Sequential deregulation of NK cell subset distribution and function starting in acute HIV-1 infection

Author:

Alter Galit1,Teigen Nickolas1,Davis Benjamin T.1,Addo Marylyn M.1,Suscovich Todd J.1,Waring Michael T.1,Streeck Hendrik1,Johnston Mary N.1,Staller Kyle D.1,Zaman M. Tauheed1,Yu Xu G.1,Lichterfeld Mathias1,Basgoz Nesli1,Rosenberg Eric S.1,Altfeld Marcus1

Affiliation:

1. From the Partners AIDS Research Center, Infectious Disease Unit, Massachusetts General Hospital and Division of AIDS, Harvard Medical School, Boston, MA.

Abstract

AbstractNatural killer (NK) cells are critical in the first-line defense against viral infections. Chronic HIV-1 infection leads to a perturbation in the NK cell compartment, yet the kinetics of this deregulation and the functional consequences are unclear. Here, we characterized changes in the NK cell compartment longitudinally by multiparameter flow cytometry, starting in acute HIV-1 infection. Acute HIV-1 infection was associated with elevated NK cell numbers, with an expansion of CD3negCD56dimCD16pos NK cells and an early depletion of CD3negCD56brightCD16neg NK cells. Ongoing viral replication resulted in a depletion of CD3negCD56dimCD16pos NK cells with a paralleled increase in functionally anergic CD3negCD56negCD16pos NK cells, accompanied by reduced functional activity, as measured by CD107a expression and cytokine secretion. Taken together, these studies demonstrate a sequential impairment of NK cell function with persistent viral replication resulting from a progressive deregulation of NK cell subsets with distinct functional properties.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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