Inhalable nanobody shows potent anti-SARS-CoV-2 activity in vivo

By Dr. Ramya Dwivedi, Ph.D.Feb 26 2021

Vaccines against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the causative agent of coronavirus disease 2019 (COVID-19), are being administered worldwide. A successful, safe and targeted therapeutic drug to treat this infection is yet to emerge.

Convalescent plasma, repurposed antivirals, neutralizing monoclonal antibodies, and highly selected nanobodies (Nbs) and multivalent forms are some of the innovative therapeutics tried against this virus.

However, these attempts to arrive at a cost-effective and highly efficient drug have been met with many challenges, such as poor supply-limit, high dose requirements, high production costs, and inefficient delivery across the plasma-lung/blood-brain barrier, etc.

To date, close to 112 million people have been infected by this highly transmissible virus. Over 2.44 million lives were lost to the severity of this disease caused by this virus. The immediate need for a therapeutic drug cannot be understated during this pandemic.

Many scientists have researched the nanobodies - the camelid-originated, single-domain antibody fragments, that binds selectively to a specific antigen. For anti-SARS-CoV-2, these nanobodies are generated such that they primarily target the receptor-binding domain (RBD) of the SARS-CoV-2 spike (S) glycoprotein for virus neutralization.

The highly selected Nbs and the multivalent forms are found to have high neutralization potency – comparable to, or even better per-mass than, some of the most successful SARS-CoV-2 neutralizing mAbs. Also, Nbs are cheaper to produce.

Study: Inhalable Nanobody (PiN-21) prevents and treats SARS-CoV-2 infections in Syrian hamsters at ultra-low doses. Image Credit: Huen Structure Bio / Shutterstock

This news article was a review of a preliminary scientific report that had not undergone peer-review at the time of publication. Since its initial publication, the scientific report has now been peer reviewed and accepted for publication in a Scientific Journal. Links to the preliminary and peer-reviewed reports are available in the Sources section at the bottom of this article. View Sources

Ultrapotent homotrimeric Pittsburgh inhalable Nanobody 21 (PiN-21)

In a paper published on the bioRxiv* preprint server, researchers presented their results with a stable and ultrapotent homotrimeric Pittsburgh inhalable Nanobody 21 (PiN-21) against SARS-CoV-2 infection in Syrian hamsters. They demonstrated the high therapeutic efficacy of this homotrimeric Nb, leveraging both intranasal and aerosol delivery.

In a previous study, the researchers showed that this ultrapotent homotrimeric construct (PiN-21) efficiently blocked the SARS-CoV-2 infectivity at below 0.1 ng/ml in vitro.

The monomeric Nbs show poor pharmacokinetics due to their small size (~15 kDa) and a lack of Fc-mediated immune effectors’ function. With these concerns for an Nb-based therapy, the researchers investigated if a high in vitro neutralization potency of SARS-CoV-2 Nbs can be translated into in vivo therapeutic benefits.

Therapeutic efficacy against SARS-CoV-2 infection in Syrian hamsters

The researchers used Syrian hamsters for the in vivo studies. The Syrian hamsters model moderate to severe COVID-19 disease. The PiN-21 was delivered intranasally and via inhalation.

The concurrent delivery of PiN-21 also eliminated any weight loss in the infected animals. Consistent protection and a reduction of the viral genomic RNA (gRNA) by reverse transcriptase (RT)-qPCR was observed in these animals.

On day two post-injection, the virus was undetectable in the upper respiratory tract (URT), including both nasal washes and throat swabs of all the PiN-21-treated animals. In contrast, the control group presented varying levels of infectious virus.

The researchers reconstructed the PiN-21 for aerosolization and found that it retained high neutralization potency. Critically, the researchers observed that the aerosolization treatment diminished the infectious viruses in the lung, indicating that the Nb administration by aerosolization may limit human-to-human transmission of SARS-CoV-2.

We envision that PiN-21 aerosolization treatment could provide both a convenient and cost-effective solution to alleviate disease onset and reduce virus transmission, especially for mild COVID-19 patients who constitute major populations of infections.”

The researchers have found that the PiN-21 can efficiently protect SARS-CoV-2 infection in hamsters by rapidly and drastically suppressing viral replication in both the URT and lower respiratory tract (LRT).

Importantly, the researchers underscored the requirement of an ultra-low dose of the PiN-21 construct to neutralize SARS-CoV-2 infectivity in vivo efficiently.

Importance of the PiN-21 construct

This study demonstrated that the high in vitro neutralization potency of PiN-21 can be translated into therapeutic benefits in vivo independent of Fc-mediated immune responses.

The researchers believe that this construct may benefit high-risk groups, such as seniors, immunocompromised individuals, and infants, in both inpatient and outpatient settings.

The affinity-matured, ultrapotent Nbs are also characterized by excellent physicochemical properties: high solubility and stability (facilitates drug scaling, storage, and transportation). These are critical during responses to pandemics.

Treatment efficacy of aerosolized PiN-21 in the hamster model of SARS-CoV-2. A. Overview of the experiment design. 3 x 104 p.f.u. of SARS-CoV-2 was IN inoculated. PiN-21 or a control Nb was aerosolized to hamsters in the cage 6 h.p.i. Animal weight changes were monitored, nasal washes and throat swabs were taken daily. Animals were euthanized for necropsy on 3 d.p.i. B. The percentage of body weight change of PiN-21 aerosol-treated animals compared to the control (n=6). C. Reduction of viral titers in hamster lungs (3 d.p.i.). Significant differences were observed between treated and control groups. **, P < 0.01; *, P < 0.05. The dashed line indicates the detection limit of the assay. D. Lung pathology scores of treated and control groups. Significant difference was denoted by ****, P < 0.0001. E. H&E staining of necrotizing bronchointerstitial pneumonia affiliate with abundant SARS-CoV-2 S antigen in bronchiole epithelium and alveolar type 1 and 2 pneumocytes in the control group. All images acquired at 20 x, scale bar = 100 µm. Areas marked by boxes are shown at higher magnification in the right-most panel (scale bar = 25 µm). F. Immunostainings of bronchointerstitial compartments (3 d.p.i.). Orange, SARS-CoV-2 S; magenta, CD68/macrophages; red, CD3e+ T cells; teal, ACE2; Grey, DAPI. The bronchiole is outlined by white hash. Total magnification 200x, scale bar = 100 µm.

These properties and small sizes of Nbs are an exciting possibility of efficient pulmonary delivery by aerosolization with characteristics of rapid onset of action, high local drug concentration/bioavailability, and improved patient compliance (needle-free) that may benefit a large population of SARS-CoV-2 infected patients, the researchers highlighted in their study.

In this study, the researchers systematically evaluated the efficacy of PiN-21 for prophylaxis and treatment of SARS-CoV-2 infected Syrian hamsters. They provided direct evidence that ultra-low administration of PiN-21 efficiently treats the virus infection. Notably, PiN-21 aerosols can be inhaled to target respiratory infection.

This study warrants further investigating of the Nb construct for effectively fighting the SARS-CoV-2 infection in humans. This is a proof-of-concept study that sheds light on the use of stable, multi-epitope and multivalent Nb constructs, in combination with PiN-21, as a novel aerosol cocktail to effectively block virus mutational escape, the researchers write.

This news article was a review of a preliminary scientific report that had not undergone peer-review at the time of publication. Since its initial publication, the scientific report has now been peer reviewed and accepted for publication in a Scientific Journal. Links to the preliminary and peer-reviewed reports are available in the Sources section at the bottom of this article. View Sources