iScience (Jul 2020)

A NKp80-Based Identification Strategy Reveals that CD56neg NK Cells Are Not Completely Dysfunctional in Health and Disease

  • Ane Orrantia,
  • Iñigo Terrén,
  • Alicia Izquierdo-Lafuente,
  • Juncal A. Alonso-Cabrera,
  • Victor Sandá,
  • Joana Vitallé,
  • Santiago Moreno,
  • María Tasias,
  • Alasne Uranga,
  • Carmen González,
  • Juan J. Mateos,
  • Juan C. García-Ruiz,
  • Olatz Zenarruzabeitia,
  • Francisco Borrego

Journal volume & issue
Vol. 23, no. 7
p. 101298

Abstract

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Summary: Natural killer (NK) cells are usually identified by the absence of other lineage markers, due to the lack of cell-surface-specific receptors. CD56neg NK cells, classically identified as CD56negCD16+, are very scarce in the peripheral blood of healthy people but they expand in some pathological conditions. However, studies on CD56neg NK cells had revealed different results regarding the phenotype and functionality. This could be due to, among others, the unstable expression of CD16, which hinders CD56neg NK cells’ proper identification. Hence, we aim to determine an alternative surface marker to CD16 to better identify CD56neg NK cells. We have found that NKp80 is superior to CD16. Furthermore, we found differences between the functionality of CD56negNKp80+ and CD56negCD16+, suggesting that the effector functions of CD56neg NK cells are not as diminished as previously thought. We proposed NKp80 as a noteworthy marker to identify and accurately re-characterize human CD56neg NK cells.

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