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Shizuo Akira

Researcher at Osaka University

Publications -  1330
Citations -  344469

Shizuo Akira is an academic researcher from Osaka University. The author has contributed to research in topics: Innate immune system & Immune system. The author has an hindex of 261, co-authored 1308 publications receiving 320561 citations. Previous affiliations of Shizuo Akira include University of California, Berkeley & Wakayama Medical University.

Papers
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Journal ArticleDOI

Lipocalin 2 bolsters innate and adaptive immune responses to blood-stage malaria infection by reinforcing host iron metabolism.

TL;DR: It is determined that Lipocalin 2 (Lcn2), a host protein that sequesters iron, is abundantly secreted during human and mouse blood-stage malaria infections and is essential to control P. yoeliiNL parasitemia, anemia, and host survival.
Book ChapterDOI

TIR domain-containing adaptors regulate TLR signaling pathways.

TL;DR: Accumulating evidence clearly demonstrates that Toll-like receptors serve as pattern recognition receptors to detect invading microbes.
Journal ArticleDOI

Increased atherosclerotic lesions and Th17 in interleukin-18 deficient apolipoprotein E-knockout mice fed high-fat diet.

TL;DR: It is suggested that in IL-18 deficiency, cholesterol in HCD synergize mechanistically with homocysteine to accelerate atherosclerosis via the alternative IL-23/Th17 pathway, demonstrating a new role for Th17 in Atherosclerosis.
Journal ArticleDOI

Th2 allergic immune response to inhaled fungal antigens is modulated by TLR-4-independent bacterial products

TL;DR: It is shown that oropharyngeal aspiration of fungal lysates promotes airway eosinophilia, secretion of Th2 cytokines and mucus cell metaplasia, and the immunomodulatory effect that bacterial lysate have on the response to fungi is TLR4 independent but MyD88 dependent.
Journal ArticleDOI

Downregulation of STAT3 activation is required for presumptive rod photoreceptor cells to differentiate in the postnatal retina.

TL;DR: In this paper, it was shown that STAT3 activation, but not SHP2 activation, is responsible for the CNTF/gp130 signaling that inhibits expression of Rhodopsin and its upstream activator, crx, in the retinal explants derived from P0 mice.