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A Field Researcher addresses participants at the 2024 EMaBS participant meeting held at the Entebbe General Hospital, Uganda, engaging them in discussions about the study’s progress and upcoming research activities.

A Field Researcher addresses participants at the 2024 EMaBS participant meeting held at the Entebbe General Hospital, Uganda, engaging them in discussions about the study’s progress and upcoming research activities.

Entebbe Mother and Baby Study (EMaBS)

A unique Ugandan birth cohort initiated in 2001

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About

The Entebbe Mother and Baby Study (EMaBS) began as a trial [ISRCTN32849447] aimed at investigating the potential benefits of treating worm infections during pregnancy and early childhood.  Today, this cohort has evolved into a unique platform for understanding how early life exposures influence health outcomes in tropical settings.  

Recent and ongoing research

EMaBS participants are currently involved in the EMaBS@21 project, which examines how early-life infections, undernutrition, and socio-economic factors influence the risk of developing cardiovascular diseases (CVDs) in adulthood. Other recent research studies nested within the cohort include the POPVAC C trial, which assessed the impact of BCG revaccination on immune responses to unrelated vaccines, and the TB042 trial, which evaluated the safety and efficacy of a candidate tuberculosis vaccine.

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About
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Established in 2003, the Entebbe Mother and Baby Study (EMaBS) began with a focused mission: to investigate the effects of worm infections during pregnancy and early childhood. These infections are known to cause significant immune modulation in their mammalian hosts, an adaptation believed to protect the worms from being eliminated by the immune system.

The study hypothesized that this immune modulation might extend beyond the worms themselves, potentially influencing responses to immunisations, unrelated infections and allergens. Additionally, it posited that worm infections in mothers could shape the development of immune responses in their children.

To test these hypotheses, EMaBS was designed to explore the effects of deworming treatments during pregnancy and early childhood on infant immune response to immunisation, as well as susceptibility to infectious diseases and allergy related diseases. The interventions concluded when the children reached five years of age, and follow up studies have continued into adolescence and adulthood.

Beyond its original scope, EMaBS has become a vital resource for examining how early life exposures impact health outcomes later in life. Situated in a tropical region encompassing both urban and rural settings, participants face unique environmental exposures uncommon in resource rich areas, such as worms, malaria, and other infectious diseases.

With over two decades of comprehensive data and samples collected from its cohort, alongside strong participant and community engagement, EMaBS now serves as an invaluable platform for addressing a wide array of research questions. Whether leveraging existing data and samples or initiating new studies, EMaBS continues to provide critical insights into the interplay between early life exposures and long term health.

Who we are
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Study team

EMaBS Principal Investigator
  • Professor Alison Elliott, MRC/UVRI and LSHTM Uganda Research Unit
Entebbe Hospital Directors
  • Dr John Bosco Nsubuga (current)
  • Dr Peterson Kyebambe
  • Dr Moses Muwanga
EMaBS@21 Principal investigator
  • Professor Emily Webb, London school of Hygiene and Tropical Medicine
EMaBS@21 Co-Principal investigator
  • Bridgious Walusimbi, MRC/UVRI and LSHTM Research Unit Uganda
EMaBS@21 Co investigators MRC/UVRI and LSHTM Research Unit Uganda
  • Professor Alison Elliott
  • Professor Moffat Nyirenda
  • Dr Anxious Niwaha
  • Dr Anne Wajja
  • Professor Nambusi Kyegombe
EMaBS@21 Co investigators KEMRI-Wellcome Research Program
  • Professor Sarah Atkinson
EMaBS@21 Coordinator
  • Dr Ronald Komata
Statistician
  • Isaac Sekitoleko
Data manager
  • Racheal Nakyesige      
  • Hellen Akurut  
Internal Monitor
  • Mirriam Akello
Administration and Community Engagement
  • Moses Kizza
Communications and Engagement officer
  • Trust Debbie Lenia
Laboratory
  • Jacent Nassuuna         
  • Ivan Ssali        
  • Carol Promise Biyinzika
  • Gloria Oduru   
  • Grace Kabami  
Medical officers
  • Joel Serubanja
  • Nelson Twinamasiko   
  • Pius Tumwesige
Clinicians
  • Christopher Zziwa       
  • Milly Namutebi
Study nurses
  • Florence Akello
  • Josephine Tumusiime
  • Susan Amongi
  • Caroline Onen
  • Caroline Ninsiima        
  • Barbra Apule
  • Esther Nakazibwe
  • Christine Nankabirwa Musoke
  • Christine Kukundakwe
  • Ruth Nyanzi Katende
Fieldworkers
  • Loyce Kisakye Namusobya       
  • Denis Nsubuga
  • Fred David Kiwudhu
  • Tony Katongole
  • Sewankambo Moses
  • Marble Naluwooza
  • Samuel Kiwanuka
  • Chrisostome Akantorana    

Entebbe Hospital staff

The staff at Entebbe Hospital play a crucial role in our team, particularly in recruiting study participants at the antenatal clinic, assisting with childbirth, and administering immunizations.

EMaBS community field workers

The EMaBS community field workers are vital members of our team. Selected by local council executives from each village within the EMaBS catchment area, they played a key role in following up with EMaBS children twice a month until the age of five. These field workers received certified initial training and participated in monthly update meetings. Each was provided with a bicycle to facilitate their work. Even today, they continue to offer valuable support to EMaBS by assisting with follow-up activities and maintaining strong connections with the community.

Collaborators and funders

  • Uganda Virus Research Institute
  • Entebbe General Hospital
  • Mulago Hospital, Uganda
  • Ministry of Health, Uganda
  • University of Cambridge
  • Oxford University
  • Leiden University Medical Center
  • KEMRI-Wellcome Trust Research Programme
  • Wellcome Trust Sanger Institute
  • Makerere University
  • Lancaster University
  • Copenhagen University
  • University of Colorado
  • Frederick National Laboratory for Cancer Research
  • University of York
  • International Agency for Research on Cancer (IARC)
  • University of the Witwatersrand
  • Amsterdam University Medical Center
Research
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As the burden of non-communicable diseases (NCDs) continues to rise in sub-Saharan Africa, the EMaBS cohort offers a critical opportunity to address the interplay between early exposures and adulthood health outcomes.

Explore detailed findings and related publications on the main research and ongoing projects highlighted below on our Publications page.

