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The surprising ways food packaging is exposing us to microplastics

The surprising ways food packaging is exposing us to microplastics

Washington Post7 hours ago

At this point, most people know that microplastics are everywhere. Scientists have shown that tiny particles, amounting to the weight of a plastic spoon, can be found in our brains; hundreds of fragments of plastic are in each breath we take.
But the exact origins of those tiny pieces of plastic have been unclear. Are they coming from plastics discarded in landfills and decomposing over dozens of years? Or are they spilling out of the plastic water bottles and containers we seal our food in? The answer matters — for individuals hoping to avoid the particles and politicians who may want to restrict the microplastics we eat, drink and breathe.

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Cue Biopharma Receives FDA Feedback on Pre-IND Briefing Document Reinforcing Company's Intention to Advance IND Submission for CUE-401 to Address Unmet Need in the Treatment of Autoimmune Disease
Cue Biopharma Receives FDA Feedback on Pre-IND Briefing Document Reinforcing Company's Intention to Advance IND Submission for CUE-401 to Address Unmet Need in the Treatment of Autoimmune Disease

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Cue Biopharma Receives FDA Feedback on Pre-IND Briefing Document Reinforcing Company's Intention to Advance IND Submission for CUE-401 to Address Unmet Need in the Treatment of Autoimmune Disease

CUE-401, a first-in-class bispecific molecule designed to induce and expand Tregs in vivo through the co-activity of transforming TGF-β and a modified variant of IL-2 BOSTON, June 24, 2025 (GLOBE NEWSWIRE) -- Cue Biopharma, Inc. (Nasdaq: CUE), a clinical-stage biopharmaceutical company developing a novel class of therapeutic biologics to selectively engage and modulate disease-specific T cells for the treatment of autoimmune disease, today announced it has received Pre-Investigational New Drug (Pre-IND) feedback from the U.S. Food and Drug Administration (FDA). The FDA reviewed the first-in-human trial design, including the Company's plan for dose escalation, proposed populations and safety monitoring plan. On the basis of the FDA feedback, the Company, intends to file an IND pending completion of final IND enabling studies. CUE-401 is the Company's lead autoimmune asset, a first-in-class bispecific fusion protein/molecule designed to induce and expand regulatory T cells (Tregs) in vivo through the co-activity of transforming growth factor beta (TGF-β) and a modified variant of interleukin 2 (IL-2). 'We are highly encouraged by the FDA's positive feedback on our proposed development plan for this important program. We believe CUE-401, with its first-in-class mechanism exploiting the combined activities of TGF-β and IL-2 is a potentially disruptive approach differentiated from other Treg-directed therapies, and has the potential to provide durable, long-lasting immune rebalance and tolerance addressing multiple, significant disease indications,' said Daniel Passeri, chief executive officer of Cue Biopharma. Dr. Dan Baker, chief development officer of Cue Biopharma commented, 'CUE-401's mechanistic design extends beyond nTreg proliferation by transforming effector/autoreactive responses to an anti-inflammatory and/or suppressive response, with the prospects of establishing tolerance. The combination of interleukin 2 (IL-2) and transforming growth factor beta (TGF-ß) is considered the 'master switch' for conversion of activated T effector cells into T cells with a regulatory phenotype.' About CUE-401CUE-401 is a preclinical, bispecific fusion protein designed to induce and expand regulatory T cells (Tregs) through the co-activity of modified variants of transforming growth factor beta (TGF-β) and interleukin 2 (IL-2) with therapeutic potential across a range of T-cell mediated autoimmune and inflammatory diseases. CUE-401 has been engineered to harness the Treg induction capacity of TGF-β combined with IL-2 signaling to provide what Cue Biopharma believes to be superior quality and stability of Tregs. The design and specifications of CUE-401 have been guided by leading scientific publications demonstrating that both IL-2 and TGF-β are required for stable and efficient production of active and durable Tregs. CUE-401 is designed to overcome multiple hurdles required to exploit the therapeutic potential of a master switch with a first-in-class, bispecific molecule integrating a masked TGF-ß, with our clinically validated, attenuated IL-2 with an antibody Fc fragment. This novel design provides for 'conditional binding' and avoids off target activity, simplifies manufacturing and has highly differentiated findings in multiple pre-clinical models. In these models, CUE-401 behaves as a master switch to convert autoreactive