Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2019 Mar;71(3):273-282.
doi: 10.1007/s00251-019-01106-z. Epub 2019 Jan 31.

Class I transactivator, NLRC5: a central player in the MHC class I pathway and cancer immune surveillance

Affiliations
Review

Class I transactivator, NLRC5: a central player in the MHC class I pathway and cancer immune surveillance

Saptha Vijayan et al. Immunogenetics. 2019 Mar.

Abstract

Major histocompatibility complex (MHC) class I and class II molecules play critical roles in the activation of the adaptive immune system by presenting antigens to CD8+ and CD4+ T cells, respectively. Although it has been well known that CIITA (MHC class II transactivator), an NLR (nucleotide-binding domain, leucine-rich-repeat containing) protein, as a master regulator of MHC class II gene expression, the mechanism of MHC class I gene transactivation was unclear. Recently, another NLR protein, NLRC5 (NLR family, CARD domain-containing 5), was identified as an MHC class I transactivator (CITA). NLRC5 is a critical regulator for the transcriptional activation of MHC class I genes and other genes involved in the MHC class I antigen presentation pathway. CITA/NLRC5 plays a crucial role in human cancer immunity through the recruitment and activation of tumor killing CD8+ T cells. Here, we discuss the molecular function and mechanism of CITA/NLRC5 in the MHC class I pathway and its role in cancer.

Keywords: CIITA; CITA/NLRC5; Cancer; MHC class I; NLR proteins.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Cell. 1994 Jan 28;76(2):287-99 - PubMed
    1. Cell. 1993 Oct 8;75(1):135-46 - PubMed
    1. Cell. 2002 Apr;109 Suppl:S21-33 - PubMed
    1. Proc Natl Acad Sci U S A. 1983 Apr;80(7):1982-6 - PubMed
    1. J Immunol. 2010 Feb 15;184(4):1990-2000 - PubMed

Publication types

MeSH terms

Substances

LinkOut - more resources