A potential agent for treating preeclampsia
It usually begins after the 20th week of pregnancy: The affected women suddenly develop high blood pressure. They excrete increased amounts of protein in their urine (called proteinuria) – a sign that the small blood vessels in the kidneys are damaged. It can also cause life-threatening damage to the liver and bone marrow. Moreover, the unborn baby is not adequately nourished, which can interfere with the baby’s growth and development. About five percent of all pregnant women in Western countries suffer from some form of preeclampsia.
Nadine Haase analyzes microscopic images.
“Preeclampsia is the most common pregnancy-related disease that today in Germany still causes a significant number of deaths among women, and it is also the leading cause of premature births, with some births occurring between the 24th and 30th weeks of pregnancy,” says Dr. Nadine Haase from the Experimental and Clinical Research Center (ECRC), a joint institution of the Max Delbrück Center for Molecular Medicine in the Helmholtz Association (MDC) and Charité – Universitätsmedizin Berlin. Haase is the lead author of a study on preeclampsia that is now being published in the Journal of Clinical Investigation. She is a member of the Hypertension-Mediated End-Organ Damage Lab, led by Professors Dominik Müller and Ralf Dechend, the latter of whom is the senior author of the paper.
The disease has previously been untreatable
There are not yet any medications for treating preeclampsia. “We know that the endogenous renin-angiotensin-aldosterone system (RAAS), which regulates blood pressure as well as water and electrolyte balance, is disrupted in women with the disease,” Haase says. “However, those agents already known to intervene in the RAAS system cannot be administered to pregnant women, because they could harm the unborn baby, especially impairing kidney development.” And other antihypertension drugs, such as methyldopa, have only a minimal effect on preeclampsia. “Often the only option is preterm delivery, and many of these premature babies don’t survive or have disabilities,” Haase says.
So, together with colleagues from Berlin, Essen, Hamburg, and Jackson, Mississippi, as well as a team from the Cambridge, Massachusetts-based medical research firm Alnylam Pharmaceuticals, Haase began to search for more effective drugs to treat preeclampsia. The researchers wanted to find out if the small interfering RNA (siRNA) molecules developed by Alnylam could alleviate the symptoms of preeclampsia without harming the fetus. “The siRNA we are using slows the production of the hormone angiotensinogen (AGT) in the liver,” Haase explains. “AGT is a precursor of angiotensin. As a result, the siRNA acts on the RAAS system in regulatory manner.” Alnylam has already successfully employed this mechanism of action to treat other diseases in humans.
Members of the Müller/Dechend Lab that work on preeclampsia.
Two animal models of preeclampsia
Haase and her colleagues tested the siRNA on two animal models. In the first model, the team of researchers used female rats that had been genetically altered so that they produced human AGT. They crossed these animals with male rats that produce human renin. Such a procedure leads to hyperactivity of the RAAS system with corresponding symptoms of preeclampsia during the gestation of the female rats.
In the other model, which was developed in the United States and goes by the name of reduced uteroplacental perfusion (RUPP), clips that reduce blood flow in the placenta were applied to the gestating rats. This caused the rat fetuses to be undernourished. In addition, the maternal rats treated with the clip developed – as did the genetically altered animals – high blood pressure and proteinuria, albeit at a lower level. Two clinical biomarkers – PlGF and sFlt-1 – that are used in the diagnosis of preeclampsia were also altered in the rats.
Histological image of a rat placenta: This image helps researchers analyze, among other things, the spiral arteries in order to gain insights into fetal nutrition.
Lower blood pressure, larger fetuses
For the therapeutic experiment, the researchers injected siRNA under the skin of the rats. They had chemically altered the molecules so that they would only act on the liver – i.e., where the hormone AGT is produced. “As hoped, we observed a decrease in the symptoms of preeclampsia in the treated rats, and this was true for both models,” Haase says. “Their blood pressure fell and the proteinuria disappeared.” Moreover, the biomarker ratio, PlGF/sFlt-1, returned to normal. Consequently, the offspring in the womb were also better nourished.
Developing an RAAS blocker that does not cross the placental barrier and cause harm to the child is one of the greatest challenges in prenatal medicine.
In addition, Haase reports that it was possible to show that the siRNA molecules only blocked the production of the hormone AGT in the liver of the rats. The siRNA was not detectable in the placenta. The researchers also studied whether the treatment administered to maternal rats affected organ development (e.g., brain, lung, heart, kidney) in the offspring. “We did not find any negative effects in the rat fetuses nor in the fetuses that were delivered,” Haase says. “The siRNA therapy thus appears to be safe, at least in animals.”
First clinical trial with pregnant women
“Our study provided the data required to take the next step toward a clinical trial,” Haase says. But further basic research is also needed. “Developing an RAAS blocker that does not cross the placental barrier and cause harm to the child is one of the greatest challenges in prenatal medicine,” says Ralf Dechend, the senior author of the study. He reports that the US company Alnylam is now planning to conduct its first therapeutic trial with pregnant women in which he will be involved in a medical advisory role. Haase, on the other hand, is already contemplating her next research project: a preclinical study in which she wants to test how a peptide (a small protein molecule) affects the treatment of preeclampsia.
Text: Anke Brodmerkel
Further information
- MDC press release: Preeclampsia triggered by an overdose of gene activity
- MDC press release: Preeclampsia: Inflammation of the placenta interferes with fetal development
Literature
Haase, Nadine et al. (2020): ”RNA interference therapeutics targeting angiotensinogen ameliorate preeclamptic phenotype in rodent models”, Journal of Clinical Investigation, DOI: 10.1172/JCI99417
Downloads
- Histological image of a rat placenta: This image helps researchers analyze, among other things, the spiral arteries in order to gain insights into fetal nutrition. Photo: Nadine Haase, MDC
- Nadine Haase analyzes microscopic images. Photo: Markus Altmann
- Members of the Müller/Dechend Lab that work on preeclampsia. Photo: Florian Herse, MDC
Contact
Dr. Nadine Haase
Member of the Müller/Dechend Lab
Experimental and Clinical Research Center (ECRC) and Max Delbrück Center for Molecular Medicine (MDC)
nadine.haase@mdc-berlin.de
Christina Anders
Editor, Communications Department
Max Delbrück Center for Molecular Medicine in the Helmholtz Association (MDC)
+49 (0)30 9406 2118
christina.anders@mdc-berlin.de
- The Max Delbrück Center for Molecular Medicine (MDC)
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The Max Delbrück Center for Molecular Medicine in the Helmholtz Association (MDC) is one of the world’s leading biomedical research institutions. Max Delbrück, a Berlin native, was a Nobel laureate and one of the founders of molecular biology. At the MDC’s locations in Berlin-Buch and Mitte, researchers from some 60 countries analyze the human system – investigating the biological foundations of life from its most elementary building blocks to systems-wide mechanisms. By understanding what regulates or disrupts the dynamic equilibrium in a cell, an organ, or the entire body, we can prevent diseases, diagnose them earlier, and stop their progression with tailored therapies. Patients should benefit as soon as possible from basic research discoveries. The MDC therefore supports spin-off creation and participates in collaborative networks. It works in close partnership with Charité – Universitätsmedizin Berlin in the jointly run Experimental and Clinical Research Center (ECRC), the Berlin Institute of Health (BIH) at Charité, and the German Center for Cardiovascular Research (DZHK). Founded in 1992, the MDC today employs 1,600 people and is funded 90 percent by the German federal government and 10 percent by the State of Berlin.
