Category Archives: Immunology

Assistant, Department of Immunology and Allergology job with RUDN UNIVERSITY | 273626 – Times Higher Education (THE)

Department: Department of Immunology and AllergologyFaculty: Institute of MedicineEmployment: Part-time (0.25)

Requirements to the candidate

Required knowledge:

Requirements:

The position of assistant of the department is assigned to a person who possesses the following criteria:

Working conditions (job description, KPI)

Responsibilities:

Conditions:

Accommodation at RUDN

For the full term of the employment contract, invited scientists who passed the competitive selection are provided with a campus apartment of the University.

According to local documents of the University, the deadline for submitting applications for vacant positions of teaching staff is one month from the date of posting information on the website of RUDN.

10.01.2022

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Assistant, Department of Immunology and Allergology job with RUDN UNIVERSITY | 273626 - Times Higher Education (THE)

Grouping of immunological T-cell receptors may be key to identifying patients’ history of infection – News-Medical.net

Grouping of pathogen-recognizing proteins on immune T cells may be key to identifying if someone has had an infection in the past, suggests a study published today in eLife.

While tests measuring antibodies against a pathogen are often used to detect signs of a previous infection, it is more difficult for researchers to measure the strength and targets of a person's T-cell response to infection or vaccination, but the findings hint at a potential new approach. This patient information could one day be useful for detecting infections, guiding treatments or supporting the research and development of new therapies and vaccines.

Immune T cells help the body find and destroy harmful viruses and bacteria. Proteins on the outer surface of T cells called receptors allow the T cells to recognize and eliminate human cells that have been infected by specific pathogens.

While the abundance of specific receptors could provide clues about past infection, the enormous molecular diversity of T-cell receptors makes it incredibly challenging to assess which receptors recognise which pathogens. Not only is each pathogen recognised by a distinct set of receptors, but each individual develops a personalised set of receptors for each pathogen. We developed a new computational approach that allows us to find similarities among pathogen-specific T-cell receptors across individuals. Ultimately, we hope this will help develop signatures of past infection despite the enormous diversity of T-cell receptors."

Koshlan Mayer-Blackwell, Study First Author and Senior Data Scientist, Fred Hutchinson Cancer Research Center

The team tested their approach using data from the immuneRACE study of T-cell receptors in patients with COVID-19. Using their new software for rapidly comparing large sets of receptors, they were able to generate 1,831 T-cell receptor groupings based on similarities in the receptors' amino acid sequences that suggest they have similar functions.

In an independent group of COVID-19 patients, the team found that the common molecular patterns associated with receptor groupings were more robustly detected than individual receptor sequences that were previously hypothesised to recognise parts of the SARS-CoV-2 virus, demonstrating a major improvement on existing approaches.

"Our study introduces and validates a flexible approach to identify sets of similar T-cell receptors, which we hope will be broadly useful for scientists studying T-cell immunity," Mayer-Blackwell says. "Grouping receptors together in this way makes it possible to compare responses to infection or vaccination across a diverse population."

To help other researchers use this approach to develop T-cell biomarkers with their own data, the team has created free customisable software called tcrdist3.

"Our software provides flexible tools that will enable scientists to analyse and integrate the rapidly growing libraries of T-cell receptor sequencing data that are needed to identify the features of pathogen-specific T-cell receptors," concludes senior author Andrew Fiore-Gartland, Co-Director of the Vaccines and Immunology Statistical Center at the Fred Hutchinson Cancer Research Center. "We hope it will open new opportunities not only to identify patients' immunological memories of past infections and vaccinations but also to predict their future immune responses."

Source:

Journal reference:

Mayer-Blackwell, K., et al. (2021) TCR meta-clonotypes for biomarker discovery with tcrdist3 enabled identification of public, HLA-restricted clusters of SARS-CoV-2 TCRs. eLife. doi.org/10.7554/eLife.68605.

