<P>Human cytomegalovirus (HCMV) establishes a lifelong chronic latent infection and often reactivates in immunocompromised patients. In addition, HCMV reactivates in patients with sepsis or other critical illnesses, particularly in patients with...
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https://www.riss.kr/link?id=A107711021
2017
-
SCOPUS,KCI등재,SCIE
학술저널
e382
0
상세조회0
다운로드다국어 초록 (Multilingual Abstract)
<P>Human cytomegalovirus (HCMV) establishes a lifelong chronic latent infection and often reactivates in immunocompromised patients. In addition, HCMV reactivates in patients with sepsis or other critical illnesses, particularly in patients with...
<P>Human cytomegalovirus (HCMV) establishes a lifelong chronic latent infection and often reactivates in immunocompromised patients. In addition, HCMV reactivates in patients with sepsis or other critical illnesses, particularly in patients with poor prognoses. However, the immunological characteristics of sepsis patients with HCMV reactivation have not been elucidated. In the present study, we examined T-cell responses in severe sepsis patients with and without HCMV reactivation. First, HCMV pp65-specific T-cell functions were assessed by intracellular cytokine staining (ICS) for IFN-γ, TNF-α, and MIP-1β and by CD107a staining. We analyzed the ICS data for each function individually and found no difference between the patient groups. However, the relative frequency of polyfunctional CD8<SUP>+</SUP> T cells was significantly decreased in sepsis patients with HCMV reactivation. Next, we examined programmed cell death protein 1 (PD-1) expression. It was significantly increased in the CD8<SUP>+</SUP> T-cell population in severe sepsis patients with HCMV reactivation, indicating CD8<SUP>+</SUP> T-cell exhaustion. Interestingly, the frequency of PD-1<SUP>+</SUP> cells in the CD8<SUP>+</SUP> T-cell population was inversely correlated with the relative frequency of polyfunctional CD8<SUP>+</SUP> T cells. Herein, we demonstrate that HCMV reactivation in severe sepsis patients is associated with PD-1 expression and impaired polyfunctionality of CD8<SUP>+</SUP> T cells.</P>
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