Angiotensin converting enzyme 2 (ACE2) is the crucial severe acute respiratory syndrome
coronavirus 2 (SARS-CoV-2) receptor and protects multiple tissues, including the lung,
from injury as a regulator of the renin–angiotensin system.
1
Therefore, ACE2 has become the focus of COVID-19 research and a plethora of drug development
efforts. Among the novel compounds under development is human recombinant soluble
ACE2 (hrsACE2 [APN01; Apeiron Biologics, Vienna, Austria]), which has two mechanisms
of action that theoretically should be of benefit in COVID-19.
2
The first involves binding the viral spike protein and thereby neutralising SARS-CoV-2,
3
and the second is minimising injury to multiple organs, including the lungs, kidneys,
and heart, because of unabated renin–angiotensin system hyperactivation and increased
angiotensin II concentrations.4, 5, 6 hrsACE2 has been tested in 89 patients, namely
in healthy volunteers in phase 1 studies and in patients with acute respiratory distress
syndrome (ARDS) in phase 2 clinical studies, with a good safety profile.7, 8 Moreover,
hrsACE2 can reduce SARS-CoV-2 load by a factor of 1000–5000 in in-vitro cell-culture
experiments and engineered organoids, directly demonstrating that ACE2 can effectively
neutralise SARS-CoV-2.
3
We describe in this Case Report the first course of treatment with hrsACE2 of a patient
with severe COVID-19.
A 45-year-old woman was admitted to hospital with a 7-day history of cough, weakness,
myalgia, fever, and dyspnoea, and a 4-day history of nausea and diarrhoea. Past medical
history revealed type 2 diabetes, controlled non-pharmacologically by exercise and
diet, and Grave's disease for which thyroidectomy had been done; the patient was euthyroid
on thyroxin. She had a normal body-mass index and reported good exercise tolerance
before her present illness. On admission she was febrile (38·1°C), mildly hypoxaemic
(PaO2 56 mm Hg on room air), and was started on oxygen by nasal cannula. A chest x-ray
showed bilateral patchy consolidations indicative of viral pneumonia (appendix p 6).
Diagnosis of SARS-CoV-2 infection was made by RT-PCR from a nasopharyngeal swab, and
treatment with hydroxychloroquine (400 mg twice daily) and anticoagulation with nadroparin
(0·4 mg once daily) were started. The following day, the patient's chest x-ray showed
increasing bilateral, multifocal, and peripheral ground glass patterns (appendix p
6
). Her fractional concentration of oxygen in inspired air (FiO2) was 153 mm Hg, and
she showed signs of exhaustion while on high flow nasal cannula, with a FiO2 of 70%.
We therefore intubated her and used a lung protective ventilatory strategy. Initial
laboratory tests showed mild leukopenia and thrombocytopenia with a profound lymphopenia
(0·54 g/L); serum lactate dehydrogenase (636 U/L), ferritin (880 μg/L), C-reactive
protein (103 mg/L), and D-dimer (1·3 mg/L) concentrations were all markedly elevated
(appendix p 4).
9 days after symptom onset (baseline, day 2 after hospital admission), treatment with
hrsACE2 (APN01; 0·4 mg/kg) intravenous infusion for 5 min twice daily was started.
This compassionate use treatment was initiated after consultations among attending
physicians, the patient's family, and external infectious disease and ARDS experts.
After administration of the first hrsACE2 dose, the patient became afebrile within
hours. Her temperature increased the following day with purulent respiratory secretions,
suggesting a bacterial pneumonia, which was treated with cefuroxime. A tracheal aspirate
subsequently grew methicillin-sensitive Staphylococcus aureus (MSSA). Renin–angiotensin
system fingerprinting and angiotensin-based markers, as well as cytokines and injury
biomarkers, were measured once daily during the 7-day administration of hrsACE2 and
thereafter for a total of 14 days. SARS-CoV-2 viral load and neutralising antibodies
were measured once daily in plasma. The presence of viral RNA was also measured in
nasopharyngeal swabs and tracheal aspirations (appendix p 2).
Therapy with hrsACE2 was continued as planned for 7 days and was well tolerated without
obvious drug-related side-effects. Her clinical course was complicated by slowly resolving
pneumonia with repeated detection of MSSA in tracheal suctions and Enterobacter aerogenes
bacteraemia, and her antibiotics were changed to linezolid and aztreonam. Her clinical
condition improved gradually and extubation was done on day 21 after baseline. The
patient was then transferred to neurological rehabilitation for treatment of critical
illness myopathy, which improved after physiotherapy. On day 57, she was discharged
from the hospital.
After the first injection of hrsACE2 we observed a marked reduction of angiotensin
II (figure 1A, B
; appendix p 4). hrsACE2 administration resulted in a profound increase of the ACE2
products angiotensin 1–7 and angiotensin 1–9 (figure 1B) and their major downstream
metabolite angiotensin 1–5 (appendix p 7) throughout the entire observation period.
