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. 2012 Sep 17;24(1):19–26. doi: 10.1089/hum.2012.108

FIG. 3.

FIG. 3.

Safety of AAV8.TBG.hLDLR in LA-DKO/hApoB-Tg mice. (A) Hematoxylin–eosin (H&E) and (B) oil red O staining of samples from mice 35 days after vector administration. (C) Serum alanine aminotransferase (ALT) levels were monitored over a 35-day period. Lymphocytes were harvested from the (C) liver and (D) spleen of mice treated with 1×1012 AAV8.TBG.hLDLR or 1×1012 AAV8.TBG.nLacZ and stimulated with either the immunodominant nLacZ epitope or a human LDLR peptide library to determine the transgene-specific response. Cells were stimulated with the capsid peptide library of AAV8 to determine the capsid response. Data represent means±SD for four mice per group.

HHS Vulnerability Disclosure