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Tuesday, January 12, 2021

Gilead, Vir To Collaborate To Find Hep B Cure

 Gilead Sciences, Inc. (GILD) and Vir Biotechnology, Inc. (VIR) have entered into a clinical collaboration to evaluate therapeutic combination strategies aimed at developing a functional cure for chronic hepatitis B virus. The companies plan to initiate a phase 2 trial evaluating combination therapy for both treatment-experienced and treatment-naïve people living with hepatitis B virus.

The multi-arm trial will evaluate different combinations of selgantolimod, Gilead's investigational TLR-8 agonist; VIR-2218, Vir's investigational small interfering ribonucleic acid. The companies will discuss the potential path forward for any future combination studies based on the outcome of the phase 2 trial.

https://www.nasdaq.com/articles/gilead-vir-announce-collaboration-to-find-cure-for-hepatitis-b-virus-quick-facts-2021-01

S. Korea Nears Deal to Buy Novavax COVID-19 Vaccines

 South Korea is close to striking a deal to purchase COVID-19 vaccines for 10 million people from U.S. drugmaker Novavax, according to informed sources Tuesday.

The Seoul government has been negotiating with Novavax to secure its vaccines as early as in the second quarter of this year, sources with knowledge of the issue said.

In August 2020, Novavax signed a development and supply deal with Korean bio firm SK Bioscience Co. to supply vaccines in global markets.

The government earlier said it has secured access to COVID-19 vaccines for 56 million people from four pharmaceutical companies and the World Health Organization’s global vaccine project, known as COVAX.

The deals include 20 million doses each from AstraZeneca, Pfizer and Moderna, which require two shots, and 6 million doses from Johnson & Johnson’s Janssen, which requires one shot.

While the secured quantity is more than the nation’s 52 million population, authorities have been working to secure an additional volume of vaccines due to lingering uncertainties surrounding inoculation, Prime Minister Chung Sye-kyun said earlier in the day.

Novavax vaccines can be shipped and stored at standard refrigeration temperatures as opposed to mRNA vaccines from Pfizer and Moderna that require freezing temperatures.

President Moon Jae-in said Monday that the government will provide all South Korean people with free-of-charge COVID-19 vaccines in phases starting next month.

http://koreabizwire.com/s-korea-nears-deal-to-buy-novavax-covid-19-vaccines/179218

AstraZeneca Covid vax could be distributed across Europe by mid-February: EU

 

Lipocine Has Positive Topline Phase 2 Results in NASH Study

  Lipocine Inc. (NASDAQ: LPCN), a clinical-stage biopharmaceutical company focused on metabolic and endocrine disorders, today announced positive topline results from its LiFT ("Liver Fat intervention with oral Testosterone") Phase 2 clinical study (NCT04134091), investigating LPCN 1144 in biopsy-confirmed non-cirrhotic non-alcoholic steatohepatitis ("NASH") male subjects. Currently, there are no approved treatments for NASH, a silent killer that affects ~30 million Americans. LPCN 1144 is an oral prodrug of endogenous testosterone. 

In the ongoing randomized, double-blind, placebo-controlled 36-week treatment LiFT study, subjects with F1-F3 fibrosis were randomized 1:1:1 to one of three arms (Treatment A is a twice daily oral dose of 142 mg testosterone equivalent, Treatment B is a twice daily oral dose of 142 mg testosterone equivalent formulated with 217 mg of d-alpha tocopherol equivalent, and the third arm is twice daily matching placebo). The primary endpoint is change in hepatic fat fraction via Magnetic Resonance Imaging Proton Density Fat Fraction ("MRI-PDFF") and exploratory liver fat/marker end points post 12 weeks of treatment. Additionally, key secondary endpoints post 36 weeks of treatment include assessment of histological change for NASH resolution and/or fibrosis improvement as well as liver fat data.