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Grouping of immunological T-cell receptors may be key to identifying patients' history of infection - News-Medical.net

Research Fellow in Cancer Immunology job with UNIVERSITY OF SOUTHAMPTON | 273475 – Times Higher Education (THE)

Cancer Sciences

Location: Southampton General HospitalSalary: 31,406 to 37,467 Per annumFull Time Fixed Term for 12 monthsClosing Date: Tuesday 14 December 2021Interview Date: To be confirmedReference: 1620021CM

Antibody and Vaccine Group, Centre for Cancer Immunology, University of Southampton, Faculty of Medicine, School of Cancer Sciences

The Antibody and Vaccine Group based in the recently opened Centre for Cancer Immunology in Southampton has a strong track-record in basic and translational immunology. One of its central aims is to develop new and more effective antibody reagents for treating cancer.

An exciting opportunity now presents itself for a research fellow to work on a Cancer Research UK funded programme to determine how a family of key receptors (Fc receptors) are regulated and serve to deliver antibody-mediated cancer cell destruction. The post-holder will leverage expertise in antibody biology, myeloid cells, transcriptomics, immunology, and cell biology in order to gain new understanding of this critical receptor family with the aim of improving cancer treatments.

You will be motivated, educated to PhD level in a relevant subject area and ideally have practical laboratory experience of antibody biology, myeloid cells, bioinformatics and in vivo methodology.

Applications for Research Fellow positions will be considered from candidates who are working towards or nearing completion of a relevant PhD qualification. The title of Research Fellow will be applied upon successful completion of the PhD. Prior to the qualification being awarded the title of Senior Research Assistant will be given.

This post is offered on a full-time fixed term contract for 12 months.

Informal queries should be directed to Professor Mark Cragg (msc@soton.ac.uk)

Details about the School of Cancer Sciences and Centre for Cancer Immunology can be found at http://www.southampton.ac.uk/medicine/research/themes/cancer-sciences.page

Application Procedure

You should submit your completed online application form at https://jobs.soton.ac.uk. The application deadline will be midnight on the closing date stated above. If you need any assistance, please call Michelle (HR Recruitment Team) on +44 (0) 23 8059 2750 or email recruitment@soton.ac.uk Please quote reference 1620021CM on all correspondence.

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Research Fellow in Cancer Immunology job with UNIVERSITY OF SOUTHAMPTON | 273475 - Times Higher Education (THE)

INmune Bio, Inc. Announces Two Presentations at the 2021 British Society of Immunology Congress and Provides 119-day data on First patient in MDS…

Boca Raton, Florida, Dec. 01, 2021 (GLOBE NEWSWIRE) -- INmune Bio, Inc. (NASDAQ: INMB) (the Company), a clinical-stage immunology company focused on developing treatments that harness the patients innate immune system to fight disease, today announced two poster presentations at the 2021 British Society of Immunology Congress, which was held November 28-December 1, in Edinburgh, UK.

Mark Lowdell, PhD, Chief Scientific Officer of INmune Bio, stated, Im delighted to have two of our team presenting our latest data on the mechanism of action of INKmune. These are the first comprehensive data showing that INKmune-mediated priming generates NK cells with memory-like phenotype (mlNK). Before this, mlNK cells could only be produced using multiple combinations of cytokines. These are the data which led us to the concept that INKmune is a pseudokine that provides multiple signals to NK cells, akin to the multi-cytokine cocktails used by others. We also show that INKmune priming promotes significant proliferation of mlNK cells in vitro. These in vitro data have been replicated in the first patient treated with three, weekly doses of INKmune for high risk MDS. At 119 days post first treatment, 60% of the patients NK cells showed the activated, tumor killing phenotype compared to fewer than 15% before INKmune therapy. The patient remains well and with a significantly improved ECOG status.

Details of the presentations are as follows:

Title: Tumor-priming generates memory-like natural killer cells with universal anti-tumor functions

Poster: P-107

Session: Poster session 1

Natural killer (NK) cells are innate lymphocytes that target virus-infected and tumor cells. NK cells are exciting candidates for cancer immunotherapy due to their fast-acting innate ability to mount anti-tumor responses and recently highlighted adaptive properties including priming and memory-like functions. Tumor-priming of NK cells through in-vitro exposure to tumor target cells pre-activates NK cells to demonstrate enhanced tumor cell lysis upon restimulation, generating long-term memory-like features. The generation of memory-like NK cells was previously reported following exposure to cytomegalovirus (CMV), interleukin (IL)-12/15/18 combinations or the tumor cell line NALM-16.

