» Articles » PMID: 30565241

Emerging Insights into Human Health and NK Cell Biology from the Study of NK Cell Deficiencies

Overview
Journal Immunol Rev
Date 2018 Dec 20
PMID 30565241
Citations 86
Authors
Affiliations
Soon will be listed here.
Abstract

Human NK cells are innate immune effectors that play a critical roles in the control of viral infection and malignancy. The importance of their homeostasis and function can be demonstrated by the study of patients with primary immunodeficiencies (PIDs), which are part of the family of diseases known as inborn defects of immunity. While NK cells are affected in many PIDs in ways that may contribute to a patient's clinical phenotype, a small number of PIDs have an NK cell abnormality as their major immunological defect. These PIDs can be collectively referred to as NK cell deficiency (NKD) disorders and include effects upon NK cell numbers, subsets, and/or functions. The clinical impact of NKD can be severe including fatal viral infection, with particular susceptibility to herpesviral infections, such as cytomegalovirus, varicella zoster virus, and Epstein-Barr virus. While NKD is rare, studies of these diseases are important for defining specific requirements for human NK cell development and homeostasis. New themes in NK cell biology are emerging through the study of both known and novel NKD, particularly those affecting cell cycle and DNA damage repair, as well as broader PIDs having substantive impact upon NK cells. In addition, the discovery of NKD that affects other innate lymphoid cell (ILC) subsets opens new doors for better understanding the relationship between conventional NK cells and other ILC subsets. Here, we describe the biology underlying human NKD, particularly in the context of new insights into innate immune cell function, including a discussion of recently described NKD with accompanying effects on ILC subsets. Given the impact of these disorders upon human immunity with a common focus upon NK cells, the unifying message of a critical role for NK cells in human host defense singularly emerges.

Citing Articles

Single-chain variable fragment affinity tuning can optimize anti-AML CAR-NK cell functionality.

Rahnama R, Kizerwetter M, Yang H, Christodoulou I, Guaraca C, Holl N J Immunother Cancer. 2025; 13(2).

PMID: 39915004 PMC: 11804205. DOI: 10.1136/jitc-2024-010763.


The Golgi complex governs natural killer cell lytic granule positioning to promote directionality in cytotoxicity.

Pedroza L, van den Haak F, Frumovitz A, Hernandez E, Hegewisch-Solloa E, Orange T Cell Rep. 2025; 44(1):115156.

PMID: 39813120 PMC: 11844255. DOI: 10.1016/j.celrep.2024.115156.


Phenotypic characterization of NK cells in 5-year-old children exposed to maternal HIV and antiretroviral therapy in early-life.

Mataramvura H, Jger J, Jordan-Paiz A, Mazengera L, Gumbo F, Bunders M BMC Immunol. 2024; 25(1):82.

PMID: 39702040 PMC: 11658373. DOI: 10.1186/s12865-024-00674-4.


Entry into the lytic cycle exposes EBV-infected cells to NK cell killing via upregulation of the MICB ligand for NKG2D and activation of the CD56 and NKG2AKIRCD56 subsets.

Desimio M, Covino D, Cancrini C, Doria M Front Immunol. 2024; 15:1467304.

PMID: 39676862 PMC: 11638013. DOI: 10.3389/fimmu.2024.1467304.


Immune-Related Genes Associated with Interstitial Lung Disease in Dermatomyositis.

Liu C, Ge Y Int J Gen Med. 2024; 17:5261-5271.

PMID: 39563787 PMC: 11573690. DOI: 10.2147/IJGM.S490294.


References
1.
Ballew B, Yeager M, Jacobs K, Giri N, Boland J, Burdett L . Germline mutations of regulator of telomere elongation helicase 1, RTEL1, in Dyskeratosis congenita. Hum Genet. 2013; 132(4):473-80. PMC: 3600110. DOI: 10.1007/s00439-013-1265-8. View

2.
Markel G, Mussaffi H, Ling K, Salio M, Gadola S, Steuer G . The mechanisms controlling NK cell autoreactivity in TAP2-deficient patients. Blood. 2003; 103(5):1770-8. DOI: 10.1182/blood-2003-06-2114. View

3.
Hazenberg M, Spits H . Human innate lymphoid cells. Blood. 2014; 124(5):700-9. DOI: 10.1182/blood-2013-11-427781. View

4.
Ibarra A, Schwob E, Mendez J . Excess MCM proteins protect human cells from replicative stress by licensing backup origins of replication. Proc Natl Acad Sci U S A. 2008; 105(26):8956-61. PMC: 2449346. DOI: 10.1073/pnas.0803978105. View

5.
De Maria A, Bozzano F, Cantoni C, Moretta L . Revisiting human natural killer cell subset function revealed cytolytic CD56(dim)CD16+ NK cells as rapid producers of abundant IFN-gamma on activation. Proc Natl Acad Sci U S A. 2010; 108(2):728-32. PMC: 3021076. DOI: 10.1073/pnas.1012356108. View