Endo, Y., Hasegawa, I., Igi, A., Onodera, A., Mita, S., Higashi, K., Kurokawa, K., Toyoda, A., Kiuchi, M., Shinzawa, M., Wang, Y., Koyama-Nasu, R., Hirahara, K., Motohashi, S., Nakayama, T., Kimura, M.Y.: SLAMF6 regulates basal T cell receptor signaling and influences invariant natural killer T cell lineage diversity. Int. Immunol. dxaf030 (2025).
Koyama-Nasu, R., Wang, Y., Miyano, H., Kimura, M. Y.: Differentiation of Cytotoxic CD8+ T Cell Subsets Under Tumor Progression: Can CD69 Be a New Therapeutic Target? Cancer Science. 0:1–8 (2025).
Kobayashi, H., Kimura, M.Y., Hasegawa, I., Suganuma, E., Ikehara, Y., Azuma, K., Ito, T., Ebata, R., Kurashima, Y., Kawasaki, Y., Shiko, Y., Saito, N., Iwase, H., Lee, Y., Noval Rivas, M., Arditi, M., Zuka, M., Hamada, H.*, and Nakayama, T.: Increased Myosin light chain 9 expression during Kawasaki disease vasculitis. Front. Immunol. 13:1036672 (2023).
Koyama-Nasu, R., Kimura, M.Y., Kiuchi, M., Aoki, A., Wang, Y., Mita, Y., Hasegawa, I., Endo, Y., Onodera, A., Hirahara, K., Motohashi, S., Nakayama, T.: CD69 imposes tumor-specific CD8+ T cell fate in tumor-draining lymph nodes. Cancer Immunol. Res. 11(8):1085-1099 (2023).
Koyama-Nasu, R., Wang, Y., Hasegawa, I., Endo, Y., Nakayama, T. and *Kimura, M. Y.: The cellular and molecular basis of CD69 function in anti-tumor immunity. Int. Immunol. dxac024 (2022). *Corresponding author
Yokoyama, M., *Kimura, M.Y., Ito, T., Hayashizaki, K., Endo, Y., Wang, Y., Yagi, R., Nakagawa, T., Kato, N., Matsubara, H. and *Nakayama, T.: Myosin light chain 9/12 regulates the pathogenesis of inflammatory bowel disease. Front. Immunol. 11: 594297 (2021). *Co-corresponding Author
Mita, Y., *Kimura, M.Y., Hayashizaki, K., Koyama-Nasu, R., Ito, T., Motohashi, S., Okamoto, Y. and Nakayama, T.: Crucial role of CD69 in anti-tumor immunity through regulating the exhaustion of tumor-infiltrating T cells. Int. Immunol. dxy050 (2018). *Corresponding author, Awarded the “Outstanding Merit Award 2018” by the Editor-in-Chief and Editorial Board of International Immunology.
*Kimura, M.Y., Igi, A., Hayashizaki, K., Mita, Y., Shinzawa, M., Kadakia, T., Endo, Y., Ogawa, S., Yagi, R., Motohashi, S., Singer, A., and Nakayama, T.: CD69 prevents PLZFhi innate precursors from prematurely exiting the thymus and aborting NKT2 cell differentiation. Nat. Commun. 9: 3749 (2018). *Corresponding author
#Hayashizaki, K., #Kimura, M.Y., #Tokoyoda. K., Hosokawa, H., Shinoda, K., Hirahara, K., Ichikawa, T., Onodera, A., Hanazawa, A., Iwamura, C., Kakuta, J., Muramoto, K., Motohashi, S., Tumes, D.J., Iinuma, T., Yamamoto, H., Ikehara, Y., Okamoto, Y. and *Nakayama, T.: Myosin light chain 9 and 12 are functional ligands for CD69 that regulate airway inflammation. Sci Immunol. 1:eaaf9154 (2016). #Co-first Author
*Kimura, M.Y., Thomas, J., Tai, X., Cuinter, T.I., Shinzawa, M., Etzensperger, R., Li, Z., Love, P., Nakayama, T. and *Singer, A.: Timing and duration of MHC I positive selection signals are adjusted in the thymus to prevent lineage errors. Nat. Immunol, 17:1415-23 (2016). *Co-corresponding author
Luckey M., Kimura M.Y., Waickman AT., Feigenbaum L., Singer A and *Park JH.: The transcription factor ThPOK suppresses Runx3 and imposes CD4 lineage fate by inducing Suppressors Of Cytokine Signaling, Nat. Immunol, 15(7):638-45 (2014).