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Here, we report a novel type of tumor-induced memory-like (TIML) NK cell induced by the acute lymphoblastic leukemia (ALL) cell line, INB16. These TIML NK cells are generated in vitro over a period of seven days to show better expansion, survival, and proliferation relative to other memory-like NK cells, maintaining similar levels of enhanced NK cell anti-tumor functional abilities including tumor lysis, and pro-inflammatory cytokine secretion against a wide range of tumor targets. Their unique phenotypic and gene expression signatures suggest a novel and distinct form of memory-like NK cell governed by tumor-specific signaling pathways. The universal and wide-acting function of these highly expanded NK cells may have important implications in the clinical setting to better mitigate challenges in low NK cell number and lytic ability.

A link to the abstract can be found here.

Title: Tumor-priming defines an intermediate stage in natural killer cell activity between resting and lytic stages for enhanced NK cell function upon re-stimulation

Poster: P-597

Session: Poster session 1

Natural killer (NK) cells are critical effector cells of the innate immune system belonging to the family of group one innate lymphocytes (ILCs). They display direct cytotoxicity against sensitive tumor targets and secrete a wide array of cytokines that help mount an effective immune response against cancer development and progression, making them attractive candidates for cancer immunotherapy.

We previously reported a tumor-priming approach to NK cell activation, whereby exposure to the acute lymphoblastic leukemia cell line CTV-1 specifically activates NK cells to display more enhanced anti-tumoral functions. This has yielded encouraging results in clinical trials against acute myeloid leukemia and myelodysplastic syndrome. Other groups reported a similar tumor-priming strategy for specific activation of NK cell anti-tumor responses using NALM-16. Still, the mechanisms involved in tumor-priming of NK cells remain to be elucidated, and it is unclear how the primed state can be achieved for optimal clinical benefit.

Here, we show that tumor-priming stimulates NK cells to a point along the lytic activation pathway for enhanced NK cell function upon re-stimulation. The primed state is achieved through exposure to less sensitive tumor targets that form fewer conjugates, and induce lower levels of avidity, degranulation, activation marker expression, pro-inflammatory cytokine secretion and lysis by NK cells. This tumor-primed state leads to enhanced NK cell function upon re-stimulation and potent NK cell killing of previously insensitive tumor targets. Interestingly, tumor-priming of NK cells is achieved in the presence of inhibitory signals and can be achieved using whole cell or cell lysate preparations, which generate differential activation signatures relative to cytokine stimulation.

This may have important implications in the clinic, where continuous cytokine exposure is associated with a dose-limiting toxicity in patients. These findings help define the tumor-primed NK cell activation state for the development of more optimal NK cell-based immunotherapeutic strategies in cancer.

A link to the abstract can be found here.

About INKmune

INKmune is a pharmaceutical-grade, replication-incompetent human tumor cell line (derived from CTV-1) which conjugates to resting NK cells and delivers multiple, essential priming signals akin to treatment with at least three cytokines in combination. INKmune is stable at -80oC and is delivered by a simple IV infusion. The INKmune:NK interaction ligates multiple activating and co-stimulatory molecules on the NK cell and enhances its avidity of binding to tumor cells; notably those resistant to normal NK-mediated lysis. Tumor-primed NK (TpNK) cells can lyse a wide variety of NK-resistant tumors including leukemias, lymphomas, myeloma, ovarian cancer, breast cancer.

About INmune Bio, Inc.

