SELECTED PUBLICATIONS
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Tatsumi N, Kumamoto Y. Role of mouse dendritic cell subsets in priming naive CD4 T cells. Curr Opin Immunol. 2023; 83:102352, DOI: 10.1016/j.coi.2023.102352, Review article
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Tatsumi N, Davila-Pagan A, Kumamoto Y. Protocol to quantify and characterize contact between T cells and antigen-presenting cells in the antigen-draining lymph nodes of mice using flow cytometry. STAR Protoc. 2022 Dec 16;3(4):101845. doi: 10.1016/j.xpro.2022.101845.
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Tatsumi N, Cogrington AL, El-Fenej J, Phondge V, Kumamoto Y. Effective CD4 T cell priming requires repertoire scanning by CD301b+ migratory cDC2 cells upon lymph node entry. Sci Immunol. 2021 Dec 10; DOI: 10.1126/sciimmunol.abg0336
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Shin H, Kumamoto Y, Gopinath S, Iwasaki A. CD301b+ dendritic cells stimulate tissue-resident memory CD8+ T cells to protect against genital HSV-2. Nature Commun 2016; 7:13346
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Kumamoto Y, Hirai T, Wong PW, Kaplan DH, Iwasaki A. CD301b+ dendritic cells suppress T follicular helper cells and antibody responses to protein antigens. eLife 2016; 5:e17979
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Kumamoto Y, Camporez JPG, Jurczak MJ, Shanabrough M, Horvath T, Shulman GI, Iwasaki A. CD301b+ mononuclear phagocytes maintain positive energy balance through secretion of resistin-like molecule alpha. Immunity 2016; 45:583-596
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Shook B, Xiao E, Kumamoto Y, Iwasaki A, Horsley V. CD301b+ macrophages are essential for effective skin wound healing. J Invest Dermatol 2016; 136:1885-1891
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Kumamoto Y, Linehan M, Weinstein JS, Laidlaw BJ, Craft JE, Iwasaki A. CD301b+ dermal dendritic cells drive T helper 2 cell-mediated immunity. Immunity 2013; 39:733-743
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Kumamoto Y, Iwasaki A. Unique features of antiviral immune system of the vaginal mucosa. Curr Opin Immunol 2012; 24:411-416 , Review article
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Kumamoto Y*, Mattei LM*, Sellers S, Payne GW, Iwasaki A. CD4+ T cells support cytotoxic T lymphocyte priming by controlling lymph node input. Proc Natl Acad Sci USA 2011; 108:8749-8754 (*equal contribution)
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Kumamoto Y, Denda-Nagai K, Aida S, Higashi N, Irimura T. MGL2+ dermal dendritic cells are sufficient to initiate contact hypersensitivity in vivo. PLoS One 2009; 4:e5619