EMaBS@21

EMaBS@21 is a ground-breaking research project nested within the long-standing Entebbe Mother and Baby Study (EMaBS) cohort at the MRC/UVR and LSHTM Uganda Research Unit. The study investigates how early-life infections, undernutrition, and socio-economic factors influence the risk of developing cardiovascular diseases (CVDs) in adulthood.

By analysing physical determinants (e.g. blood pressure, blood lipids, glucose levels, Body Mass Index (BMI) alongside behavioural risk factors (diet, physical activity, alcohol and tobacco use), the study aims to uncover critical life-course factors contributing to CVD susceptibility in sub-Saharan Africa. The insights derived from this work aim to inform preventive health interventions and policies tailored to the unique exposures and challenges of the region.

Our main objective:

To determine how early-life infections and undernutrition impact cardiovascular disease (CVD) risk in adulthood. The study will assess physiological determinants of CVD (blood pressure, lipid levels, glucose, and BMI) and behavioural risk factors such as diet and physical inactivity.

Our specific objectives are to:

1. Determine the effect of early-life exposures on physiological determinants of CVDs, measured in young Ugandan adults

2. Assess (a) determinants of behavioral risk factors for CVDs, and (b) their associations with physiological determinants of CVDs in young Ugandan adults

3. Investigate nutritional and metabolic pathways through which early-life exposures may influence physiological determinants of CVDs

4. Explore participants’ understanding of CVDs including their awareness of behavioral CVD risk factors, their subjective assessment of their own CVD risk profile and where they obtain information about NCDs

Childhood infection, Epigenetics and Long-term health

Can common childhood infections have lasting effects on a person’s health later in life?

This pioneering study led by researchers from the MRC/UVRI and LSHTM Uganda Research Unit, the London School of Hygiene & Tropical Medicine, and the University of Oxford seeks to answer this critical question. While the immediate consequences of severe childhood infections, such as death or disability, are well-recognized, the long-term effects of repeated infections, even when a child appears to recover, remain unclear. This collaborative study aims to explore whether recurrent infections in childhood cause chemical modifications to a person’s DNA—known as epigenetic changes. Epigenetic changes are alterations in DNA that do not affect the genetic sequence but can influence how genes are expressed. These changes accumulate throughout a person’s life and are shaped by environmental factors like diet, smoking, or obesity.

The researchers will use data from the Entebbe Mother and Baby Study (EMaBS) to investigate whether frequent childhood infections lead to specific epigenetic changes.

In a second phase, the team will use data from the Uganda General Population Cohort (GPC) to assess whether these infection-related epigenetic changes increase the risk of non-communicable diseases, such as cancer, in adulthood.

The project is led by Dr. James Gilchrist, a clinician-scientist at the University of Oxford, in collaboration with Bridgious Walusimbi, a Research Fellow at the London School of Hygiene & Tropical Medicine. Funding for this research is provided by a Wellcome Career Development Award.

This study holds the potential to uncover how childhood health experiences shape lifelong disease risk, offering critical insights that could inform future public health interventions.

POPVAC C

POPVAC C comprises a trial designed to determine the effect of BCG re-vaccination on the response to unrelated vaccines in adolescents participating in the Entebbe Mother and Baby Study birth cohort, and an observational study on life-course exposures that impact vaccine responses.

Adolescents who were enrolled prenatally into the Entebbe Mother and Baby Study birth cohort were recruited and randomised to receive either BCG revaccination (150 participants) or no BCG revaccination (150 participants). We found that BCG revaccination did not impact on immune responses to an array of other vaccines against tetanus, diphtheria, HPV, yellow fever and typhoid. However, participants in POPVAC C generally had higher vaccine responses than their contemporaries living in two rural Ugandan settings; supporting the hypothesis, that rural environment is associated with reduced vaccine immunogenicity.

Co-Host

The Co-Host study aims to identify determinants of susceptibility and response to SARS-CoV-2 infection, and to investigate the role of adolescents in disease transmission. Co-Host enrolled 500 participants from the EMaBS cohort, and followed them up for one year, documenting COVID-19 incidence and vaccination, and collecting blood samples for measurement of SARS-CoV-2 antibodies. Analysis is ongoing.

TB042

BCG confers variable protection against pulmonary tuberculosis, reduced in countries near the equator and rural, compared to urban, settings. A more effective vaccine is needed. The TB042 trial was a proof-of-concept study evaluating the safety and immunogenicity of a ChAdOx1 85A-MVA85A boost compared with BCG revaccination, among adolescents residing in a tuberculosis-endemic area in the topics. Following ChAdOx1 85A dose escalation and age de-escalation, TB042 recruited 60 adolescents from the EMaBS cohort. The trial found that the ChAdOx1 85A–MVA85A regimen was safe and induced stronger Ag85A-specific responses than BCG revaccination.

Allergy and asthma work at 9 years

Following the original EMaBS trial findings, we wanted to find out whether the effects of worms and their treatment during pregnancy continued as children grow up.  When EMaBS children were nine years of age, we collected data on history of allergy-related diseases, and used skin prick tests and IgE measurements to assess responses to allergens (Protocol). We found that allergen sensitisation started early in childhood and increased with age, but that eczema, wheeze were common in infancy, and declined with age, suggesting that environmental exposures during childhood may dissociate atopy and allergy-related diseases. We found no evidence that prenatal and early-life treatment of helminths altered the risk of atopic diseases later in childhood.

Earlier blood pressure work

There is good evidence that exposures while still in the womb, and factors such as growth patterns in early life, can influence blood pressure. In addition, that blood pressure in adolescents can predict blood pressure in later life.  We measured blood pressure and lipid levels at age 10 or 11 years to see how factors such as birth weight and exposures to infection influence these parameters. We found that post-natal weight gain was important in the developmental programming of blood pressure, with fast-growing low birth weight children at particular risk. Regarding infections, we found associations between either current or early-life malaria and reduced blood pressure and modified lipid levels.

Original EMaBS trial

In the original EMaBS trial, we expected that treatment of the mothers’ worms would result in improved responses to vaccines in the children, but this was not generally the case. The only result that fitted in with our hypothesis was that albendazole treatment modified the response to tetanus immunisation among children of mothers with hookworm. We discuss the possible explanation for this in our papers on this topic. The most striking result of the trial was that treatment of worms during pregnancy resulted in increased rates of eczema in the children. This result fits in with the “Hygiene Hypothesis” which proposes that infections, including worm infections, influence the human immune response, protecting from the excessive inflammation that causes allergy (and other diseases such as inflammatory bowel disease and type I diabetes).

