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. Author manuscript; available in PMC: 2007 Dec 26.
Published in final edited form as: Clin Cancer Res. 2006 Oct 15;12(20 Pt 1):6106–6115. doi: 10.1158/1078-0432.CCR-06-1183

Table 2.

Anti-FR and anti-allo responses of transduced T cells from patients in cohort 1 and 2 of the study

Cohort 2
Cohort 1, median
Pt. 9 Pt. 10 Pt. 11 Pt. 12 Pt. 13 Pt. 14 Median
Media alone 36 60 34 42 0 19 35 153
Melanoma (FR) 35 54 28 26 14 27 28 139
IGROV-1 (FR+) 1,375 2,960 8,010 1295 1,340 9,050 2,168 6,501
Allogeneic stimulator PBMCs 2,270 1,555 2,995 5625 >4,320 603 2,633
Autologous PBMCs 210 456 36 140 39 298 175
OKT3 5,784 13,317 9,620 2890 >3,760 >59,000 7,702 7,457

NOTE: T cell reactivity towards the FR tumor antigen and allogeneic stimulator PBMCs was determined by assaying IFN-γ secretion (pg/mL) using ELISA following overnight incubation of Tcells with the targets listed. Plastic-coated anti-CD3 (OKT3) was used as an indicator of maximal T cell response. Transduced T cells from all patients were reactive with FR, and T cells from patients in cohort 2 were reactive with allogeneic PBMCs. Nontransduced Tcells did not respond against IGROV-1, except for patient 14 in whom 548 pg/mL IFN-γ was secreted (data not shown).