Kimura, M.Y., Pobezinsky, L.A., Guinter, T.I., Thomas, J., Adams, A., Park, J.H., Tai, X. and *Singer, A.; IL-7 signaling must be intermittent, not continuous, during CD8+ T cell homeostasis to promote cell survival instead of cell death. Nat. Immunol. 14:143-151 (2013).
Kimura, M.Y., Iwamura, C., Suzuki, A., Miki, T., Hasegawa, A., Sugaya, K., Yamashita, M., Ishii, S. and *Nakayama, T.: Schnurri-2 controls memory Th1 and Th2 cell numbers in vivo. J. Immunol. 178:4926-4936 (2007).
Iwamura, C., Kimura, M.Y., Shinoda, K., Endo, Y., Hasegawa, A., Yamashita, M. and *Nakayama, T.: Schnurri-2 regulates Th2-dependent airway inflammation and airway hyperresponsiveness. Int. Immunol. 19:755-762 (2007).
Kimura, M.Y., Hosokawa, H., Yamashita, M., Hasegawa, A., Iwamura, C., Watarai, H., Taniguchi, M., Takagi, T., Ishii, S. and *Nakayama, T.: Regulation of Th2 cell differentiation by murine Schnurri-2. J. Exp. Med. 201:397-408 (2005).
Kimura, M., Koseki, Y., Yamashita, M., Watanabe, N., Shimizu, C., Katsumoto, T., Taniguchi M., Koseki, H. and *Nakayama, T.: Regulation of Th2 cell differentiation by mel-18, a mammalian polycomb group gene. Immunity. 15:275-287 (2001).
Kimura, M., Yamashita, M., Kubo, M., Iwashima, M., Shimizu, C., Chiba, J., Taniguchi, M., Katsumata, M. and *Nakayama, T.: Impaired Ca/calcineurin pathway in in vivo anergized CD4 T cells. Int. Immunol. 12:817-824 (2000).
2025年
Kadariswantiningsih, I.N., Okunaga, I., Yamasaki, K., Empitu, M. A., Yamada, H., Makino, S., Hotta, A., Yagita, H., Aizawa, M., Koyama-Nasu, R., Kimura, M.Y., Tatsumoto, N., Asanuma, K.: CCL5 paradoxically regulates glomerular injury by skewing macrophage polarization. JCI Insight. e173742 (2025).
Ozaki , K., Aoki, T., Kobayashi, M., Takami, M., Kobayashi , M., Ito, T., Ogawa, K., Tanaka, H., Nishii, K., Nishimura, K., Motoyoshi, K., Kojima, I., Katsumi, D., Shimizu, D., Wang, H., Kimura, M. Y., Hirahara, K., Koseki, H., Higuchi, Y., Motohashi, S.: Anti-tumor effect of intratumoral administration of induced pluripotent stem cell-derived NKT cells on glioblastoma through CD155/DNAM-1 interaction. Stem Cells Transl Med. 14(9): szaf036 (2025).
Endo, Y., Hasegawa, I., Igi, A., Onodera, A., Mita, S., Higashi, K., Kurokawa, K., Toyoda, A., Kiuchi, M., Shinzawa, M., Wang, Y., Koyama-Nasu, R., Hirahara, K., Motohashi, S., Nakayama, T., Kimura, M.Y.: SLAMF6 regulates basal T cell receptor signaling and influences invariant natural killer T cell lineage diversity. Int. Immunol. dxaf030 (2025).
Koyama-Nasu, R., Wang, Y., Miyano, H., Kimura, M. Y.: Differentiation of Cytotoxic CD8+ T Cell Subsets Under Tumor Progression: Can CD69 Be a New Therapeutic Target? Cancer Science. 0:1–8 (2025).