Subjects will have access to LPCN 1144 through an open label extension study (NCT04685993). The extension study will enable the collection of additional data on LPCN 1144 for up to a total of 72 weeks of therapy

Treatments with LPCN 1144 post 12 weeks of treatment resulted in robust liver fat reduction, assessed by MRI-PDFF, and showed improvement of liver injury markers with no observed tolerability issues. Inclusion of d-alpha tocopherol formulated with the testosterone prodrug resulted in additional liver benefits, notably improved key liver markers without compromising tolerability.

https://www.biospace.com/article/releases/lipocine-announces-positive-topline-phase-2-results-from-lpcn-1144-ongoing-lift-study-in-biopsy-confirmed-nash-subjects/

Monday, January 11, 2021

How COVID-19 overpowers the immune system

 Seeking to understand why COVID-19 is able to suppress the body's immune response, new research from the USC Leonard Davis School of Gerontology suggests that mitochondria are one of the first lines of defense against COVID-19 and identifies key differences in how SARS-CoV-2, the virus that causes COVID-19, affects mitochondrial genes when compared to other viruses. These differences offer possible explanations as to why older adults and people with metabolic disfunction have more severe responses to COVID-19 than other individuals and they also provide a starting point for more targeted approaches that may help identify therapeutics, says senior author Pinchas Cohen, professor of gerontology, medicine and biological sciences and dean of the USC Leonard Davis School.

"If you already have mitochondrial and metabolic dysfunction, then you may, as a result, have a poor first line of defense against COVID-19. Future work should consider mitochondrial biology as a primary intervention target for SARS-CoV-2 and other coronaviruses," he said.

The study, published in the Nature journal Scientific Reports, expands on recent findings that COVID-19 mutes the body's innate inflammatory response and reports that it does so by diverting  from their normal function.

"We already knew that our immune response was not mounting a successful defense to COVID-19, but we didn't know why," said lead author Brendan Miller, a senior doctoral student at the USC Leonard Davis School. "What we did differently was look at how the virus specifically targets mitochondria, a cellular organelle that is a crucial part of the body's innate immune system and energy production."

Making use of the vast amounts of public data being uploaded in the early days of the virus outbreak, the research team performed RNA sequencing analyses that compared mitochondrial-COVID interactions to those of other viruses: respiratory syncytial virus, seasonal influenza A virus, and human parainfluenza virus 3. These reanalyses identified three ways in which COVID-19, but not the other viruses, mutes the body's cellular protective response.

Chief among their findings is that SARS-CoV-2 uniquely reduces the levels of a group of mitochondrial proteins, known as Complex One, that are encoded by nuclear DNA. It is possible that this effect "quiets" the cell's metabolic output and reactive oxygen species generation, that when functioning correctly, produces an inflammatory response that can kill a virus, they say.

"COVID-19 is reprogramming the cell to not make these Complex One-related proteins. That could be one way the virus continues to propagate," says Miller, who notes that this, along with the study's other observations, still needs to be validated in future experiments.

The study also revealed that SARS-CoV-2 does not change the levels of the messenger protein, MAVS mRNA, that usually tells the cell a viral attack has happened. Normally, when this protein gets activated it functions as an alarm system, warning the cell to self-destruct so that the virus cannot replicate, says Miller.

In addition, the researchers found that genes encoded by the mitochondria were not being turned on or off by SARS-CoV-2—a process that is believed to produce energy that can help the cell evade a virus—at rates to be expected when confronted with a .

"This study adds to a growing body of research on mitochondrial-COVID interactions and presents tissue and cell-specific effects that should be carefully considered in future experiments," said Cohen.

Explore further

Uracil switch in SARS-CoV-2 genome alters innate immune responses
More information: Brendan Miller et al, Host mitochondrial transcriptome response to SARS-CoV-2 in multiple cell models and clinical samples, Scientific Reports (2021). DOI: 10.1038/s41598-020-79552-z
https://medicalxpress.com/news/2021-01-covid-overpowers-immune.html

Augmented immune response explains adverse course of COVID-19 with hypertension

 COVID-19 patients who also suffer from high blood pressure are more likely to fall severely ill with the disease, which also leaves them at greater risk of death. Scientists from the Berlin Institute of Health (BIH) and Charité–Universitätsmedizin Berlin, in collaboration with partners in Heidelberg and Leipzig, have now found that the immune cells of patients with hypertension are already pre-activated, and that this pre-activation is greatly enhanced under COVID-19. This most likely explains the augmented response of the immune system and the more severe disease progression. However, certain hypertension-reducing drugs known as ACE inhibitors can have a beneficial effect. They not only lower blood pressure, but also counteract immune hyperactivation. The scientists have now published their findings in the journal Nature Biotechnology.

