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PLoS Pathog . Elevated cytokines and chemokines in peripheral blood of patients with SARS-CoV-2 pneumonia treated with high-titer convalescent plas

tetano

Editor, Senior Moderator
PLoS Pathog


. 2021 Oct 29;17(10):e1010025.
doi: 10.1371/journal.ppat.1010025. Online ahead of print.
Elevated cytokines and chemokines in peripheral blood of patients with SARS-CoV-2 pneumonia treated with high-titer convalescent plasma


Stacey L Fanning[SUP] 1 [/SUP], Robert Korngold[SUP] 2 3 [/SUP], Zheng Yang[SUP] 2 [/SUP], Kira Goldgirsh[SUP] 2 [/SUP], Steven Park[SUP] 2 [/SUP], Joshua Zenreich[SUP] 3 [/SUP], Melissa Baker[SUP] 3 [/SUP], Phyllis McKiernan[SUP] 3 [/SUP], Ming Tan[SUP] 4 [/SUP], Bingsong Zhang[SUP] 4 [/SUP], Michele L Donato[SUP] 3 [/SUP], David S Perlin[SUP] 2 [/SUP]



Affiliations

Abstract

The global SARS-CoV-2 coronavirus pandemic continues to be devastating in many areas. Treatment options have been limited and convalescent donor plasma has been used by many centers to transfer passive neutralizing antibodies to patients with respiratory involvement. The results often vary by institution and are complicated by the nature and quality of the donor plasma itself, the timing of administration and the clinical aspects of the recipients. SARS-CoV-2 infection is known to be associated with an increase in the blood concentrations of several inflammatory cytokines/chemokines, as part of the overall immune response to the virus and consequential to mediated lung pathology. Some of these correlates contribute to the cytokine storm syndrome and acute respiratory distress syndrome, often resulting in fatality. A Phase IIa clinical trial at our institution using high neutralizing titer convalescent plasma transfer gave us the unique opportunity to study the elevations of correlates in the first 10 days after infusion. Plasma recipients were divided into hospitalized COVID-19 pneumonia patients who did not (Track 2) or did (Track 3) require mechanical ventilation. Several cytokines were elevated in the patients of each Track and some continued to rise through Day 10, while others initially increased and then subsided. Furthermore, elevations in MIP-1α, MIP-1β and CRP correlated with disease progression of Track 2 recipients. Overall, our observations serve as a foundation for further study of these correlates and the identification of potential biomarkers to improve upon convalescent plasma therapy and to drive more successful patient outcomes.
 
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