Skip NavigationSkip to Content

Long-Term Delivery of an Anti-SIV Monoclonal Antibody With AAV

  1. Author:
    Martinez-Navio, José M
    Fuchs, Sebastian P
    Mendes, Desiree E
    Rakasz, Eva G
    Gao, Guangping
    Lifson,Jeffrey
    Desrosiers, Ronald C
  2. Author Address

    Department of Pathology, Miller School of Medicine, University of Miami, Miami, FL, United States., Wisconsin National Primate Research Center, University of Wisconsin, Madison, WI, United States., Gene Therapy Center, University of Massachusetts Medical School, Worcester, MA, United States., AIDS and Cancer Virus Program, Frederick National Laboratory for Cancer Research, Frederick, MD, United States.,
    1. Year: 2020
    2. Date: MAR 17
    3. Epub Date: 2020 03 17
  1. Journal: Frontiers in immunology
    1. 11
    2. Pages: 449
  2. Type of Article: Article
  3. Article Number: 449
  4. ISSN: 1664-3224
  1. Abstract:

    Long-term delivery of anti-HIV monoclonal antibodies using adeno-associated virus (AAV) holds promise for the prevention and treatment of HIV infection. We previously reported that after receiving a single administration of AAV vector coding for anti-SIV antibody 5L7, monkey 84-05 achieved high levels of AAV-delivered 5L7 IgG1 in vivo which conferred sterile protection against six successive, escalating dose, intravenous challenges with highly infectious, highly pathogenic SIVmac239, including a final challenge with 10 animal infectious doses (1). Here we report that monkey 84-05 has successfully maintained 240-350 µg/ml of anti-SIV antibody 5L7 for over 6 years. Approximately 2% of the circulating IgG in this monkey is this one monoclonal antibody. This monkey generated little or no anti-drug antibodies (ADA) to the AAV-delivered antibody for the duration of the study. Due to the nature of the high-dose challenge used and in order to rule out a potential low-level infection not detected by regular viral loads, we have used ultrasensitive techniques to detect cell-associated viral DNA and RNA in PBMCs from this animal. In addition, we have tested serum from 84-05 by ELISA against overlapping peptides spanning the whole envelope sequence for SIVmac239 (PepScan) and against recombinant p27 and gp41 proteins. No reactivity has been detected in the ELISAs indicating the absence of naturally arising anti-SIV antibodies; moreover, the ultrasensitive cell-associated viral tests yielded no positive reaction. We conclude that macaque 84-05 was effectively protected and remained uninfected. Our data show that durable, continuous antibody expression can be achieved after one single administration of AAV and support the potential for lifelong protection against HIV from a single vector administration. Copyright © 2020 Martinez-Navio, Fuchs, Mendes, Rakasz, Gao, Lifson and Desrosiers.

    See More

External Sources

  1. DOI: 10.3389/fimmu.2020.00449
  2. PMID: 32256496
  3. PMCID: PMC7089924
  4. WOS: 000525548600001

Library Notes

  1. Fiscal Year: FY2019-2020
NCI at Frederick

You are leaving a government website.

This external link provides additional information that is consistent with the intended purpose of this site. The government cannot attest to the accuracy of a non-federal site.

Linking to a non-federal site does not constitute an endorsement by this institution or any of its employees of the sponsors or the information and products presented on the site. You will be subject to the destination site's privacy policy when you follow the link.

ContinueCancel