More than 600,000 people worldwide have fallen victim to the lung disease COVID-19 so far, which is caused by the SARS coronavirus-2 (SARS-CoV-2).
In order to obtain an effective therapy for COVID-19 as quickly as possible, drugs that are being used to treat other diseases are currently being repurposed for COVID-19 treatment.
In a new study, researchers found that the malaria drug chloroquine, which has been demonstrated to inhibit the SARS-CoV-2 infection of African green monkey kidney cells, is not able to prevent infection of human lung cells with the novel coronavirus.
Chloroquine is therefore unlikely to prevent the spread of the virus in the lung and should not be used for the treatment of COVID-19.
The research was conducted by a team at Leibniz Institute for Primate Research in Göttingen and elsewhere.
It is known that SARS-CoV-2 is able to use two different routes to enter cells.
First, after attaching to the cells, the virus can fuse directly with the plasma membrane and introduce its genetic material into the host cell.
Second, it can enter the interior of the cells upon uptake via transport structures, called endosomes.
In both cases, the attachment of the virus to the cells and subsequent entry is mediated by the viral spike protein.
Chloroquine is a drug that is used to treat malaria.
Since chloroquine inhibits the infection of monkey kidney cells with SARS-CoV-2, chloroquine has been tested in clinical trials as a possible candidate for the treatment of COVID-19.
However, how chloroquine inhibits the infection of monkey kidney cells was not clear.
The current study showed that chloroquine inhibits viral entry into these cells. This raised the question whether chloroquine also inhibits the infection of lung cells.
The team found that chloroquine does not prevent SARS-CoV-2 entry into human lung cells and subsequent spread of the virus in these cells.
They found that the antiviral activity of chloroquine is cell type-specific and that chloroquine does not block the infection of lung cells.
This means that in future tests of potential COVID-19 drugs, care should be taken that relevant cell lines are used for the research in order not to waste unnecessary time and resources in our search for effective COVID-19 therapies.
One author of the study is Stefan Pöhlmann, head of the Infection Biology Unit.
The study is published in Nature.
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