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. 2015 Feb 12;8(1):40–61. doi: 10.3390/ph8010040

Table 2.

Ex vivo expansion conditions for adoptive immunotherapy using ex vivo activated Vγ9Vδ2 T cells.

Reference Number of Patients Disease Cell Source Culture condition
IL-2 Stimulant (Concentration) Serum Culture days
Kobayashi et al., 2007 Cancer Immunol. Immunother. [22] 7 RCC PB 100 U/mL 2M3B1-PP 100 μM 2% Auto serum 14 days
Bennouna et al., 2008 Cancer Immunol. Immunother. [21] 10 RCC Leukapheresis 328 U/mL: d1, 984 U/mL: d4–14 BrHPP 3 μM 9% FCS 14 days
Kobayashi et al., 2011 Cancer Immunol. Immunother. [23] 11 RCC Leukapheresis (1 leukapheresis for 2 treatments) 100 U/mL 2M3B1-PP 100 μM 2% Auto serum 11 days
Nicol et al., 2011 Br. J. Cancer [24] 18 Melanoma: 4, Ovarian cancer: 1, Colon cancer: 1 Luekapheresis 1 leukapheresis for 8 treatments 700 IU/mL, d0; 350 IU/mL, every 2–3 days Zol 1 μM 10% AB serum 7–14 days
Melanoma: 3
Adenocarcinoma: 1
Cholangiocarcinoma: 1
Ovarian carcinoma: 1
Colon cancer: 2
Duodenal cancer: 1
Breast cancer: 2, Cervical cancer: 1
Nakajima et al., 2010 Eur. J. Cardiothorac. Surg. [26] 10 Non-small-cell lung cancer Peripheral blood 70 mL 1000 U/mL Zol 5 μM 10% Auto serum 14 days
Abe et al., 2009 Exp. Hematol. [25] 6 Multiple myeloma Peripheral blood 1000 U/mL Zol 5 μM Auto serum 14 days
Wada et al., 2014 Cancer Med. [27] 7 Gastric cancer Leukapheresis 1000 U/mL Zol 5 μM Auto serum 14 days