Resources
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Data and sample archive of EMaBS

This is currently being updated, for urgent enquires please contact Alison Elliott at Alison.Elliott@lshtm.ac.uk or Alison.Elliott@mrcuganda.org.

Information to the participants

Publications
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Preparatory work and other ancillary or descriptive studies
  • Bukusuba JW, Hughes P, Kizza M, Muhangi L, Muwanga M, Whitworth JAG, Elliott AM. Screening for intestinal helminth infection in a semi-urban cohort of pregnant women in Uganda.  Tropical Doctor, 2004; 34:27-28.
  • Kizito D, Woodburn PW, Kesande B, Ameke C, Nabulime J, Muwanga M, Grosskurth H, Elliott AM.  Uptake of HIV and syphilis testing by pregnant women and their male partners in a programme for Prevention of Mother-to-Child HIV transmission in Uganda. Tropical Medicine and International Health, 2008; 13:680-682.
  • Mpairwe H, Muhangi L, Namujju PB, Kisitu A, Tumusiime A, Muwanga M, Whitworth JAG, Onyango S, Biryahwaho B. Elliott AM. HIV risk perception and prevalence in a programme for prevention of mother-to-child HIV transmission: comparison of women who accept voluntary counselling and testing and those tested anonymously. Journal of Acquired Immune Deficiency Syndromes, 2005; 39:354-358.
  • Hillier SD, Booth M, Muhangi L, Nkurunziza P, Khihembo M, Kakande M, Sewankambo M, Kizindo R, Kizza M, Muwanga M, Bambury M, Elliott AM.  Plasmodium falciparum and helminth co-infection in a semi-urban population of pregnant women in Uganda. Journal of Infectious Diseases 2008; 198:920-927.
  • Woodburn PW, Muhangi L, Hillier S, Ndibazza J, Namujju P, Kizza M, Ameke C, Omoding NE, Booth M, Elliott AM.  Risk factors for helminth, malaria and HIV infection in pregnancy in Entebbe, Uganda.  PLoS Neglected Tropical Diseases 2009; 3:e473.
  • Millard JD, Muhangi L, Sewankambo M, Ndibazza J, Elliott AM, Webb EL. Assessing the external validity of a randomised, controlled trial of anthelminthics in mothers and their children in Entebbe, Uganda, using a two-stage cluster sample community survey. Trials 2014, 15:310.
  • Elliott AM, Namujju PB, Mawa PA, Quigley MA, Nampijja M, Nkurunziza PM, Belisle JT, Muwanga M, Whitworth JAG.  A randomised controlled trial of the effects of albendazole in pregnancy on maternal responses to mycobacterial antigens and infant responses to bacille Calmette-Guerin (BCG) immunisation [ISRCTN32849447]. BMC Infectious Diseases 2005, 5:115.
  • Elliott AM, Kizza M, Quigley MA, Ndibazza J, Nampijja M, Muhangi L, Morison L, Namujju PB, Muwanga M, Kabatereine N, Whitworth JAG. The impact of helminths on the response to immunisation and on the incidence of infection and disease in childhood in Uganda: design of a randomised, double-blind, placebo-controlled, factorial trial of de-worming interventions delivered in pregnancy and early childhood [ISRCTN32849447], Clinical Trials 2007; 4:42-57.
Safety of treating worms during pregnancy
  • Ndibazza J, Lule S, Nampijja M, Mpairwe H, Oduru G, Kiggundu M, Akello M, Muhangi L, Elliott AM.  A Description of Congenital Anomalies among Infants in Entebbe, Uganda. Birth Defects Research Part A: Clinical and Molecular Teratology, 2011; doi:10.1002/bdra.20838.
  • Ndibazza J, Muhangi L, Akishule D, Kiggundu M, Ameke C, Oweka J, Kizindo R, Duong T, Kleinschmidt I, Muwanga M, Elliott AM.  The effects of de-worming in pregnancy on maternal and perinatal outcomes in Entebbe Uganda: a randomised controlled trial. Clinical Infectious Diseases 2010; 50:531-540.
  • Friedman JF, Olveda RM, Mirochnik MH, Bustinduy AL, Elliott AM. Praziquantel for the treatment of schistosomiasis during human pregnancy.  Bull World Health Organ. 2018 Jan 1;96(1):59-65. doi: 10.2471/BLT.17.198879. Epub 2017 Nov 27. PubMed PMID: 29403101; PubMed Central PMCID: PMC5791873
  • Luty AJF, Elliott AM.  Tackling neglect: treating schistosomiasis during pregnancy. Lancet Infectious Diseases, 2015 Oct 23. pii: S1473-3099(15)00379-5. doi: 10.1016/S1473-3099(15)00379-5. [Epub ahead of print] PMID: 26771653
  • Muhangi L, Woodburn P, OmaraM, Omoding N, Kizito D, Mpairwe H, Nabulime J, Ameke C, Morison LA, Elliott AM.  Associations between mild-moderate anaemia in pregnancy and helminth, malaria and HIV infection in Entebbe, Uganda.  Transactions of the Royal Society of Tropical Medicine and Hygiene 2007; 101:899-907.
Vaccines (plus infectious diseases in some papers)
  • Elliott AM, Mawa PA, Webb EL, Nampijja M, Lyada N, Bukusuba J, Kizza M, Namujju P, Nabulime J, Ndibazza J, Muwanga M, Whitworth JAG. Effects of maternal and infant co-infections, and of maternal immunisation, on the infant response to BCG and tetanus immunisation in a birth cohort in Uganda. Vaccine 2010; 29:247-255.
