New BioAge Drug Prevents Death From COVID-19 in Old Mice by Reversing Immune Aging

Immunity Boost Concept

A Phase 2 clinical trial is testing the new drug’s ability to reduce mortality in older people hospitalized with COVID-19. By directly targeting immune aging, BGE-175 could effectively treat emerging COVID variants that evade vaccine-based immunity.

The immune system deteriorates with age, making COVID-19 particularly deadly in older people — but to date, no clinically available medication addresses this key risk factor. A study published today (March 21, 2022) in Nature shows that an oral drug that reverses multiple aspects of immune aging effectively prevents death in a mouse model of COVID-19, suggesting that the medication could be used to protect the elderly patients who are at greatest risk in the pandemic.

In the study, daily doses of BGE-175 (asapiprant) protected aged mice from a lethal dose of SARS-CoV-2, the virus that causes COVID-19. Ninety percent of mice that received the drug survived, whereas all untreated control mice died. BGE-175 treatment was initiated two days after infection, when the mice were already ill, a time-frame relevant to real-life clinical situations in which patients would receive medication only after becoming symptomatic.

The mouse model used in the study closely mirrored the pathological progression of human COVID-19. The mouse-adapted strain of SARS-CoV-2 generated by the researchers caused a disease that shared many of the hallmarks of human COVID-19: accumulation of fluid in the air sacs of the lungs, extensive infiltration of lung tissue by immune cells, and high levels of pro-inflammatory factors called cytokines.

BGE-175 is currently in a Phase 2 clinical trial to test whether it can prevent disease progression and mortality in older patients hospitalized with COVID-19. BGE-175 is being clinically developed by BioAge Labs, a California-based biotechnology company devoted to creating drugs that treat human disease and extend healthspan by targeting the molecular mechanisms of aging.

“The COVID-19 pandemic has devastated elderly populations around the world,” said Kristen Fortney, PhD, CEO of BioAge and an author of the study. “The promising preclinical data in this paper show that BGE-175 almost completely protects aged mice from lethality in a compelling model of human COVID-19. By reversing age-related declines in critical immune mechanisms, BGE-175 could allow older patients to more effectively fight off this disease.”

Reversing immune aging via a dual mechanism

As we age, a biochemical pathway involving the signaling molecule PGD2 becomes more active, impairing immunity in two major ways: First, antigen-presenting cells called dendritic cells migrate less efficiently, slowing the adaptive T-cell and antibody responses. Second, white blood cells called neutrophils infiltrate infected tissues more aggressively, leading to damaging inflammation. Thus, the aged immune system is both slower to respond to new infections and more likely to overreact once it does mount a response.

BGE-175 inhibits this pathway by blocking the interaction between PGD2 and its receptor, a protein called DP1. BioAge’s AI-based drug discovery platform identified the PGD2-DP1 pathway as a key target for immune aging. In the study described in the Nature paper, BGE-175 increased migration of dendritic cells from the lungs into the lymph nodes, decreased the levels of neutrophils in lung tissue, and dramatically improved overall survival. From the standpoint of PGD2 pathway activity, the drug restored the immune system to a more youthful state.

As with the drug-treated animals, genetically engineered mice that were unable to synthesize PGD2 or lacked DP1 had lower viral loads, exhibited less inflammation and tissue damage, and were less susceptible to death from viral infection, confirming that BGE-175 acts through the PGD2 pathway.

“Our findings clearly show that the therapeutic target of BGE-175 plays a key role in making the aged lung environment conducive for optimal immune function, and thereby counters immune aging,” said Stanley Perlman, MD, PhD, Professor of Microbiology and Immunology and Pediatric Infectious Physician at the University of Iowa, who was an author of the Nature paper. “The drug’s protective effect in mice supports the idea that BGE-175 corrects age-related declines in immunity, providing a strong rationale for testing in older patients who are hospitalized with COVID-19.”

Clinical applications in human beings — for COVID and beyond

A Phase 2 clinical trial, initiated in March 2021, is testing whether BGE-175 can prevent respiratory failure and mortality in older patients hospitalized with COVID-19. Because some cases of COVID-19 are associated with uncontrolled inflammation, which increases disease severity and morbidity, the trial will also measure BGE-175’s effect on levels of inflammatory markers, providing insight into BGE-175’s ability to restore normal regulation of the immune system. Full details of the trial are available at ClinicalTrials.gov, and efficacy data are anticipated in the first half of 2022.

Antiviral drugs against COVID-19, as well as antibodies raised by vaccines, bind to specific viral proteins to exert their effect, and could therefore could lose efficacy if the SARS-CoV-2 virus continues to mutate — as already observed for the highly contagious omicron variant.

Because BGE-175 targets the host immune system rather than the invading virus, it has the potential to retain its efficacy against emerging strains that can resist antiviral drugs or evade vaccine-based immunity. Similarly, because its mechanism of action is not specific to COVID-19, the drug could help older patients fight off other viruses. Consistent with this, in the Nature study, BGE-175 prevented lethality from SARS-CoV, the original SARS virus, which like SARS-CoV-2 also causes more severe disease in older animals.

