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10.1016/j.jaci.2020.05.003

http://scihub22266oqcxt.onion/10.1016/j.jaci.2020.05.003
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32407836!7212968!32407836
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suck abstract from ncbi


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pmid32407836      J+Allergy+Clin+Immunol 2020 ; 146 (1): 89-100
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  • Longitudinal hematologic and immunologic variations associated with the progression of COVID-19 patients in China #MMPMID32407836
  • Chen R; Sang L; Jiang M; Yang Z; Jia N; Fu W; Xie J; Guan W; Liang W; Ni Z; Hu Y; Liu L; Shan H; Lei C; Peng Y; Wei L; Liu Y; Hu Y; Peng P; Wang J; Liu J; Chen Z; Li G; Zheng Z; Qiu S; Luo J; Ye C; Zhu S; Zheng J; Zhang N; Li Y; He J; Li J; Li S; Zhong N
  • J Allergy Clin Immunol 2020[Jul]; 146 (1): 89-100 PMID32407836show ga
  • BACKGROUND: Crucial roles of hematologic and immunologic responses in progression of coronavirus disease 2019 (COVID-19) remain largely unclear. OBJECTIVE: We sought to address the dynamic changes in hematologic and immunologic biomarkers and their associations with severity and outcomes of COVID-19. METHODS: A retrospective study including 548 patients with COVID-19 with clarified outcome (discharged or deceased) from a national cohort in China was performed. Cross-sectional and longitudinal variations were compared and the associations with different severity and outcomes were analyzed. RESULTS: On admission, the counts of lymphocytes, T-cell subsets, eosinophils, and platelets decreased markedly, especially in severe/critical and fatal patients. Increased neutrophil count and neutrophils-to-lymphocytes ratio were predominant in severe/critical cases or nonsurvivors. During hospitalization, eosinophils, lymphocytes, and platelets showed an increasing trend in survivors, but maintained lower levels or dropped significantly afterwards in nonsurvivors. Nonsurvivors kept a high level or showed an upward trend for neutrophils, IL-6, procalcitonin, D-dimer, amyloid A protein, and C-reactive protein, which were kept stable or showed a downward trend in survivors. Positive correlation between CD8(+) T-cell and lymphocytes count was found in survivors but not in nonsurvivors. A multivariate Cox regression model suggested that restored levels of lymphocytes, eosinophils, and platelets could serve as predictors for recovery, whereas progressive increases in neutrophils, basophils, and IL-6 were associated with fatal outcome. CONCLUSIONS: Hematologic and immunologic impairment showed a significantly different profile between survivors and nonsurvivors in patients with COVID-19 with different severity. The longitudinal variations in these biomarkers could serve to predict recovery or fatal outcome.
  • |Adult[MESH]
  • |Aged[MESH]
  • |Betacoronavirus[MESH]
  • |Biomarkers/*blood[MESH]
  • |COVID-19[MESH]
  • |China[MESH]
  • |Cohort Studies[MESH]
  • |Coronavirus Infections/*blood/*immunology/mortality[MESH]
  • |Cross-Sectional Studies[MESH]
  • |Disease Progression[MESH]
  • |Female[MESH]
  • |Humans[MESH]
  • |Longitudinal Studies[MESH]
  • |Male[MESH]
  • |Middle Aged[MESH]
  • |Pandemics[MESH]
  • |Pneumonia, Viral/*blood/*immunology/mortality[MESH]
  • |Prognosis[MESH]
  • |Retrospective Studies[MESH]


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