  • Webb EL, Mawa PA, Ndibazza J, Kizito D, Namatovu A, Kyosiimire-Lugemwa J, Nanteza B, Nampijja M, Muhangi L, Woodburn PWW, Akurut H, Mpairwe H, Akello M, Lyadda N, Bukusuba J, Kihembo M, Kizza M, Kizindo R, Nabulime J, Ameke C, Namujju PB, Tweyongyere R, Muwanga M, Whitworth JAG, Elliott AM. Effect of single-dose anthelmintic treatment during pregnancy on an infant's response to immunisation and on susceptibility to infectious diseases in infancy: a randomised, double-blind, placebo-controlled trial. Lancet 2011; 377:52-62.
  • Ndibazza J, Mpairwe H, Webb EL, Mawa PA, Nampijja M, Muhangi L, Kihembo M, Lule SA, Rutebarika D, Apule B, Akello F, Akurut H, Oduru G, Naniima P, Kizito D, Kizza M, Kizindo R, Tweyongyere R, Alcock K, Muwanga M, Elliott AM. Impact of anthelminthic treatment in pregnancy and early childhood on response to immunisation and on the incidence of infectious diseases and eczema in early childhood: results of a randomised, double-blind, placebo-controlled trial. PLoS One 2012, 7:e50325.
  • Nash S, Mentzer AJ, Lule SA, Kizito D, van der Klis FRM, Elliott AM.  The impact of prenatal exposure to parasitic infections and to anthelminthic treatment on antibody responses to routine immunisations given in infancy: secondary analysis of a randomised controlled trial. PLoS Negl Trop Dis 2017; 11(2):e0005213.
  • Kizito D, Tweyongyere R, Namatovu A, Webb EL, Muhangi L, Lule SA, Bukenya H, Cose S, Elliott AM. Factors affecting the infant antibody response to measles immunisation in Entebbe-Uganda. BMC Public Health. 2013,13(1):619.
  • Anderson EJ, Webb EL, Mawa PA, Kizza M, Lyadda N, Nampijja M, Elliott AM. The influence of BCG vaccine strain on mycobacteria-specific and non-specific immune responses in a prospective cohort of infants in Uganda. Vaccine 2012, 30:2083-2089.
Tuberculosis
  • Lule SA, Mawa P, Nkurunungi G, Nampijja M, Kizito D, Akello F, Muhangi L, Elliott AM, Webb EL. Factors associated with tuberculosis infection, and with anti-mycobacterial immune responses, among five year olds BCG-immunised at birth in Entebbe, Uganda. Vaccine 2015, 33(6):796-804.
  • Nkurunungi G, Lutangira JE, Lule SA, Akurut H, Kizindo R, Fitchett JR, Kizito D, Sebina I, Muhangi L, Webb EL, Cose S, Elliott AM.  Determining Mycobacterium tuberculosis Infection among BCG-immunised Ugandan Children by T-SPOT.TB and tuberculin skin testing. PLoS One 2012, 7:e47340. 
Malaria
  • Ndibazza J, Webb EL, Lule S, Mpairwe H, Akello M, Oduru G, Kizza M, Akurut H, Muhangi L, Magnussen P, Vennervald B, Elliott AM.  Associations between maternal helminth and malaria infections in pregnancy, and clinical malaria in the offspring: a birth cohort in Entebbe, Uganda. Journal of Infectious Diseases 2013, 208:2007-16.
HIV infection
  • Muhangi L, Lule SA, Mpairwe H, Ndibazza J, Kizza M, Nampijja M, Nakazibwe E, Kihembo M, Webb EL, Elliott AM.  Maternal HIV infection and other factors associated with growth outcomes of HIV-uninfected infants in Entebbe, Uganda. Public Health and Nutrition 2013, 16:1548-57.
  • Webb EL, Kyosiimire-Lugemwa J, Kizito D, Nkurunziza P, Lule S, Muhangi L, Muwanga M, Kaleebu P, Elliott AM.  The effect of anthelminthic treatment during pregnancy on HIV plasma viral load; results from a randomised, double blinded, placebo-controlled trial in Uganda. Journal of Acquired Immune Deficiency Syndromes, 2012, 60:307-13.
Impact of parasitic infections on viral infections and cancer disease risk
  • Nalwoga A, Webb EL, Muserere C, Chihota B, Miley W, Labo N, Elliott A, Cose S, Whitby D, Newton R, Variation in KSHV prevalence between geographically proximate locations in Uganda. Infect Agent Cancer, 2020. 15: p. 49.
  • Wakeham K, Webb EL, Sebina I, Muhangi L, Miley W, Johnson WT, Ndibazza J, Elliott AM, Whitby D, Newton R.  Parasite infection is associated with Kaposi’s sarcoma associated herpesvirus (KSHV) in Ugandan women. Infectious Agents and Cancer 2011, 6:15.
  • Wakeham K, Webb EL, Sebina I, Nalwoga A, Muhangi L, Miley W, Johnston WT, Ndibazza J, Whitby D, Newton R, Elliott AM.  Risk factors for seropositivity to Kaposi’s sarcoma associated herpesvirus (KSHV) among children in Uganda. Journal of Acquired Immune Deficiency Syndromes 2013, 63:228-33.
  • Nalwoga A, Cose S, Wakeham K, Miley W, Ndibazza J, Drakeley C, Elliott A, Whitby D, Newton R.  Association between malaria exposure and Kaposi's sarcoma-associated herpes virus seropositivity in Uganda. Trop Med Int Health. 2015 May;20(5):665-672.      PMID: 25611008
  • Nalwoga A, Miley W, Labo N, Elliott A, Cose S, Whitby D, Newton R.  Age of Infection with Kaposi Sarcoma Associated Herpesvirus and Subsequent Antibody Values Among Children in Uganda.      Ped Infect Dis J 2018 Aug;37(8):e225-e228.
  • Newton R, Labo N, Wakeham K, Marshall V, Roshan R, Nalwoga A, Sebina I, Muhangi L, Webb E, Miley W, Rochford R, Elliott A, Whitby D.  Determinants of -herpesvirus shedding in saliva among Ugandan children and their mothers.  Journal of Infectious Diseases, 2018 May 12. doi: 10.1093/infdis/jiy262. [Epub ahead of print]
  • Thorne L, Nalwoga A, Mentzer AJ, de Rougemont A, Hosmillo M, Webb E, Nampiija M, Muhwezi A, Carstensen T, Gurdasani D, Hill AV, Sandhu MS, Elliott A, Goodfellow I. The First Norovirus Longitudinal Seroepidemiological Study from Sub-Saharan Africa Reveals High Seroprevalence of Diverse Genotypes Associated with Host Susceptibility Factors.  J Infect Dis 2018 Apr 18. doi: 10.1093/infdis/jiy219. [Epub ahead of print]
