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DOI 10.2174/1871530317666170613125009

Медицинская библиотека · Endocrine, metabolic & immune disorders drug targets · 2017

A Review on Defects of Dendritic Cells in Common Variable Immunodeficiency.

Sharifi Laleh, Tavakolinia Naeimeh, Kiaee Fatemeh, Rezaei Nima, Mohsenzadegan Monireh, Azizi Gholamreza, Yazdani Reza, Shariat Mansoureh, Mirshafiey Abbas, Aghamohammadi Asghar

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Аннотация

BACKGROUND AND

OBJECTIVES

Common variable immunodeficiency (CVID) is the most important primary disorder that is associated with clinical complications including recurrent infections, malignancy and autoimmune diseases. The genetic cause of CVID is mostly unknown and only a few genetic causes are identified. The various options are proposed for determining the etiology of CVID patients, such as T- and B-cell defects, Toll-like receptors (TLRs) impairments, altered cytokine production as well as blemished dendritic cells (DCs). The patients with CVID show a reduction in number and frequency of DCs in blood, an altered expression of cell surface molecules, and defective activation through toll-like receptors (TLRs). Also loss of IFNα has a critical role in B-cell impairments of CVID patients. The aim of this review is to collect under one umbrella, all the recent knowledge about DCs defects of CVID patients.

METHODS

This review covers basic information about physiology of DCs followed by reports of DCs situation in CVID.

CONCLUSION

According to the results of researches assessing DCs frequency and function in CVID, the roll of DCs in the pathogenesis of CVID cannot be ruled out. The article is expected to encourage the researchers to do comprehensive researches about complex connections between DCs and other immune cells in CVID.

Для цитирования: Sharifi Laleh, Tavakolinia Naeimeh, Kiaee Fatemeh, Rezaei Nima, Mohsenzadegan Monireh, Azizi Gholamreza, Yazdani Reza, Shariat Mansoureh, Mirshafiey Abbas, Aghamohammadi Asghar. A Review on Defects of Dendritic Cells in Common Variable Immunodeficiency.. Endocrine, metabolic & immune disorders drug targets. 2017. DOI: 10.2174/1871530317666170613125009.

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