2024年
Aoki, A., Iwamura, C., Kiuchi, M., Tsuji, K., Sasaki, A., Hishiya, T., Hirasawa, R., Kokubo, K., Kuriyama, Sachiko., Onodera, A., Shimada, T., Nagaoka, T., Ishikawa, S., Kojima, A., Mito, H., Hase, R., Kasahara, Y., Kuriyama, N., Nakamura, S., Urushibara, T., Kaneda, S., Sakao, S., Nishida, O., Takahashi, K., Kimura, M.Y., Motohashi, S., Igari, H., Ikehara, Y., Nakajima, H., Suzuki, T., Hanaoka, H., Nakada, T., Kikuchi, T., Nakayama, T., Yokote, K, Hirahara, K.: Suppression of Type I Interferon Signaling in Myeloid Cells by Autoantibodies in Severe COVID-19 Patients. J Clin Immunol. 44(4):104 (2024).
Ahmad, I., Omura, S., Sato, F., Park, A.M., Khadka, S., Gavins F.N.E., Tanaka, H., Kimura, M.Y., Tsunoda, I.: Exploring the Role of Platelets in Virus-Induced Inflammatory Demyelinating Disease and Myocarditis. Int. J. Mol. Sci. 25(6): 3460 (2024).
Onodera, A., Kokubo. K., Okano, M., Onoue, M. Kiuchi, M., Iwamura, C.,Iinuma, T., Kimura,M.Y., Ebihara, N., Hanazawa, T., Nakayama, T., Hirahara, K.: Pathogenic helper T cells as the novel therapeutic targets for immune-mediated intractable diseases. Pharmacol Ther. 247:108445 (2023).
Koyama-Nasu, R., Kimura, M.Y., Kiuchi, M., Aoki, A., Wang, Y., Mita, Y., Hasegawa, I., Endo, Y., Onodera, A., Hirahara, K., Motohashi, S., Nakayama, T.: CD69 imposes tumor-specific CD8+ T cell fate in tumor-draining lymph nodes. Cancer Immunol. Res. 11(8):1085-1099(2023).
Kobayashi, H., Kimura, M.Y., Hasegawa, I., Suganuma, E., Ikehara, Y., Azuma, K., Ito, T., Ebata, R., Kurashima, Y., Kawasaki, Y., Shiko, Y., Saito, N., Iwase, H., Lee, Y., Noval Rivas, M., Arditi, M., Zuka, M., Hamada, H.*, and Nakayama, T.: Increased Myosin light chain 9 expression during Kawasaki disease vasculitis. Front. Immunol. 13:1036672(2023).
2022年
Koyama-Nasu, R., Wang, Y., Hasegawa, I., Endo, Y., Nakayama, T. and Kimura, M. Y.: The cellular and molecular basis of CD69 function in anti-tumor immunity. Int. Immunol.: dxac024(2022).
2021年
Nakayama T, Hirahara K, Kimura MY, Iwamura C, Kiuchi M, Kokubo K, Onodera A, Hashimoto K, Motohashi S.: CD4+ T cells in inflammatory diseases: pathogenic T- helper cells and the CD69–Myl9 system. Int. Immunol. 33(12):699-704(2021).
Sarkar MH, Yagi R, Endo Y, Koyama-Nasu R, Wang Y, Hasegawa I, Ito T, Junttila IS, Zhu J, Kimura MY, Nakayama T.:IFNγ suppresses the expression of GFI1 and thereby inhibits Th2 cell proliferation. PLoS ONE 16(11): e0260204(2021).
Yokoyama, M., Kimura, M.Y., Ito, T., Hayashizaki, K., Endo, Y., Wang, Y., Yagi, R., Nakagawa, T., Kato, N., Matsubara, H. and Nakayama, T.: Myosin light chain 9/12 regulates the pathogenesis of inflammatory bowel disease. Front. Immunol. 11: 594297(2021).
2020年
Suzuki, A.S., Yagi, R., Kimura, M.Y., Iwamura, C., Shinoda, K., Onodera, A., Hirahara, K., Tumes, D.J., Koyama-Nasu, R., Lismaa, S.E., Graham, R.M., Motohashi, S. and Nakayama, T.: Essential role for CD30-Transglutaminase 2 axis in memory Th1 and Th17 cell generation. Front. Immunol. 11:1536(2020).
Aoki, T., Takami, M., Takatani, T., Motoyoshi, K., Ishii, A., Hara, A., Toyoda, T., Okada, R., Hino, M., Koyama-Nasu, R., Kiuchi, M., Hirahara, K., Kimura, M.Y., Nakayama, T., Shimojo, N., and Motohashi, S.: Activated invariant natural killer T cells directly recognize leukemia cells in a CD1d-independent manner. Cancer Sci. 111(7):2223-2233(2020).