Normalising the sum of these three renin–angiotensin system peptides to renin activity
resulted in an angiotensin-based marker that was associated with soluble plasma ACE2
activity (figure 1C), which was confirmed by an angiotensin II-to-angiotensin 1–7
conversion assay (figure 1D); ACE2 activity remained increased up to 7 days following
administration of the last dose of hrsACE2. Additionally, the angiotensin 1–7/angiotensin
II and angiotensin 1–5/angiotensin II ratios showed a marked skewing towards ACE2-generated
peptides (appendix p 7). The sum of all five angiotensin metabolites as determined
by renin–angiotensin system equilibrium analysis showed a strong correlation with
renin concentration, as validated in pooled human plasma spiked with different concentrations
of renin and hrsACE2, respectively (appendix p 7). We also observed soluble ACE2 present
in tracheal fluid throughout the observation period, showing an increase towards day
6 that peaked 36 h following administration of the final dose of hrsACE2 (figure 1D);
whether this reflects shedding of endogenous ACE2 or accumulation of hrsACE2, or both,
remains to be elucidated.
Figure 1
Human recombinant soluble ACE2 pharmacodynamics and drug concentrations
(A) Renin–angiotensin system fingerprinting of angiotensin metabolites in relation
to human recombinant soluble ACE2 dosing. Circle sizes and angiotensin values correspond
to metabolite concentrations (pmol/L). Black arrows mark the catalysing reactions
mediated by the indicated enzymes. (B) Plasma concentrations of various ACE2 substrates
and catalysed products. (C) ACE2 activity as the sum of ACE2 products and downstream
metabolites related to plasma renin activity. (D) ACE2 activity (angiotensin II-to-angiotensin
1–7 catalytic conversion assays) in plasma and tracheal suctions. First dose administered
on day 0; red triangles indicate days on which drug was administered. ACE2=angiotensin
converting enzyme 2. AT1R=angiotensin II type 1 receptor. MAS=G protein coupled receptor
Mas. NEP=neutral endopeptidase.
Concurrent with reduced angiotensin II concentrations we detected a marked reduction
in the inflammatory cytokine interleukin (IL)-6 and chemokine IL-8 (figure 2A
; appendix p 4), both of which play an important role in lung injury and cytokine
storm.
9
Furthermore, concentrations of soluble advanced glycosylation end product-specific
receptor, a marker for lung epithelial injury associated with higher mortality in
ARDS,
10
and the inflammation marker ferritin, were markedly decreased following hrsACE2 administration
(figure 2A). Serum concentrations of the inflammatory marker tumour necrosis factor
α and the lung damage biomarker serum surfactant protein D showed an initial increase
followed by a marked decrease.
11
A similar increase but delayed decrease (possibly because of the bacterial complications)
were noted for C-reactive protein and for the endothelial injury marker angiopoietin
2 concentrations (figure 2B; appendix p 4). Therefore, hrsACE2 treatment was associated
with a marked decrease in concentrations of critical cytokines implicated in COVID-19
pathology, and hrsACE2 remains catalytically active in the scenario of severe COVID-19.
Figure 2
Inflammatory, endothelial, and alveolar biomarkers
(A) Plasma concentrations of IL-6, IL-8, sRAGE, and ferritin. (B) Plasma concentrations
of C-reactive protein, TNFα, surfactant protein D, and angiopoietin-2. Red triangles
indicate days on which drug was administered. IL=interleukin. sRAGE=soluble advanced
glycation end product receptor. TNFα=tumour necrosis factor.
SARS-CoV-2 was detectable in the plasma 2 days before administration (day −2, 32 000
copies per mL) and on the first day of administration (day 0, 2500 copies per mL;
figure 3A
). 1 day later, plasma viraemia had decreased to a very low level (270 copies per
mL) and thereafter remained undetectable during daily testing, until the end of the
observation period when viral RT-PCR plasma testing was stopped. In tracheal aspirates,
SARS-CoV-2-specific RT-PCR revealed an increase of the measured viral RNA within 2
days of starting hrsACE2 treatment, followed by rapid clearance until the end of the
treatment period (figure 3B; appendix p 4).
Figure 3
Viral load and neutralising antibodies
Viral load (blue circles) and neutralising antibodies (green squares) in plasma (A)
and tracheal suctions and nasopharyngeal swabs (B). PCR LOD was 100 copies per mL.
Red triangles indicate days on which drug was administered. LOD=limit of detection.
hrsACE2 binds to the spike glycoprotein of SARS-CoV-2 at an affinity calculated to
be approximately 1·2 nM,
12
an affinity similar to high affinity antibody binding. Because hrsACE2 does not have
an Fc region to directly link to the immune system, assessing whether hrsACE2 treatment
for 1 week might interfere with the formation of antibodies against the virus was
crucial. Therefore, we assessed plasma neutralising anti-SARS-CoV-2 antibodies, which
were first detected 7 days after symptom onset and reached a plateau 5 days later
(figure 3A)—at a similar timepoint as previously reported.
13
Moreover, hrsACE2 infusions did not interfere with the generation of anti-viral IgA
and IgG antibodies in the patient's plasma (appendix p 4). Thus, intravenous treatment
with hrsACE2 has no apparent effect on anti-SARS-CoV-2 seroconversion.
