scholarly journals Comparison of the innate immune responses of porcine monocyte-derived dendritic cells and splenic dendritic cells stimulated with LPS

2014 ◽  
Vol 21 (3) ◽  
pp. 242-254 ◽  
Author(s):  
Xueqi Qu ◽  
Mehmet U Cinar ◽  
Huitao Fan ◽  
Maren Pröll ◽  
Dawit Tesfaye ◽  
...  
Keyword(s):  
Dendritic Cells ◽  
Immune Responses ◽  
Innate Immune ◽  
Innate Immune Responses

scholarly journals Innate cell profiles during the acute and convalescent phase of SARS-CoV-2 infection in children

2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Melanie R. Neeland ◽  
Samantha Bannister ◽  
Vanessa Clifford ◽  
Kate Dohle ◽  
Kim Mulholland ◽  
...  
Keyword(s):  
Immune Response ◽  
Dendritic Cells ◽  
Immune Responses ◽  
Acute Phase ◽  
Innate Immune ◽  
Low Density ◽  
Innate Immune Responses ◽  
Immunological Mechanisms ◽  
Activated Neutrophils ◽  
Classical Monocytes

AbstractChildren have mild severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) confirmed disease (COVID-19) compared to adults and the immunological mechanisms underlying this difference remain unclear. Here, we report acute and convalescent innate immune responses in 48 children and 70 adults infected with, or exposed to, SARS-CoV-2. We find clinically mild SARS-CoV-2 infection in children is characterised by reduced circulating subsets of monocytes (classical, intermediate, non-classical), dendritic cells and natural killer cells during the acute phase. In contrast, SARS-CoV-2-infected adults show reduced proportions of non-classical monocytes only. We also observe increased proportions of CD63+ activated neutrophils during the acute phase to SARS-CoV-2 in infected children. Children and adults exposed to SARS-CoV-2 but negative on PCR testing display increased proportions of low-density neutrophils that we observe up to 7 weeks post exposure. This study characterises the innate immune response during SARS-CoV-2 infection and household exposure in children.

scholarly journals Multifaceted innate immune responses engaged by astrocytes, microglia and resident dendritic cells against Chikungunya neuroinfection

2015 ◽  
Vol 96 (2) ◽  
pp. 294-310 ◽  
Author(s):  
Trina Das ◽  
Jean Jacques Hoarau ◽  
Marie Christine Jaffar Bandjee ◽  
Marianne Maquart ◽  
Philippe Gasque
Keyword(s):  
Dendritic Cells ◽  
Immune Responses ◽  
Innate Immune ◽  
Innate Immune Responses

scholarly journals Asian and African lineage Zika viruses show differential replication and innate immune responses in human dendritic cells and macrophages

2019 ◽  
Vol 9 (1) ◽  
Author(s):  
Pamela Österlund ◽  
Miao Jiang ◽  
Veera Westenius ◽  
Suvi Kuivanen ◽  
Riia Järvi ◽  
...  
Keyword(s):  
Dendritic Cells ◽  
Immune Responses ◽  
Asian American ◽  
Pacific Islands ◽  
Fetal Brain ◽  
Innate Immune ◽  
Host Protein ◽  
Cytokine Gene Expression ◽  
Innate Immune Responses ◽  
African Lineage

Abstract Zika virus (ZIKV) infections in humans are considered to be mild or subclinical. However, during the recent epidemics in the Pacific Islands and the Americas, the infection was associated with Quillain-Barré syndrome and congenital infections with fetal brain abnormalities, including microcephaly. Thus, more detailed understanding of ZIKV-host cell interactions and regulation of innate immune responses by strains of differential evolutionary origin is required. Here, we characterized the infection and immune responses triggered by two epidemic Asian/American lineage viruses, including an isolate from fetal brains, and a historical, low passage 1947 African lineage virus in human monocyte-derived dendritic cells (DCs) and macrophages. The epidemic Asian/American ZIKV replicated well and induced relatively good antiviral responses in human DCs whereas the African strain replicated less efficiently and induced weaker immune responses. In macrophages both the African and Asian strains showed limited replication and relatively weak cytokine gene expression. Interestingly, in macrophages we observed host protein degradation, especially IRF3 and STAT2, at early phases of infection with both lineage viruses, suggesting an early proteasomal activation in phagocytic cells. Our data indicates that ZIKV evolution has led to significant phenotypic differences in the replication characteristics leading to differential regulation of host innate immune responses.