INmune Bio, Inc. is a publicly traded (NASDAQ: INMB), clinical-stage biotechnology company focused on developing treatments that target the innate immune system to fight disease. INmune Bio has two product platforms that are both in clinical trials. The DN-TNF product platform utilizes dominant-negative technology to selectively neutralize soluble TNF, a key driver of innate immune dysfunction and mechanistic target of many diseases. DN-TNF is in clinical trial to determine if it can treat cancer (INB03), Mild Alzheimers disease, Mild Cognitive Impairment and treatment resistant depression (XPro). The Natural Killer Cell Priming Platform includes INKmune aimed at priming the patients NK cells to eliminate minimal residual disease in patients with cancer. INmune Bios product platforms utilize a precision medicine approach for the treatment of a wide variety of hematologic malignancies, solid tumors and chronic inflammation. To learn more, please visit http://www.inmunebio.com.

Forward Looking Statements

Clinical trials are in early stages and there is no assurance that any specific outcome will be achieved. Any statements contained in this press release that do not describe historical facts may constitute forward-looking statements as that term is defined in the Private Securities Litigation Reform Act of 1995. Any statements contained in this press release that do not describe historical facts may constitute forward-looking statements as that term is defined in the Private Securities Litigation Reform Act of 1995. Any forward-looking statements contained herein are based on current expectations but are subject to a number of risks and uncertainties. Actual results and the timing of certain events and circumstances may differ materially from those described by the forward-looking statements as a result of these risks and uncertainties. INB03, XPro1595, and INKmune are still in clinical trials or preparing to start clinical trials and have not been approved and there cannot be any assurance that they will be approved or that any specific results will be achieved. The factors that could cause actual future results to differ materially from current expectations include, but are not limited to, risks and uncertainties relating to the Companys ability to produce more drug for clinical trials; the availability of substantial additional funding for the Company to continue its operations and to conduct research and development, clinical studies and future product commercialization; and, the Companys business, research, product development, regulatory approval, marketing and distribution plans and strategies. These and other factors are identified and described in more detail in the Companys filings with the Securities and Exchange Commission, including the Companys Annual Report on Form 10-K, the Companys Quarterly Reports on Form 10-Q and the Companys Current Reports on Form 8-K. The Company assumes no obligation to update any forward-looking statements in order to reflect any event or circumstance that may arise after the date of this release.

INmune Bio Contact:

David Moss, CFO (858) 964-3720info@inmunenbio.com

Investor Contact: Chuck Padala LifeSci Advisors (646) 627-8390

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INmune Bio, Inc. Announces Two Presentations at the 2021 British Society of Immunology Congress and Provides 119-day data on First patient in MDS...

Sanofi to acquire Origimm Biotechnology, gaining therapeutic acne vaccine candidate – BioPharma-Reporter.com

It marks Sanofis first move into skin immunology and the skin microbiome as it champions its strategy to build an industry-leading vaccines pipeline.

Founded in 2012, Origimm specializes in the discovery of virulent skin microbiome components and antigens from bacteria causing skin disease, such as acne. Its therapeutic vaccine candidate for acne vulgaris ORI-001, is based on recombinant proteins, and entered preliminary clinical studies in Q3 this year.

In parallel, Sanofi is working to develop additional antigen versions and expects to leverage its mRNA platform in a Phase 1/2 trial to start in 2023.

The acquisition of Origimm further broadens our vaccines R&D pipeline with a first vaccine candidate against acne, a high medical need for millions of teenagers and adults, says Thomas Triomphe, Executive Vice President, Global Head of Sanofi Pasteur.

Welcoming Origimm within Sanofi expands our area of expertise by bringing extensive know-how in the field of skin microbiome and skin immunology. We look forward to unlocking the full potential of this candidate.

Origimm develops preventive and therapeutic products that act against those skin-colonizing bacteria that can induce skin disease. Unlike acne treatments, its therapy would address the root cause of the disease, rather than treat the symptoms.

Diseases caused by skin microbes are more complex than classic infections because the same microbes that appear harmless, or even beneficial, on the surface of skin can become pathogenic under certain conditions.

Origimm has identified the proteins produced by bacteria when it reacts to an increase in sebum secretion from the skin's pores, thus creating a specific immune response for when the bacterium breaches the skin.

