| Guidelines for the use of flow cytometry and cell sorting in immunological studies (second edition) |
188 |
| The Gasdermin-D pore acts as a conduit for IL-1 secretion in mice |
42 |
| Contributions of the intestinal microbiome in lung immunity |
31 |
| T-bet and Eomes govern differentiation and function of mouse and human NK cells and ILC1 |
25 |
| Targeting Treg cells in cancer immunotherapy |
24 |
| Function and mechanism of the pyrin inflammasome |
22 |
| Untangling NETosis from NETs |
21 |
| Role of AIM2 inflammasome in inflammatory diseases, cancer and infection |
21 |
| A catch-22: Interleukin-22 and cancer |
19 |
| CMV and natural killer cells: shaping the response to vaccination |
18 |
| Helios(+) and Helios(-) Treg subpopulations are phenotypically and functionally distinct and express dissimilar TCR repertoires |
18 |
| Tissue-resident MAIT cell populations in human oral mucosa exhibit an activated profile and produce IL-17 |
17 |
| Mechanisms of CD8(+) Tcell-mediated suppression of HIV/SIV replication |
16 |
| Expression of c-Kit discriminates between two functionally distinct subsets of human type 2 innate lymphoid cells |
15 |
| Infection with a Brazilian isolate of Zika virus generates RIG-I stimulatory RNA and the viral NS5 protein blocks type I IFN induction and signaling |
15 |
| Short-chain fatty acids: Bacterial messengers modulating the immunometabolism of T cells |
14 |
| The gut microbiota: An emerging risk factor for cardiovascular and cerebrovascular disease |
13 |
| The vaccine adjuvant alum promotes IL-10 production that suppresses Th1 responses |
13 |
| Nanoparticle-based approaches to immune tolerance for the treatment of autoimmune diseases |
13 |
| Sca-1(+) cardiac fibroblasts promote development of heart failure |
12 |
| Plasma cells: The programming of an antibody-secreting machine |
12 |
| Serotonin decreases the production of Th1/Th17 cytokines and elevates the frequency of regulatory CD4(+) T-cell subsets in multiple sclerosis patients |
12 |
| Eomes controls the development of Th17-derived (non-classic) Th1 cells during chronic inflammation |
12 |
| The enigmatic function of IgD: some answers at last |
12 |
| Omalizumab dampens type 2 inflammation in a group of long-term treated asthma patients and detaches IgE from Fc epsilon RI |
11 |
| IL-1 activation in response to Staphylococcus aureus lung infection requires inflammasome-dependent and independent mechanisms |
11 |
| Regulatory Tcells are required for normal and activin-promoted wound repair in mice |
11 |
| GM-CSF therapy inhibits chronic graft-versus-host disease via expansion of regulatory T cells |
10 |
| Dock2 in the development of inflammation and cancer |
10 |
| Human milk oligosaccharides promote immune tolerance via direct interactions with human dendritic cells |
10 |
| Blimp-1 induces and Hobit maintains the cytotoxic mediator granzyme B in CD8 Tcells |
9 |
| Suppressive oligodeoxynucleotides containing TTAGGG motifs inhibit cGAS activation in human monocytes |
9 |
| Airway epithelial TSLP production of TLR2 drives type 2 immunity in allergic airway inflammation |
9 |
| Microglial MHC class II is dispensable for experimental autoimmune encephalomyelitis and cuprizone-induced demyelination |
9 |
| USP14 promotes K63-linked RIG-I deubiquitination and suppresses antiviral immune responses |
9 |
| Axl and MerTK receptor tyrosine kinases maintain human macrophage efferocytic capacity in the presence of viral triggers |
9 |
| Microbial metabolites, short-chain fatty acids, restrain tissue bacterial load, chronic inflammation, and associated cancer in the colon of mice |
9 |
| Proteasome inhibition with bortezomib induces a therapeutically relevant depletion of plasma cells in SLE but does not target their precursors |
9 |
| Murine macrophage chemokine receptor CCR2 plays a crucial role in macrophage recruitment and regulated inflammation in wound healing |
9 |
| Proteome analysis of human CD56(neg) NK cells reveals a homogeneous phenotype surprisingly similar to CD56(dim) NK cells |
8 |
| Detailed characterization of human Mycobacterium tuberculosis specific HLA-E restricted CD8(+) T cells |
8 |
| ILC-poiesis: Ensuring tissue ILC differentiation at the right place and time |
8 |
| T cells and ILC2s are major effector cells in influenza-induced exacerbation of allergic airway inflammation in mice |
8 |
| No strict requirement for eosinophils for bone marrow plasma cell survival |
8 |
| Eosinophils are not essential for maintenance of murine plasma cells in the bone marrow |
8 |
| Th2 cell-derived IL-4/IL-13 promote ILC2 accumulation in the lung by ILC2-intrinsic STAT6 signaling in mice |
7 |
| Suppression of Aiolos and Ikaros expression by lenalidomide reduces human ILC3-ILC1/NK cell transdifferentiation |
7 |
| The role of IL-23 receptor signaling in inflammation-mediated erosive autoimmune arthritis and bone remodeling |
7 |
| Human dendritic cells activated with MV130 induce Th Th17 and IL-10 responses via RIPK2 and MyD88 signalling pathways |
7 |
| Characterization of regulatory T cells in obese omental adipose tissue in humans |
7 |
