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FullText URL fulltext20220630-11.pdf Tables20220630-11.pdf SI20220630-11.pdf
Author Uchida, Tetsuya| Nishioka, Ryohei| Yanai, Risa|
Keywords cellulose nanocrystals composite dispersibility mechanical properties surface treatment
Note This is the peer reviewed version of the following article: [Uchida, T, Nishioka, R, Yanai, R. Preparation of cellulose nanocrystals coated with polymer crystals and their application in composite films. Polym Adv Technol. 2022; 1- 8.], which has been published in final form at [https://doi.org/10.1002/pat.5705]. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions. This article may not be enhanced, enriched or otherwise transformed into a derivative work, without express permission from Wiley or by statutory rights under applicable legislation. Copyright notices must not be removed, obscured or modified. The article must be linked to Wiley’s version of record on Wiley Online Library and any embedding, framing or otherwise making available the article or pages there of by third parties from platforms, services and websites other than Wiley Online Library must be prohibited.
This fulltext is available in April 2023.|
Published Date 2022-04-26
Publication Title Polymers for Advanced Technologies
Volume volume33
Issue issue8
Publisher Wiley
Start Page 2511
End Page 2518
ISSN 1042-7147
NCID AA10838191
Content Type Journal Article
language English
OAI-PMH Set 岡山大学
Copyright Holders © 2022 John Wiley & Sons Ltd.
File Version author
DOI 10.1002/pat.5705
Web of Science KeyUT 000787505800001
Related Url isVersionOf https://doi.org/10.1002/pat.5705
FullText URL fulltext20220630-10.pdf
Author Sumi, Nanako| Nagahiro, Shota| Nakata, Eiji| Watanabe, Kazunori| Ohtsuki, Takashi|
Keywords Ultrasound Sonosensitizer Rose Bengal RNAi RNA delivery
Note © 2022 Elsevier Ltd. This manuscript version is made available under the CC-BY-NC-ND 4.0 License. http://creativecommons.org/licenses/by-nc-nd/4.0/. This is the accepted manuscript version. The formal published version is available at https://doi.org/10.1016/j.bmcl.2022.128767.
This fulltext is available in May 2024. |
Published Date 2022-07
Publication Title Bioorganic & Medicinal Chemistry Letters
Volume volume68
Publisher Elsevier BV
Start Page 128767
ISSN 0960-894X
NCID AA1079577X
Content Type Journal Article
language English
OAI-PMH Set 岡山大学
Copyright Holders © 2022 Elsevier Ltd.
File Version author
PubMed ID 35513220
DOI 10.1016/j.bmcl.2022.128767
Web of Science KeyUT 000800009100005
Related Url isVersionOf https://doi.org/10.1016/j.bmcl.2022.128767
FullText URL fulltext20220630-9.pdf
Author Naito, Hiromichi| Nojima, Tsuyoshi| Yorifuji, Takashi| Fujisaki, Noritomo| Nakao, Atsunori|
Keywords Post cardiac arrest syndrome Hypoxic ischemic brain injury Cardiopulmonary resuscitation Prognosis
Published Date 2022-8
Publication Title The American Journal of Emergency Medicine
Volume volume58
Publisher Elsevier BV
Start Page 27
End Page 32
ISSN 0735-6757
NCID AA10642870
Content Type Journal Article
language English
OAI-PMH Set 岡山大学
Copyright Holders © 2022 The Authors.
File Version publisher
PubMed ID 35623180
DOI 10.1016/j.ajem.2022.05.017
Web of Science KeyUT 000808614800006
FullText URL fulltext20220630-8.pdf
Author Nishimura, Takeshi| Nojima, Tsuyoshi| Naito, Hiromichi| Ishihara, Satoshi| Nakayama, Shinichi| Nakao, Atsunori|
Keywords JTDB Prehospital Emergency life-saving technician Trauma
Published Date 2022-06
Publication Title The American Journal of Emergency Medicine
Volume volume56
Publisher Elsevier BV
Start Page 218
End Page 222
ISSN 0735-6757
Content Type Journal Article
language English
OAI-PMH Set 岡山大学
Copyright Holders © 2022 The Authors.