Maternal schistosome infection on responses to schistosomiasis in the offspring
  • Tweyongyere R, Naniima P, Mawa PA, Jones FM, Webb EL, Cose S, Dunne DW, Elliott AM. Effect of maternal Schistosoma mansoni infection and praziquantel treatment during pregnancy on Schistosoma mansoni infection and immune responsiveness among offspring at age five years.  PLoS Neglected Tropical Diseases 2013, 7(10): e2501.
  • Tweyongyere R, Mawa PA, Kihembo M, Jones FM, Webb EL, Cose S, Dunne DW, Vennervald BJ, Elliott AM.  Effect of praziquantel treatment of Schistosoma mansoni during pregnancy on immune responses to schistosome antigens among the offspring: results of a randomised, placebo-controlled trial. BMC Infectious Diseases 2011; 11:234.
  • Tweyongyere R, Mawa PA, Emojong NO, Mpairwe H, Jones FM, Duong T, Dunne DW, Vennervald BJ, Katunguka-Rwakishaya E, Elliott AM.      Effect of praziquantel treatment of Schistosoma mansoni during pregnancy on intensity of infection and antibody responses to schistosome antigens: results of a randomised, placebo-controlled trial. BMC Infectious Diseases 2009, 9:32.
  • Tweyongyere R, Mawa PA, Ngom-Wegi S, Ndibazza J, Duong T, Vennervald BJ, Dunne DW, Katunguka-Rwakishaya E, Elliott AM.  Effect of praziquantel treatment during pregnancy on cytokine responses to schistosome antigens: results of a randomised, placebo-controlled trial. Journal of Infectious Diseases 2008, 198:1870-1879.
Genetics of infant vaccine responses
  • Mentzer AJ, Dilthey AT, Pollard M, Gurdasani D, Karakoc E, Carstensen T, Muhwezi A, Cutland C, Diarra A, da Silva Antunes R, Paul S, Smits G, Wareing S, Kim H, Pomilla C, Chong AY, Brandt DYC, Nielsen R, Neaves S, Timpson N, Crinklaw A, Lindestam Arlehamn CS, Rautanen A, Kizito D, Parks T, Auckland K, Elliott KE, Mills T, Ewer K, Edwards N, Fatumo S, Webb E, Peacock S, Jeffery K, van der Klis FRM, Kaleebu P, Vijayanand P, Peters B, Sette A, Cereb N, Sirima S, Madhi SA, Elliott AM, McVean G, Hill AVS, Sandhu MS. High-resolution African HLA resource uncovers HLA-DRB1 expression effects underlying vaccine response. Nat Med. 2024 May;30(5):1384-1394. doi: 10.1038/s41591-024-02944-5. Epub 2024 May 13. PMID: 38740997; PMCID: PMC11108778. 
Vaccines in adolescence - POPVAC
  • Zirimenya L, Nkurunungi G, Nassuuna J, Natukunda A, Mutebe A, Oduru G, Kabami G, Akurut H, Onen C, Namutebi M, Serubanja J, Nakazibwe E, Akello F, Tumusiime J, Sewankambo M, Kiwanuka S, Kiwudhu F, Kizindo R, Kizza M, Wajja A, Cose S, Muwanga M, Webb E, Elliott AM. Impact of BCG revaccination on the response to unrelated vaccines in a Ugandan adolescent birth cohort: randomised controlled trial protocol C for the 'POPulation differences in VACcine responses' (POPVAC) programme. BMJ Open. 2021;11(2):e040430.
  • Nkurunungi G, Zirimenya L, Natukunda A, Nassuuna J, Oduru G, Ninsiima C, Zziwa C, Akello F, Kizindo R, Akello M, Kaleebu P, Wajja A, Luzze H, Cose S, Webb E, Elliott AM. Population differences in vaccine responses (POPVAC): scientific rationale and cross-cutting analyses for three linked, randomised controlled trials assessing the role, reversibility and mediators of immunomodulation by chronic infections in the tropics. BMJ Open. 2021;11(2):e040425.
  • Natukunda A, Nkurunungi G, Zirimenya L, Nassuuna J, Zziwa C, Ninsiima C, Tumusiime J, Nyanzi R, Namutebi M, Kiwudhu F, van Dam GJ, Corstjens P, Kizindo R, Nkangi R, Kabagenyi J, Nassanga B, Cose S, Wajja A, Kaleebu P, Elliott AM, Webb E. Does Schistosome or Malaria Exposure Contribute to Urban-Rural Differences in Vaccine Responses in Uganda? A Causal Mediation Analysis Using Data from Three Linked Randomised Controlled Trials. Lancet Glob Health. 2024 Nov; 12(11): e1860–e1870.
  • Nassuuna J, Zirimenya L, Nkurunungi G, Natukunda A, Zziwa C, Ninsiima C, Apule B, Onen C, Amongi S, Serubanja J, Tumwesige P, Nsubuga D, Amongin R, van Dam GJ, Corstjens P, Kayiwa J, Kabagenyi J, Cose S, Wajja A, Kaleebu P, Webb E, Elliott AM. The Effect of Bcg Revaccination on the Response to Unrelated Vaccines in Urban Ugandan Adolescents: Results of the Popvac C Randomised, Controlled Trial. Lancet Glob Health. 2024 Nov; 12(11): e1849–e1859.
  • Nassuuna J, Sterk J, Walusimbi B, Natukunda A, Nkangi R, Amongin R, Zirimenya L, Webb EL, Elliott AM, Nkurunungi G✉. Helminth-driven gut inflammation and microbial translocation are linked to altered vaccine responses in rural Uganda. 2024. PREPRINT available at Research Square [https://doi.org/10.21203/rs.3.rs-5201954/v1].
Vaccines in adolescence – TB
  • Wajja A, Francis BN, Natukunda A, Serubanja J, Tumusiime J, Akurut H, Oduru G, Nassuuna J, Kabagenyi J, Morrison H, Scott H, Powell Doherty R, Marshall JL, Puig IC, Cose S, Kaleebu P, Webb EL, Satti I, McShane H, Elliott AM, TB042 Study Team. Safety and immunogenicity of ChAdOx1 85A prime followed by MVA85A boost compared to BCG revaccination among Ugandan adolescents who received BCG at birth: a randomised, open-label trial. Lancet Infect Dis. 2024 Mar;24(3):285-296.
