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Home » Topics » Disease categories and therapies » Respiratory

Respiratory
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Microscopic view of P. aeruginosa infection of mouse lung
Infection

What stops a bad guy in the lung? A good guy in the lung, of course

Jan. 20, 2023
By Anette Breindl
Researchers at the Barcelona Institute of Science and Technology’s Center for Genomic Regulation (CRG) and Pulmobiotics Ltd. have used one bacterium to fight another. In mouse models, the team used engineered Mycoplasma pneumoniae to treat Pseudomonas aeruginosa, the chief culprit in ventilator-associated pneumonia (VAP).
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Cross-section of a mouse lung infected with P. aeruginosa and treated with engineered M. pneumoniae
Newco news

Pulmobiotics is developing cell therapy for lung diseases, but with a twist

Jan. 19, 2023
By Anette Breindl
Pulmobiotics Ltd., which was founded in 2019, is developing cell therapy for lung diseases, including lung cancer. But unlike other cell therapies for cancer, this one is based not on harnessing T cells but on engineering bacteria. The team has engineered Mycoplasma pneumoniae to deliver various therapeutic proteins to the lung, depending on the therapeutic indication.
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Biomarkers

CMKLR1 PET imaging found tied to experimental acute lung injury

Jan. 19, 2023
Chemokine-like receptor 1 (CMKLR1) is a G protein-coupled receptor for chemerin and resolvin E1 that plays a key role in the recruitment and activation of macrophages, natural killer cells and plasmacytoid dendritic cells in inflammatory diseases.
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3D renderings of RSV
Respiratory

Targeting prefusion state is better bet for RSV vaccines

Jan. 5, 2023
By Mar de Miguel
After comparing the response to the two types of vaccines for the respiratory syncytial virus (RSV) based on its fusion protein (F), prefusion (pre-F) versus postfusion (post-F) vaccines, scientists at the National Institutes of Health (NIH) and Astrazeneca plc have demonstrated that targeting the pre-F protein led to better protection. No more bets on RSV immunization based on the post-F protein of the virus. Laboratories can now bet all on red for the pre-F technology.
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Respiratory

Genentech patents new LATS1 and/or LATS2 inhibitors for ARDS

Jan. 3, 2023
Genentech Inc. has disclosed 2,8-diazaspiro [4.5] decane compounds acting as serine/threonine-protein kinase LATS1 and/or LATS2 inhibitors reported to be useful for the treatment of acute respiratory distress syndrome (ARDS).
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Xenoview in lungs in MRI

Polarean Imaging wins FDA nod for hyperpolarized MRI contrast agent

Dec. 30, 2022
By Meg Bryant
The U.S. FDA has approved Polarean Imaging plc’s drug-device combination product, Xenoview, for use with magnetic resonance imaging (MRI) in evaluating lung ventilation in adults and children aged 12 and older. The hyperpolarized contrast agent, which is prepared from the Xenon Xe 129 gas blend, is expected to be commercially available in the U.S. starting next month.
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Respiratory

Azcuris reports development of TSLP/TSLPR interaction inhibitors

Dec. 29, 2022
Research at Azcuris Co. Ltd. has led to the development of thymic stromal lymphopoietin (TSLP)/cytokine receptor-like factor 2 (CRLF2; TSLPR) interaction inhibitors, which are reported to be useful for the treatment of autoimmune diseases, chronic obstructive pulmonary disease (COPD), allergy, asthma, allergic rhinitis and chronic rhinosinusitis.
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Respiratory

NLRP3 inflammasome inhibitors described in Roche patent

Dec. 29, 2022
F. Hoffmann-La Roche Ltd. and Hoffmann-La Roche Inc. have described NLRP3 inflammasome inhibitors reported to be useful for the treatment of asthma and chronic obstructive pulmonary disease (COPD).
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Colorized scanning electron micrograph of human respiratory syncytial virus.
Infection

Poolbeg's collaboration with Onethree Biotech identifies potential RSV drug candidates

Dec. 22, 2022
Poolbeg Pharma plc has identified potential new drug candidates from its respiratory syncytial virus (RSV) artificial intelligence (AI) program with Onethree Biotech Inc.
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The two phase IIIs of Verona: more positive data prompts NDA talk

Dec. 20, 2022
By Lee Landenberger
After posting positive top-line data in August from its phase III ENHANCE-2 study of ensifentrine for treating chronic obstructive pulmonary disease (COPD), Verona Pharma plc now has positive results from the companion phase III study. The ENHANCE-1 trial of ensifentrine as a COPD maintenance treatment hit its primary and key secondary endpoints, prompting the company to say it plans to submit an NDA for the treatment to the U.S. FDA sometime in the first half of 2023.
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