Dendritic Cells in Sepsis: Pathological Alterations and Therapeutic Implications

Joint Authors

Wu, Dongdong
Ji, Xinying
Li, Tao

Source

Journal of Immunology Research

Issue

Vol. 2017, Issue 2017 (31 Dec. 2017), pp.1-9, 9 p.

Publisher

Hindawi Publishing Corporation

Publication Date

2017-09-18

Country of Publication

Egypt

No. of Pages

9

Main Subjects

Biology

Abstract EN

Sepsis is the leading cause of death for critically ill patients in recent years.

Dendritic cells (DCs) are important antigen-presenting cells and play a key role in immune response by regulating the innate and adaptive immunity.

The number of DCs, the differentiation of monocytes into DCs, and the levels of surface molecules associated with the function of DCs are changed in the development of sepsis.

There are many mechanisms involved in the alterations of DCs during sepsis, including the induction of apoptosis, reactive oxygen species generation, activation of the Wnt signaling pathway, epigenetic regulation, and variation in Toll-like receptor-dependent signaling.

In this review, we present the classifications of DC subsets and mechanisms involved in the alterations of DCs in sepsis, as well as further discuss the therapeutic strategies targeting DCs in sepsis to improve the aberrant immune response and prolong the life during sepsis progression.

American Psychological Association (APA)

Wu, Dongdong& Li, Tao& Ji, Xinying. 2017. Dendritic Cells in Sepsis: Pathological Alterations and Therapeutic Implications. Journal of Immunology Research،Vol. 2017, no. 2017, pp.1-9.
https://search.emarefa.net/detail/BIM-1181725

Modern Language Association (MLA)

Wu, Dongdong…[et al.]. Dendritic Cells in Sepsis: Pathological Alterations and Therapeutic Implications. Journal of Immunology Research No. 2017 (2017), pp.1-9.
https://search.emarefa.net/detail/BIM-1181725

American Medical Association (AMA)

Wu, Dongdong& Li, Tao& Ji, Xinying. Dendritic Cells in Sepsis: Pathological Alterations and Therapeutic Implications. Journal of Immunology Research. 2017. Vol. 2017, no. 2017, pp.1-9.
https://search.emarefa.net/detail/BIM-1181725

Data Type

Journal Articles

Language

English

Notes

Includes bibliographical references

Record ID

BIM-1181725