More than one billion people worldwide suffer from high blood pressure, or hypertension. Of the more than 75 million people around the world who have become infected with the SARS-CoV-2 virus worldwide so far, more than 16 million also have hypertension. These patients are more likely to become severely ill, which in turn results in an increased risk of death. It was previously unclear to what extent treatment with antihypertensive drugs could be continued during a SARS-CoV-2 infection—and whether they were more likely to benefit or harm the patients. This is because antihypertensives interfere with the exact same regulatory mechanism that the novel  SARS-CoV-2 uses to enter the  and trigger COVID-19.

Professor Ulf Landmesser is Medical Director of the CharitéCenter 11 for Cardiovascular Diseases, Director of the Medical Department of Cardiology and BIH Professor of Cardiology on the Charité's Campus Benjamin Franklin in Berlin. He recognized early on that patients with hypertension or cardiovascular diseases often experienced a particularly critical disease progression with COVID-19. "The virus uses the receptor ACE2 as an entry portal into the cells, and the formation of this receptor is potentially influenced by the administration of antihypertensive drugs," explains Landmesser. "We had therefore initially feared that patients receiving ACE inhibitors or  might have more ACE2 receptors on their cell surfaces and thus become more easily infected."

Certain drugs that lower blood pressure could also help with COVID-19

To clarify this suspicion, the scientists analyzed individual cells from the respiratory systems of COVID-19 patients who were also taking medication for high blood pressure. Dr. Sören Lukassen, a scientist in Professor Christian Conrad's group at the BIH Digital Health Center, explains that they were subsequently able to give the all-clear: "We found that the drugs do not seem to cause more receptors to form on the cells. As a result, we do not believe that they make it easier for the virus to enter the cells in this way and thus cause the more severe course of COVID-19." On the contrary, cardiovascular patients taking ACE inhibitors actually displayed a lower risk of becoming severely ill with COVID-19. In fact, they displayed almost the same level of risk as COVID-19 patients without cardiovascular problems.

Severe course of COVID-19 linked to pre-activation of the immune system

The blood of hypertensive patients usually shows elevated levels of inflammation, which can be fatal in the case of a SARS-CoV-2 infection. "Elevated inflammation levels are always a warning signal that COVID-19 will be more severe, regardless of any cardiovascular issues," explains Landmesser. The scientists therefore employed single-cell sequencing methods to investigate the immune response of hypertensive patients with COVID-19.

"We analyzed a total of 114,761 cells from the nasopharynx of 32 COVID-19 patients and 16 non-infected controls, with both groups including cardiovascular patients as well as people without cardiovascular problems," reports Dr. Saskia Trump, research group leader in the lab of Irina Lehmann, who is BIH Professor for Environmental Epigenetics and Lung Research. "We found that the immune cells of the cardiovascular patients displayed strong pre-activation even before infection with the novel coronavirus," explains Lehmann. "After contact with the virus, these patients were more likely to develop an augmented immune response, which was associated with the severe disease progression of COVID-19. However, our results also showed that treatment with ACE inhibitors, though not with angiotensin receptor blockers, could prevent this augmented immune response following infection by the coronavirus. ACE inhibitors could thus reduce the risk of patients with hypertension from experiencing severe disease progression."