  • Wajja A, Nassanga B, Natukunda A, Serubanja J, Tumusiime J, Akurut H, Oduru G, Nassuuna J, Kabagenyi J, Morrison H, Scott H, Powell Doherty R, Marshall JL, Cabrera Puig I, Cose S, Kaleebu P, Webb EL, Satti I, McShane H, Elliott AM; TB042 Study Team. Optimising the vaccine strategy of BCG, ChAdOx1 85A, and MVA85A for tuberculosis control. (letter) Lancet Infect Dis. 2024 Feb;24(2):e78-e79. 
Infections and allergy-related disease
  • Elliott AM, Mpairwe H, Quigley M, Nampijja M, Muhangi L, Owek-Onyee J, Muwanga M, Ndibazza J, Whitworth JAG.  Helminth infection during pregnancy and development of infantile eczema.      JAMA 2005; 294:2032-2034.
  • Mpairwe H, Muhangi L, Ndibazza J, Tumusiime J, Muwanga M, Rodrigues LC, Elliott AM. Skin prick test reactivity to common allergens among women in a peri-urban area in Uganda. Transactions of the Royal Society of Tropical Medicine 2008; 102:367-373.
  • Mpairwe H, Webb E, Muhangi L, Ndibazza J, Akishule D, Nampijja M, Ngom-wegi S, Tumusime J, Muwanga M, Rodrigues LC, Elliott AM: Anthelminthic treatment during pregnancy is associated with an increased risk of allergic conditions in infancy: results from a randomised controlled trial. Pediatric Allergy and Immunology 2011; 22:305-12.
  • Mpairwe H, Ndibazza J, Webb EL, Nampijja M, Muhangi L, Apule B, Lule S, Akurut H, Kizito D, Kakande M, Jones FM, Fitzsimmons CM, Muwanga M, Rodrigues LC, Dunne DW, Elliott AM. Maternal hookworm modifies the risk factors for eczema in childhood: birth cohort in Uganda.  Pediatric Allergy and Immunology 2014, 25(5):481-8.
  • Namara B, Nash S, Lule SA, Akurut H, Mpairwe H, Akello F, Tumusiime J, Kizza M, Nkurunungi G, Muhangi L, Webb E, Muwanga M, Elliott AM.  Effects of treating helminths during pregnancy and early childhood on risk of allergy-related outcomes: follow up of a randomized controlled trial.  Pediatr Allergy Immunol. 2017 Dec;28(8):784-792
  • Lule SA, Mpairwe H, Nampijja M, Akello F, Kabagenyi J, Namara B, Nkurunungi G, Kizito D, Kahwa J, Muhangi L, Nash S, Muwanga M, Webb EL, Elliott AM, Life-course of atopy and allergy-related disease events in tropical sub-Saharan Africa: A birth cohort study. Pediatr Allergy Immunol, 2017. 28(4): p. 377-83.
  • Lubyayi L, Mpairwe H, Nkurunungi G, Lule SA, Nalwoga A, Webb EL, Levin J, Elliott AM. Infection-exposure in infancy is associated with reduced allergy-related disease in later childhood in a Ugandan cohort. eLife 2021; 10: e66022.
Infections, nutrition and cognitive development
  • Muriuki JM, Mentzer AJ, Webb EL, Morovat A, Kimita W, Ndungu FM, Macharia AW, Crane RJ, Berkley JA, Lule SA, Cutland C, Sirima SB, Diarra A, Tiono AB, Bejon P, Madhi SA, Hill AVS, Prentice AM, Suchdev PS, Elliott AM, Williams TN, and Atkinson SH. Estimating the burden of iron deficiency among African children. BMC Medicine, 2020. 18(1): p. 31-31.
  • Muriuki JM, Mentzer AJ, Kumita W, Ndungu FM, Macharia AW, Webb EL, Lule SA, Morovat A, Hill AVS, Bejon P, Elliott AM, Williams TN, Atkinson SH.  Iron status and associated malaria risk among African children. Clin Infect Dis. 2019 May 17;68(11):1807-1814.
  • Muriuki JM, Mentzer AJ, Band G, Gilchrist JJ, Carstensen T, Lule SA, Goheen MM, Joof F, Kimita W, Mogire R, Cutland C, Diarra A, Rautanen A, Pomilla C, Gurdasani D, Rockett K, Mturi N, Ndungu FM, Scott AG, Sirima SB, Morovat A, Prentice AM, Madhi SA, Webb EL, Elliott AM, Bejon P, Sandhu MS, Hill AVS, Kwiatkowski DP, Williams TN, Cerami C, Atkinson SH.  The ferroportin Q248H mutation protects from anemia, but not malaria or bacteremia.  Science Advances 2019 Sep 4;5(9):eaaw0109.
  • Muriuki JM, Mentzer AJ, Mitchell R, Webb EL, Etyang AO, Kyobutungi C, Morovat A, Kimita W, Ndungu FM, Macharia AW, Ngetsa CJ, Makale J, Lule SA, Musani SK, Raffield LM, Cutland CL, Sirima SB, Diarra A, Tiono AB, Fried M, Gwamaka M, Adu-Afarwuah S, Wirth JP, Wegmüller R, Madhi SA, Snow RW, Hill AVS, Rockett KA, Sandhu MS, Kwiatkowski DP, Prentice AM, Byrd KA, Ndjebayi A, Stewart CP, Engle-Stone R, Green TJ, Karakochuk CD, Suchdev PS, Bejon P, Duffy PE, Davey Smith G, Elliott AM, Williams TN, Atkinson SH. Malaria is a cause of iron deficiency in African children. Nature Medicine. 2021;27(4):653-8.
  • Bundi CK, Nalwoga A, Lubyayi L, Muriuki JM, Mogire RM, Opi H, Mentzer AJ, Mugyenyi CK, Mwacharo J, Webb EL, Bejon P, Williams TN, Gikunju JK, Beeson JG, Elliott AM, Ndungu FM, Atkinson SH. Iron Deficiency Is Associated With Reduced Levels of Plasmodium falciparum-specific Antibodies in African Children. Clinical Infectious Diseases 2020; 73(1): 43-9.
  • Mogire RM, Muriuki JM, Morovat A, Mentzer AJ, Webb EL, Kimita W, Ndungu FM, Macharia AW, Cutland CL, Sirima SB, Diarra A, Tiono AB, Lule SA, Madhi SA, Prentice AM, Bejon P, Pettifor JM, Elliott AM, Adeyemo A, Williams TN, Atkinson SH. Vitamin D Deficiency and Its Association with Iron Deficiency in African Children. Nutrients. 2022 Mar 25;14(7):1372.
