Literature DB >> 24136735

The prevalence of neutralizing antibodies against adeno-associated virus capsids is reduced in young Japanese individuals.

Jun Mimuro1, Hiroaki Mizukami, Midori Shima, Tadashi Matsushita, Masashi Taki, Shinji Muto, Satoshi Higasa, Michio Sakai, Tsukasa Ohmori, Seiji Madoiwa, Keiya Ozawa, Yoichi Sakata.   

Abstract

Pre-existing antibodies against adeno-associated virus (AAV), caused by natural AAV infections, interfere with recombinant AAV vector-mediated gene transfer. We studied the prevalence of neutralizing antibodies against AAV serotypes 1, 2, 5, 8, and 9 in healthy subjects (n = 85) and hemophilia patients (n = 59) in a Japanese population. For healthy subjects, the prevalence of neutralizing antibodies against AAV serotypes 1, 2, 5, 8, and 9 was 36.5%, 35.3%, 37.6%, 32.9%, and 36.5%, respectively, while that in hemophilia patients was 39.7%, 28.8%, 35.6%, 32.9%, and 27.4%, respectively. There was no difference in the prevalence of neutralizing antibody against each AAV serotype between the healthy subjects and the hemophilia patients. The prevalence of neutralizing antibodies against all AAV serotypes increased with age in both healthy subjects and hemophilia patients. High titers of neutralizing antibodies against AAV2 (≥1:224) and AAV8 (≥1:224) were more evident in older individuals (≥42 years old). Approximately 50% of all screened individuals were seronegative for neutralizing antibodies against each AAV tested, while approximately 25% of individuals were seropositive for each AAV serotype tested. The prevalence of seronegativity for all AAV serotypes was 67.0% (healthy subjects, 68.6%; hemophilia patients, 65.0%) and 18.6% (healthy subjects, 20.5%; hemophilia patients, 15.7%) in young (<42 years old) and older subjects (≥42 years old), respectively. The findings from this study suggested that young subjects are more likely to be eligible for gene therapy based on AAV vectors delivered via an intravascular route because of the low prevalence of antibodies to AAV capsids.
© 2013 Wiley Periodicals, Inc.

Entities:  

Keywords:  AAV vector; epidemiology; gene therapy

Mesh:

Substances:

Year:  2013        PMID: 24136735     DOI: 10.1002/jmv.23818

Source DB:  PubMed          Journal:  J Med Virol        ISSN: 0146-6615            Impact factor:   2.327


  18 in total

1.  Endothelial cells derived from patients' induced pluripotent stem cells for sustained factor VIII delivery and the treatment of hemophilia A.

Authors:  Melanie Rose; Kewa Gao; Elizabeth Cortez-Toledo; Emmanuel Agu; Alicia A Hyllen; Kelsey Conroy; Guangjin Pan; Jan A Nolta; Aijun Wang; Ping Zhou
Journal:  Stem Cells Transl Med       Date:  2020-03-12       Impact factor: 6.940

2.  Neutralizing Antibodies Against Adeno-Associated Viral Capsids in Patients with mut Methylmalonic Acidemia.

Authors:  Elizabeth A Harrington; Jennifer L Sloan; Irini Manoli; Randy J Chandler; Mark Schneider; Peter J McGuire; Roberto Calcedo; James M Wilson; Charles P Venditti
Journal:  Hum Gene Ther       Date:  2016-03-22       Impact factor: 5.695

Review 3.  Advances in gene therapy for hemophilia: basis, current status, and future perspectives.

Authors:  Tsukasa Ohmori
Journal:  Int J Hematol       Date:  2018-08-06       Impact factor: 2.490

4.  Platelet-targeted hyperfunctional FIX gene therapy for hemophilia B mice even with preexisting anti-FIX immunity.

Authors:  Jocelyn A Schroeder; Juan Chen; Yingyu Chen; Yuanhua Cai; Hongyin Yu; Jeremy G Mattson; Paul E Monahan; Qizhen Shi
Journal:  Blood Adv       Date:  2021-03-09

5.  Prevalence of anti-adeno-associated virus serotype 8 neutralizing antibodies and arylsulfatase B cross-reactive immunologic material in mucopolysaccharidosis VI patient candidates for a gene therapy trial.

Authors:  Rita Ferla; Pamela Claudiani; Marco Savarese; Karen Kozarsky; Rossella Parini; Maurizio Scarpa; Maria Alice Donati; Giovanni Sorge; John J Hopwood; Giancarlo Parenti; Simona Fecarotta; Vincenzo Nigro; Hatice Serap Sivri; Ans Van Der Ploeg; Generoso Andria; Nicola Brunetti-Pierri; Alberto Auricchio
Journal:  Hum Gene Ther       Date:  2015-03       Impact factor: 5.695

6.  CRISPR/Cas9-mediated genome editing via postnatal administration of AAV vector cures haemophilia B mice.

Authors:  Tsukasa Ohmori; Yasumitsu Nagao; Hiroaki Mizukami; Asuka Sakata; Shin-Ichi Muramatsu; Keiya Ozawa; Shin-Ichi Tominaga; Yutaka Hanazono; Satoshi Nishimura; Osamu Nureki; Yoichi Sakata
Journal:  Sci Rep       Date:  2017-06-23       Impact factor: 4.379

7.  Synthetic DNA delivery by electroporation promotes robust in vivo sulfation of broadly neutralizing anti-HIV immunoadhesin eCD4-Ig.

Authors:  Ziyang Xu; Megan C Wise; Hyeree Choi; Alfredo Perales-Puchalt; Ami Patel; Edgar Tello-Ruiz; Jacqueline D Chu; Kar Muthumani; David B Weiner
Journal:  EBioMedicine       Date:  2018-08-30       Impact factor: 8.143

8.  Adenovirus-associated antibodies in UK cohort of hemophilia patients: A seroprevalence study of the presence of adenovirus-associated virus vector-serotypes AAV5 and AAV8 neutralizing activity and antibodies in patients with hemophilia A.

Authors:  Sophia Stanford; Ruth Pink; Desmond Creagh; Amanda Clark; Gillian Lowe; Nicola Curry; John Pasi; David Perry; Sylvia Fong; Gregory Hayes; Kandiah Chandrakumaran; Savita Rangarajan
Journal:  Res Pract Thromb Haemost       Date:  2019-01-25

9.  Determination of Anti-Adeno-Associated Viral Vector Neutralizing Antibodies in Patients With Heart Failure in the Cardiovascular Foundation of Colombia (ANVIAS): Study Protocol.

Authors:  Melvin Y Rincon; Carlos E Prada; Marcos Lopez; Victor Castillo; Luis Eduardo Echeverria; Norma Serrano
Journal:  JMIR Res Protoc       Date:  2016-06-09

10.  [Research advances on gene therapy for hemophilia].

Authors:  X Y Dai; L Zhang
Journal:  Zhonghua Xue Ye Xue Za Zhi       Date:  2018-04-14
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