<?xml version="1.0" encoding="UTF-8"?>
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  <title>DSpace Collection: 833 - 972</title>
  <link rel="alternate" href="http://localhost:8080/xmlui/handle/123456789/9709" />
  <subtitle>833 - 972</subtitle>
  <id>http://localhost:8080/xmlui/handle/123456789/9709</id>
  <updated>2026-04-09T00:48:15Z</updated>
  <dc:date>2026-04-09T00:48:15Z</dc:date>
  <entry>
    <title>Validation of a modified enrichment broth for efficient screening of group B Streptococcus in pregnant women</title>
    <link rel="alternate" href="http://localhost:8080/xmlui/handle/123456789/9724" />
    <author>
      <name>Tanno, Daiki</name>
    </author>
    <author>
      <name>Saito, Kyoichi</name>
    </author>
    <author>
      <name>Tomii, Yasuaki</name>
    </author>
    <author>
      <name>Nakatsuka, Yukari</name>
    </author>
    <author>
      <name>Uechi, Kohei</name>
    </author>
    <author>
      <name>Ohashi, Kazutaka</name>
    </author>
    <id>http://localhost:8080/xmlui/handle/123456789/9724</id>
    <updated>2025-02-21T08:29:22Z</updated>
    <published>2024-08-01T00:00:00Z</published>
    <summary type="text">Title: Validation of a modified enrichment broth for efficient screening of group B Streptococcus in pregnant women
Authors: Tanno, Daiki; Saito, Kyoichi; Tomii, Yasuaki; Nakatsuka, Yukari; Uechi, Kohei; Ohashi, Kazutaka
Abstract: Abstract We validated a modified enrichment broth that changes its color when group B&#xD;
Streptococcus (GBS) grows. No GBS was detected in any of the non-yellow samples. Thus,&#xD;
the non-yellow samples were considered GBS-negative without conducting further examinations,&#xD;
potentially reducing medical costs and workload.</summary>
    <dc:date>2024-08-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Unveiling the dynamics of respiratory infections revealed by multiplex PCR testing during the COVID-19 pandemic in Taiwan, 2020e2023</title>
    <link rel="alternate" href="http://localhost:8080/xmlui/handle/123456789/9723" />
    <author>
      <name>Su, Hung-Chieh</name>
    </author>
    <author>
      <name>Chang, Yu-Chang</name>
    </author>
    <author>
      <name>Chen, Chih-Hao</name>
    </author>
    <author>
      <name>Cheng, Meng-Yu</name>
    </author>
    <author>
      <name>Hsih, Wen-Hsin</name>
    </author>
    <author>
      <name>Chen, Yi-Jhen</name>
    </author>
    <id>http://localhost:8080/xmlui/handle/123456789/9723</id>
    <updated>2025-02-21T08:28:39Z</updated>
    <published>2024-08-01T00:00:00Z</published>
    <summary type="text">Title: Unveiling the dynamics of respiratory infections revealed by multiplex PCR testing during the COVID-19 pandemic in Taiwan, 2020e2023
Authors: Su, Hung-Chieh; Chang, Yu-Chang; Chen, Chih-Hao; Cheng, Meng-Yu; Hsih, Wen-Hsin; Chen, Yi-Jhen
Abstract: Abstract Background: The emergence of SARS-CoV-2 in late 2019 sparked the global COVID-&#xD;
19 pandemic, leading to varied vaccine policies worldwide. The evolving patterns of respiratory&#xD;
pathogens, aside from SARS-CoV-2, during the pandemic have had a significant impact&#xD;
on the development of vaccine strategies.&#xD;
Methods: This study explores the landscape of respiratory pathogens, encompassing SARS-CoV-&#xD;
2, respiratory syncytial virus (RSV), and influenza viruses, through a retrospective analysis of&#xD;
data obtained from the BioFire Respiratory Panel 2.1 (RP 2.1) at China Medical University Hospital&#xD;
(Taichung, Taiwan) spanning from January 2020 to November 2023.&#xD;
Results: Among the 7950 respiratory samples studied, pediatric cases exhibited higher positivity (64.9%, 2488/3835) and mixed detection rates (43.8%, 1090/2488) than adults.&#xD;