File Version publisher
PubMed ID 35447563
DOI 10.1016/j.ajem.2022.04.004
Web of Science KeyUT 000799775900035
Related Url isVersionOf https://doi.org/10.1016/j.ajem.2022.04.004
FullText URL fulltext20220630-1.pdf
Author Udono, Heiichiro| Nishida, Mikako|
Keywords Mitochondrial ROS Oxidative stress Apoptosis Ageing Nrf2
Note © 2022 Elsevier B.V. This manuscript version is made available under the CC-BY-NC-ND 4.0 License. http://creativecommons.org/licenses/by-nc-nd/4.0/. This is the accepted manuscript version. The formal published version is available at [https://doi.org/10.1016/j.bbagen.2022.130171] .
This fulltext is available in Aug. 2023.|
Published Date 2022-08
Publication Title Biochimica et Biophysica Acta (BBA) - General Subjects
Volume volume1866
Issue issue8
Publisher Elsevier BV
Start Page 130171
ISSN 0304-4165
NCID AA00564679
Content Type Journal Article
language English
OAI-PMH Set 岡山大学
Copyright Holders © 2022 Elsevier B.V.
File Version author
PubMed ID 35588955
DOI 10.1016/j.bbagen.2022.130171
Web of Science KeyUT 000806942900004
Related Url isVersionOf https://doi.org/10.1016/j.bbagen.2022.130171
FullText URL fulltext20220630-7.pdf figure20220630-7.pdf
Author Nagasaki, Joji| Togashi, Yosuke|
Keywords CD4(+) T cell cytotoxic CD4(+ )T cell regulatory T cell T-cell exhaustion
Note This is a pre-copyedited, author-produced version of an article accepted for publication in [International Immunology] following peer review. The version of record [Joji Nagasaki, Yosuke Togashi, A variety of ‘exhausted’ T cells in the tumor microenvironment, International Immunology, Volume 34, Issue 11, November 2022, Pages 563–570, https://doi.org/10.1093/intimm/dxac013] is available online at: [https://doi.org/10.1093/intimm/dxac013]
This fulltext is available in April 2023.|
Published Date 2022-4-23
Publication Title International Immunology
Volume volume34
Issue issue11
Publisher Oxford University Press
Start Page 563
End Page 570
ISSN 1460-2377
Content Type Journal Article
language English
OAI-PMH Set 岡山大学
Copyright Holders © The Author(s) 2022.
File Version author
PubMed ID 35460561
DOI 10.1093/intimm/dxac013
Web of Science KeyUT 000805278200001
Related Url isVersionOf https://doi.org/10.1093/intimm/dxac013
FullText URL fulltext20220630-6.pdf
Author Tsunata, Ren| Takemoto, Masatsugu| Ogasawara, Satoshi| Saito, Tatsuya| Ueno, Tomoyuki|
Note © 2022 IEEE. Personal use of this material is permitted. Permission from IEEE must be obtained for all other uses, in any current or future media, including reprinting/republishing this material for advertising or promotional purposes, creating new collective works, for resale or redistribution to servers or lists, or reuse of any copyrighted component of this work in other works. |
Published Date 2022-5
Publication Title IEEE Transactions on Industry Applications
Volume volume58
Issue issue3
Publisher Institute of Electrical and Electronics Engineers (IEEE)
Start Page 3470
End Page 3485
ISSN 0093-9994
NCID AA00667900
Content Type Journal Article
language English
OAI-PMH Set 岡山大学
Copyright Holders Copyright © 2022, IEEE
File Version author
DOI 10.1109/tia.2022.3154336
Web of Science KeyUT 000799279300052
Related Url isVersionOf https://doi.org/10.1109/tia.2022.3154336
FullText URL fulltext20220630-5.pdf figure20220630-5.pdf
Author Okazaki, Yuki| Furumatsu, Takayuki| Kodama, Yuya| Hiranaka, Takaaki| Kintaka, Keisuke| Kamatsuki, Yusuke| Ozaki, Toshifumi|
Keywords Anterior cruciate ligament Coronal inclination Knee kinematics Magnetic resonance imaging Medial meniscus Posterior root tear
Note This version of the article has been accepted for publication, after peer review (when applicable) and is subject to Springer Nature’s AM terms of use, but is not the Version of Record and does not reflect post-acceptance improvements, or any corrections. The Version of Record is available online at: http://dx.doi.org/10.1007/s00590-022-03285-0