effector T cells (inflammatory cells) into stable, induced T-regulatory cells (iTregs). These findings suggest that CUE-401 acts by establishing a 'tolerance positive feedback loop' that not only increases nonspecific Treg populations, but critically, reduces and converts specific autoreactive T cells into transdifferentiated iTregs that are specific for the disease-causing autoantigens. About Cue BiopharmaCue Biopharma, a clinical-stage biopharmaceutical company, is developing a novel class of injectable biologics to selectively engage and modulate disease-specific T cells directly within the patient's body. The company's proprietary platform, Immuno-STAT™ (Selective Targeting and Alteration of T cells), and biologics are designed to harness the curative potential of the body's intrinsic immune system without the adverse effects of broad systemic immune in Boston, Massachusetts, we are led by an experienced management team with deep expertise in immunology and immuno-oncology as well as the design and clinical development of protein biologics. For more information please visit and follow us on X and LinkedIn. Forward-Looking StatementsThis press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. Such forward-looking statements include, but are not limited to, those regarding: the company's expectations regarding the planned IND filing for CUE-401; the Company' expectations regarding the potential characteristics and benefit of CUE-401; the company's belief that the Immuno-STAT platform stimulates targeted immune modulation through the selective modulation of disease-relevant T cell and the applicability of the company's platform across many cancers and autoimmune diseases; and the company's business strategies, plans and prospects. Forward-looking statements, which are based on certain assumptions and describe the company's future plans, strategies and expectations, can generally be identified by the use of forward-looking terms such as 'believe,' 'expect,' 'may,' 'will,' 'should,' 'would,' 'could,' 'seek,' 'intend,' 'plan,' 'goal,' 'project,' 'estimate,' 'anticipate,' 'strategy,' 'future,' 'likely' or other comparable terms, although not all forward-looking statements contain these identifying words. All statements other than statements of historical facts included in this press release regarding the company's pipeline of product candidates and platforms, and its strategies, prospects, plans and objectives are forward-looking statements. Important factors that could cause the company's actual results and financial condition to differ materially from those indicated in the forward-looking statements include, among others, the Company's ability to successfully advance is development plan for CUE-401; potential setbacks in the company's research and development efforts including negative or inconclusive results from its preclinical studies or clinical trials or the company's ability to replicate in later clinical trials positive results found in preclinical studies and early-stage clinical trials of its product candidates; serious and unexpected drug-related side effects or other safety issues experienced by participants in clinical trials; its ability to secure required U.S. Food and Drug Administration ('FDA') or other governmental approvals for its product candidates, including FDA clearance of any future IND submission for CUE-401, and the breadth of any approved indication; adverse effects caused by public health pandemics, including possible effects on the company's trials; delays and changes in regulatory requirements, policy and guidelines including potential delays in submitting required regulatory applications to the FDA; the company's reliance on licensors, collaborators, contract research organizations, suppliers and other business partners; the company's ability to obtain adequate financing to fund its business operations in the near term; the company's ability to maintain and enforce necessary patent and other intellectual property protection; competitive factors; general economic and market conditions and the other risks and uncertainties described in the Risk Factors and in Management's Discussion and Analysis of Financial Condition and Results of Operations sections of the company's most recently filed Annual Report on Form 10-K and any subsequently filed Quarterly Report(s) on Form 10-Q. Any forward-looking statement made by the company in this press release is based only on information currently available to the company and speaks only as of the date on which it is made. The company undertakes no obligation to publicly update any forward-looking statement, whether written or oral, that may be made from time to time, whether as a result of new information, future developments or otherwise. Investor Contact Marie Campinell Senior Director, Corporate CommunicationsCue Biopharma, Media ContactJonathan PappasLifeSci Communicationsjpappas@