Comparability study of monocyte derived dendritic cells, primary monocytes, and THP1 cells for innate immune responses

2021 ◽  
Vol 498 ◽  
pp. 113147
Author(s):  
Yi Wen ◽  
Xiaoli Wang ◽  
Suntara Cahya ◽  
Paul Anderson ◽  
Candyd Velasquez ◽  
...  
Keyword(s):  
Dendritic Cells ◽  
Immune Responses ◽  
Innate Immune ◽  
Innate Immune Responses

scholarly journals Sulforaphane Epigenetically Regulates Innate Immune Responses of Porcine Monocyte-Derived Dendritic Cells Induced with Lipopolysaccharide

PLoS ONE ◽  
2015 ◽  
Vol 10 (3) ◽  
pp. e0121574 ◽  
Author(s):  
Xueqi Qu ◽  
Maren Pröll ◽  
Christiane Neuhoff ◽  
Rui Zhang ◽  
Mehmet Ulas Cinar ◽  
...  
Keyword(s):  
Dendritic Cells ◽  
Immune Responses ◽  
Innate Immune ◽  
Innate Immune Responses

scholarly journals Phagocytosis of Enterovirus-Infected Pancreatic  -Cells Triggers Innate Immune Responses in Human Dendritic Cells

Diabetes ◽  
2010 ◽  
Vol 59 (5) ◽  
pp. 1182-1191 ◽  
Author(s):  
B. M. Schulte ◽  
M. Kramer ◽  
M. Ansems ◽  
K. H. W. Lanke ◽  
N. van Doremalen ◽  
...  
Keyword(s):  
Dendritic Cells ◽  
Immune Responses ◽  
Innate Immune ◽  
Innate Immune Responses ◽  
Pancreatic Cells ◽  
Human Dendritic Cells

scholarly journals SARS-CoV-2 Impairs Dendritic Cells and Regulates DC-SIGN Gene Expression in Tissues

2021 ◽  
Vol 22 (17) ◽  
pp. 9228
Author(s):  
Guoshuai Cai ◽  
Mulong Du ◽  
Yohan Bossé ◽  
Helmut Albrecht ◽  
Fei Qin ◽  
...  
Keyword(s):  
Gene Expression ◽  
Dendritic Cells ◽  
Immune Responses ◽  
Single Cell ◽  
Upper Airway ◽  
Innate Immune ◽  
Healthy Controls ◽  
Innate Immune Responses ◽  
Current Spreading ◽  
Plasmacytoid Dcs

The current spreading coronavirus SARS-CoV-2 is highly infectious and pathogenic. In this study, we screened the gene expression of three host receptors (ACE2, DC-SIGN and L-SIGN) of SARS coronaviruses and dendritic cells (DCs) status in bulk and single cell transcriptomic datasets of upper airway, lung or blood of COVID-19 patients and healthy controls. In COVID-19 patients, DC-SIGN gene expression was interestingly decreased in lung DCs but increased in blood DCs. Within DCs, conventional DCs (cDCs) were depleted while plasmacytoid DCs (pDCs) were augmented in the lungs of mild COVID-19. In severe cases, we identified augmented types of immature DCs (CD22+ or ANXA1+ DCs) with MHCII downregulation. In this study, our observation indicates that DCs in severe cases stimulate innate immune responses but fail to specifically present SARS-CoV-2. It provides insights into the profound modulation of DC function in severe COVID-19.

scholarly journals Severe Acute Respiratory Syndrome Coronavirus Fails To Activate Cytokine-Mediated Innate Immune Responses in Cultured Human Monocyte-Derived Dendritic Cells

2005 ◽  
Vol 79 (21) ◽  
pp. 13800-13805 ◽  
Author(s):  
Thedi Ziegler ◽  
Sampsa Matikainen ◽  
Esa Rönkkö ◽  
Pamela Österlund ◽  
Maarit Sillanpää ◽  
...  
Keyword(s):  
Dendritic Cells ◽  
Severe Acute Respiratory Syndrome ◽  
Immune Responses ◽  
A549 Cells ◽  
Human Monocyte ◽  
Innate Immune ◽  
Lung Epithelial Cells ◽  
Cytokine Gene Expression ◽  
Innate Immune Responses ◽  
Necrosis Factor Alpha

ABSTRACT Activation of host innate immune responses was studied in severe acute respiratory syndrome coronavirus (SCV)-infected human A549 lung epithelial cells, macrophages, and dendritic cells (DCs). In all cell types, SCV-specific subgenomic mRNAs were seen, whereas no expression of SCV proteins was found. No induction of cytokine genes (alpha interferon [IFN-α], IFN-β, interleukin-28A/B [IL-28A/B], IL-29, tumor necrosis factor alpha, CCL5, or CXCL10) or IFN-α/β-induced MxA gene was seen in SCV-infected A549 cells, macrophages, or DCs. SCV also failed to induce DC maturation (CD86 expression) or enhance major histocompatibility complex class II expression. Our data strongly suggest that SCV fails to activate host cell cytokine gene expression in human macrophages and DCs.

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