Delayed reduction in viral load

Furthermore, the scientists found that the anti-hypertensive drugs can also impact how quickly the immune system is able to reduce the viral load, i.e., the concentration of the virus in the body. "Here, we observed a clear difference between the different forms of treatment for high blood pressure," notes Roland Eils, Director of the BIH Digital Health Center. "In the patients treated with angiotensin II receptor blockers, the reduction in viral load was significantly delayed, which could also contribute to a more severe course of COVID-19. We did not observe this delay in the patients who were receiving ACE inhibitors to treat their hypertension."

Interdisciplinary collaboration speeds up research

More than 40 scientists have been working at a breakneck pace on this . "The ability to quickly provide answers to urgent questions during the ongoing pandemic requires interdisciplinary collaboration among many committed individuals," explains Eils. "COVID-19 is such a complex disease that we brought together experts from cardiology, immunology, virology, pulmonary medicine, intensive care and computer science for this study. Our goal was to provide a scientifically sound answer as quickly as possible to the question of whether simultaneous treatment with ACE inhibitors or angiotensin receptor blockers could have beneficial or even adverse effects during the COVID-19 pandemic."

No evidence of increased risk of infection

Thanks to the study, the teams from the BIH, Charité and collaborating institutions in Leipzig and Heidelberg can now reassure both patients and the physicians treating them: "Our study provides no evidence that treatment with anti-hypertensive drugs increases the risk of infection by the novel coronavirus," says Ulf Landmesser, summarizing the results. "However, treating hypertension with ACE inhibitors could be more beneficial for patients suffering from COVID-19 than treatment with angiotensin II receptor blockers—a hypothesis that is currently being further investigated in randomized trials."

More information: Saskia Trump et al, Hypertension delays viral clearance and exacerbates airway hyperinflammation in patients with COVID-19, Nature Biotechnology (2020). DOI: 10.1038/s41587-020-00796-1

https://medicalxpress.com/news/2021-01-augmented-immune-response-adverse-covid-.html

JPM: Microsoft signs on to Verily, Broad Institute's Terra open research platform

 Verily and the Broad Institute of MIT and Harvard hope to dramatically boost the reach of their open-source biomedical research platform through a new partnership with Microsoft.

The scalable Terra platform includes digital tools currently used by over 15,600 researchers, to analyze and collaborate on data gathered from nearly 2 million study participants spanning cancer genomics to infectious disease projects.

Now, Microsoft is signing on as an equal partner in Terra’s operation and development—and the computing giant plans to help drive its global adoption, by pulling it through its established network of AI and cloud-computing customers that includes over 168,000 healthcare organizations.

“Terra simplifies the process so researchers can analyze and share data they have generated, and access and analyze data others have made available without needing to duplicate datasets,” said Eric Lander, president and founding director of the Broad Institute. 

“As an interoperable, open-source system, Terra is designed to work across many different types of biomedical information—moving aside barriers to storage, permissions and computing to enable collaboration and generate insights,” Lander said.


Terra will work with Microsoft’s Azure services as well as the cloud-based offerings from Verily’s corporate sibling, Google. Additionally, Microsoft plans to dedicate its own software engineering resources and lend its machine learning expertise to Terra’s efforts, while also using open application interfaces and internationally recognized modular software components.

“Terra’s adoption of [Global Alliance for Genomics and Health] standards is an important step forward,” said Helen Parkinson, head of molecular archival resources at the European Bioinformatics Institute. “By following these standards, Terra supports modularity and interoperability, which are key to creating a global and federated data ecosystem.”

Together, Verily, Microsoft and the Broad Institute expect to see the rate of new healthcare data—including all the information generated from genomic tests, digital scans, biometric signals and electronic health records—to reach dozens of exabytes by 2025, with each being equal to 1 billion gigabytes.

“Our three organizations share the goals of improving patient care, driving innovation in biomedical research, and lowering costs across healthcare and life sciences,” Verily Chief Operating Officer Stephen Gillett said. “This partnership combines multimodal data, secure analytics and scalable cloud computing to improve insight and evidence generation, allowing us to ultimately impact more patients’ lives."

https://www.fiercebiotech.com/medtech/microsoft-signs-to-verily-broad-institute-s-terra-open-research-platform