Recent scientific findings about the role ofPropionibacterium acnes (P. acnes)in acne vulgaris have opened the path for the development of a new, highly specific and efficacious acne therapy,"notes Origimm.

"Our therapeutic product is designed to support the human immune system in controllingthe growth ofP. acneson the skin and prevent it from damaging the cellular lining of the pores.

"Our intention is not just to provide a more effective treatment of acne, but also to prevent its formation in the first place, thereby avoiding any potential skin damage (scarring). Therefore, both therapeutic and prophylactic immunotherapymay be possible.

The acquisition is expected to close early December 2021.

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Sanofi to acquire Origimm Biotechnology, gaining therapeutic acne vaccine candidate - BioPharma-Reporter.com

The Importance of Immunology by Joe Murphy, Hampton School – This is Local London

Due to a challenging winter in the presence of the COVID pandemic, new variants of concern such as Omicron and an increase in the number of colds and flu, immunology has never been more important; hence, there has been a large rise in interest in this area of science. Immunology is the study of the immune system and how it can protect us from disease. This brief article derives from an interview with Dr Robert Busch who is a Senior Lecturer from the School of Life and Health Sciences at the University of Roehampton, whose research focuses on the immune system.

Immunology is very important in current times as it is essential for maintaining general human health, responding to disease and also for developing COVID-19 vaccines that can make the virus more survivable and less transmissible. Dr Busch recognises this as a difficult and tragic time for many people, and knowledge of immunology is of great importance.

Dr Buschs current research is focused on tissue antigens, which are molecules that trigger immune responses by activating other cells of the immune system. In particular he studies how the immune system kicks in when it is faced with infection, but is quiet at other times so that the body doesn't fight itself. Tissue antigens vary from one person to the next and this variation can influence the risk of autoimmunity (when the immune system attacks the bodys own tissues).

Other research that Dr Busch conducts is on Vitamin D which is also important for immune regulation and can influence how many tissue antigens are produced and their ability to function in response to different diseases. Vitamin D has also been of interest in relation to COVID; however, so far results have been contradictory and no clear conclusions can be drawn.

Dr Busch stated, There is much to discover in the future, such as studying new and existing diseases and creating new vaccines. Another aspect of immunology that needs to be researched further is the question of how to turn off an immune cell once it has been activated, without compromising the immune systems ability to fight infections. Dr Busch describes this as the Holy Grail of immunology. Essentially, the more we know about how our immune system reacts, the better we can make the interventions that will combat viruses and protect people.

Immunology is important now and will remain so in the future, and scientists such as Dr Robert Busch are paving the way in helping broaden our understanding of the immune system so that we can fight disease and stay healthy.

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The Importance of Immunology by Joe Murphy, Hampton School - This is Local London

Western News – Western researcher helping bring HIV cure within reach – Western News

At first, in the medical fight against AIDS, there was only uncertainty.

Then researchers brought hope in the form of life-saving treatment antiretrovirals that stop HIV from replicating in an infected person and reduce the risk of transmission.

Now, as the international community marks World AIDS Day on Dec. 1, a cure could be within REACH.

Western University researcher Jessica Prodger is a collaborator in Research Enterprise to Advance a Cure for HIV (REACH), an ambitious multi-institutional project funded through the U.S. National Institutes of Health (NIH).

HIV is resilient and has, so far, been resistant to a cure. One key issue is that some of the virus, as it integrates itself into human DNA, becomes invisible to the immune system if the infected cells go dormant.But the cells retain the viral DNA, and if a person stopped taking antiretroviral treatment, the infection would reactivate and the virus would again replicate.

The work of REACH focuses on understanding this latent reservoir of infected cells and figuring out how to eliminate it.

Prodger, a professor of immunology and microbiology at Westerns Schulich School of Medicine & Dentistry, is a co-lead investigator in Weill Cornell Medicines new five-year, US$28.5million Martin Delaney Collaboratory grant from the NIH.

