Here, we demonstrate that
KIR2DL4
copy number variation (CNV) is associated with CD4
+
T-cell decline and functionality of cytokine-producing NK cells during primary simian immunodeficiency virus (SIV) infection in
Mamu-A
*
01
−
Indian-origin rhesus macaques, with higher
KIR2DL4
copy numbers being associated with a better preservation of CD4
+
T cells and an increased gamma interferon (IFN-γ) production from stimulated cytokine-producing NK cell subsets during acute SIVmac251 infection. These findings underscore the crucial role of activating killer-cell immunoglobulin-like receptors (KIRs) in NK cell-mediated SIV responses during early SIV infection.