Annual mixed detection rates increased (27.9e48%). Prevalence analysis revealed diverse patterns&#xD;
across age groups, with higher rates in pediatrics. Notably, human rhinovirus/enterovirus&#xD;
predominated (48.1%). Mixed detection illustrated viral co-detections, notably with parainfluenza&#xD;
viruses and adenovirus. Government policies and pandemic dynamics influenced infection&#xD;
patterns, with RSV resurgence after May 2022. Age-specific RSV detection demonstrated a&#xD;
shift, influencing vaccine considerations. Amid global vaccine initiatives, RSV’s increasing&#xD;
trend in adults warrants attention.&#xD;
Conclusions: This comprehensive analysis emphasizes the importance of multiplex PCR testing&#xD;
in shaping targeted vaccination strategies during evolving respiratory pathogen landscapes.</summary>
    <dc:date>2024-08-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>The persistence of low CD4/CD8 ratio in chronic HIV-infection, despite ART suppression and normal CD4 levels, is associated with pre-therapy values of inflammation and thymic function</title>
    <link rel="alternate" href="http://localhost:8080/xmlui/handle/123456789/9722" />
    <author>
      <name>Garrido-Rodrı´guez, Vanesa</name>
    </author>
    <author>
      <name>Bulnes-Ramos, A´ngel</name>
    </author>
    <author>
      <name>Olivas-Martı´nez, Israel</name>
    </author>
    <author>
      <name>Pozo-Balado, Marı´a del Mar</name>
    </author>
    <author>
      <name>A´lvarez-Rı´os, Ana Isabel</name>
    </author>
    <author>
      <name>Gutie´rrez, Fe´lix</name>
    </author>
    <id>http://localhost:8080/xmlui/handle/123456789/9722</id>
    <updated>2025-02-21T08:23:48Z</updated>
    <published>2024-08-01T00:00:00Z</published>
    <summary type="text">Title: The persistence of low CD4/CD8 ratio in chronic HIV-infection, despite ART suppression and normal CD4 levels, is associated with pre-therapy values of inflammation and thymic function
Authors: Garrido-Rodrı´guez, Vanesa; Bulnes-Ramos, A´ngel; Olivas-Martı´nez, Israel; Pozo-Balado, Marı´a del Mar; A´lvarez-Rı´os, Ana Isabel; Gutie´rrez, Fe´lix
Abstract: Abstract Background: Persistence of a low CD4/CD8 ratio is associated with an increased&#xD;
morbimortality in people living with HIV (PLWH) under effective antiretroviral therapy. We&#xD;
aimed to explore the immunological significance of a persistently low CD4/CD8 ratio, even&#xD;
despite normal CD4 levels, and assess whether these features vary from those associated to&#xD;
a low nadir-CD4, another well-established predictor of disease progression.&#xD;
Methods: CD4-recovered PLWH were classified by CD4/CD8 ratio after three-years of ART (viral&#xD;
suppression, CD4 500; R &lt; 0.8, n Z 24 and R &gt; 1.2, n Z 28). sj/b-TRECs ratio and&#xD;
inflammatory-related markers were quantified. PBMCs were immunophenotyped by CyTOF&#xD;
and functionally characterized by ELISPOT. Subjects were also reclassified depending on&#xD;
nadir-CD4 (N   350/N &gt; 350).&#xD;
Results: R &lt; 0.8 showed a differential inflammatory profile compared to R &gt; 1.2 (increased b2-&#xD;
microglobulin, D-dimers and IP-10 before ART). R &lt; 0.8 presented lower baseline thymic function,&#xD;
being inversely correlated with post-ART inflammation. R &lt; 0.8 at follow-up showed most&#xD;
alterations in CD8 subsets (increasing frequency and exhibiting a senescent phenotype [e.g.,&#xD;
CD57þ, CD95þ]) and enhanced T-cell IFNg/IL-2 secretion. However, comparing N   350 to&#xD;
N &gt; 350, the main features were altered functional markers in CD4 T-cells, despite no differences&#xD;
in maturational subsets, together with a restricted T-cell cytokine secretion pattern.&#xD;