Angelou, C.C., Wells, A.C., Vijayaraghavan, J., Dougan, C.E., Lawlor, R., Iverson, E., Lazarevic, V., Kimura, M.Y., Peyton, S.R., Minter, L.M., Osborne, B.A., Pobezinskaya, E.L., *Pobezinsky, L.A.: Differentiation of Pathogenic Th17 Cells is Negatively Regulated by Let-7 MicroRNAs in a Mouse Model of Multiple Sclerosis. Front. Immunol. 17;10:3125(2020).
〜2019年
Tumes, D., Hirahara, K., Papadopoulos, M., Shinoda, K., Onodera, A., Kumagai, J., Ho Yip, K., Pant, H., Kokubo, K., Kiuchi, M., Aoki, A., Obata-Ninomiya, K., Tokoyoda, K., Endo, Y., Kimura, M.Y. and *Nakayama, T.: Ezh2 controls development of natural killer T cells that cause spontaneous asthma-like pathology. J. Allergy Clin. Immunol.144(2):549-560.e10(2019).
Pobezinskaya, E.L., Wells, A.C., Angelou, C.C., Fagerberg, E., Aral, E., Iverson, E., Kimura, M.Y. and Pobezinsky, L.A.: Survival of naïve T cells requires the expression of let-7 miRNAs. Front. Immunol. 3;10:955(2019).
Kimura, M.Y., Koyama-Nasu, R., Yagi, R. and Nakayama, T.: A new therapeutic target: the CD69-Myl9 system in immune responses. Semin. Immunopathol. 41(3):349-358(2019).
Mita, Y., Kimura, M.Y., Hayashizaki, K., Koyama-Nasu, R., Ito, T., Motohashi, S., Okamoto, Y. and Nakayama, T.: Crucial role of CD69 in anti-tumor immunity through regulating the exhaustion of tumor-infiltrating T cells. Int. Immunol. dxy050(2018).
Kimura, M.Y., Igi, A., Hayashizaki, K., Mita, Y., Shinzawa, M., Kadakia, T., Endo, Y., Ogawa, S., Yagi, R., Motohashi, S., Singer, A., and Nakayama, T.: CD69 prevents PLZFhi innate precursors from prematurely exiting the thymus and aborting NKT2 cell differentiation. Nat. Commun. 9: 3749(2018).
Kimura, M.Y., Hayashizaki, K., Tokoyoda, K., Takamura, S., Motohashi, S. and Nakayama, T.: Crucial role for CD69 in allergic inflammatory responses. Immunol. Rev. 278:87-100(2017).
Hayashizaki, K., Kimura, M.Y., Tokoyoda. K., Hosokawa, H., Shinoda, K., Hirahara, K., Ichikawa, T., Onodera, A., Hanazawa, A., Iwamura, C., Kakuta, J., Muramoto, K., Motohashi, S., Tumes, D.J., Iinuma, T., Yamamoto, H., Ikehara, Y., Okamoto, Y. and Nakayama, T.: Myosin light chain 9 and 12 are functional ligands for CD69 that regulate airway inflammation. Sci Immunol. 1:eaaf9154(2016).
Kimura, M.Y., Thomas, J., Tai, X., Cuinter, T.I., Shinzawa, M., Etzensperger, R., Li, Z., Love, P., Nakayama, T. and Singer, A.: Timing and duration of MHC I positive selection signals are adjusted in the thymus to prevent lineage errors. Nat. Immunol, 17:1415-23(2016).
Luckey M., Kimura M.Y., Waickman AT., Feigenbaum L., Singer A and Park JH.: The transcription factor ThPOK suppresses Runx3 and imposes CD4 lineage fate by inducing Suppressors Of Cytokine Signaling, Nat. Immunol, 15(7):638-45(2014).
Kimura, M.Y., Pobezinsky, L.A., Guinter, T.I., Thomas, J., Adams, A., Park, J.H., Tai, X. and Singer, A.; IL-7 signaling must be intermittent, not continuous, during CD8+ T cell homeostasis to promote cell survival instead of cell death. Nat. Immunol. 14:143-151(2013).