This fulltext is available in May 2023.|
Published Date 2022-05-20
Publication Title European Journal of Orthopaedic Surgery and Traumatology
Volume volume33
Issue issue4
Publisher Springer Science and Business Media LLC
Start Page 1255
End Page 1262
ISSN 1432-1068
NCID AA11622799
Content Type Journal Article
language English
OAI-PMH Set 岡山大学
Copyright Holders © The Author(s), under exclusive licence to Springer-Verlag France SAS, part of Springer Nature 2022
File Version author
PubMed ID 35593940
DOI 10.1007/s00590-022-03285-0
Web of Science KeyUT 000800795900002
Related Url isVersionOf https://doi.org/10.1007/s00590-022-03285-0
FullText URL fulltext20220630-4.pdf
Author Kato, Kosaku| Uemura, Yohei| Asakura, Kiyotaka| Yamakata, Akira|
Note This document is the Accepted Manuscript version of a Published Work that appeared in final form in The Journal of Physical Chemistry C, copyright © 2022 American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see https://doi.org/10.1021/acs.jpcc.2c01662
This fulltext is available in May 2023.|
Published Date 2022-05-25
Publication Title The Journal of Physical Chemistry C
Volume volume126
Issue issue22
Publisher American Chemical Society
Start Page 9257
End Page 9263
ISSN 1932-7447
NCID AA1217589X
Content Type Journal Article
language English
OAI-PMH Set 岡山大学
Copyright Holders © 2022 American Chemical Society
File Version author
DOI 10.1021/acs.jpcc.2c01662
Web of Science KeyUT 000810253900001
Related Url isVersionOf https://doi.org/10.1021/acs.jpcc.2c01662
FullText URL fulltext20220630-3.pdf
Author Maki, Yuta| Kawata, Kazuki| Liu, Yanbo| Goo, Kang‐Ying| Okamoto, Ryo| Kajihara, Yasuhiro| Satoh, Ayano|
Keywords glycoprotein N-glycan cholera toxin native chemical ligation live imaging
Note This is the peer reviewed version of the following article: [Y. Maki, K. Kawata, Y. Liu, K.-Y. Goo, R. Okamoto, Y. Kajihara, A. Satoh, Chem. Eur. J. 2022, 28, e202201253], which has been published in final form at [https://doi.org/10.1002/chem.202201253]. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions. This article may not be enhanced, enriched or otherwise transformed into a derivative work, without express permission from Wiley or by statutory rights under applicable legislation. Copyright notices must not be removed, obscured or modified. The article must be linked to Wiley’s version of record on Wiley Online Library and any embedding, framing or otherwise making available the article or pages there of by third parties from platforms, services and websites other than Wiley Online Library must be prohibited.
This fulltext is available in May 2023.|
Published Date 2022-05-23
Publication Title Chemistry - A European Journal
Volume volume28
Issue issue37
Publisher Wiley
Start Page e202201253
ISSN 0947-6539
NCID AA11076269
Content Type Journal Article
language English
OAI-PMH Set 岡山大学
Copyright Holders © 2022 Wiley-VCH GmbH
File Version author
PubMed ID 35604098
DOI 10.1002/chem.202201253
Web of Science KeyUT 000798823300001
Related Url isVersionOf https://doi.org/10.1002/chem.202201253
FullText URL fulltext20220620-4.pdf
Author Ren, Jianchao| Kaneta, Takashi|
Note This version of the article has been accepted for publication, after peer review (when applicable) and is subject to Springer Nature’s AM terms of use, but is not the Version of Record and does not reflect post-acceptance improvements, or any corrections. The Version of Record is available online at: http://dx.doi.org/10.1007/s44211-022-00078-7
This fulltext is available in Feb. 2023.|
Published Date 2022-02-25
Publication Title Analytical Sciences
Volume volume38
Issue issue4
Publisher Springer Science and Business Media LLC
Start Page 651
End Page 655
ISSN 0910-6340
NCID AA10500785
Content Type Journal Article
language English
OAI-PMH Set 岡山大学
Copyright Holders © 2022. The Author(s), under exclusive licence to The Japan Society for Analytical Chemistry.
