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. 2010 Jul;32(7):512–527. doi: 10.1111/j.1365-3024.2010.01225.x

Table 1.

Assessment of IFN-γ levels at approximately 24 h after the start of schizont rupture in three independent experiments using multiple parasite strains

Experimenta Parasite Strain Parasitaemia and maturity at start of experiment Time point approx 24 h after schizont rupture IFN-γ 1 pg/mLb IFN-γ 2 pg/mLb Mean IFN-γ pg/mL
A Palo Alto 4·0% mature pigmented trophozoites 30 h 86·1 128·3 107·2
A TM284 4·5% mature pigmented trophozoites 42 h 158·5 109·5 134·0
A R29 4·0% mature pigmented trophozoites 42 h 171·9 174·4 173·2
B Palo Alto 2·0% bursting schizonts, 22·0% small rings 18 h 1459·7 ND 1459·7
B TM284 4·4% bursting schizonts, 3·8% small rings 18 h 3670·1 3370·1 3520·1
B Field isolate A 5·8% schizonts 32 h 851·9 828·6 840·3
B Field isolate B 5·1% schizonts 32 h 762·3 1015·6 889·0
B Field isolate C 4·4% mature pigmented trophozoites Mean of 32 and 40 h 939·6 801·3 870·5
C Palo Alto 1·3% large rings 42 h 5·0 38·3 21·7
C TM284 0·5% mature pigmented trophozoites 42 hc 5·2 2·5 3·9
C Field isolate D 0·5% mature pigmented trophozoites 42 hc 70·9 58·4 64·6
C Field isolate E 0·7% schizonts 24 h 65·0 58·2 61·6
a

Each experiment used a different single donor. Experiment A is shown in detail in Figure 4. Experiments B and C are as described in the text;

b

IFN-γ levels in culture supernatants of two replicate wells were measured at each time point by ELISA;

c

For both TM284 and Field isolate D, the final time point studied (42 h) was about 18 h after schizont rupture began. Ideally, a 48-h time point (giving data 24 h after schizont rupture) would have been optimal; however, this was not available for this experiment.