Wisconsin Supreme Court sides with environmentalists in fight over PFAS "forever chemicals"
Wisconsin Supreme Court sides with environmentalists in fight over PFAS "forever chemicals"

CBS News

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  • CBS News

Wisconsin Supreme Court sides with environmentalists in fight over PFAS "forever chemicals"

How scientists are working to clean up PFAS How scientists are working to clean up PFAS How scientists are working to clean up PFAS The Wisconsin Supreme Court delivered a victory for environmentalists on Tuesday in the fight over "forever chemicals" known as PFAS, issuing a ruling that advocates said will hold polluters accountable. The liberal-controlled court ruled that state regulators can force landowners to clean up emerging pollutants such as PFAS before they are officially designated as hazardous substances. The 5-2 ruling is a defeat for the state's powerful group representing businesses and manufacturers, which had argued the state couldn't enforce regulations on substances before they were officially designated as hazardous. It is the latest development in a yearslong battle in Wisconsin and nationally involving regulators, environmentalists, politicians and businesses over how to deal with PFAS contamination. Cities large and small across Wisconsin, from Madison to Marinette and La Crosse to Wausau, are grappling with PFAS contamination. PFAS, or perfluoroalkyl and polyfluoroalkyl substances, are a group of chemicals that have been around for decades and have now spread into the nation's air, water and soil. The chemicals helped eggs slide across nonstick frying pans, ensured that firefighting foam suffocates flames and helped clothes withstand the rain and keep people dry. They resist breaking down, however, which means they stay around in the environment and have a hard time breaking down in the body. There is a wide range of health harms now associated with exposure to certain PFAS, including low birth weight, cancer and liver disease. The Wisconsin Supreme Court ruled in a case brought by the state's largest business group, Wisconsin Manufacturers & Commerce, which sued the DNR in 2021 on behalf of Leather Rich, a dry cleaning business in Oconomowoc. Leather Rich became aware of PFAS contamination in 2018 and was working on cleaning it up when the DNR posted a message online in 2019 saying it now considered PFAS chemicals a hazardous substance. The agency ordered the dry cleaner to test its groundwater for PFAS but didn't tell the business which compounds it needed to test for or what levels would be considered dangerous. Leather Rich argued the DNR can't force businesses to test and clean up contamination from emerging pollutants like PFAS without first designating them as hazardous substances. That process can take years and requires approval from the Legislature. All that time, polluters could harm the environment and put people's health and safety at risk with no obligation to begin cleanup, the DNR argued. A Waukesha County judge and the state appeals court sided with Leather Rich. The DNR appealed, saying the lower court's ruling would neuter the state's "spills law," which was designed to confront pollution. That law, enacted about 50 years ago, requires anyone who causes, possesses or controls a hazardous substance that's been released into the environment to clean it up. "Wisconsin's Spills Law safeguards human health and the environment in real time by directly regulating parties responsible for a hazardous substance discharge," Justice Janet Protasiewicz wrote for the majority. No state law required the DNR to implement a rule before requiring Leather Rich to begin cleaning up the site, she wrote. "The DNR has explicit authority to enforce a threshold for reporting the discharge of hazardous substances," Protasiewicz wrote. The court's four liberal justices were joined by conservative Justice Brian Hagedorn in the majority. Conservative justices Annette Ziegler and Rebecca Bradley dissented. They said the ruling allows bureaucrats to "impose rules and penalties on the governed without advance notice, oversight, or deliberation. In doing so, the majority violates three first principles fundamental to preserving the rule of law — and liberty." Democratic Gov. Tony Evers and environmental advocates hailed the decision. Evers called it "a historic victory for the people of Wisconsin and my administration's fight against PFAS and other harmful contaminants." Rob Lee, attorney for Midwest Environmental Advocates, called the ruling "a victory for the health and wellbeing of the people of Wisconsin" that reinforces "a bedrock environmental and public health protection that has kept Wisconsinites safe from toxic contamination for almost fifty years." But Scott Manley, a vice president at WMC, said the ruling leaves it up to businesses and homeowners to guess about what is hazardous, leaving them subject to "crushing fines and endless, costly litigation." "This ruling blesses a regulatory approach that is fundamentally unfair, unworkable, and impossible to comply with," Manley said. Federal regulators placed the first-ever national standards on PFAS in drinking water last year, but the Trump administration said in May that it planned to weaken those limits. The state has imposed less restrictive limits on PFAS in surface and drinking water, defined as piped water delivered through public systems and noncommunity systems that serve places such as factories, schools and hotels. But it has not implemented PFAS standards for groundwater, the source of drinking water for about two-thirds of Wisconsin residents. The agency stopped efforts to draft them in 2023 after determining that compliance would be too expensive.

Is Florida on the list of states expected to see northern lights on Tuesday night?
Is Florida on the list of states expected to see northern lights on Tuesday night?

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Is Florida on the list of states expected to see northern lights on Tuesday night?

The National Oceanic and Atmospheric Administration (NOAA) upgraded its geomagnetic storm watch for June 25 and 26, and as many as 14 states could catch a glimpse of the northern lights overnight on Tuesday into Wednesday. Unfortunately for Floridians, the Sunshine State isn't on the list. NOAA's Space Weather Prediction Center's latest three-day forecast shows that a hole in the sun's atmosphere will be directed toward Earth, sparking a stream of solar wind toward the pale blue dot. The storm's Kp index is about a five for Tuesday and Wednesday night, indicating that the northern lights will be 'brighter and there will be more auroral activity' for the places that can see them. Parts of the United States encompassing about 14 states will be able to catch a glimpse of aurora borealis: Northern Idaho Iowa Maine Michigan Minnesota Montana New Hampshire New York North Dakota South Dakota Vermont Washington Wisconsin Wyoming Florida and the northern lights aren't exactly well acquainted, but they do cross paths in rare occasions. The northern lights were spotted in Florida twice in 2024: First in May and then again in November, thanks to a pair of powerful solar storms. Though rare, Florida has seen northern lights before 2024. In 1989, the aurora borealis appeared on the First Coast and was visible in a red glow tinged with pale green and white streaks, the Florida Times-Union reported. Northern lights were visible as far as South Florida in 1981, though reports indicate they were much less impressive. Then there was the Carrington Event of 1859 tinting the sky bright red and green, which may have been the most powerful solar flare on record, according to NOAA. Contributors: Cheryl McCloud, Eric Lagatta — USA TODAY NETWORK - Florida This article originally appeared on Pensacola News Journal: Florida not on the list to see northern lights tonight

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