Immune Netw.  2004 Dec;4(4):205-215. 10.4110/in.2004.4.4.205.

The Emerging Role of Natural Killer Cells in Innate and Adaptive Immunity

Affiliations
  • 1School of Biological Sciences and Technology, Hormone Research Center, Chonnam National University, Gwangju, Korea. kanghs@jnu.ac.kr
  • 2Department of Pharmacy & Research Center for Transgenic cloned Pig, Chungnam National University, Daejeon, Korea.
  • 3Department of Life Science, Sookmyung Women's University, Seoul, Korea.
  • 4Laboratory of Immunology, Korea Research Institute of Bioscience and Biotechnology, Daejeon, Republic of Korea.

Abstract

In the early host defense system, effector function of natural killer (NK) cells results in natural killing against target cells such as microbe-infected, malignant, and certain allogenic cells without prior stimulation. NK cell cytotoxicity is selectively regulated by homeostatic prevalence between a repertoire of both activating and inhibitory receptors, and the discrimination of untransformed cells is achieved by recognition of major histocompatibility complex (MHC) class I alleles through inhibitory signals. Although it is well known that the bipotential T/NK progenitors are derived from the common precusor, functional mechanisms in terms of the development of NK cells remain to be further investigated. NK cells are mainly involved in innate immunity, but recent studies have been reported that they also play a critical role in adaptive immune responses through interaction with dendritic cells (DC). This interaction will provide effector functions and development of NK cells, and elucidation of its precise mechanism may lead to therapeutic strategies for effective treatment of several immune diseases.

Keyword

Natural killer cells; innate immunity; adaptive immunity; development; function; NK receptors; tumor; major histocompatibility complex; dendritic cells

MeSH Terms

Adaptive Immunity*
Alleles
Dendritic Cells
Discrimination (Psychology)
Homicide
Immune System Diseases
Immunity, Innate
Killer Cells, Natural*
Major Histocompatibility Complex
Prevalence
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