  • Mogire RM, Morovat A, Muriuki JM, Mentzer AJ, Webb EL, Kimita W, Ndungu FM, Macharia AW, Cutland CL, Sirima SB, Diarra A, Tiono AB, Lule SA, Madhi SA, Sandhu MS, Prentice AM, Bejon P, Pettifor JM, Elliott AM, Adeyemo A, Williams TN, Atkinson SH. Prevalence and predictors of vitamin D deficiency in young African children. BMC medicine. 2021;19(1):115.
Cognition
  • Nampijja M, Apule B, Lule S, Akurut H, Muhangi L, Elliott AM, Alcock KJ. Adaptation of Western measures of cognition for assessing 5-year-old semi-urban Uganda children. British Journal of Educational Psychology 2010; 80:15-30.
  • Nampijja M, Apule B, Lule S, Akurut H, Muhangi L, Webb EL, Lewis C, Elliott AM, Alcock KJ. Effects of maternal worm infections and anthelminthic treatment during pregnancy on infant motor and neurocognitive functioning. Journal of the International Neuropsychological Society 2012, 18: 1019-1030.
  • Nampijja M, Kizindo R, Apule B, Lule S, Muhangi L, Titman A, Elliott A, Alcock K, Lewis C. The role of the home environment in neurocognitive development of children living in extreme poverty and with frequent illnesses: a cross-sectional study [version 1; referees: awaiting peer review]. Wellcome Open Res 2018, 3:152 (https://doi.org/10.12688/wellcomeopenres.14702.1)
  • Nampijja M, Mutua AM, Elliott AM, Muriuki JM, Abubakar A, Webb EL, Atkinson SH. Low Hemoglobin Levels Are Associated with Reduced Psychomotor and Language Abilities in Young Ugandan Children. Nutrients. 2022 Mar 30;14(7):1452.
  • Mutua A, Nampijja M, Elliott A, Pettifor J, Williams T, Abubakar A, Webb E, Atkinson S.  Vitamin D Status Is Not Associated with Cognitive or Motor Function in Pre-School Ugandan Children. Nutrients 2020 Jun 3;12(6):E1662. doi: 10.3390/nu12061662.
Early life exposures and cardiovascular disease risk
  • Lule SA, Webb EL, Ndibazza J, Nampijja M, Muhangi L, Akello F, Kakande M, Kizindo R, Elliott AM.  Maternal recall of birth weight and birth size in Entebbe, Uganda. Tropical Medicine and International Health, 2012, 17:1465-1469.
  • Lule SA, Namara B, Akurut H, Muhangi L, Lubyayi L, Nampijja M, Akello F, Tumusiime J, Aujo JC, Oduru G, Smeeth L, Elliott AM, Webb EL.  Are birth weight and postnatal weight gain in childhood associated with blood pressure in early adolescence? Results from a Ugandan birth cohort.  International Journal of Epidemiology, 2018 Jul 3. doi: 10.1093/ije/dyy118. [Epub ahead of print]
  • Lule S, Namara B, Akurut H, Lubyayi L, Nampijja M, Akello F, Tumusiime J, Aujo J, Oduru G, Mentzer A, Smeeth L, Elliott A, Webb E.  Blood pressure risk factors in early adolescents: results from a Ugandan birth cohort. Journal of Human Hypertension, 2019 Feb 25. doi: 10.1038/s41371-019-0178-y. [Epub ahead of print]
  • Koopman JPR, Lule SA, Zziwa C, Akurut H, Lubyayi L, Nampijja M, Akello F, Balungi P, Tumusiime J, Oduru G, Elliott AM, Webb EL, Bradley J. The determinants of lipid profiles in early adolescence in a Ugandan birth cohort. Scientific reports 2021; 11(1): 16503.
  • Lule SA, Mentzer AJ, Namara B, Muwhezi A, Nassanga B, Akurut H, Lubyayi L, Tumusiime J, Akello F, Smeeth L, Elliott AM, Webb EL. A genome-wide association and replication study of blood pressure in Ugandan early adolescents.      Molecular Genetics & Genomic Medicine 2019 Oct;7(10):e00950.
  • Nsamba J, Lule SA, Namara B Zziwa C, Akurut H, Lubyayi L, Akello F, Tumusiime J, Elliott AM, Webb EL. Effect of birth weight, exclusive breastfeeding and growth in infancy on fat mass and fat free mass indices in early adolescence: an analysis of the Entebbe Mother and Baby Study (EMaBs) cohort [version 1; referees: awaiting peer review]. AAS Open Res 2019, 2:11 
Reviews - overviews
  • Lule SA, Elliott AM, Smeeth L, Webb EL.  Is birth weight associated with blood pressure among African children and adolescents? A systematic review.  J Dev Orig Health Dis. 2018 Jun;9(3):270-280.
  • Sanya RE, Nkurunungi G, Biraro IA, Mpairwe H, Elliott AM.  A life without worms.  Transactions of the Royal Society for Tropical Medicine and Hygiene 2017 Jan 1;111(1):3-11
  • Wammes L, Mpairwe H, Elliott AM, Yazdanbakhsh M.  Helminth therapy or elimination: epidemiological, immunological, and clinical considerations.  Lancet Infectious Diseases 2014; 14(11):1150-1162.
  • Mpairwe H, Tweyongyere R, Elliott A.  Pregnancy and helminth infections.  Parasite Immunology, 2014, 36(8):328-37.
  • Elliott AM, Ndibazza J, Mpairwe H, Muhangi L, Webb EL, Kizito D, Mawa P, Tweyongyere R, Muwanga M for the Entebbe Mother and Baby Study Team. Treatment with anthelminthics during pregnancy: what gains and what risks for the mother and child? Parasitology, 2011; 138(12):1499-507
Updates
Updates List Block
Updates List
EMaBS@21 achieves remarkable progress in extending follow-up to adulthood
EMaBS@21 Principal Investigator, Professor Emily Webb addressing participants at a stakeholder meeting for the project
EMaBS@21 Principal Investigator, Professor Emily Webb addressing participants at a stakeholder meeting for the project

