All products and services are For Research Use Only and CANNOT be used in the treatment or diagnosis of disease.
The vector of anti-CD5 chimeric antigen receptor (CAR) is constructed for the engineering of T cells to target Human CD5. The T cells are genetically modified through transduction with a lentiviral vector expressing scFv of anti-CD5 antibody linked to 41BB and CD3ζ signaling domains. And the vector product was designed for the treatment of Acute lymphoblastic leukemia (ALL).
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CAR Construction : H65-41BB-CD3ζ
Fig.4 The immunophenotype of CD5CAR T cells. The majority of CD5KO anti-CD5 CAR-T cells displayed a naive-like surface phenotype that might have an enhanced capacity for expansion, differentiation, and self-renewal upon antigen stimulation. Dai, Zhenyu, et al. "The rational development of CD5-targeting biepitopic CARs with fully human heavy-chain-only antigen recognition domains." Molecular Therapy 29.9 (2021): 2707-2722. Distributed under Open Access license CC BY 4.0, without modification. |
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CAR Construction : H65-41BB-CD3ζ
Fig.5 Cytotoxicity assay in vitro. Anti-CD5 CAR-T cells exhibited cytotoxicity in vitro when co-incubated with malignant T cell lines with moderate expression of CD5 antigen at relatively low effector to target (E:T) ratios Dai, Zhenyu, et al. "The rational development of CD5-targeting biepitopic CARs with fully human heavy-chain-only antigen recognition domains." Molecular Therapy 29.9 (2021): 2707-2722. Distributed under Open Access license CC BY 4.0, without modification. |
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CAR Construction : H65-41BB-CD3ζ
Fig.6 Cytokine secretion and repeated stimulation assay of CD5-targeting CAR-T cells in vitro. CAR-T cells produced the pro-inflammatory cytokines tumor necrosis factor alpha (TNF-α) and interferon (IFN)-γ and elevated levels of interleukin-2 (IL-2) release when co-incubated with CCRF-CEM cells. Dai, Zhenyu, et al. "The rational development of CD5-targeting biepitopic CARs with fully human heavy-chain-only antigen recognition domains." Molecular Therapy 29.9 (2021): 2707-2722. Distributed under Open Access license CC BY 4.0, without modification. |
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CAR Construction : H65-41BB-CD3ζ
Fig.7 The in vivo antitumor activity of CD5-targeting CAR-T cells in the tumor model established by CCRF-CEM. A mouse tumor model of T cell acute lymphoblastic leukemia (T-ALL) by tail intravenous injection of CCRF-CEM-ffLuc cells was established to verify the in vivo efficacy of CD5 CAR-T cells. Dai, Zhenyu, et al. "The rational development of CD5-targeting biepitopic CARs with fully human heavy-chain-only antigen recognition domains." Molecular Therapy 29.9 (2021): 2707-2722. Distributed under Open Access license CC BY 4.0, without modification. |
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CAR Construction : H65-41BB-CD3ζ
Fig.8 The in vivo antitumor activity of CD5-targeting CAR-T cells in the tumor model established by SUP-T1. A xenograft mouse tumor model was established by SUP-T1 cells with moderate CD5 expression to verify the in vivo efficacy of CD5 CAR-T cells. Dai, Zhenyu, et al. "The rational development of CD5-targeting biepitopic CARs with fully human heavy-chain-only antigen recognition domains." Molecular Therapy 29.9 (2021): 2707-2722. Distributed under Open Access license CC BY 4.0, without modification. |
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Fig.9 The binding affinity measurement of H65 antibody to CD5 antigen. The affinity of H65 to recombinant human CD5 was determined using bio-layer interferometry. Dai, Zhenyu, et al. "The rational development of CD5-targeting biepitopic CARs with fully human heavy-chain-only antigen recognition domains." Molecular Therapy 29.9 (2021): 2707-2722. Distributed under Open Access license CC BY 4.0, without modification. |
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