
Articles
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3 weeks ago |
nature.com | Laurie A. Dempsey
Tissues such as the skin, lungs and gut are constantly exposed to diverse microbial communities and must maintain tight barriers to prevent infection of underlying tissues. In Nature, Vicanolo et al. identify a unique subset of tissue-resident neutrophils found in barrier tissues that are capable of synthesizing extracellular matrix (ECM) components, such as collagen and fibronectin, that contribute to barrier formation.
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1 month ago |
nature.com | Laurie A. Dempsey
Hematopoietic stem cell transplantation (HSCT) offers potentially curative therapies for patients with in-borne hematopoietic disorders or those undergoing treatments for hematological malignancies. However, notable morbidity or mortality can occur in patients receiving HSCT, owing to graft-versus-host disease (GVHD). In Science Translational Medicine, Omdahl et al.
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2 months ago |
nature.com | Laurie A. Dempsey
Circulating naive lymphocytes are recruited from the blood to homeostatic lymph nodes (LNs) by the chemokines CCL19 and CCL21, which are ligands for the CCR7 receptor. However, upon infection and inflammation, reactive LNs undergo structural changes and alter their gene expression to facilitate lymphocyte activation. In Cell, Chen et al. examine how inflammation alters the chemotactic signals for LN recruitment of naive lymphocytes.
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Oct 28, 2024 |
nature.com | Laurie A. Dempsey
X chromosome inactivation (XCI) occurs in female mammals to normalize gene expression of sex chromosomes. This process is known to involve cis-mediated interactions by the long-noncoding RNA Xist on the inactive X (Xi) chromosome. This process is often incomplete with some genes that escape XCI (such as Xist) and many immune-relevant genes are expressed on the X chromosome, which might contribute to sex biases in autoimmune diseases and immune responses. In Science Immunology, Forsyth et al.
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Sep 4, 2024 |
nature.com | Laurie A. Dempsey
Protease allergens, such as papain or found in extracts of mosquito saliva or fire ants, induce an itch response. How skin-resident innate immune cells influence this cutaneous sensory neuron response is unclear. In Nature, Flayer et al. identify a distinct IL-3-expressing γδ T cell subset (termed GD3) that resides in the skin epidermis and interacts with PEP1 neurons to enhance itch responses and subsequent TH2 allergic immune responses to protease allergens.
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