Intra-amniotic FVIII mRNA delivery produced detectable fetal FVIII protein in a rat model of potential perinatal treatment.
Evidence
This controlled preclinical rat experiment injected 166 fetuses with hFVIII mRNA lipopolyplex or mRNA-free control on gestational day 17 and measured fetal liver and serum hFVIII through term.
Caveat
The evidence is limited to fetal protein expression in rats, not bleeding prevention or clinical benefit in human infants.
Simplified
is an X-linked monogenic disease resulting in insufficient pro-coagulant factor VIII (FVIII) levels. Hemophiliac infants are at risk for life-threatening hemorrhage, especially during birth. No perinatal treatment for Hemophilia A is currently available. It has been previously shown that the transamniotic route is a viable option to deliver exogenous mRNA to the fetus. We sought to determine whether FVIII mRNA so delivered could be translated by the fetus, leading to the presence of FVIII in the fetal circulation. Time-dated pregnant Sprague Dawley dams underwent volume-matched intra-amniotic injections in all their fetuses ( = 166) of either a human FVIII (hFVIII) mRNA encapsulated by lipopolyplex (mRNA; = 115) or of the same lipopolyplex without mRNA (control; = 51) on gestational day 17 (E17; term = E21-22). Fetal liver and serum samples were procured daily until term and screened for hFVIII protein by ELISA. There was no maternal mortality. Overall survival was 90% (149/166). Controlled by the mRNA-free injections, fetal serum levels of hFVIII were statistically significantly higher overall in the mRNA group ( = 0.002), peaking at E20 (24.4 ± 2.4 ng/mL in the mRNA group vs. 10.5 ± 1.9 ng/mL for control; < 0.001). In the fetal liver, there was variability in statistically significant differences between the groups, with the shorter time point showing significance ( = 0.003). Encapsulated exogenous mRNA encoding for factor VIII can be incorporated and translated by the fetus following simple intra-amniotic injection in a rat model. Transamniotic mRNA delivery could become a novel strategy for the perinatal management of Hemophilia A. n n n p p p
Key numbers
16.0 ± 0.9 ng/mL
Increase in Levels
Fetal serum levels in the group vs. .
24.4 ± 2.4 ng/mL
Peak Levels
Observed at E20 in the group vs. .
90%
Overall Fetal Survival
Survival rate across all time points for both groups.
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