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TABLE 1.

The relationship between the course of infection and antibody assays in malaria-naive animals

Vaccine Monkey no. Parasite challenge inoculation Prepatent period (days) % Peak parasitemiaa Day of cure
Course of infection Prechallenge sera
Secondary processing assaye
Dayb % Parasitemia % Hematocrit ImFc ELISAd 1st 2nd
P30P2MSP-119 2581 104 9 0.05 Self-resolved 105 1/500,000 +++ +
2582 104 20 0.05 Self-resolved 105 1/450,000 +++ ++
2590 104 8 0.05 Self-resolved 106 1/500,000 +++ +++
2593 104 8 4.3 18 4.3 30 Virulent 105 1/180,000 ++
2586 105 12 0.05 Self-resolved 106 1/1,000,000 +++ +++
2571 105 4 1.2 22 1.2 21 Anemic 106 1/200,000
2578 105 11 0.1 17 22 Anemic 105 1/250,000 +++ +++
2572 105 5 6.0 10 6.0 48 Virulent 104 1/16,000
TBVg 2521f 104 10 0.2 11 0.2 19 Anemic 104 1/16,000
TBV T580 104 8 5.0 12 5.0 39 Virulent 103 1/700
None 2570 104 6 6.2 11 6.2 44 Virulent
None 2584 104 5 5.3 12 5.2 55 Virulent
TBV T562 105 6 6.9 15 6.9 30 Virulent 103 1/700
None 2592 105 4 5.9 9 5.9 44 Virulent
None 2594 105 6 5.0 9 5.0 46 Virulent
a

Parasitemia of 0.05% indicates that a total of one or two parasites were seen in the 50 high-power light microscopy fields of a blood smear. 

b

Cured all remaining monkeys on day 44. 

c

ImF, immunofluorescence for pRBCs. 

d

ELISA titration on P30P2MSP-119; titers giving an OD of 1, which is on the linear part of the titration curve. 

e

Secondary processing assay: −, no detectable processing inhibition; +/−, just-detectable inhibition; +, significant inhibition; ++, strong inhibition, +++, apparently complete inhibition. 

f

Control monkey 2521 received one vaccination of P30P2MSP-119 instead of TBV25H at the third vaccination. 

g

TBV, TBV25H.