{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Kgoadi K"],"funding":["U.S. Department of Health & Human Services | NIH | National Institute of Allergy and Infectious Diseases (NIAID)"],"pagination":["2397"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC11894076"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["16(1)"],"pubmed_abstract":["People living with HIV (PLWH) have an increased risk for developing tuberculosis after M. tuberculosis infection, despite anti-retroviral therapy (ART). To delineate the underlying mechanisms, we conducted single cell transcriptomics on bronchoalveolar lavage cells from PLWH on ART and HIV uninfected healthy controls infected with M. tuberculosis ex vivo. We identify an M1-like proinflammatory alveolar macrophage subset that sequentially acquires TNF signaling capacity in controls but not in PLWH. Cell-cell communication analyses reveal interactions between M1-like macrophages and effector memory T cells within TNF superfamily, chemokine, and costimulatory networks in the airways of controls. These interaction networks were lacking in PLWH infected with M. tuberculosis, where anti-inflamma"],"journal":["Nature communications"],"pubmed_title":["Alveolar macrophages from persons with HIV mount impaired TNF signaling networks to M. tuberculosis infection."],"pmcid":["PMC11894076"],"funding_grant_id":["R01AI166305","P30AI168386"],"pubmed_authors":["Kgoadi K","Rengarajan J","Ibegbu CC","Dkhar HK","Dawa S","Cribbs SK","Bajpai P","Enriquez AB"],"additional_accession":[]},"is_claimable":false,"name":"Alveolar macrophages from persons with HIV mount impaired TNF signaling networks to M. tuberculosis infection.","description":"People living with HIV (PLWH) have an increased risk for developing tuberculosis after M. tuberculosis infection, despite anti-retroviral therapy (ART). To delineate the underlying mechanisms, we conducted single cell transcriptomics on bronchoalveolar lavage cells from PLWH on ART and HIV uninfected healthy controls infected with M. tuberculosis ex vivo. We identify an M1-like proinflammatory alveolar macrophage subset that sequentially acquires TNF signaling capacity in controls but not in PLWH. Cell-cell communication analyses reveal interactions between M1-like macrophages and effector memory T cells within TNF superfamily, chemokine, and costimulatory networks in the airways of controls. These interaction networks were lacking in PLWH infected with M. tuberculosis, where anti-inflamma","dates":{"release":"2025-01-01T00:00:00Z","publication":"2025 Mar","modification":"2025-04-20T01:49:07.9Z","creation":"2025-04-20T01:49:07.9Z"},"accession":"S-EPMC11894076","cross_references":{"pubmed":["40064940"],"doi":["10.1038/s41467-025-57668-y"]}}