This is a huge endeavour involving 37 co-investigators, all of us attacking HIV from one important angle, Prodger said. The NIH Martin Delaney funding removes competition between individual groups, allowing us to organize cure research into large, well-funded teams, and I think were going to make huge strides.

Her research includes a study group of HIV-positive women and men in Uganda who are receiving antiretroviral therapy.

Her team has been tracking and quantifying the HIV reservoir in this cohort, and has made important discoveries, such as that latent HIV is not as easily reactivated in females.

Its one small, but vital, part in solving the larger HIV puzzle and finding a cure, said Prodger, who also holds a Canada Research Chair in genital immunology and prevention of sexually transmitted infections.

Burden of infection

Around the world, 38 million people live with human immunodeficiency syndrome (HIV) and require daily, lifelong medication.

In 2020 alone, about two million people contracted HIV and 690,000 died from AIDS-related illnesses, UNAIDS notes.

All told, 80 million people have contracted the virus; half of those have died from AIDS-related illnesses.

The heaviest burden of infection is still borne by people in low-income countries where different strains of HIV are in circulation, while most of the research is taking place in high-income countries among high-income populations with predominantly one HIV strain.

Shifting focus

But progress is taking place.

AIDS-related deaths have dropped by 64 per cent since the peak in 2004. Infection numbers last year were about half the number of infected in 1997.

Antiretrovirals and other medications are transforming HIV infection into a manageable chronic condition, and people who are on effective treatment cannot transmit the virus to others.

Scientists around the world, including many at Western, are working towards new treatments, cures and potential vaccines.

The focus of HIV research for the first 30 years (since HIV was first identified) was on treatment and prevention, to save lives and stop people from dying of AIDS.This has been hugely successful, Prodger said. The discovery of the reservoir came decades after the discovery of the virus, and the field has only just begun to focus on a cure, now that highly effective treatments have been developed.

The REACH team is composed of investigators with expertise in virology, immunology, clinical studies and community advocates.

With 18 different institutions involved, the REACH program is a model for harnessing the great power of many scientific communities and minds, said a news release from Weill CornellMedicine, based in New York.

The project team, led by Dr. Brad Jones,associateprofessor ofimmunology inmedicine in the Division of Infectious Diseases at Weill Cornell Medicine, received the Delaney Collaboratory grant in August 2021. The REACH Collaboratoryis co-led by Dr. Marina Caskey of The Rockefeller University.

This award represents a remarkable vote of confidence and recognition of Weill Cornell Medicine as an international hub of HIV cure research, Jones said in the news release. With this funding we will leverage novel technological and analytical methods to redefine how the immune system interacts with the HIV reservoir in people on therapy.

A cure either eradicating the virus in the body or suppressing the virus by boosting the immune system would end the need for lifelong medication.We believe that both of these outcomes are possible, but that they are complex andthere arechallenging problems to solve, Jones said.

Prodger emphasized its the collaboratorys collective work, not any one individuals, that will make the difference and, ultimately, lead to a cure.

Research is very much about building an enormous structure, brick by brick. You begin to see what an amazing thing this is when everyone adds their brick to the whole, she said.

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Western News - Western researcher helping bring HIV cure within reach - Western News

UK professor impacted by Omicron travel restrictions – LEX18 Lexington KY News

LEXINGTON, Ky. (LEX 18) First detected in the United States Wednesday, Omicron has rapidly become the dominant variant of the coronavirus in South Africa, a country that has held a special place in Dr. Zach Porterfield's heart.

An assistant professor of immunology and infectious diseases at the University of Kentucky, Dr. Porterfield told LEX 18 he has lived in South Africa on and off over the last 21 years. He has studied as an HIV virologist in the country, where he said doctors and scientists have been doing exceptional work researching COVID-19.

"We probably found [Omicron] in South Africa because there was a concerted effort to look," Dr. Porterfield said. "We have the expertise and technology to do that [genetic] sequencing."

Dr. Porterfield said he was planning to travel to South Africa next week, before learning about new travel restrictions imposed on South Africa and seven other African countries.

"I still have an apartment in Durban and projects and laboratory collaborations in South Africa that I was planning to return and try and set right," he said.

