Virus World
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Virus World
Virus World provides a daily blog of the latest news in the Virology field and the COVID-19 pandemic. News on new antiviral drugs, vaccines, diagnostic tests, viral outbreaks, novel viruses and milestone discoveries are curated by expert virologists. Highlighted news include trending and most cited scientific articles in these fields with links to the original publications. Stay up-to-date with the most exciting discoveries in the virus world and the last therapies for COVID-19 without spending hours browsing news and scientific publications. Additional comments by experts on the topics are available in Linkedin (https://www.linkedin.com/in/juanlama/detail/recent-activity/)
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Scientists Used Crispr To Edit HIV-Like Viruses In Monkey DNA

Scientists Used Crispr To Edit HIV-Like Viruses In Monkey DNA | Virus World | Scoop.it

Using gene-editing to remove a retrovirus is a step towards a cure for HIV infection in humans. Scientists have used Crispr gene-editing to remove an HIV-like virus from monkey DNA, a major step towards a cure for HIV infection in humans. In a study led by neurovirologist Kamel Khalili of Temple University in Philadelphia, researchers constructed a modified adenovirus containing a Crispr-Cas9 gene-editing system. That 'construct' (called 'AAV9-CRISPR-Cas9') was then injected into rhesus macaque monkeys to deliver the Crispr system into cells. The monkey cells were infected with SIV (Simian Immunodeficiency Virus), a close relative of HIV (Human Immunodeficiency Virus). Both are retroviruses — viral parasites that cut-and-paste their genetic material into a host's DNA. SIV infects macaques and other non-human primates in the same way that HIV infects people, making it a good model for studying retroviral infection — and testing how to remove those viruses from the human genome.

 

The gene-editing construct was designed to target specific sites where the retrovirus was integrated into the macaque genome. It was able to reach tissues where viruses like SIV and HIV can hide for years without being detected, known as reservoirs, such as bone marrow, lymph nodes, T cells of the immune system and the brain. According to the study, the construct was precise and has a low risk of cutting the wrong places in DNA ('off-target' sites). The research has obvious implications for preventing or treating AIDS (Acquired Immunodeficiency Syndrome) in humans by curing a patient of HIV infection.

 

Original study published in Nature Comm. (November 27, 2020):

https://doi.org/10.1038/s41467-020-19821-7

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Inovio Reports Long-Term Positive Results for COVID-19 Vaccine in Rhesus Macaques

Inovio Reports Long-Term Positive Results for COVID-19 Vaccine in Rhesus Macaques | Virus World | Scoop.it

Inovio released results of a nonhuman primate study for its COVID-19 DNA vaccine, Ino-4800. The vaccine protected the animals 13 weeks after vaccinations and mediated T- and B-cell immune responses, according to the firm. The results, published on bioRxiv, demonstrated that Ino-4800 reduced viral load in the lungs and nasal passages of macaques that received two doses of Ino-4800 (one mg) four weeks apart followed by live virus challenge 13 weeks after the second dose. The vaccinated macaques demonstrated seroconversion after a single dose, with neutralizing antibodies and T cells found in their blood more than four months after the initial dose. Moreover, the levels of antibodies were similar to or greater than those who have recovered from COVID-19. The study showed that the vaccine induced acute and memory T- and B-cell responses, including neutralizing antibodies against the early virus strain as well as the now dominant G614 variant.

 

The company anticipates beginning phase II/III efficacy trials this summer. A separate nonhuman primate study evaluating the durability of Ino-4800 at 12 months postvaccination is currently underway and is supported by the federal government's Operation Warp Speed to accelerate development of a vaccine for SARS-CoV-2.

 

Preprint of the study available in bioRxiv (July 29, 2020):

https://doi.org/10.1101/2020.07.28.225649

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Macaques Show Protective Immunity Against SARS-CoV-2 After Infection or After Vaccine 

Macaques Show Protective Immunity Against SARS-CoV-2 After Infection or After Vaccine  | Virus World | Scoop.it

Two new studies in macaques offer hope that humans could develop protective immunity against SARS-CoV-2, either as the result of a natural infection or by way of a vaccine. While there are differences between SARS-CoV-2 infection in macaques and humans, these findings - some of the first to show that non-human primates can develop protective immunity to SARS-CoV-2 - are promising in light of the ongoing efforts around the world to develop a vaccine and antibody treatments for COVID-19. An understanding of protective immunity to SARS-CoV-2 is critical for vaccine and public health strategies. A key unanswered question is whether infection with SARS-CoV-2 results in protective immunity against re-exposure; there is currently no data on whether humans are protected from re-exposure in this way. 

 

Earlier this year, research investigating cynomolgus macaques found these animals to be promising models for testing COVID-19 therapeutics. Here, in two new studies in rhesus macaques, researchers explored whether initial exposure to SARS-CoV-2 protected against reinfection and whether vaccination protected against infection, respectively. In a macaque model of SARS-CoV-2 infection they developed, and which recapitulated certain aspects of human SARS-CoV-2 infection, Abishek Chandrashekar, Ralph Baric, Dan Barouch and colleagues tested whether 9 adult animals who had cleared the virus were immune to viral re-challenge 35 days later. All 9 animals showed little to no symptoms after re-challenge and exhibited immune responses that protected against the second infection (given at the same doses as the first). Additional research will be required to define the durability of natural immunity shown here, the authors note. "Rigorous clinical studies will be required to determine whether SARS-CoV-2 infection effectively protects against SARS-CoV-2 re-exposure in humans," they say....

