Innate Lymphoid Cells Are Depleted Irreversibly during Acute HIV-1 Infection in the Absence of Viral Suppression

Biology Biology
Genomics Genomics
Immunology Immunology
Infectious Disease Infectious Disease
Alex K. Shalek Alex K. Shalek
Sam Kazer Sam Kazer

Kløverpris et al.▾ Kløverpris, H.N., Kazer, S.W., Mjösberg, J., Mabuka, J.M., Wllmann, A., Ndhlovu, Z., Yadon, M.C., Nhamoyebonde, S., Muenchhoff, M., Simoni, Y., Andersson F., Kuhn, W., Garrett, N., Burgers, W.A., Kamya, P., Pretorius, K., Dong, K., Moodly, A., Newell, E.W., Kasprowicz, V., Abdool Karim, S.S., Goulder, P., Shalek, A.K., Walker, B.D., Ndung'u, T., Leslie, A.

Immunity , Volume 44

February, 2016


Innate lymphoid cells (ILCs) play a central role in the response to infection by secreting cytokines crucial for immune regulation, tissue homeostasis, and repair. Although dysregulation of these systems is central to pathology, the impact of HIV-1 on ILCs remains unknown. We found that human blood ILCs were severely depleted during acute viremic HIV-1 infection and that ILC numbers did not recover after resolution of peak viremia. ILC numbers were preserved by antiretroviral therapy (ART), but only if initiated during acute infection. Transcriptional profiling during the acute phase revealed upregulation of genes associated with cell death, temporally linked with a strong IFN acutephase response and evidence of gut barrier breakdown. We found no evidence of tissue redistribution in chronic disease and remaining circulating ILCs were activated but not apoptotic. These data provide a potential mechanistic link between acute HIV-1 infection, lymphoid tissue breakdown, and persistent immune dysfunction.