Dr Hilligan joined the Malaghan Institute in 2012 to undertake post-graduate research in the Ronchese Lab. Her research has centred around a rare population of innate immune cells, known as antigen-presenting cells (APC), that play vital role in initiating and shaping immune responses. She will return to the Malaghan Institute in late 2022.
"I am interested in understanding the innate immune pathways involved in initiating and shaping adaptive immune responses. I have a particular interest in antigen-presenting cell populations, which are known play an important role in dictating the outcome of immune responses. I am working to understand the mechanisms by which various antigen-presenting cell subsets recognise and respond to material from different pathogens and allergens, and ultimately, regulate the function of effector immune cells. The aim of this research is to inform vaccine design and assist with therapeutic strategies for autoimmune and allergic diseases.
"I am currently investigating how the immunological history of an individual may shape the composition and function of their antigen-presenting cells compartment. I am using pre-clinical models to test the effects of various inflammatory and infectious stimuli on the developmental trajectory and functional capacity of APC populations in both the short- and long-term."
Dr Kerry Hilligan awarded HRC Emerging Researcher First Grant
31 May 2022
Preclinical study finds TB vaccine effective at preventing serious COVID-19 illness
25 January 2022
Discovery points to the skin as ‘ground zero’ for allergic disease
19 November 2021
Royal Society Te Apārangi Fellowship to investigate relationship between germs and the development of allergies
2 November 2021
Immune system discovery could lead to better treatments and vaccines
10 November 2020
Research under lockdown: Keeping an eye on dendritic cells in the skin
26 May 2020
Lage SL, Amaral EP, Hilligan KL, Laidlaw E, Rupert A, Namasivayan S, Rocco J, Galindo F, Kellogg A, Kumar P, Poon R, Wortmann GW, Shannon JP, Hickman HD, Lisco A, Manion M, Sher A, Sereti I (2022). Persistent Oxidative Stress and Inflammasome Activation in CD14highCD16- Monocytes From COVID-19 Patients. Front Immunol. 12:799558
Hilligan KL, Namasivayam S, Clancy CS, O'Mard D, Oland SD, Robertson SJ, Baker PJ, Castro E, Garza NL, Lafont BAP, Johnson R, Ronchese F, Mayer-Barber KD, Best SM, Sher A (2022). Intravenous administration of BCG protects mice against lethal SARS-CoV-2 challenge. J Exp Med. 219(2):e20211862.
Mayer JU, Hilligan KL, Chandler JS, Eccles DA, Old SI, Domingues RG, Yang J, Webb GR, Munoz-Erazo L, Hyde EJ, Wakelin KA, Tang SC, Chappell SC, von Daake S, Brombacher F, Mackay CR, Sher A, Tussiwand R, Connor LM, Gallego-Ortega D, Jankovic D, Le Gros G, Hepworth MR, Lamiable O, Ronchese F (2021). Homeostatic IL-13 in healthy skin directs dendritic cell differentiation to promote TH2 and inhibit TH17 cell polarization. Nat Immunol. 2021 Nov 18
Hilligan KL, Ronchese F (2020). Antigen presentation by dendritic cells and their instruction of CD4+ T helper cell responses. Cell Mol Immunol. 17(6):587-599
Ronchese F, Hilligan KL, Mayer JU (2020). Dendritic Cells and the Skin Environment. Curr Opin Immunol. 64:56-62.
R Blecher-Gonen, P Bost, KL Hilligan, E David, T Meir-Salame, B Cohen-Toth, E Roussel, JU Mayer, LM Connor, S Itzkovitz, B Schikowski, F Ronchese, I Amit, (2019). Single-Cell Analysis of Diverse Pathogen Responses Defines a Molecular Roadmap for Generating Antigen-Specific Immunity. Cell Syst. doi: 10.1016/j.cels.2019.01.001.
LM Connor, S-C Tang, E Cognard, S Ochiai, KL Hilligan, SI Old, C Pellefigues, RF White, D Patel, AAT Smith, DA Eccles, O Lamiable, MJ McConnell and F Ronchese, (2017). Th2 responses are primed by skin dendritic cells with distinct transcriptional profiles. J Exp Med. doi: 10.1084/jem.20160470
KL Hilligan, LM Connor, AJ Schmidt and F Ronchese, (2016). Activation-Induced TIM-4 Expression Identifies Differential Responsiveness of Intestinal CD103+ CD11b+ Dendritic Cells to a Mucosal Adjuvant. PLoS ONE 11(7): e0158775. doi:10.1371/journal.pone.0158775.