File Version author
PubMed ID 35286641
DOI 10.1007/s44211-022-00078-7
Web of Science KeyUT 000808551700004
Related Url isVersionOf https://doi.org/10.1007/s44211-022-00078-7
FullText URL fulltext20220630-2.pdf
Author Takahashi, Misa| Hagiya, Hideharu| Tanaka, Shuichi| Yamamoto, Koichiro| Honda, Hiroyuki| Hasegawa, Kou| Otsuka, Fumio|
Note © 2022 Elsevier B.V. This manuscript version is made available under the CC-BY-NC-ND 4.0 License. http://creativecommons.org/licenses/by-nc-nd/4.0/. This is the accepted manuscript version. The formal published version is available at [https://doi.org/10.1016/j.jiac.2022.02.021] .
This fulltext is available in March 2023.|
Published Date 2022-7
Publication Title Journal of Infection and Chemotherapy
Volume volume28
Issue issue7
Publisher Elsevier BV
Start Page 978
End Page 981
ISSN 1341-321X
NCID AA11057978
Content Type Journal Article
language English
OAI-PMH Set 岡山大学
Copyright Holders © 2022 Elsevier B.V.
File Version author
PubMed ID 35277342
DOI 10.1016/j.jiac.2022.02.021
Web of Science KeyUT 000808081000003
Related Url isVersionOf https://doi.org/10.1016/j.jiac.2022.02.021
FullText URL fulltext.pdf
Author Tamura, Katsunori| Oshima, Yuri| Fuse, Yuta| Nagaoka, Noriyuki| Kunoh, Tatsuki| Nakanishi, Makoto| Fujii, Tatsuo| Nanba, Tokuro| Takada, Jun|
Published Date 2022-04-10
Publication Title ACS Omega
Volume volume7
Issue issue15
Publisher American Chemical Society
Start Page 12795
End Page 12802
ISSN 2470-1343
Content Type Journal Article
language English
OAI-PMH Set 岡山大学
Copyright Holders © 2022 The Authors.
File Version publisher
PubMed ID 35474768
DOI 10.1021/acsomega.1c07390
Web of Science KeyUT 000812569200001
Related Url isVersionOf https://doi.org/10.1021/acsomega.1c07390
FullText URL fulltext.pdf
Author Yamada, Yuto| Fujiwara, Masaki| Shimazu, Taichi| Etoh, Tsuyoshi| Kodama, Masafumi| So, Ryuhei| Matsushita, Takanori| Yoshimura, Yusaku| Horii, Shigeo| Fujimori, Maiko| Takahashi, Hirokazu| Nakaya, Naoki| Miyaji, Tempei| Hinotsu, Shiro| Harada, Keita| Okada, Hiroyuki| Uchitomi, Yosuke| Yamada, Norihito| Inagaki, Masatoshi|
Published Date 2022-06
Publication Title BMJ Open
Volume volume12
Issue issue6
Publisher BMJ Publishing Group
Start Page e060621
ISSN 2044-6055
Content Type Journal Article
language English
OAI-PMH Set 岡山大学
Copyright Holders © Author(s) (or their employer(s)) 2022.