Conclusion: Persistence of low CD4/CD8 ratio in successfully-treated PLWH, with normal CD4&#xD;
counts, is associated with baseline inflammation and low thymic function, and it features&#xD;
post-therapy alterations specific to CD8 T-cells. Differently, subjects recovered from low&#xD;
nadir-CD4 in this setting feature post-therapy alterations on CD4 T-cells. Hence, different&#xD;
mechanisms of disease progression could underlie these biomarkers, potentially requiring&#xD;
different clinical approaches.</summary>
    <dc:date>2024-08-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>The clinical impact of primary granulocytecolony stimulating factor prophylaxis in children with acute lymphoblastic leukemia who underwent induction chemotherapy</title>
    <link rel="alternate" href="http://localhost:8080/xmlui/handle/123456789/9721" />
    <author>
      <name>Lu, Yi-An</name>
    </author>
    <author>
      <name>Liu, Hsi-Che</name>
    </author>
    <author>
      <name>Hou, Jen-Yin</name>
    </author>
    <author>
      <name>Chiu, Nan-Chang</name>
    </author>
    <author>
      <name>Huang, Ting-Huan</name>
    </author>
    <author>
      <name>Yeh, Ting-Chi</name>
    </author>
    <id>http://localhost:8080/xmlui/handle/123456789/9721</id>
    <updated>2025-02-21T07:54:35Z</updated>
    <published>2024-08-01T00:00:00Z</published>
    <summary type="text">Title: The clinical impact of primary granulocytecolony stimulating factor prophylaxis in children with acute lymphoblastic leukemia who underwent induction chemotherapy
Authors: Lu, Yi-An; Liu, Hsi-Che; Hou, Jen-Yin; Chiu, Nan-Chang; Huang, Ting-Huan; Yeh, Ting-Chi
Abstract: Abstract Background: Data describing the risk factors for the occurrence of severe infections&#xD;
in acute lymphoblastic leukemia (ALL) patients following induction chemotherapy and&#xD;
the role of prophylactic granulocyte-colony stimulating factor (G-CSF) in the era of antimicrobials&#xD;
prophylaxis are limited.&#xD;
Methods: This study enrolled 188 children aged  18 years with newly diagnosed ALL who&#xD;
received Taiwan Pediatric Oncology Group ALL-2002 and 2013 treatments between January&#xD;
1, 2010 and June 30, 2021. Prophylactic G-CSF was administered when a patient continues neutropenia&#xD;
after achieving the first bone marrow remission since June 1, 2015. Clinical factors&#xD;
were assessed for their association with severe infections.&#xD;
Results: From January 2010 to May 2015, 80 children experienced a total of 11 (13.5%) episodes&#xD;
of severe infections; while 10 (9.2%) episodes were reported to occur in 108 patients who&#xD;
received prophylactic G-CSF. Reduction of severe infections occurrence did not achieve statistical&#xD;
significance during prophylactic G-CSF administration in ALL patients. Compared with&#xD;
ALL-high risk (HR) and very high risk patients with no G-CSF prophylaxis, the use of G-CSF prophylaxis&#xD;
significantly reduced episodes of febrile neutropenia. Occurrence of grade III-IV intestinal ileus, grade II-III oral mucositis, prolonged neutropenia, central venous catheter&#xD;
(CVC) placement, or the requirement insulin therapy for hyperglycemia were associated with&#xD;
higher risk of bloodstream infections.&#xD;
Conclusions: ALL-HR patients with G-CSF prophylaxis were associated with reduction of febrile&#xD;
neutropenia episodes. Occurrence of severe ileus, oral mucositis, hyperglycemia, CVC placement,&#xD;
or prolonged neutropenia were associated with severe infections in ALL patients&#xD;
receiving induction chemotherapy.</summary>
    <dc:date>2024-08-01T00:00:00Z</dc:date>
  </entry>
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