Innate lymphoid cells in intestinal inflammation Dahkki Geremia, A, Arancibia-Cárcamo, C

A functionally specialized population of mucosal CD103+ DCs induces Foxp3+ regulatory T cells via a TGF-beta and retinoic acid-dependent mechanism. Dahkki Coombes, J, Siddiqui, K, Arancibia-Cárcamo, C, Hall, J, Sun, C, Belkaid, Y, Powrie, F

Interleukin-23 restrains regulatory T cell activity to drive T cell-dependent colitis. Dahkki Izcue, A, Hue, S, Buonocore, S, Arancibia-Cárcamo, C, Ahern, P, Iwakura, Y, Maloy, K, Powrie, F

IL-23-responsive innate lymphoid cells are increased in inflammatory bowel disease. Dahkki Geremia, A, Arancibia-Cárcamo, C, Fleming, M, Rust, N, Singh, B, Mortensen, N, Travis, S, Powrie, F

Th1 and innate lymphoid cells accumulate in primary sclerosing cholangitis-associated inflammatory bowel disease Dahkki Gwela, A, Siddhanathi, P, Oxford IBD Cohort Investigators, Chapman, R, Travis, S, Powrie, F, Arancibia-Cárcamo, C, Geremia, A

The short chain fatty acid butyrate imprints an antimicrobial program in macrophages Dahkki Schulthess, J, Pandey, S, Capitani, M, Rue-Albrecht, K, Arnold, I, Franchini, F, Chomka, A, Ilott, N, Johnston, D, Pires, E, McCullagh, J, Sansom, S, Arancibia-Carcamo, C, Uhlig, H, Powrie, F

RORγt inhibitors suppress TH17 responses in inflammatory arthritis and inflammatory bowel disease. Dahkki de Wit, J, Al-Mossawi, M, Hühn, M, Arancibia-Cárcamo, C, Doig, K, Kendrick, B, Gundle, R, Taylor, P, Mcclanahan, T, Murphy, E, Zhang, H, Barr, K, Miller, J, Hu, X, Aicher, T, Morgan, R, Glick, G, Zaller, D, Correll, C, Powrie, F, Bowness, P

CD161 defines a functionally distinct subset of pro-inflammatory natural killer cells Dahkki Kurioka, A, Cosgrove, C, Simoni, Y, van Wilgenburg, B, Geremia, A, Björkander, S, Sverremark-Ekström, E, Thurnheer, C, Günthard, H, Khanna, N, Swiss HIV Cohort Study (50 Others), Oxford IBD Cohort Investigators et al., Walker, L, Arancibia-Cárcamo, C, Newell, E, Willberg, C, Klenerman, P

SARS-CoV-2 RNA detected in blood products from patients with COVID-19 is not associated with infectious virus Dahkki Andersson, M, Arancibia-Carcamo, C, Auckland, K, Baillie, K, Barnes, E, Beneke, T, Bibi, S, Brooks, T, Carroll, M, Crook, D, Dingle, K, Dold, C, Downs, L, Dunn, L, Eyre, D, Gilbert Jaramillo, J, Harvala, H, Hoosdally, S, Ijaz, S, James, T, James, W, Jeffery, K, Justice, A, Klenerman, P, Knight, J, Knight, M, Liu, X, Lumley, S, Matthews, P, McNaughton, A, Mentzer, A, Mongkolsapaya, J, Oakley, S, Oliveira, M, Peto, T, Ploeg, R, Ratcliff, J, Robbins, M, Roberts, D, Rudkin, J, Russell, R, Screaton, G, Semple, M, Skelly, D, Simmonds, P, Stoesser, N, Turtle, L, Wareing, S, Zambon, M

Constructing custom-made radiotranscriptomic signatures of vascular inflammation from routine CT angiograms: a prospective outcomes validation study in COVID-19 Dahkki Kotanidis, CP, Xie, C, Alexander, D, Rodrigues, JCL, Burnham, K, Mentzer, A, O’Connor, D, Knight, J, Siddique, M, Lockstone, H, Thomas, S, Kotronias, R, Oikonomou, EK, Badi, I, Lyasheva, M, Shirodaria, C, Lumley, SF, Constantinides, B, Sanderson, N, Rodger, G, Chau, KK, Lodge, A, Tsakok, M, Gleeson, F, Adlam, D, Rao, P, Indrajeet, D, Deshpande, A, Bajaj, A, Hudson, BJ, Srivastava, V, Farid, S, Krasopoulos, G, Sayeed, R, Ho, L-P, Neubauer, S, Newby, DE, Channon, KM, Deanfield, J, Antoniades, C, Ahern, DJ, Ai, Z, Ainsworth, M, Allan, C, Allcock, A, Angus, B, Ansari, MA, Arancibia-Cárcamo, C, Aschenbrenner, D, Attar, M