Infection, modulation and responses of antigen-presenting cells to African swine fever viruses

生物 抗原 病毒学 免疫学
作者
Giulia Franzoni,Silvia Dei Giudici,Annalisa Oggiano
出处
期刊:Virus Research [Elsevier BV]
卷期号:258: 73-80 被引量:48
标识
DOI:10.1016/j.virusres.2018.10.007
摘要

African swine fever (ASF) is a devastating viral disease of domestic pigs and wild boar for which there is no vaccine available. The aetiological agent ASF virus (ASFV) has a predilection for cells of the myeloid lineage. Macrophages provide a first line defence against pathogens and are the main target of ASFV, thus several studies analysed their response to infection in terms of cytokine/chemokine expression and modulation of functionality. These studies have typically used macrophages differentiated in vitro from blood or bone marrow progenitors and few studies have focused on responses of polarized macrophages (M1, M2) or functional macrophage subsets isolated from different tissues. ASFV can also infect dendritic cells (DC), but regardless of their central role in the induction of adaptive immune responses, their role in ASFV infection was only partially analysed. Future studies on ASFV-DC interaction are needed, which should take into consideration the heterogeneity within this family, composed of different subsets whose phenotype is also organ specific. Other porcine immune cells such as γδ-T cells, NK cells and fibrocytes, can act as ‘non-conventional’ antigen-presenting cells (APCs). In particular, γδ-T cells from ASFV immune pigs were shown to present viral antigens to T cells, but no studies have further explored the interaction of ASFV with this cell type or other non-conventional APCs. In this review we will provide an overview of the interaction of APCs with ASFV, describing the differences between virulent and attenuated strains, and suggesting areas for possible future studies.

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
Brook1985完成签到,获得积分10
刚刚
1秒前
mo_完成签到,获得积分20
1秒前
Hao发布了新的文献求助100
1秒前
NexusExplorer应助Anna采纳,获得10
2秒前
3秒前
3秒前
4秒前
cosmol发布了新的文献求助10
4秒前
高兴的小完成签到,获得积分0
5秒前
5秒前
多多发布了新的文献求助20
5秒前
十二月发布了新的文献求助10
7秒前
爱动脑筋的小孩完成签到,获得积分10
7秒前
7秒前
8秒前
8秒前
8秒前
8秒前
9秒前
anzahi应助纯情的浩然采纳,获得10
10秒前
猪头肉发布了新的文献求助10
10秒前
11秒前
破晓发布了新的文献求助10
11秒前
独闯江湖应助明天天明采纳,获得10
12秒前
13秒前
zhang发布了新的文献求助10
13秒前
毛毛虫发布了新的文献求助10
14秒前
莹0000发布了新的文献求助10
14秒前
偏偏完成签到,获得积分10
15秒前
15秒前
15秒前
fabea完成签到,获得积分0
16秒前
16秒前
16秒前
eseme完成签到,获得积分10
17秒前
Anna发布了新的文献求助10
17秒前
wanci应助111采纳,获得10
17秒前
18秒前
18秒前
高分求助中
Adhesion Science: Principles & Practice 1234
Signals, Systems, and Signal Processing 610
Introduction to Cosmetic Formulation and Technology, 2nd Edition 400
Petrology and Plate Tectonics,2025 400
Burger's Medicinal Chemistry and Drug Discovery 400
A Step-by-Step Guide to Qualitative Data Coding 2nd Edition 400
Programming for Chemical Engineers Using C, C++, and MATLAB 320
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 物理 内科学 复合材料 催化作用 物理化学 光电子学 电极 细胞生物学 基因 无机化学
热门帖子
关注 科研通微信公众号,转发送积分 6700887
求助须知:如何正确求助?哪些是违规求助? 8442623
关于积分的说明 18035432
捐赠科研通 5936071
什么是DOI,文献DOI怎么找? 2988835
邀请新用户注册赠送积分活动 1964618
关于科研通互助平台的介绍 1908154