Although his plans may have been upended, Dr. Porterfield said he understands why President Joe Biden's administration implemented the latest travel bans.

"I think the right thing to do is take a moment to pause and think through what does this mean," he said.

President Biden explained earlier this week that while travel restrictions will not prevent the arrival of the variant, they could buy the administration time to prepare.

Health experts around the world, including representatives from the World Health Organization, have criticized the restrictions, suggesting they are ineffective and punitive.

"Blanket travel bans will not prevent the international spread of Omicron," said Dr. Tedros Adhanom Ghebreyesus, the Director-General of the WHO. "And they place a heavy burden on lives and livelihoods."

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UK professor impacted by Omicron travel restrictions - LEX18 Lexington KY News

Viral evolution in animals could reveal future of COVID-19 – Jill Lopez

When animals catch COVID-19 from humans, new SARS-CoV-2 variants can arise. To evaluate this phenomenon, an interdisciplinary team at the College of Veterinary Medicine and Biomedical Sciences systematically analyzed mutation types occurring in the virus after infection of cats, dogs, ferrets, and hamsters.

Confirmed COVID-19 cases in a variety of wild, zoo, and household animals demonstrate cross-species transmission, which is a rare occurrence for most viruses.

SARS-CoV-2, in the realm of coronaviruses, has a very broad species range, said Laura Bashor, one of the first authors and a doctoral student in the Department of Microbiology, Immunology and Pathology. Generally speaking, many types of viruses cant infect other species of animals, they evolved to be very specific.

Humans have so much exposure to many different animals which permitted this virus to have the opportunity to expose a variety of different species, said Erick Gagne, a first author and now an assistant professor of wildlife disease ecology at the University of Pennsylvania.

The global reach and spillover of the virus have given researchers a unique opportunity to investigate the viral evolution of SARS-CoV-2, including in University Distinguished Professor Sue VandeWoudes laboratory at Colorado State University.

These specialists in disease transmission in wild and domestic cats applied their experience in sequence analysis and studying a collection of genomes to SARS-CoV-2.The studywas recently published in PNAS, the official journal of the National Academy of Sciences.

Researchers in the VandeWoude lab worked with Assistant Professor Angela Bosco-Lauth and Professor Dick Bowen in the Department of Biomedical Sciences, who used their animal modeling expertise to develop a test for SARS-CoV-2 susceptibility of animal species.

Also key to the findings was a newer sequencing technique of the virus at different stages of the study, now common to detect variants in the human population. Mark Stenglein, associate professor in the Department of Microbiology, Immunology, and Pathology, provided computational skills in analyzing biological molecule sequences, known as bioinformatics, to the study.

We found there was evolution, we saw selection on the virus, and we saw a lot of variants emerge in the genome sequence of the virus, said Bashor.

To provide ample viral material for the study, Bosco-Lauth and Bowen cultivated a SARS-CoV-2 human sample in cells grown in the lab. Bashor and Gagne determined that multiple mutations developed, and became a greater percentage of the genetic population, at each step of this process.

Then the virus was introduced to the four household species, and samples of the virus were collected from their nasal passages after infection.

In the animals, the cell culture variants reverted back to the initial human type, which indicates that likely there is adaption occurring in that cell culture and environment that was selected for those variants, said Gagne.

Not all these mutations within the cell culture SARS-CoV-2 variant transferred in the new hosts. Instead, different mutations emerged within the virus shed by the live animals.

The initial viral sample in the study was isolated in early 2020. The team observed mutations that have since formed wide-spread SARS-CoV-2 strains in the human population at an accelerated rate throughout the study.

Among those were a number that weve since seen in humans in the alpha, beta, delta variants, said Dr. Sue VandeWoude, senior author. There were specific genetic code changes that mimicked what other scientists have reported in people.

Contact exposure between two cats demonstrated the SARS-CoV-2 variant can be transmitted with the possibility of producing a new strain within the species.