File Version publisher
PubMed ID 35701062
DOI 10.1136/bmjopen-2021-060621
Web of Science KeyUT 000811702800009
Related Url isVersionOf https://doi.org/10.1136/bmjopen-2021-060621
JaLCDOI 10.18926/AMO/63722
FullText URL 76_3_281.pdf
Author Yu, Bo| Wang, Rui| Luo, Huikun| Yang, Di| Wang, Simo| Yu, Yaqiong| Okamura, Hirohiko| Qiu, Lihong|
Abstract Periodontal ligament (PDL) cells are critical for the bone remodeling process in periapical lesions since they can differentiate into osteoblasts and secrete osteoclastogenesis-promoting cytokines. Post-translational histone modifications including alterations of the methylation status of H3K27 are involved in cell differentiation and inflammatory reaction. The histone demethylase Jumonji domain-containing 3 (Jmjd3) specifically removes methylation of H3K27. We investigated whether Jmjd3 is involved in the osteogenic differentiation and secretion of PDL cells’ inflammatory factors. Jmjd3 expression in periapical lesions was examined by immunostaining. Using siRNA specific for Jmjd3 or the specific Jmjd3 inhibitor GSK-J4, we determined Jmjd3’s roles in osteogenic differentiation and cytokine production by real-time RT-PCR. The locations of Jmjd3 and NF-κB were analyzed by immunocytochemistry. Compared to healthy PDLs, the periapical lesion samples showed higher Jmjd3 expression. Treatment with GSK-J4 or Jmjd3 siRNA suppressed PDL cells’ osteogenic differentiation by suppressing the expressions of bone-related genes (Runx2, Osterix, and osteocalcin) and mineralization. Jmjd3 knockdown decreased the expressions of cytokines (TNF-α, IL-1β, and IL-6) induced by lipopolysaccharide extracted from Porphyromonas endodontalis (Pe-LPS). Pe-LPS induced the nuclear translocations of Jmjd3 and NF-κB; the latter was inhibited by GSK-J4 treatment. Jmjd3 appears to regulate PDL cells’ osteogenic differentiation and proinflammatory cytokine expressions.
Keywords periapical lesions histone demethylase Jmjd3 periodontal ligament cell osteogenic differentiation proinflammatory cytokines
Amo Type Original Article
Publication Title Acta Medica Okayama
Published Date 2022-06
Volume volume76
Issue issue3
Publisher Okayama University Medical School
Start Page 281
End Page 290
ISSN 0386-300X
NCID AA00508441
Content Type Journal Article
language English
Copyright Holders Copyright Ⓒ 2022 by Okayama University Medical School
File Version publisher
Refereed True
PubMed ID 35790358
Web of Science KeyUT 000823568300007
JaLCDOI 10.18926/AMO/63721
FullText URL 76_3_273.pdf
Author Furuichi, Shuro| Mitani, Shigeru| Endo, Hirosuke| Namba, Yoshifumi| Kawamoto, Toyohiro|
Abstract Following total hip arthroplasty (THA), some patients exhibit anterior or posterior pelvic tilt (PT). This case– control study investigated whether changes to PT following THA can be preoperatively predicted. Methods: 135 patients with hip osteoarthritis who underwent THA were assessed. The parameters measured preoperatively and one year postoperatively were lumbar lordosis (LL) based on plain X-ray and pelvic incidence (PI), PT, and sacral slope (SS), all of which were measured as pelvic morphological angles. Patients were classified into groups (A–E) based on the degree of post-THA PT, and their preoperative conditions were compared. PI minus LL was used to evaluate spinal alignment and pelvic balance. Results: Overall, 33%, 30%, 21%, 13%, and 3% of the hips of patients in Groups A, B, C, D, and E were postoperatively assessed. In Groups A–E, the SS values were 34.6°±8.9°, 37.6°±8.4°, 37.9°±8.9°, 42.6°±9.5°, and 60.0°±11.1°, whereas the PI minus LL values were 2.9°±15.0°, 1.2°±13.6°, 3.6°±17.7°, 12.7°±13.1°, and −1.3°±11.7°, respectively. Conclusions: Following THA, 70% of patients experienced posterior PT. Pre-THA SS ≥45° or PI minus LL ≥15° signified marked postoperative posterior tilt and could predict postoperative PT following THA. These findings are useful for implant placement, as they can predict pelvic inclination.
