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. Author manuscript; available in PMC: 2012 Oct 1.
Published in final edited form as: Clin Cancer Res. 2011 Aug 19;17(19):6174–6184. doi: 10.1158/1078-0432.CCR-11-1111

Table 1.

In vitro recognition of ALDH+ and ALDHbright cells present in human carcinoma cell lines, xenograft and surgically removed lesion by HLA-A2-restricted, ALDH1A188–96 peptide- CD8+ T cells in flow cytometry-based CMC assaysa.

Cells Cells only Cells + ALDH1A1-specific CD8+
T cell + isotype mAb
Cells + ALDH1A1-specific CD8+ T
cells + KS1 mAb
Cell
number
%
ALDH+
%
ALDHbright
Cell
number
%
ALDH+
%
ALDHbright
Cell
number
%
ALDH+
%
ALDHbright
PCI-13 380,000 17.6 3.2 302,000
(−22%)
5.3
(−70%)
0.5
(−83%)
350,000
(−8%)
13.6
(−23%)
3.5
(+10%)
MDA-MB-231 204,000 28.3 0.4 188,000
(−8%)
14.2
(−50%)
0.3
(−75%)
200,000
(−2%)
31.1
(+11%)
0.3
(−25%)
MIA PaCa-2 365,000 43.2 4.6 194,000
(−47%)
37.2
(−14%)
1.8
(−60%)
299,000
(−18%)
40
(−7%)
3.8
(−18%)
PCI-13 xenograft 350,000 13.1 2.1 213,000
(−29%)
3.5
(−73%)
0.6
(−72%)
298,000
(−15%)
13
(−5%)
7-Jan
(−22%)
SCCHN lesion 084124 150,000 3.4 0.9 100,000
(−33%)
0.9
(−74%)
0.1
(−89%)
NDb ND ND
a

Flow cytometry analyses of ALDH+ and ALDHbright cells present in SCCHN PCI-13, breast carcinoma MDA-MB-231 and pancreatic carcinoma MIA PaCa-2 cells, and digests of a PCI-13-derived xenograft and a SCCHN lesion following incubation with HLA-A2-restricted, ALDH1A188–96 peptide--specific CD8+ T cells at an E/T cell ratio of 2.5:1, followed by flow cytometry analysis with ALDEFLUOR±DEAB. 5×10 target cells were used with the exception of the analysis of the SCCHN lesion. Lysis was blocked by HLA-A2, A28-specific KS1 mAb. The percentages of ALDH+ and ALDHbright cells in each sample following incubation with HLA-A2-restricted, ALDH1A188–96 peptide-specific CD8+ T cells in the presence of isotype mAb or KS1 mAb are indicated. The decreases in these values compared to the “Cells only” control are indicated in parentheses

b

ND indicates not done due to insufficient cells