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. 2002 Dec;70(12):6961–6967. doi: 10.1128/IAI.70.12.6961-6967.2002

TABLE 1.

Course of infection in A. vociferans monkeys challenged with P. falciparum parasites

Vaccine group and monkey ELISA titera to:
Days to:
% Parasitemia
Outcomed
AMA1 MSP142 Patencyb Treatmentc Peak At treatment
Pvs25H
    T1119 206 982 5 11 6.20 6.20 Virulent
    T1172 63 4,160 5 11 6.25 6.25 Virulent
    T907 7,450 22,750 6 11 6.50 6.50 Virulent
    T978 75 12,280 6 11 20.15 20.15 Virulent
    T1136 11,020 42,800 7 14 7.55 7.55 Virulent
        Meane 603 8,665 6 12 (Δ = 7) 9 9
Naïve
    T1146 4 11 25.05 25.05 Virulent
    T1091 5 9 9.05 9.05 Virulent
    T1169 5 11 17.1 17.1 Virulent
    T960 7 11 8.05 8.05 Virulent
        Mean 5 11 (Δ = 7) 15 15
MSP142
    T1139 149 135 7 15 3.35 3.35 Anemic (V)
    T1115 51 136 6 15 4.60 4.60 Virulent
    T891 16 73 6 14 10.05 10.05 Virulent
    T1096 37 109 5 28 0.07 0.00 Self-cured
        Mean 52 96,438 6 18 (Δ = 13) 5 5
AMA1
    T979 311,200 168 28 0.00 0.00 Subpatent (Dp)
    T1089 152,600 1,975 10 18 0.60 0.60 Anemic (Dp)
    T1185 336,800 419 28 0.00 0.00 Subpatent (Dp)
    T1152 87,200 7,000 6 12 7.60 7.60 Virulent
    T1102 328,400 11,130 9 21 5.10 5.10 Virulent (Dp)
    T1112 82,600 1,000 22 36 0.55f 0.35 Controlled (Dp)
        Mean 183,222 1,487 17 23 (Δ = 7) 2 2
AMA1 + MSP142
    T1138 38,600 77,500 7 14 6.80 6.80 Virulent
    T964 161,400 87,100 24 33 0.65f 4.0 Controlled (Dp)
    T1173 13,850 199,100 10 20 0.16 0.16 Anemic (Dp, C)
    T1188 39,000 146,600 7 20 0.02 0.00 Anemic (Sc)
    T914 72,200 164,400 11 20 5.70 5.70 Virulent (Dp)
    T1155 260,400 90,500 28 0.00 0.00 Subpatent (Dp)
    T986 110,975 188,700 14 5.60 5.60 Virulent
        Mean 61,567 108,375 13 21 (Δ = 9) 3 3
a

Expressed in arbitrary antibody units, calculated by reference to a standard Aotus serum against the plate antigen. A serum dilution of the reciprocal of the antibody units reported would give an approximate absorbance at 405 nm of 1.0. —, not measured.

b

Monkeys T979, T1185, and T1155 were subpatent (parasitemia, <0.01%) for the 28-day course of the challenge.

c

If not already treated, all monkeys were treated on day 28, except T1112 and T964, which were subpatent for 22 and 24 days, respectively, so treatment was deferred in order to monitor the course of their parasitemia. Shown also are the numbers of days between treatment and patency (Δ).

d

Describes course of infection. Virulent, a sharply rising, uncontrolled parasitemia requiring treatment (parasitemia, >5%); subpatent, no parasites observed per 10,000 RBCs over the course of the challenge; self-cured, parasites cleared by the animal without intervention; controlled, parasite growth controlled to low levels for the 28 days of the study; anemic, monkey required treatment for anemia (hematocrit, <25%). At the time of treatment for anemia, the course of the parasitemia could be virulent (V), controlled (C), or self-cured (Sc). The course of the infection was also modified in some animals by a delay to patency (Dp), where the animal became patent after all control animals had become patent (>7 days).

e

Shown are geometric mean ELISA titers and arithmetic means for each of the other columns, including only data from the 28 days of challenge. Thus for this purpose, T979, T1185, and T1155 are considered to have 28 days to patency; T1112 and T964 are considered to have 28 days to treatment, with peak parasitemias and parasitemias at day 28 of 0.55 and 0.65, respectively.

f

Shown is the peak parasitemia within the 28-day challenge period. Monkeys T1112 and T964 were monitored for an additional period, when they eventually had peak parasitemias of 0.75% (T1112) and 4.0% (T964).