Keywords hip total hip arthroplasty arthroplasty radiography lordosis
Amo Type Original Article
Publication Title Acta Medica Okayama
Published Date 2022-06
Volume volume76
Issue issue3
Publisher Okayama University Medical School
Start Page 273
End Page 280
ISSN 0386-300X
NCID AA00508441
Content Type Journal Article
language English
Copyright Holders Copyright Ⓒ 2022 by Okayama University Medical School
File Version publisher
Refereed True
PubMed ID 35790357
Web of Science KeyUT 000823568300006
JaLCDOI 10.18926/AMO/63720
FullText URL 76_3_265.pdf
Author Kosaki, Yoshinori| Naito, Hiromichi| Iida, Atsuyoshi| Ihoriya, Hiromi| Nojima, Tsuyoshi| Yamada, Taihei| Yamamoto, Hirotsugu| Nakamura, Shunsuke| Mandai, Yasuhiro| Nakao, Atsunori|
Abstract Basic life support (BLS) courses for laypersons, including cardiopulmonary resuscitation (CPR) training, is known to improve outcomes of out-of-hospital cardiac events. We asked medical students to provide BLS training for laypersons as a part of their emergency medicine education and evaluated the effects of training on the BLS skills of laypersons. We also used a questionnaire to determine whether the medical students who provided the BLS training were themselves more confident and motivated to perform BLS compared to students who did not provide BLS training. The proportions of laypersons who reported confidence in checking for a response, performing chest compressions, and automated external defibrillator (AED) use were significantly increased after the BLS training. The proportions of medical students who reported increased confidence/motivation in terms of understanding BLS, checking for a response, chest compression, use of AED, and willingness to perform BLS were significantly greater among medical students who provided BLS instructions compared to those who did not. BLS instruction by medical students was associated with an improvement in laypersons’ CPR accuracy and confidence in responding to cardiac arrest. The results indicate that medical students could gain understanding, confidence, and motivation in regard to their BLS skills by teaching BLS to laypersons.
Keywords BLS medical education emergency medicine resuscitation
Amo Type Original Article
Publication Title Acta Medica Okayama
Published Date 2022-06
Volume volume76
Issue issue3
Publisher Okayama University Medical School
Start Page 265
End Page 271
ISSN 0386-300X
NCID AA00508441
Content Type Journal Article
language English
Copyright Holders Copyright Ⓒ 2022 by Okayama University Medical School
File Version publisher
Refereed True
PubMed ID 35790356
Web of Science KeyUT 000823568300005
JaLCDOI 10.18926/AMO/63719
FullText URL 76_3_255.pdf
Author Nakatsuka, Kosuke| Matsuoka, Yoshikazu| Kurita, Masako| Wang, Ruilin| Tsuboi, Chika| Sue, Nobutaka| Kaku, Ryuji| Morimatsu, Hiroshi|
Abstract Mirror image pain (MIP) is a type of extraterritorial pain that results in contralateral pain or allodynia. Glutamate transporter-1 (GLT-1) is expressed in astrocytes and plays a role in maintaining low glutamate levels in the synaptic cleft. Previous studies have shown that GLT-1 dysfunction induces neuropathic pain. Our previous study revealed bilateral GLT-1 downregulation in the spinal cord of a spared nerve injury (SNI) rat. We hypothesized that spinal GLT-1 is involved in the mechanism of MIP. We also previously demonstrated noradrenergic GLT-1 regulation. Therefore, this study aimed to investigate the effect of an α1 adrenergic antagonist on the development of MIP. Rats were subjected to SNI. Changes in pain behavior and GLT-1 protein levels in the SNI rat spinal cords were then examined by intrathecal administration of the α1 adrenergic antagonist phentolamine, followed by von Frey test and western blotting. SNI resulted in the development of MIP and bilateral downregulation of GLT-1 protein in the rat spinal cord. Intrathecal phentolamine increased contralateral GLT-1 protein levels and partially ameliorated the 50% paw withdrawal threshold in the contralateral hind paw. Spinal GLT-1 upregulation by intrathecal phentolamine ameliorates MIP. GLT-1 plays a role in the development of MIPs.
