Evaluation of Cellular Immune Response to Adeno-Associated Virus-Based Gene Therapy

Springer Science and Business Media LLC - Tập 25 - Trang 1-25 - 2023
Boris Gorovits1, Mitra Azadeh2, George Buchlis3, Michele Fiscella4, Travis Harrison5, Mike Havert6, Sylvia Janetzki7, Vibha Jawa8, Brian Long9, Yolanda D. Mahnke10, Andrew McDermott11, Mark Milton12, Robert Nelson13, Christian Vettermann9, Bonnie Wu14
1Sana Biotechnology, Cambridge, USA
2Ultragenyx Pharmaceutical Inc., Novato, USA
3University of Pennsylvania, Philadelphia, USA
4Regenxbio Inc, Rockville, USA
5Precision for Medicine, Inc, Redwood City, USA
6Gene Therapy Partners, San Diego, USA
7ZellNet Consulting Inc, Fort Lee, USA
8Bristol Myers Squibb Pharmaceutical, Princeton, USA
9BioMarin Pharmaceutical Inc, Novato, USA
10FlowKnowHow LLC, Brooklyn, USA
11Labcorp Early Development Laboratories Inc, Indianapolis, USA
12Lake Boon Pharmaceutical Consulting LLC, Hudson, USA
13BioAgilytix Europe GmbH, Hamburg, Germany
14Janssen Pharmaceuticals, Raritan, USA

Tóm tắt

The number of approved or investigational late phase viral vector gene therapies (GTx) has been rapidly growing. The adeno-associated virus vector (AAV) technology continues to be the most used GTx platform of choice. The presence of pre-existing anti-AAV immunity has been firmly established and is broadly viewed as a potential deterrent for successful AAV transduction with a possibility of negative impact on clinical efficacy and a connection to adverse events. Recommendations for the evaluation of humoral, including neutralizing and total antibody based, anti-AAV immune response have been presented elsewhere. This manuscript aims to cover considerations related to the assessment of anti-AAV cellular immune response, including review of correlations between humoral and cellular responses, potential value of cellular immunogenicity assessment, and commonly used analytical methodologies and parameters critical for monitoring assay performance. This manuscript was authored by a group of scientists involved in GTx development who represent several pharma and contract research organizations. It is our intent to provide recommendations and guidance to the industry sponsors, academic laboratories, and regulatory agencies working on AAV-based GTx viral vector modalities with the goal of achieving a more consistent approach to anti-AAV cellular immune response assessment.

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