J
Jacob E. Kohlmeier
Researcher at Emory University
Publications - 31
Citations - 1924
Jacob E. Kohlmeier is an academic researcher from Emory University. The author has contributed to research in topics: Cytotoxic T cell & Population. The author has an hindex of 21, co-authored 31 publications receiving 1361 citations.
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Journal ArticleDOI
Type I and Type III Interferons Restrict SARS-CoV-2 Infection of Human Airway Epithelial Cultures.
Abigail Vanderheiden,Philipp Ralfs,Philipp Ralfs,Tatiana Chirkova,Amit A. Upadhyay,Amit A. Upadhyay,Matthew G. Zimmerman,Shamika Bedoya,Hadj S. Aoued,Hadj S. Aoued,Gregory M. Tharp,Gregory M. Tharp,Kathryn L. Pellegrini,Kathryn L. Pellegrini,Candela Manfredi,Eric J. Sorscher,Bernardo A. Mainou,Jenna L. Lobby,Jacob E. Kohlmeier,Anice C. Lowen,Pei Yong Shi,Vineet D. Menachery,Larry J. Anderson,Arash Grakoui,Steven E. Bosinger,Steven E. Bosinger,Mehul S. Suthar +26 more
TL;DR: The studies demonstrate the utility of pHAE cultures to model SARS-CoV-2 infection and that both type I and III IFNs can serve as therapeutic options to treat COVID-19 patients.
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Airway-Resident Memory CD8 T Cells Provide Antigen-Specific Protection against Respiratory Virus Challenge through Rapid IFN-γ Production.
TL;DR: Direct evidence of airway CD8 TRM cell–mediated protection demonstrates the importance of these cells as a first line of defense for optimal immunity against respiratory pathogens and suggests they should be considered in the development of future cell-mediated vaccines.
Journal ArticleDOI
CXCR6 regulates localization of tissue-resident memory CD8 T cells to the airways
Alexander N. Wein,Sean R. McMaster,Shiki Takamura,Paul Dunbar,Emily K. Cartwright,Sarah L. Hayward,Daniel T. McManus,Takeshi Shimaoka,Satoshi Ueha,Tatsuya Tsukui,Tomoko Masumoto,Makoto Kurachi,Kouji Matsushima,Jacob E. Kohlmeier +13 more
TL;DR: This work shows that the CXCR6/CXCL16 axis governs the partitioning of TRM cells to different compartments of the lung and maintains the airway TRM cell pool.
Journal ArticleDOI
Specific niches for lung-resident memory CD8+ T cells at the site of tissue regeneration enable CD69-independent maintenance.
Shiki Takamura,Hideki Yagi,Yoshiyuki Hakata,Chihiro Motozono,Sean R. McMaster,Tomoko Masumoto,Makoto Fujisawa,Tomomi Chikaishi,Junko Komeda,Jun Itoh,Miki Umemura,Ami Kyusai,Michio Tomura,Toshinori Nakayama,David L. Woodland,Jacob E. Kohlmeier,Masaaki Miyazawa +16 more
TL;DR: It is shown that most lung CD8+ TRM cells are not maintained in the inducible bronchus-associated lymphoid tissue (iBALT) but are maintained in specific niches created at the site of tissue regeneration, which are termed as repair-associated memory depots (RAMDs).
Journal ArticleDOI
Antigen-Specific Memory Regulatory CD4+Foxp3+ T Cells Control Memory Responses to Influenza Virus Infection
Erik L. Brincks,Alan D. Roberts,Tres Cookenham,Stewart Sell,Stewart Sell,Jacob E. Kohlmeier,Marcia A. Blackman,David L. Woodland +7 more
TL;DR: The existence of a previously undescribed population of Ag-specific memory Tregs that shape the cellular immune response to secondary influenza virus challenges are demonstrated and offer an additional parameter to consider when determining the efficacy of vaccinations.