“A properly functioning immune system is our first defense against any virus, and we know that age-associated immune abnormalities place the elderly at a much increased risk for death and complications from COVID-19,” said Eric Verdin, MD, President and CEO of the Buck Institute for Research on Aging, who was not involved in the study. “New therapeutics that target age-associated pathways, especially those involved in immunity, will provide important tools for decreasing the burden of mortality and disability caused by COVID-19, as well as other infections that disproportionately harm the elderly.”

Pending positive results in the Phase 2 trial, BioAge intends to pursue broad clinical applications for BGE-175, including diseases such as influenza and viral pneumonia.

Reference: “Eicosanoid signaling blockade protects middle-aged mice from severe COVID-19” by Lok-Yin Roy Wong, Jian Zheng, Kevin Wilhelmsen, Kun Li, Miguel E. Ortiz, Nicholas J. Schnicker, Andrew Thurman, Alejandro A. Pezzulo, Peter J. Szachowicz, Pengfei Li, Ruangang Pan, Klaus Klumpp, Fred Aswad, Justin Rebo, Shuh Narumiya, Makoto Murakami, Sonia Zuniga, Isabel Sola, Luis Enjuanes, David K. Meyerholz, Kristen Fortney, Paul B. McCray Jr. and Stanley Perlman, 21 March 2022, Nature.
DOI: 10.1038/s41586-022-04630-3

About BioAge

BioAge is a clinical-stage biotechnology company developing a pipeline of treatments to extend healthy lifespan by targeting the molecular causes of aging with a large and mechanistically diverse portfolio of drugs. The company uses its discovery platform, which combines quantitative analysis of samples from proprietary longitudinal human cohorts, to map out the key molecular pathways that impact healthy human aging, thus revealing the causes of age-related disease.

3 Comments on "New BioAge Drug Prevents Death From COVID-19 in Old Mice by Reversing Immune Aging"

  1. There has never been a better time to be a mouse!

  2. Very Interesting. Some Thoughts.

    1. Why do people age and why does immunity decline with age?

    2. The human body is a complex interaction of sub-systems . However we are all mortals and mortality ( death is certain!). Becoming immortal is a dream of humaans.

    3. BGE-175 (asapiprant) is a potent and selective DP1 receptor antagonist

    4. Reportedly earlier research in Sheep and Pigs, this substance Suppresses the increase in nasal resistance. Oral administration of Asapiprant suppresses Prostaglandin (PG) D2 (PGD)2-induced nasal resistance.

    5.The prostaglandins are a group of lipids made at sites of tissue damage or infection that are involved in dealing with injury and illness. They control processes such as inflammation, blood flow, the formation of blood clots and the induction of labour in woman.

    6.The Covid-19 affected Men much more than Women. The relationship between Prostaglandins, Progesterone and Estrogen in the Human Reproductive system , and regulation of Prostaglandins and Progesterone mechanism is probably responsible for this and providing greater protection against Covid-19 for the female gender compared to the male gender.

    7. Now coming to the article about Immunity of BGE-175 (asapiprant) and its impact on Aged Mice in providing protection against Covid-19, lung function and collection of fluids and cytokine storm, etc. reported :
    (a) attributing it exclusively to “BGE-175 increased migration of dendritic cells from
    the lungs into the lymph nodes, decreased the levels of neutrophils in lung tissue,
    and it dramatically improving overall survival against Covid 19 Virus” and
    conclusion drawn that from the standpoint of PGD2 pathway activity, and stating that
    the drug restored the immune system to a more youthful state is a big stretch.
    (b) It may be a subset ofthe understanding of the complex Immmune system.

    8. The reason for this is that in youthful persons the Telomers have a long tail. In Elderly persons the tail appears impaired and sickly.

    9. We need a much more comprehensive understanding of the immune system . Cells age and die. If cell functioning goes awry we fall sick , and if the protective systems (Immune system ) doesn’t kick in sub-systems fail.

    Views expressed are personal and not binding on anyone.

  3. @Sekar,

    While many parts of the body and immune system weaken over time, one organ that has a major impact is your thymus gland which is primarily responsible for “teaching” certain immune cells how to recognize and respond to threats, both from outside as well as within. After about the age of thirty, the thymus begins to shut down and around sixty years of age, the thymus is almost nonfunctional; this directly correlates to a rise in the incidence of various cancers and other diseases among the elderly since at this point no new immune cells are being “taught”.

    Immunology is insanely complex, with multiple interlocking systems, each with multiple components and organs, that interact in ways that researchers still haven’t completely uncovered. The lack of a comprehensive understanding isn’t due to a lack of effort.

    If we could find a way to successfully “rewind the clock” on the immune system, we would be well on the way to figuring out how to tackle the larger issue of senescence.

Leave a Reply to Tao Cancel reply

Email address is optional. If provided, your email will not be published or shared.