Keywords alpha adrenergic receptor glutamate transporter-1 mirror image pain neuropathic pain spared nerve injury
Amo Type Original Article
Publication Title Acta Medica Okayama
Published Date 2022-06
Volume volume76
Issue issue3
Publisher Okayama University Medical School
Start Page 255
End Page 263
ISSN 0386-300X
NCID AA00508441
Content Type Journal Article
language English
Copyright Holders Copyright Ⓒ 2022 by Okayama University Medical School
File Version publisher
Refereed True
PubMed ID 35790355
Web of Science KeyUT 000823568300004
JaLCDOI 10.18926/AMO/63718
FullText URL 76_3_247.pdf
Author Yoshida, Shohei| Fujii, Nobuharu| Kamoi, Chihiro| Kitamura, Wataru| Fujiwara, Hideaki| Asada, Noboru| Nishimori, Hisakazu| Fujii, Keiko| Matsuoka, Ken-ichi| Maeda, Yoshinobu|
Abstract Vaccine-preventable disease (VPD) infections are more severe in immunocompromised hosts. Vaccination against measles, mumps, rubella, and varicella zoster (VZV) (MMRV) is therefore recommended for hematopoietic stem cell transplantation (HCT) recipients. However, studies on adult HCT recipients with VPD infections are limited. At our institution, we have systematically conducted serological MMRV tests as a part of check-up examinations during long-term follow-up (LTFU) after HCT since 2015. This retrospective study aimed to evaluate changes in the serostatus between before and 2 years after allogeneic HCT. Among 161 patients, the pre-transplant seropositivity was 82.7% for measles, 86.8% for mumps, 84.2% for rubella, and 94.3% for VZV. Among 56 patients who underwent LTFU including serological MMRV tests at 2 years after HCT, the percentages maintaining seroprotective antibody levels for measles, mumps, rubella and VZV were 71.5% (40/56), 51.8% (29/56), 48.2% (27/56), and 60.7% (34/56), respectively. Vaccination was recommended for 22 patients, and 12 were vaccinated. Among the 12 vaccinated patients, rates of seroconversion were examined in 2-6 patients for each of the four viruses. They were 100% (3/3) for measles, 33.3% (1/3) for mumps, 50% (3/6) for rubella, and 0% (0/2) for VZV. Further studies are warranted to clarify the effect of vaccination in adult HCT recipients.
Keywords vaccine-preventable disease vaccination allogeneic hematopoietic stem cell transplantation adult
Amo Type Original Article
Publication Title Acta Medica Okayama
Published Date 2022-06
Volume volume76
Issue issue3
Publisher Okayama University Medical School
Start Page 247
End Page 253
ISSN 0386-300X
NCID AA00508441
Content Type Journal Article
language English
Copyright Holders Copyright Ⓒ 2022 by Okayama University Medical School
File Version publisher
Refereed True
PubMed ID 35790354
Web of Science KeyUT 000823568300003
JaLCDOI 10.18926/AMO/63717
FullText URL 76_3_235.pdf
Author Tenta, Masafumi| Eguchi, Jun| Wada, Jun|
Abstract The combination of sarcopenia and obesity (sarcopenic obesity) is associated with the development of metabolic syndrome and cardiovascular events. The molecular pathways that develop sarcopenic obesity have studied intensively. Transmembrane protein 97 (TMEM97) is 176 amino acids conserved integral membrane protein with four transmembrane domains that is expressed in several types of cancer. Its physiological significance in adipose tissue and skeletal muscle has been unclear. We studied TMEM97-transgenic mice and mice lacking TMEM97, and our findings indicate that TMEM97 expression is regulated in adipose tissue and skeletal muscle from obesity. TMEM97 represses adipogenesis and promotes myogenesis in vitro. Fat-specific TMEM97 transgenic mice showed systemic insulin resistance. Mice overexpressing TMEM97 in skeletal muscle exhibited systemic insulin resistance. Mice lacking TMEM97 were protected against diet-induced obesity and insulin resistance. These phenotypes are associated with the effects of TMEM97 on inflammation genes in adipose tissue and skeletal muscle. Our findings indicates that there is a link between TMEM97 and chronic inflammation in obesity.
Keywords adipose tissue skeletal muscle obesity
Amo Type Original Article
Publication Title Acta Medica Okayama
Published Date 2022-06
Volume volume76
Issue issue3
Publisher Okayama University Medical School
Start Page 235
End Page 245
ISSN 0386-300X
NCID AA00508441
Content Type Journal Article
language English
Copyright Holders Copyright Ⓒ 2022 by Okayama University Medical School
File Version publisher
Refereed True
PubMed ID 35790353
Web of Science KeyUT 000823568300002