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Lab-grown human embryo models spark calls for regulation

Scientists have used stem cells to create structures that resemble human embryos in the lab, in a first that has prompted calls for stricter regulation in the rapidly advancing field.

Several different labs around the world have released pre-print studies in the past seven days describing their research, which experts said should be treated with caution as the research has not yet been peer-reviewed.

The labs used different techniques to encourage , which can become any type of cell, to self-assemble into a structure that resembles an embryo—without needing sperm, an egg or fertilization.

Pre-Clinical Study Shows Benefits to Targeting the Lymph Node for Cancer Treatment

Immune checkpoint inhibitors (ICIs) have improved the landscape of cancer research over the past decade. These therapies, which target a patient’s own immune system aiming to make it stronger and more equipped to fight cancer, have provided novel and beneficial therapeutic options for patients with advanced and metastatic disease.

While ICIs can induce long-term responses and cures in patients with limited therapeutic options, they present significant challenges. First, different patients exhibit different levels of responsiveness to ICIs. So, when one patient achieves a cure, another with a similar type of cancer may remain non-responsive. While we don’t fully understand the reasons behind the disparate responsiveness of ICIs, this remains an active area of research globally. Second, ICI use can elicit toxicities known as immune-related adverse events (irAEs). In some patients irAEs can be managed and thus tolerable, especially given the anti-cancer effects. However, some patients experience severe irAEs that can significantly hinder the quality of life of cancer survivors. In some cases, serious and life-threatening irAEs can even require treatment discontinuation.

A pre-clinical study recently published in the Journal of Clinical and Experimental Cancer Research explores a potential regimen that may help confront both of these challenges. The researchers hypothesized that ICIs, if targeted directly to the lymph node (LN), could both enhance the anti-tumor response and reduce the associated irAEs.

Unexpected discovery: Blue-green algae produce oil

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Cyanobacteria — colloquially also called blue-green algae — can produce oil from water and carbon dioxide with the help of light. This is shown by a recent study by the University of Bonn. The result is unexpected: Until now, it was believed that this ability was reserved for plants. It is possible that blue-green algae will now also become interesting as suppliers of feed or fuel, especially since they do not require arable land. The results have now been published in the journal PNAS.

What do rapeseed, avocado and olive tree have in common? They are all used by humans as producers of oil or fat. However, the ability to produce oil from water and carbon dioxide with the help of light is something that is essentially common to all plants, from unicellular algae to the giant sequoia trees. “We have now shown for the first time that cyanobacteria can do the same,” explains biologist Prof. Dr. Peter Dörmann from the Institute of Molecular Physiology and Biotechnology of Plants (IMBIO) at the University of Bonn. “This was a complete surprise, not only to us.”

Until now, experts had assumed that cyanobacteria lack this property. After all, they are actually bacteria, even if their trivial name “blue-green algae” suggests otherwise. They therefore differ considerably from plants in many respects: Cyanobacteria are closer related to the intestinal bacterium E. coli than to an olive tree. “There are indeed ancient reports in the literature that cyanobacteria can contain oil,” says Dörmann. “But these have never been verified.”

Pregnancy Hormone Estriol May Reverse Myelin Damage in Multiple Sclerosis

Summary: Treating a mouse model of multiple sclerosis (MS) with the pregnancy hormone estriol could reverse myelin breakdown in the brain’s cortex, a primary area affected in MS.

MS results in inflammation that damage the myelin coating around nerve fibers in the brain’s cortex, leading to disability worsening. Current MS treatments only target inflammation and can’t repair myelin damage.

However, the new study found that estriol not only prevented brain atrophy but also induced remyelination, suggesting it could repair MS-induced damage.

Alzheimer’s: Excessive alcohol consumption may accelerate progression

Nima Majlesi, director of Medical Toxicology at Staten Island University Hospital, also not part of the research, said the new study is “fascinating, and the more research that can be done on neurodegenerative diseases such as [Alzheimer’s disease], the more answers that can then be obtained for the betterment of everyone’s health.”

“There has never been any doubt that excessive alcohol use and recurrent intoxication [are] unhealthy in the medical community. There has occasionally been some doubt on whether a small amount of alcohol use daily can have health benefits. Even in patients not at risk for [Alzheimer’s disease], excessive alcohol use and recurrent intoxication [have] many detrimental effects on human health.” — Dr. Nima Majlesi

However, Dr. Majlesi cautioned that “in this study, they exposed mice to ethanol vapors, which is not the typical route for human consumption.”

New Research Shows HIV Can Lie Dormant in the Brain

Scientists from the HIV Cure Center at the UNC School of Medicine, University of California San Diego, Emory University, and University of Pennsylvania have been searching for where exactly these latent cells are hiding in the body. New research published in the Journal of Clinical Investigations confirms that microglial cells – which are specialized immune cells with a decade-long lifespan in the brain – can serve as a stable viral reservoir for latent HIV.


Yuyang Tang, PhD, and Guochun Jiang, PhD, in the UNC School of Medicine extracted living brain tissue to conclude that specialized immune cells in the brain can harbor latent but replication-competent HIV.

As a part of its life cycle, the human immunodeficiency virus-1 (HIV) inserts a copy of its DNA into human immune cells. Some of these newly infected immune cells can then transition into a dormant, latent state for a long period of time, which is referred to as HIV latency.

Although current therapies, such current antiretroviral therapy (ART), can successfully block the virus from replicating further, it cannot eradicate latent HIV. If treatment is ever discontinued, the virus can rebound from latency and reignite the progression of HIV infection to AIDS.