ACE2 is the crucial cell surface receptor for SARS-CoV-2.
14
We have previously shown that ACE2 counterbalances the effects of angiotensin II and
thereby protects the heart, kidney, and importantly the lung via its enzymatic activity
in the renin–angiotensin system.5, 6, 15 Furthermore, we showed that ACE2 is the crucial
SARS-CoV receptor in vivo,
4
explaining why SARS-CoV and now SARS-CoV-2 became highly pathogenic viruses, with
ACE2 being the receptor for both viruses, and downregulation of ACE2 via virus binding
resulting in loss of renin–angiotensin system tissue homoeostasis.
15
These results provide a molecular explanation as to why SARS-CoV and SARS-CoV-2 infections
cause severe and often lethal lung failure. Moreover, genetic inactivation of ACE2
causes severe lung injury in influenza A H5N1-challenged and H7N9-challenged mice,
while administration of soluble ACE2 protects from lethal avian influenza A H5N1 infections.16,
17
Angiotensin II plasma concentrations are increased in acute lung injury,
15
predict fatal outcomes in patients infected with H7N9,
18
and, importantly, are also linked to severity of COVID-19.
19
ACE2 converts angiotensin II into angiotensin 1–7, which acts via its G protein coupled
receptor Mas receptor to counterbalance induction of the renin–angiotensin system.
Angiotensin II can drive cardiac disease, hypertension, fibrotic changes in the lung
and liver, diabetic nephropathy, inflammation, blood vessel constriction, and lung
injury, all of which are worsened in ACE2 mutant mice and can be alleviated in experimental
mouse models using hrsACE2.
20
Angiotensin II infusion in patients has also been associated with increased thrombotic
events and induction of the proinflammatory cytokine IL-6.21, 22 Our compassionate
use in a patient with COVID-19 now shows that hrsACE2 is highly active in cleaving
angiotensin II into angiotensin 1–7, as well as cleaving angiotensin I into angiotensin
1–9, starting with the first infusion, and that hrsACE2 remains active throughout
the course of the 7-day treatment.
After cessation of the therapy, angiotensin II concentrations returned within 48 h
to concentrations before treatment, in line with previous data on the half-life of
hrsACE2 in humans.
7
Notably, angiotensin 1–7 concentrations remained elevated for up to 7 days after hrsACE2
therapy was stopped, suggesting long-term beneficial effects. Compared to baseline,
markedly increased soluble ACE2 activity was detected in plasma up to 7 days after
dosing was stopped, which was paralleled by sustained elevation of the ACE2-dependent
renin–angiotensin system markers. Whether low concentrations of hrsACE2 are sufficient
to enhance angiotensin 1–7 concentrations for a prolonged time or whether treatment
triggered endogenous enzyme activity that can account for these effects needs further
analysis. Of note, a second patient with severe COVID-19 symptoms received two doses
of compassionate treatment with hrsACE2 for 1 day; however, because of the short term
1-day treatment, we did not include the patient in this Case Report. Importantly,
infusion of hrsACE2 in this patient was associated with a rapid and markedly reduced
serum angiotensin II concentration, efficiently increasing angiotensin 1–7 concentration
and alternative renin–angiotensin system markers for up to 5 days. Thus, hrsACE2 maintains
its tissue protective enzymatic activity to reduce angiotensin II concentrations in
patients with COVID-19. Notably, our compassionate use treatment was started at a
late stage of the disease in which inflammatory parameters were elevated and respiratory
function had already markedly deteriorated. A phase 2/3 study of hrsACE2 is currently
ongoing and includes patients with COVID-19 at earlier stages of the disease (pre-intubation).
Multiple efforts are underway to block SARS-CoV-2 infection, with approaches including
blocking viral entry—for example, fusin or transmembrane protease serine 2 inhibitors;
soluble ACE2 or antibodies, peptides, or small molecules that mimic ACE2 binding to
the viral spike protein; and inhibiting the viral proteases and viral RNA-dependent
RNA polymerase (eg, remdesivir). Moreover, vaccines specifically targeting the spike–ACE2
interaction are in development.
23
Therefore, ACE2 is at the core of COVID-19 research and drug development. Providing
first data on the effect of blocking the viral spike glycoprotein in patients with
COVID-19 is of paramount importance. Here, we have provided data on soluble ACE2 therapy
in a patient with SARS-CoV-2 infection.
Acknowledging the limitations of our study, the data show that the virus disappeared
rapidly from the serum; and, albeit at a later time after hrsACE2 (APN01) therapy,
from the nasal cavity and lung. Whether this decrease in viral load reflects the effect
of hrsACE2 treatment or the natural history of the disease remains speculative. Importantly,
hrsACE2 treatment did not interfere with the generation of neutralising antibodies.
The same was seen for the patient receiving hrsACE2 for 1 day—rapidly undetectable
serum viraemia and generation of anti-viral IgG and IgA antibodies (data not shown).
Considering that SARS-CoV-2 can directly infect blood vessels, as determined in our
experimental organoid model
3
and post-mortem examinations,
24
intravenous delivery of hrsACE2 could have an important effect on blocking the systemic
spread of the virus from the lung to other organs.