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. 2020 Nov 17;11:609994. doi: 10.3389/fimmu.2020.609994

Table 1.

In vivo arachidonic acid therapeutic action.

Experimental host Schistosome species Ref
Schistosoma mansoni a Schistosoma haematobium b
Mice (21)
ARA dose 1,000 mg/kg 1,000 mg/kg
Worm burden decrease P = 0.007; 37.9% P = 0.003; 57.7%
ARA dose 300 mg/kg/d c for 15 d 300 mg/kg/d for 15 d
Worm burden decrease P = 0.001;63.6% P = 0.007; 81.4%
Hamsters (22)
ARA dose 300 + 2,500 mg/kg/d over 2 d 300 + 2,500 mg/kg/d over 2 d
Worm burden decrease P = 0.017; 78.9% P = 0.0002; 50.6%
Childrenc Number of cured/total number of treated children (cure rate %)
Light infection Moderate infection Heavy infection Ref
Low endemicity region (23)
PZQ 40 mg/kg once 12/14 (85) 5/6 (83)
ARA 10 mg/kg/d for 15 d 11/14 (78) 4/9 (44)
PZQ + ARA 14/16 (87) 7/7 (100)
High endemicity region (24)
PZQ 40 mg/kg once 19/32 (60) 11/26 (42) 3/15 (20)
ARA 10 mg/kg/d for 15 d 12/24 (50) 3/23 (13) 3/14 (21%)
PZQ + ARA 19/23 (83) 13/23 (57) 11/14 (78)
a

Mice and hamsters infected with S. mansoni were ARA-treated 6 weeks after infection.

b

Mice and hamsters infected with S. haematobium were ARA-treated 12 weeks after infection.

c

Children were infected with S. mansoni.

d

d = day.