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  1. Article ; Online: Transferrin Receptor-Targeted Iduronate-2-sulfatase Penetrates the Blood-Retinal Barrier and Improves Retinopathy in Mucopolysaccharidosis II Mice.

    Imakiire, Atsushi / Morimoto, Hideto / Suzuki, Hidehiko / Masuda, Tomomi / Yoden, Eiji / Inoue, Asuka / Morioka, Hiroki / Konaka, Takashi / Mori, Ayaka / Shirasaka, Ryoji / Kato, Ryo / Hirato, Tohru / Sonoda, Hiroyuki / Minami, Kohtaro

    Molecular pharmaceutics

    2023  Volume 20, Issue 11, Page(s) 5901–5909

    Abstract: Mucopolysaccharidoses (MPSs) make up a group of lysosomal storage diseases characterized by the aberrant accumulation of glycosaminoglycans throughout the body. Patients with MPSs display various signs and symptoms, such as retinopathy, which is also ... ...

    Abstract Mucopolysaccharidoses (MPSs) make up a group of lysosomal storage diseases characterized by the aberrant accumulation of glycosaminoglycans throughout the body. Patients with MPSs display various signs and symptoms, such as retinopathy, which is also observed in patients with MPS II. Unfortunately, retinal disorders in MPS II are resistant to conventional intravenous enzyme-replacement therapy because the blood-retinal barrier (BRB) impedes drug penetration. In this study, we show that a fusion protein, designated pabinafusp alfa, consisting of an antihuman transferrin receptor antibody and iduronate-2-sulfatase (IDS), crosses the BRB and reaches the retina in a murine model of MPS II. We found that retinal function, as assessed by electroretinography (ERG) in MPS II mice, deteriorated with age. Early intervention with repeated intravenous treatment of pabinafusp alfa decreased heparan sulfate deposition in the retina, optic nerve, and visual cortex, thus preserving or even improving the ERG response in MPS II mice. Histological analysis further revealed that pabinafusp alfa mitigated the loss of the photoreceptor layer observed in diseased mice. In contrast, recombinant nonfused IDS failed to reach the retina and hardly affected the retinal disease. These results support the hypothesis that transferrin receptor-targeted IDS can penetrate the BRB, thereby ameliorating retinal dysfunction in MPS II.
    MeSH term(s) Animals ; Mice ; Blood-Retinal Barrier/metabolism ; Glycosaminoglycans ; Iduronate Sulfatase/metabolism ; Iduronate Sulfatase/therapeutic use ; Iduronic Acid ; Mucopolysaccharidosis II/drug therapy ; Mucopolysaccharidosis II/diagnosis ; Receptors, Transferrin ; Retinal Diseases/drug therapy
    Chemical Substances Glycosaminoglycans ; Iduronate Sulfatase (EC 3.1.6.13) ; Iduronic Acid (3402-98-0) ; Receptors, Transferrin ; Ids protein, mouse (EC 3.1.6.13) ; Tfrc protein, mouse
    Language English
    Publishing date 2023-10-20
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2138405-8
    ISSN 1543-8392 ; 1543-8384
    ISSN (online) 1543-8392
    ISSN 1543-8384
    DOI 10.1021/acs.molpharmaceut.3c00736
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: A spinal microglia population involved in remitting and relapsing neuropathic pain.

    Kohno, Keita / Shirasaka, Ryoji / Yoshihara, Kohei / Mikuriya, Satsuki / Tanaka, Kaori / Takanami, Keiko / Inoue, Kazuhide / Sakamoto, Hirotaka / Ohkawa, Yasuyuki / Masuda, Takahiro / Tsuda, Makoto

    Science (New York, N.Y.)

    2022  Volume 376, Issue 6588, Page(s) 86–90

    Abstract: Neuropathic pain is often caused by injury and diseases that affect the somatosensory system. Although pain development has been well studied, pain recovery mechanisms remain largely unknown. Here, we found that CD11c-expressing spinal microglia appear ... ...

    Abstract Neuropathic pain is often caused by injury and diseases that affect the somatosensory system. Although pain development has been well studied, pain recovery mechanisms remain largely unknown. Here, we found that CD11c-expressing spinal microglia appear after the development of behavioral pain hypersensitivity following nerve injury. Nerve-injured mice with spinal CD11c
    MeSH term(s) Animals ; Bacterial Proteins/genetics ; CD11 Antigens/genetics ; CD11 Antigens/metabolism ; Chronic Pain/physiopathology ; Female ; Hyperalgesia/physiopathology ; Luminescent Proteins/genetics ; Male ; Mice ; Mice, Inbred C57BL ; Mice, Transgenic ; Microglia/physiology ; Neuralgia/physiopathology ; Peripheral Nerve Injuries/physiopathology ; Recurrence ; Spinal Cord/physiopathology
    Chemical Substances Bacterial Proteins ; CD11 Antigens ; Itgax protein, mouse ; Luminescent Proteins ; yellow fluorescent protein, Bacteria
    Language English
    Publishing date 2022-03-31
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 128410-1
    ISSN 1095-9203 ; 0036-8075
    ISSN (online) 1095-9203
    ISSN 0036-8075
    DOI 10.1126/science.abf6805
    Database MEDical Literature Analysis and Retrieval System OnLINE

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