Thats what were seeing in people too, said Bosco-Lauth. Hosts that are really well adapted to support SARS-CoV-2 infection are also very good at allowing these mutations to stick and to be passed on.

Bashor did not anticipate studying SARS-CoV-2 when she came to CSU to begin her doctoral studies during the pandemic. However, it provided a unique opportunity to hit the ground running as a graduate student on a really cool and viable project in disease ecology and evolution.

Gagne was completing his postdoctoral research on cross-species transmission of feline retroviruses in the VandeWoude lab when the team launched the SARS-CoV-2 study. Now an assistant professor, he has continued to investigate SARS-CoV-2 spillover with the Wildlife Futures Program at the University of Pennsylvania.

Graduate students and early career scientists like Bashor and Gagne, have made meaningful contributions to SARS-CoV-2 research, said VandeWoude.

The team has continued their investigations to focus on cats, as they have shown higher susceptibility for COVID-19 spillover from humans and can produce variants of the virus and spread to other cats.

Bashor began analyzing SARS-CoV-2 genome sequences from a large pool of cat species all over the world, including tigers, lions and snow leopards. The publicly available data of infected cats could provide additional insights on the adaptability and mutability of COVID-19 within and among cat species.

There is not evidence of transmission from cats to humans. But cats continue to be susceptible to all variants of COVID-19 in the human population.

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Viral evolution in animals could reveal future of COVID-19 - Jill Lopez

Analysis shows skin peanut allergy patch safe and well tolerated over 3-year period – Hospital Healthcare Europe

The use of Viaskin, an epicutaneous patch used for children with a peanut allergy appears to be safe and well tolerated according to a three-year analysis presented by at the American College of Allergy, Asthma and Immunology Conference, November 2021.

A peanut allergy is thought to affect around 2% of the general population and in a study of 3218 children, the incidence was found to be 24.8%. The presence of a peanut allergy is challenging for those affected and requires a high level of vigilance directed towards the avoidance of accidental ingestion of peanut-containing foods.

The use of viaskin represents epicutaneous immunotherapy and according to the manufacturer, DBV Technologies, is a proprietary technology platform that enables the delivery of biologically active compounds to the immune system through the skin.

The data presented at the American College of Allergy, Asthma and Immunology Conference was based on the REALISE trial, which included children with documented histories of peanut anaphylaxis and who were randomised, 3:1, to either viaskin peanut 250mcg (which contains 1/1000th of the protein found in a single peanut) or a placebo for a period of 6 months. Once this initial phase was completed, all subjects continued to receive the active treatment in an open-label extension, for a period of three years. For the REALISE study, the primary outcome was set as adverse Events (AEs), treatment-emergent adverse events (TEAEs) and serious adverse events (SAEs) throughout the study period.

The 6-month safety data for viaskin has already been published and showed that the patch was well-tolerated.

Findings

REALISE recruited 393 children with a median age of 7 years (gender not reported) of whom, 14 (3.6%) had a history of severe anaphylaxis. Throughout the study period, most subjects experienced at least one TEAE although these were reported as being mild (97.4%) or moderate (70.4%) in severity and commonly consisted of application site erythema and pruritus which fortunately decreased over time.

Overall, 16 children experienced a total of 17 anaphylactic reactions (none severe) considered to be due to viaskin. In addition, there were 2 serious that were viakskin-related TEAEs (2 anaphylactic reactions: one leading to permanent study discontinuation). No difference in TEAEs in subjects with severe anaphylaxis history was apparent.

The authors concluded that over 36-months, Viaskin Peanut was generally well tolerated, with decreasing frequency and intensity of local and systemic treatment-related AEs over time.

The product is yet to be approved by the FDA, which has requested more data or the EMA.

Citation

Brown-Whitehorn T et al. D030 REALISE (REAL-LIFE USE AND SAFETY OF EPIT) STUDY: 3 YEAR RESULTS IN PEANUT-ALLERGIC CHILDREN. Ann Allergy Asthma Immunol 2021

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Analysis shows skin peanut allergy patch safe and well tolerated over 3-year period - Hospital Healthcare Europe