The Entebbe Mother and Baby Study at 21 years (EMaBS@21) is not just a continuation of a long-term cohort study, it is a crucial opportunity to answer pressing global and regional questions about how early-life infections and environmental exposures shape long-term health. With 500 out of 900 participants enrolled within five months, recruitment has been promising.

Globally, longitudinal cohort studies have provided vital evidence on the lasting effects of early-life physical and social exposures, guiding policy on disease prevention, and chronic illness management. However, Africa has a limited number of such long-term studies, making EMaBS one of the few cohorts to provide regional data tailored to local health challenges. The findings from EMaBS@21 will contribute to global knowledge while offering targeted recommendations for Uganda and the wider region, where the burden of infectious and non-communicable diseases remains high.

Navigating the challenge of retention

A key factor in the success of EMaBS@21 is the strong foundation of participant engagement built over the years with the EMaBS cohort. The ability to bring back 900 participants at this stage is not about new retention efforts within EMaBS@21, but rather a reflection of the long-term relationships, trust, and strategic engagement that have been in place throughout EMaBS.

Young adults aged 18-21 are navigating major life transitions, such as higher education, employment, and family responsibilities, making their continued participation in research a significant achievement. Over the years, the study team has addressed challenges like participant mobility, scheduling conflicts, and skepticism about clinical research. Personalized follow-ups, flexible scheduling, and continuous community engagement have helped sustain interest and involvement.

Additionally, peer networks, ambassador programs, and incentives have reinforced the importance of participation. The commitment to building trust within local communities has been central to success ensuring that participants feel valued and understand the impact of their contribution to scientific research.

By maintaining these strong relationships, the study has successfully reached this milestone, with over half of the target group of 900 participants, already returning for follow-up at age 21.

Expanding research through the cohort

The Entebbe Mother and Baby Study (EMaBS) has grown into a vital research platform, providing long-term insights intoinfection, immunity, and overall health outcomes. Over the years, it has supported novel studies in maternal and child health, allergy, and infectious disease epidemiology, while also serving as a foundation for interdisciplinary collaborations within the MRC/UVRI & LSHTM Uganda Research Unit.

Through its long-term cohort, EMaBS has provided valuable insights into immune system development, vaccine responses, and the epidemiology of infectious diseases such as tuberculosis, malaria, and HIV. Additionally, it has also played a key role in understanding how early-life infections and environmental exposures influence long-term health, including the risk of non-communicable diseases (NCDs) like diabetes, hypertension, and asthma.

Exploring early-life exposures and their impact on cardiovascular health in sub-Saharan Africa
Social Scientist going through the study information with a participant

As non-communicable diseases (NCDs), particularly cardiovascular diseases (CVDs), continue to rise in sub-Saharan Africa, understanding their origins and risk factors remains crucial. Addressing this gap, the MRC/UVRI and LSHTM Uganda Research Unit in collaboration with London School of Hygiene & Tropical Medicine, Kenya Medical Research Institute – Wellcome Trust and the University of Manchester is conducting a study titled, “Entebbe Mothers and Babies at 21 (EMaBS@21)."

​Funded through a research grant from the Medical Research Council (MRC) UK, this study builds upon the unique Entebbe Mother and Baby Study (EMaBS) birth cohort, which has tracked the health and development of participants from pre-natal stages through childhood and adolescence for over two decades. By linking newly collected data to the vast archive of socio-demographic, genetic, immunization and nutrition information, the study will shed light on how early life exposures such as infections and undernutrition shape the cardiovascular health trajectory in adulthood.

Filling critical gaps in cardiovascular research

The EMaBS at 21 study aims to understand how early life factors, like infections and malnutrition affect the development of CVD risk factors such as blood pressure, lipid levels, glucose metabolism and body mass index. The study focuses on understanding how these factors play out in the sub-Saharan context, where early-life exposures differ from those in high-income countries. 

Professor Emily Webb, Principal Investigator, emphasizes that there are very few birth cohorts in tropical Africa, limiting our understanding of how early-life exposures impact long-term health outcomes. The EMaBS cohort offers a unique opportunity to identify critical moments in the life-course where targeted interventions could reduce future risk of CVD.  

A comprehensive approach

This ambitious study uses a mixed-methods approach, combining quantitative and qualitative research. Researchers will collect physical measurements, including anthropometry and blood pressure, along with biological samples such as blood, stool, and urine, for measurement of blood glucose and lipid profiles, infections and metabolomics. Behavioral data, including diet, physical activity, alcohol, and tobacco use will be captured through questionnaires. Cutting edge laboratory analyses will explore pathways through which early life infections influence later CVD risk, while qualitative data from in-depth interviews and focus group discussions will offer insights into participants’ perceptions of CVD risk.

Advanced statistical techniques, including regression and latent class analyses, will be used to identify the links between early-life exposures and adult CVD risk.

Evidence-based interventions

The findings from EMaBS@21 are expected to inform health policy and intervention strategies aimed at reducing the growing burden of cardiovascular diseases in sub-Saharan Africa. By addressing the specific early-life exposures affecting populations in the region, the study aims to develop targeted interventions for populations with unique health trajectories.

About the key scientists:

Professor Emily Webb (study Principal Investigator) is the Director of the MRC International Statistics and Epidemiology Group (ISEG), and co-theme leader for ISEG's work on emerging and neglected diseases. Her current research focuses on the design and analysis of intervention and observational studies in the fields of helminths, vaccines and child health. She leads capacity strengthening programmes in epidemiology and medical statistics for scientists from sub-Saharan Africa.

Bridgious Walusimbi (study Lead Investigator) is a Doctoral researcher at Makerere University, a Research Fellow at London School of Hygiene and Tropical Medicine, as well as Honorary Research Fellow at University of Manchester. He is a bioinformatician with a strong desire to become a top-level researcher committed to improving health of communities in Sub-Saharan Africa through cutting-edge research founded on statistical modelling in infection and immunity, underpinned by a strong base in genetics, epigenetics, metabolomics and microbiome science. He is also involved in Africa Bioinformatics capacity building initiatives such as H3A Africa as faculty.

About the collaborating institutions:

The Medical Research Council/Uganda Virus Institute/ London School of Hygiene & Tropical Medicine Uganda Research Unit (MRC/UVRI & LSHTM) is an internationally recognized center of excellence for research and training. Its mission is to conduct high-quality research that adds knowledge and leads to improved control of infectious and non-communicable diseases in Uganda, Africa and globally, through translation of scientific findings into policy and practice, and rigorous research capacity building.

University of Manchester is a prestigious member of the Russell Group, renowned for its world-class research, exceptional teaching, and commitment to social responsibility. Established in 1824, it has a rich history of groundbreaking achievements, including hosting 26 Nobel Prize winners and pioneering innovations such as the first nuclear reaction, the modern computer, and the isolation of graphene. With a focus on interdisciplinary collaboration and global impact, it continues to address major global challenges, provide transformative education, and shape future leaders.

Kenya Medical Research Institute (KEMRI) is a State Corporation established in Kenya in 1979 through the Science and Technology (Repealed) Act, Cap 250 of the Laws of Kenya operated under the Science Technology and Innovation Act, 2013 as the national body responsible for carrying out research in human health in Kenya. Currently, KEMRI operates under Legal Notice No. 35 of March 2021. KEMRI has grown from its humble beginning over 40 years ago to become a regional leader in human health research. The Institute currently ranks as one of the leading Centres of excellence in health research both in Africa as well as globally.

Learn more about vaccine research at the Unit.