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
. 2009 May;9(5):353-63.
doi: 10.1038/nri2545.

Immunogenic and tolerogenic cell death

Affiliations
Review

Immunogenic and tolerogenic cell death

Douglas R Green et al. Nat Rev Immunol. 2009 May.

Abstract

The immune system is routinely exposed to dead cells during normal cell turnover, injury and infection. Mechanisms must exist to discriminate between different forms of cell death to correctly eliminate pathogens and promote healing while avoiding responses to self, which can result in autoimmunity. However, an effective immune response against host tissue is often needed to eliminate tumours following treatment with chemotherapeutic agents that trigger tumour cell death. Consequently, a central problem in immunology is to understand how the immune system determines whether cell death is immunogenic, tolerogenic or 'silent'.

PubMed Disclaimer

Figures

Figure 1
Figure 1. Characteristics of immunogenic cell death
When cells succumb to the immunogenic variant of apoptosis, they expose calreticulin (CRT) on the cell surface at a pre-apoptotic state. Moreover, they may expose other chaperones including members of the heat shock protein (HSP) family. Later, they release the DAMP HMGB1 as well as other, yet-to-be-characterized factors. The surface-exposed molecules as well as soluble products from dying cells affect the function of DC through the action on specific receptors. For details see main text.
Figure 2
Figure 2. Mechanisms of tolerance induction by apoptotic cells
Apoptotic cells either do not release DAMPs or modify them (e.g., HMGB1, see text) and are engulfed by DC. TGFβ, produced by the dying cells or the engulfing cells induce the differentiation of inducible Treg, which inhibit immune responses. Alternatively, CD8+ T cells are stimulated in the absence of activated CD4+ T cells, resulting in helpless CTL. These are capable of a primary cytotoxic response, but upon restimulation produce TRAIL. As a result, they themselves die while also inhibiting new immune responses, resulting in tolerance.
Figure 2
Figure 2. Mechanisms of tolerance induction by apoptotic cells
Apoptotic cells either do not release DAMPs or modify them (e.g., HMGB1, see text) and are engulfed by DC. TGFβ, produced by the dying cells or the engulfing cells induce the differentiation of inducible Treg, which inhibit immune responses. Alternatively, CD8+ T cells are stimulated in the absence of activated CD4+ T cells, resulting in helpless CTL. These are capable of a primary cytotoxic response, but upon restimulation produce TRAIL. As a result, they themselves die while also inhibiting new immune responses, resulting in tolerance.

Similar articles

Cited by

References

    1. Medzhitov R, Janeway CA., Jr. Decoding the patterns of self and nonself by the innate immune system. Science. 2002;296:298–300. - PubMed
    1. Zitvogel L, et al. Immune response against dying tumor cells. Adv Immunol. 2004;84:131–179. - PubMed
    1. Gaipl US, et al. Clearance deficiency and systemic lupus erythematosus (SLE) J Autoimmun. 2007;28:114–121. - PubMed
    1. Matzinger P. The danger model: a renewed sense of self. Science. 2002;296:301–305. - PubMed
    1. Thompson CB. Apoptosis in the pathogenesis and treatment of disease. Science. 1995;267:1456–1462. - PubMed

Publication types

LinkOut - more resources