Literature DB >> 10804282

Cationic liposome conjugation to recombinant adenoviral vector reduces viral antigenicity.

A Natsume1, M Mizuno, Y Ryuke, J Yoshida.   

Abstract

Adenoviral (Ad) vectors are commonly used in gene therapy trials because of their efficiency in gene transfer. However, their use is limited by immune responses that reduce transgene expression and decrease the efficacy of repeated vector administration. In this study, we demonstrated that conjugation of Ad vector with our novel cationic liposomes could reduce viral antigenicity in vivo. Mice subcutaneously injected with liposome-conjugated Ad vector showed a 6.5-fold reduction of anti-Ad antibodies with neutralizing activity, compared to those with unconjugated Ad vector. Interestingly, we also found that the conjugated vector is less susceptible to inactivation by neutralizing antibodies in vitro and in vivo. Our results suggest that liposome conjugation reduces viral antigenicity, shields vectors from neutralizing antibody, and may allow repeated Ad vector administration.

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Year:  2000        PMID: 10804282      PMCID: PMC5926462          DOI: 10.1111/j.1349-7006.2000.tb00953.x

Source DB:  PubMed          Journal:  Jpn J Cancer Res        ISSN: 0910-5050


  17 in total

Review 1.  The use of DNA viruses as vectors for gene therapy.

Authors:  M Ali; N R Lemoine; C J Ring
Journal:  Gene Ther       Date:  1994-11       Impact factor: 5.250

2.  A model system for in vivo gene transfer into the central nervous system using an adenoviral vector.

Authors:  B L Davidson; E D Allen; K F Kozarsky; J M Wilson; B J Roessler
Journal:  Nat Genet       Date:  1993-03       Impact factor: 38.330

3.  Transfer of a foreign gene into the brain using adenovirus vectors.

Authors:  S Akli; C Caillaud; E Vigne; L D Stratford-Perricaudet; L Poenaru; M Perricaudet; A Kahn; M R Peschanski
Journal:  Nat Genet       Date:  1993-03       Impact factor: 38.330

4.  Transient immune blockade prevents formation of neutralizing antibody to recombinant adenovirus and allows repeated gene transfer to mouse liver.

Authors:  Y Yang; K Greenough; J M Wilson
Journal:  Gene Ther       Date:  1996-05       Impact factor: 5.250

5.  Biology of adenovirus vectors with E1 and E4 deletions for liver-directed gene therapy.

Authors:  G P Gao; Y Yang; J M Wilson
Journal:  J Virol       Date:  1996-12       Impact factor: 5.103

6.  Adenovirus-assisted lipofection: efficient in vitro gene transfer of luciferase and cytosine deaminase to human smooth muscle cells.

Authors:  J Kreuzer; S Denger; F Reifers; C Beisel; K Haack; J Gebert; W Kübler
Journal:  Atherosclerosis       Date:  1996-07       Impact factor: 5.162

7.  Direct in vivo gene transfer to ependymal cells in the central nervous system using recombinant adenovirus vectors.

Authors:  G Bajocchi; S H Feldman; R G Crystal; A Mastrangeli
Journal:  Nat Genet       Date:  1993-03       Impact factor: 38.330

8.  An adenovirus vector for gene transfer into neurons and glia in the brain.

Authors:  G Le Gal La Salle; J J Robert; S Berrard; V Ridoux; L D Stratford-Perricaudet; M Perricaudet; J Mallet
Journal:  Science       Date:  1993-02-12       Impact factor: 47.728

9.  Poly (lactic-glycolic) acid copolymer encapsulation of recombinant adenovirus reduces immunogenicity in vivo.

Authors:  S J Beer; C B Matthews; C S Stein; B D Ross; J M Hilfinger; B L Davidson
Journal:  Gene Ther       Date:  1998-06       Impact factor: 5.250

10.  Efficient, repeated adenovirus-mediated gene transfer in mice lacking both tumor necrosis factor alpha and lymphotoxin alpha.

Authors:  K Benihoud; I Saggio; P Opolon; B Salone; F Amiot; E Connault; C Chianale; F Dautry; P Yeh; M Perricaudet
Journal:  J Virol       Date:  1998-12       Impact factor: 5.103

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  5 in total

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2.  Multiple treatment cycles of liposome-encapsulated adenoviral RIP-TK gene therapy effectively ablate human pancreatic cancer cells in SCID mice.

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3.  Co-delivery of adenovirus and carmustine by anionic liposomes with synergistic anti-tumor effects.

Authors:  Zhirong Zhong; Yu Wan; Sanjun Shi; Jianfeng Han; Zhirong Zhang; Xun Sun
Journal:  Pharm Res       Date:  2011-07-26       Impact factor: 4.200

Review 4.  Clinical gene therapy for brain tumors. Liposomal delivery of anticancer molecule to glioma.

Authors:  Jun Yoshida; Masaaki Mizuno
Journal:  J Neurooncol       Date:  2003-12       Impact factor: 4.130

5.  Systemically administered liposome-encapsulated Ad-PEDF potentiates the anti-cancer effects in mouse lung metastasis melanoma.

Authors:  Hua-shan Shi; Li-ping Yang; Wei Wei; Xiao-qing Su; Xiao-peng Li; Meng Li; Shun-tao Luo; Hai-long Zhang; Lian Lu; Yong-qiu Mao; Bing Kan; Li Yang
Journal:  J Transl Med       Date:  2013-04-03       Impact factor: 5.531

  5 in total

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