scispace - formally typeset
K

Ken-ichi Isobe

Researcher at Nagoya University

Publications -  294
Citations -  18597

Ken-ichi Isobe is an academic researcher from Nagoya University. The author has contributed to research in topics: Antigen & Cytotoxic T cell. The author has an hindex of 48, co-authored 293 publications receiving 16715 citations. Previous affiliations of Ken-ichi Isobe include Nagoya Women's University & Shubun University.

Papers
More filters
Journal ArticleDOI

Immunological aspects of age-related diseases.

TL;DR: The proportion of elderly people rises in the developed countries and the increased susceptibility of the elderly to infectious diseases is caused by immune dysfunction, especially T cell functional decline, which is divided into two categories: an aging of immune cell itself and involvement of immune cells to age-related pathological changes.
Journal ArticleDOI

GADD34 induces p21 expression and cellular senescence.

TL;DR: It is found that transduction of 7EJ-Ras cells with a retroviral vector expressing GADD34 suppressed their proliferation, and that it suppresses cellular proliferation through the induction of cellular senescence.
Journal Article

Development of host-dependent high-grade tumor-specific immunity through a novel mechanism triggered by the Lyt-2+ tumor-specific T cell clone (K7L) that induces temporal growth of L1210 leukemia-K7L-variant.

TL;DR: In this article, the authors showed that the L1210-specific Lyt-2+ T cell clone, K7L, was insensitive to the antitumor activity of K7l and this property of tumor clones was stable after repeated in vitro passage, and definite tumor (L1210)-specific cytotoxic T lymphocyte (CTL) activity was developed by antigen restimulation in the culture of spleen cells from these mice.
Book ChapterDOI

Aging in the mouse and perspectives of rejuvenation through induced pluripotent stem cells (iPSCs).

TL;DR: The authors' aged iPSCs made teratomas when injected into the back skin of syngeneic mice, and differentiated to tissue cells of three germ lines in vitro, and showed strong alkaline phosphatase (AP) activity.

Characterization of antibody responses of local lymph nodes to antigen given under the oral submucosa

TL;DR: It is suggested that the oral mucosal tissue including MLN acts like Peyer's patches in GALT for IgA synthesis, which might in part explain the reason why MLN and ILN display distinct modes of response and sensitivity to the action of LPS.