Davey, Brianna, CPampusch, Mary, SCartwright, Emily, KAbdelaal, Hadia, MRakasz, Eva, GRendahl, AaronBerger, Edward, ASkinner, Pamela, J2022-11-282022-11-282022-11-28https://hdl.handle.net/11299/243377Excel files of flow cytometry data and statistics to support manuscript figuresT cells expressing a simian immunodeficiency (SIV)-specific chimeric antigen receptor (CAR) and the follicular homing molecule, CXCR5, were infused into antiretroviral therapy (ART) suppressed, SIV-infected rhesus macaques to assess their ability to localize to the lymphoid follicle and control the virus upon ART interruption. The cells did not persist in the animals beyond 28 days. Development of anti-CAR antibodies could be responsible for the lack of persistence. Potential antigenic sites on the anti-SIV CAR used in these studies included domains 1 and 2 of CD4, the carbohydrate recognition domain (CRD) of mannose-binding lectin (MBL), and an extracellular domain of the costimulatory molecule, CD28, along with short linker sequences. Using a flow cytometry based assay and target cells expressing the CAR/CXCR5 construct, we examined the serum of the CAR T-cell treated animals to determine that the animals had developed an anti-CAR antibody response after infusion. Binding sites for the anti-CAR antibodies were identified by using alternative CARs transduced into target cells and by preincubation of the target cells with a CD4 blocking antibody. All of the treated animals developed antibodies in their serum that bound to CAR-T cells and the majority were capable of inducing an ADCC response. The CD4 antibody-blocking assay suggests that the dominant immunogenic components of this CAR are the CD4 domains with a possible additional site of the CD28 domain with its linker.CC0 1.0 Universalhttp://creativecommons.org/publicdomain/zero/1.0/CAR T cellanti-drug antibodySIVrhesus macaqueimmunotherapyDatasethttps://doi.org/10.13020/d3e7-wt82