Emily Wong

Dr Emily Wong is an Infectious Disease physician-scientist whose work focuses on trying to understand the impact of HIV infection on TB pathogenesis, immunity and epidemiology.  To address these questions she uses a range of techniques that span molecular to population science.

Emily specialises in establishing unique human cohorts to address fundamental questions about infectious disease and immune responses. Emily is one of the co-Primary Investigators of Vukuzazi, AHRI’s population-based health ‘omics study that links the longstanding demographic surveillance population to next-generation science.  Designed to shed light on genetic and acquired drivers of health and disease, Vukuzazi defines deep human phenotypes using community-based health screening for HIV, TB and non-communicable diseases and collects biosamples to support genomic and transcriptomic study in a population of 30 000 people in the uMkhanyakude district of KwaZulu-Natal.  Vukuzazi enrolled 18,041 participants between 2018-2020.  Emily’s research team is involved in several collaborative projects analyzing baseline Vukuzazi data and longitudinal follow-up of individuals with specific phenotypes important to understanding TB. In collaboration with the Department of Pulmonology at Inkosi Albert Luthuli Hospital, she established Phefumula, a research bronchoscopy cohort that allows comparative study of immune cells from the mucosal surface of the lung and the peripheral blood of people with well-defined states of HIV and TB.

Emily’s clinical and research interests have focused on the intersections of the HIV and TB epidemics in South Africa since she first worked in Durban in 2003. She witnessed the profound toll of the HIV-epidemic in KZN and was inspired by health care workers and activists who fought to make antiretroviral therapy available in the public sector. To try to better understand the causes of HIV-related mortality after ARV rollout, Emily worked with colleagues in Johannesburg to conduct a post-mortem needle autopsy study to determine the causes of death of patients dying in the first months of antiretroviral therapy; this work revealed very high rates of disseminated tuberculosis and tuberculosis immune reconstitution inflammatory syndrome. Funded by a career development fellowship from the NIH, Emily then focused on trying to understand the immune response to TB in the human lung through study of immune cells in the respiratory mucosa. She particularly focused on a novel class of innate lymphocytes, Mucosal Associated Invariant T (MAIT) cells, trying to understand their role in anti-TB immunity and how HIV altered their function.  Since the launch of Vukuzazi, Emily’s research group spans the Durban and Somkhele campuses of AHRI and aims to bring together next-generation molecular techniques with population science to understand and interrupt drivers of TB infection and disease in the context of HIV hyperendemnicity.

In addition to her resident faculty appointment at AHRI, Emily is an Assistant Professor in the Department of Medicine at the University of Alabama Birmingham (UAB) School of Medicine in the Department of Medicine, Division of Infectious Diseases.  She is also an Associate Scientist in the UAB Center for AIDS Research (CFAR) and has a secondary appointment in the UAB Department of Microbiology.  When not in the lab, Emily can be found trying to keep up with her children’s interests, which these days means juggling online and in person primary school and chasing after a bicycle-riding 3-year-old on the beachfront.

Get in touch with Emily via emily.wong@ahri.org

Click here for a full list of publications.

Emily Wong

Wong Group

The Wong Group’s current projects include:

  1. Trying to understand the clinical, microbiological, radiological and immunological features of subclinical TB.
  2. Next-generation population science approaches to the intersection of infectious and non-communicable disease epidemics in rural KwaZulu-Natal.
  3. Investigations of immune responses to Mtb at the lung’s mucosal surface.

Meet the Team

Urisha Singh  - Wong Group

Urisha Singh

Postdoctoral fellow

Urisha was awarded a PhD in Virology from the University of KwaZulu-Natal for studies on HIV drug resistance and its impact on treatment outcomes. She is currently a 5th year MBCHB candidate and is interested in a physician-scientist career that will involve translational research. Her current research focus is on identifying strategies to address the intersection of infections and non-communicable diseases in South Africa. She is also interested in investigating subclinical TB and methods for its diagnosis.

Lerato Ndlovu - Wong Group

Lerato Ndlovu

Postdoctoral fellow

Dr Lerato Ndlovu did her masters in plant breeding and biochemistry before moving to Dr Al Leslie’s immunology lab at AHRI for her PhD. Her project focused on a set of innate immune cells called neutrophils, and investigating their unique phenotypic and genetic signature as a potential biomarker for TB disease status. She is currently a SANTHE and INSIGHT Fogarty postdoctoral fellow in the Wong group. Her postdoctoral project aims to characterise the impact of HIV co-infection on inflammation and anti-Mtb antibody responses in subclinical TB.

Yumna Moosa - Wong Group

Yumna Moosa

PhD student

Yumna Moosa is an amateur mathematician and qualified medical doctor, with a MBChB degree from the University of Cape Town. She also holds a Master’s degree in Virology and Bioinformatics from UKZN. Her PhD project involves applying molecular and bioinformatic techniques to understand transmission and drivers of tuberculosis and dysbiotic vaginal microbiota in the Vukuzazi study.

Jana Fehr - Wong Group

Jana Fehr

PhD student

Jana Fehr wrote her master thesis in Molecular Biotechnology about modelling the spread of HIV in different environments. She is now a PhD student at the Digital Health chair of the Hasso-Plattner-Institute in Germany and collaborates with the Wong group and the the Vukuzazi programme - AHRI's next generation population-based health research platform. Her project focuses on applying machine learning on community-based data to answer fundamental questions about tuberculosis.

