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. 1999 Nov;98(3):413–421. doi: 10.1046/j.1365-2567.1999.00888.x

Table 2.

Anti‐cytotoxic T‐lymphocyte antigen‐4 (CTLA‐4) monoclonal antibodies (mAbs) augment alloimmune response of human T cells in secondary mixed lymphocyte response (MLR)

[3H]TdR incorporation (c.p.m. × 10–3 ± SD)

Day 3 Day 4


Stimulator* S : R mAb Isotype Anti‐CTLA‐4 Isotype Anti‐CTLA‐4
RPMI 8866 1 : 20 IgG2a 53·9 ± 2·4 17·7 ± 2·4
2G12 63·0 ± 4·4 21·8 ± 2·6
4B10 64·1 ± 5·1 22·5 ± 2·6
IgG2b 56·7 ± 1·6 15·9 ± 1·6
1G3 67·3 ± 1·8 20·7 ± 3·2
1 : 50 IgG2a 27·7 ± 1·0 7·8 ± 0·6
2G12 39·0 ± 1·9 9·8 ± 1·4
4B10 34·4 ± 2·3 9·2 ± 2·0
IgG2b 29·9 ± 2·6 8·7 ± 1·5
1G3 37·1 ± 2·5 8·0 ± 2·5
KM‐H2 1 : 20 IgG2a 30·7 ± 2·4 26·7 ± 0·7
2G12 27·6 ± 3·7 29·0 ± 2·5
4B10 31·5 ± 5·9 28·9 ± 4·5
IgG2b 31·7 ± 2·2 25·5 ± 3·5
1G3 34·8 ± 3·6 28·9 ± 2·1
*

T cells were cultured for 5 days in primary mixed lymphocyte response (MLR) against irradiated RPMI 8866 cells in a stimulator–responder (S : R) ratio of 1 : 20. Subsequently they were washed and resuspended in complete medium. Forty‐eight hours later, they were restimulated with either RPMI 8866 or with a third‐party stimulator (KM‐H2) in the stimulator–responder ratio indicated, in the presence of either anti‐CTLA‐4 mAb or isotype control. [3H]‐Thymidine (TdR) incorporation on days 3 and 4 is shown as the mean± SD of quadruplicate or triplicate cultures.