carriers. Nucleic Acids Res 1994; 22: 5439–5446.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  35. Donahue RE, Kessler SW, Bodine D, McDonagh K, Dunbar C, Goodman S et al. Helper virus induced T-cell lymphoma in nonhuman primates after retroviral mediated gene transfer. J Exp Med 1992; 176: 1125–1135.

    Article  CAS  PubMed  Google Scholar 

  36. Panoskaltsis N, Abboud CN . Human immunodeficiency virus and the hematopoietic repertoire: implications for gene therapy. Front Biosci 1999; 4: D457–D467.

    Article  CAS  PubMed  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to P Schwarzenberger.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Yang, G., Zhong, Q., Huang, W. et al. Retrovirus molecular conjugates: a versatile and efficient gene transfer vector system for primitive human hematopoietic progenitor cells. Cancer Gene Ther 13, 460–468 (2006). https://doi.org/10.1038/sj.cgt.7700911

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1038/sj.cgt.7700911

Keywords

This article is cited by

Search

Quick links