AAV-1–mediated gene transfer to skeletal muscle in humans results in dose-dependent activation of capsid-specific T cells

F Mingozzi, JJ Meulenberg, DJ Hui… - Blood, The Journal …, 2009 - ashpublications.org
F Mingozzi, JJ Meulenberg, DJ Hui, E Basner-Tschakarjan, NC Hasbrouck, SA Edmonson…
Blood, The Journal of the American Society of Hematology, 2009ashpublications.org
In a clinical trial for adeno-associated virus serotype 1 (AAV-1)–mediated gene transfer to
muscle for lipoprotein lipase (LPL) deficiency, 1 subject from the high-dose cohort
experienced a transient increase in the muscle enzyme creatine phosphokinase (CPK) 4
weeks after gene transfer. Simultaneously, after an initial downward trend consistent with
expression of LPL, plasma triglyceride levels returned to baseline. We characterized B-and
T-cell responses to the vector and the transgene product in the subjects enrolled in this …
Abstract
In a clinical trial for adeno-associated virus serotype 1 (AAV-1)–mediated gene transfer to muscle for lipoprotein lipase (LPL) deficiency, 1 subject from the high-dose cohort experienced a transient increase in the muscle enzyme creatine phosphokinase (CPK) 4 weeks after gene transfer. Simultaneously, after an initial downward trend consistent with expression of LPL, plasma triglyceride levels returned to baseline. We characterized B- and T-cell responses to the vector and the transgene product in the subjects enrolled in this study. IFN-γ enzyme-linked immunosorbent spot (ELISpot) and intracellular cytokine staining assays performed on peripheral blood mononuclear cells (PBMCs) from the subject who experienced the CPK elevation showed the activation of capsid-specific CD4+ and CD8+ T cells. Four of 8 subjects had detectable T-cell responses to capsid with dose-dependent kinetics of appearance. Subjects with detectable T-cell responses to capsid also had higher anti–AAV-1 IgG3 antibody titer. No subject developed B- or T-cell responses to the LPL transgene product. These findings suggest that T-cell responses directed to the AAV-1 capsid are dose-dependent. Whether they also limit the duration of expression of the transgene at higher doses is unclear, and will require additional analyses at later time points.
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