Alison Castle - Wong Group

Alison Castle

Clinical Research Fellow

Alison is a current Fogarty global health scholar and infectious disease fellow at Massachusetts General Hospital. Her clinical research focuses on the intersection of infectious and non-communicable diseases. More specifically, she will explore the bidirectional relationship between tuberculosis, diabetes, and other comorbidities within an HIV-endemic cohort.

Maphe Mthembu - Wong Group

Maphe Mthembu

Research Study Coordinator

Dr Maphe Mthembu holds a masters and PhD from UKZN. Her work at AHRI focuses on understanding the immune response to HIV infected individuals and how infection alters immunity to M tuberculosis. She has also been working on studying the function and location of mucosal invariant T (MAIT) cells immune response from bronchoalveolar lavage fluid compared to the peripheral blood.

Thando Zulu  - Wong Group

Thando Zulu

Laboratory Technician

Thando holds a master’s degree in virology and an honours degree in medical science from the University of KwaZulu-Natal. Her work at AHRI focuses on HIV and TB immunology. Her other duties include serving as a lab coordinator, processing, and storage of human samples as well as maintenance and upkeep of BSL3 and BSL2 laboratories.

Selected Recent Publications

Wong EB. (2021). It is time to focus on asymptomatic tuberculosis. Clinical Infectious Diseases.

Wong EB, Olivier S, Gunda R, Koole O, Surujdeen A, Gereta D, Munatsi D, Modise TH, Dreyer J, Nxumalo S, Smit T, Ording-Jespersen G, Mpofana IB, Khan K, Sikhosana ZEL, Moodley S, Shen YJ, Khoza T, Mhlongo N, Bucibo S, Nyamande K, Baisley K, Cuadros D, Tanser F, Grant AS, Herbst K, Seeley J, Hanekom WA, Ndung'u T, Siedner MJ, Pillay D and the Vukuzazi Team. (corresponding author) (2021). Convergence of infectious and non-communicable disease epidemics in rural South Africa: a cross-sectional, population-based multimorbidity study. Lancet Glob Health 2021; 9: e967–76. (PMID: 34143995, PMCID: PMC8220132).

Khuzwayo S, Mthembu M, Meermeier EW, Prakadan S, Kazer SW, Bassett T, Nyamande K, Khan DF, Maharaj P, Mitha M, Suleman M, Mhlane Z, Ramjit D, Karim F, Shalek A, Lewinsohn DM, Ndung'u T, Wong EB. (corresponding author) (2021). MR1-restricted MAIT cells from the human lung mucosal surface have distinct phenotypic, functional and transcriptomic features that are preserved in HIV infection.. Frontiers in Immunology 12:1135 .

Fehr J, Konigorski S, Olivier S, Gunda R, Surujdeen A, Gareta D, Smit T, Baisley K, Moodley S, Moosa Y, Hanekom W, Koole O, Ndung'u T, Pillay D, Grant AD, Siedner MJ, Lippert C, Wong EB and the Vukuzazi Team. (corresponding author) (2021). Computer-aided interpretation of chest radiography reveals the spectrum of tuberculosis in rural South Africa. npj Digit Med.

Muema D*, Mthembu M*, Schiff A, Singh U, Bassett T, Corleis B, Nyamande K, Fakey Khan D, Maharaj P, Mitha M, Suleman M, Mhlane Z, Ramjit D, Karim F, Kwon D, Ndung'u T, Wong EB. (corresponding author) (2020). Contrasting Inflammatory Signatures in Peripheral Blood and Bronchoalveolar Cells Reveal Compartment-Specific Effects of HIV Infection.. Frontiers in Immunology 11:864 .

Wong, E. B., Gold, M. C., Meermeier, E. W., Xulu, B. Z., Khuzwayo, S., Sullivan, Z. A., … Lewinsohn, D. M. (2019). TRAV1-2+ CD8+ T-cells including oligoconal expansions of MAIT cells are enriched in the airways in human tuberculosis. Communications Biology, 2(1), 203.

Wong EB, Ndung'u T, Kasprowicz VO. (2017). The role of mucosal-associated invariant T cells in infectious diseases.  Immunology; 150(1):45-54.

Sullivan ZS*, Wong EB*, Ndung'u TN, Kasprowicz VO, Bishai WR. (2015) . Latent TB infection increases immune activation in individuals co-infected with HIV. EBioMedicine, 2(4), 334-340.

Wong EB, Akilimali NA, Govender P, Sullivan Z, Cosgrove C, Pillay M, Lewinsohn DM, Bishai WR, Walker BD, Ndung’u T, Klenerman P, Kasprowicz VO. (2013). Low levels of peripheral CD161++CD8+ Mucosal Associated Invariant T (MAIT) cells are found in HIV and HIV/TB co-infection. PLoS ONE, 8(12):e83474.

Wong EB, Omar T, Setlhako GJ, Osih R, Feldman C, Murdoch DM, Martinson NA, Bangsberg DR, Venter WD. (2012). Causes of Death on Antiretroviral Therapy: A Post-Mortem Study from South Africa. PLoS ONE, 7(10).