• FluTrackers.com Inc. does not provide medical advice. Information on this web site is collected from various internet resources, and the FluTrackers board of directors makes no warranty to the safety, efficacy, correctness or completeness of the information posted on this site by any author or poster. The information collated here is for instructional and/or discussion purposes only and is NOT intended to diagnose or treat any disease, illness, or other medical condition. Every individual reader or poster should seek advice from their personal physician/healthcare practitioner before considering or using any interventions that are discussed on this website. By continuing to access this website you agree to consult your personal physican before using any interventions posted on this website, and you agree to hold harmless FluTrackers.com Inc., the board of directors, the members, and all authors and posters for any effects from use of any medication, supplement, vitamin or other substance, device, intervention, etc. mentioned in posts on this website, or other internet venues referenced in posts on this website.
  • We are not asking for any donations. Do not donate to any entity who says they are raising funds for us.

Oxf Open Immunol . Neutrophilia, lymphopenia and myeloid dysfunction: a living review of the quantitative changes to innate and adaptive immune cell

tetano

Editor, Senior Moderator
Oxf Open Immunol


. 2021 Jul 15;2(1):iqab016.
doi: 10.1093/oxfimm/iqab016. eCollection 2021.
Neutrophilia, lymphopenia and myeloid dysfunction: a living review of the quantitative changes to innate and adaptive immune cells which define COVID-19 pathology


Amy S Codd[SUP] 1 [/SUP], Stephanie J Hanna[SUP] 1 [/SUP], Ewoud B Compeer[SUP] 2 [/SUP], Felix C Richter[SUP] 2 [/SUP], Eleanor J Pring[SUP] 1 [/SUP], Ester Gea-Mallorquí[SUP] 3 [/SUP], Mariana Borsa[SUP] 2 [/SUP], Owen R Moon[SUP] 1 [/SUP], D Oliver Scourfield[SUP] 1 [/SUP], Oxford-Cardiff COVID-19 Literature Consortium; Awen M Gallimore[SUP] 1 [/SUP], Anita Milicic[SUP] 4 [/SUP]



Affiliations

Abstract

Destabilization of balanced immune cell numbers and frequencies is a common feature of viral infections. This occurs due to, and further enhances, viral immune evasion and survival. Since the discovery of the Severe Acute Respiratory Syndrome coronavirus 2 (SARS-CoV-2), which manifests in coronavirus disease 2019 (COVID-19), a great number of studies have described the association between this virus and pathologically increased or decreased immune cell counts. In this review, we consider the absolute and relative changes to innate and adaptive immune cell numbers, in COVID-19. In severe disease particularly, neutrophils are increased, which can lead to inflammation and tissue damage. Dysregulation of other granulocytes, basophils and eosinophils represents an unusual COVID-19 phenomenon. Contrastingly, the impact on the different types of monocytes leans more strongly to an altered phenotype, e.g. HLA-DR expression, rather than numerical changes. However, it is the adaptive immune response that bears the most profound impact of SARS-CoV-2 infection. T cell lymphopenia correlates with increased risk of intensive care unit admission and death; therefore, this parameter is particularly important for clinical decision-making. Mild and severe diseases differ in the rate of immune cell counts returning to normal levels post disease. Tracking the recovery trajectories of various immune cell counts may also have implications for long-term COVID-19 monitoring. This review represents a snapshot of our current knowledge, showing that much has been achieved in a short period of time. Alterations in counts of distinct immune cells represent an accessible metric to inform patient care decisions or predict disease outcomes.

Keywords: B cells; SARS-CoV-2; cell counts; clinical; lymphocytes; lymphopenia; monocytes; neutrophilia; neutrophils; prognosis; recovery; severity.
 
Back
Top Bottom