 

Original Studies  Published in Science (May 20, 2020):

https://doi.org/10.1126/science.abc4776

 

https://doi.org/10.1126/science.abc6284

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Could a Blood Test Show if a Covid-19 Vaccine Works? - The New York Times

Could a Blood Test Show if a Covid-19 Vaccine Works? - The New York Times | Virus World | Scoop.it

A new study in monkeys suggests that a blood test could predict the effectiveness of a Covid-19 vaccine — and perhaps speed up the clinical trials needed to get a working vaccine to billions of people around the world. The study, published on Friday in Nature, reveals telltale blood markers that predict whether a monkey’s immune system is prepared to wipe out incoming coronaviruses The finding raises hope that researchers will be able to look for the same markers in people who get vaccines in clinical trials. If the markers are strong enough, they could reveal if the vaccines protect against Covid-19. And researchers would no longer have to wait for some trial volunteers to get the disease, as they do now. “It will pave the way for a much more rapid advancement of the Covid vaccine field,” said Dr. Dan Barouch, a vaccine expert at Beth Israel Deaconess Medical Center in Boston and one of the researchers behind the new study. Last month brought the stunning news that clinical trials of two new coronavirus vaccines, one from Moderna and the other from Pfizer and BioNTech, showed efficacy rates around 95 percent. The strength of these two vaccines is, paradoxically, bad news for the dozens of others in earlier stages of development. Many of them will most likely have to be compared against the robust front-runners rather than a placebo shot. Because that is a high statistical bar to clear, their trials will need a lot more volunteers, time and money. “You’d have to follow millions of people for a long time,” said Dr. Nelson Michael, the director of the Center for Infectious Diseases Research at Walter Reed Army Institute of Research, where a protein-based vaccine is being prepared for clinical trials in early 2021. “It’s just fantasy.” 

 

For some smaller companies, these comparison trials may be deal-breakers. “You’re going to see a lot of dropout,” said. Dr. Gregory Poland, a vaccine expert at the Mayo Clinic. That’s a big problem, because Pfizer and Moderna won’t have nearly enough doses to give to everyone in the United States, let alone the world. And the next wave of vaccines may turn out to be superior to the first, in one way or the other. They could cost a lot less, for example. Some might come in just one dose instead of two, and won’t need a deep freeze. Some might offer protection that lasts a lot longer. “We’d rather not have to revaccinate the world every one or two years,” Dr. Michael said. The new monkey study offers a ray of hope for these next-generation vaccines, suggesting that they could be tested not against older vaccines, but using a measurement known as a “correlate of protection.” “That’s the holy grail of vaccine research,” Dr. Michael said. Influenza vaccines are already tested this way. Every new flu season requires the design of a new flu shot, but researchers don’t have to run clinical trials comparing it with old versions. Instead, they just check whether the new vaccine triggers a person’s immune system to make enough of a certain kind of antibody against the flu. If it does, then researchers know the vaccine is adequately stimulating the immune system. If scientists could discover a correlate of protection against the coronavirus, they could follow the example of the flu. “That is an entirely plausible and feasible scenario,” said Dr. Anthony Fauci, the director of the National Institutes of Allergy and Infectious Diseases.  A spokeswoman for the Food and Drug Administration said that basing clinical trials on correlates of protection — if they turn out to exist — “possibly could be considered in the future.”

 

In their new study, Dr. Barouch and his colleagues found a correlate of protection in monkeys. They built the experiment on their previous research showing that once monkeys recover from Covid-19, they can resist a second infection. The scientists drew blood from these exposed animals and isolated an array of protective antibodies called IgG. The researchers set out to see if there was a level of IgG that reliably protected monkeys from Covid-19. If the IgG antibodies produced by vaccines were above that level, the vaccines could be judged effective. To find that line, the researchers gave monkeys varying doses of antibodies, and then exposed them all to the coronavirus and watched how well they fought off the infection. In the monkeys with the weakest dose, the viruses multiplied much as they would in an ordinary animal. But the monkeys that got a medium dose produced far fewer viruses. Some of them were able to wipe out the viruses altogether. At the highest dose, the monkeys were completely protected. Until now, scientists relied on circumstantial evidence that suggested IgG antibodies were crucial to clearing coronavirus infections. The new study puts that idea to the test — and determines the threshold of IgG antibodies required to ward off an infection. “This is the first time, to the best of my knowledge, that we’ve actually proven that antibodies protect,” Dr. Barouch said. “Everything else has been a statistical association.” The experiment revealed that a modest amount of IgG antibodies turned out to be enough. That could be heartening news for vaccine developers, because even so-so vaccines may be able to cross the threshold.....

 

Cited research published in Nature (Dec. 04, 2020):

https://doi.org/10.1038/s41586-020-03041-6

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Primary Exposure to SARS-CoV-2 Protects Against Reinfection in Rhesus Macaques

Primary Exposure to SARS-CoV-2 Protects Against Reinfection in Rhesus Macaques | Virus World | Scoop.it

Coronavirus disease 2019 (COVID-19), which is caused by infection with the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has become a global pandemic. It currently remains unclear whether convalescing patients have a risk of reinfection. We generated a rhesus macaque model of SARS-CoV-2 infection that was characterized by interstitial pneumonia and systemic viral dissemination mainly in the respiratory and gastrointestinal tracts. Rhesus macaques reinfected with the identical SARS-CoV-2 strain during the early recovery phase of the initial SARS-CoV-2 infection did not show detectable viral dissemination, clinical manifestations of viral disease, or histopathological changes.

 

Comparing the humoral and cellular immunity between primary infection and rechallenge revealed notably enhanced neutralizing antibody and immune responses. Our results suggest that primary SARS-CoV-2 exposure protects against subsequent reinfection in rhesus macaques.

 

Published in Science (July 2, 2020):

https://science.sciencemag.org/content/early/2020/07/01/science.abc5343

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