Teri Roberts

ORCID: 0000-0002-1046-2490
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About
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Research Areas
  • Tuberculosis Research and Epidemiology
  • Hepatitis C virus research
  • HIV Research and Treatment
  • HIV/AIDS Research and Interventions
  • Hepatitis B Virus Studies
  • Mosquito-borne diseases and control
  • Mycobacterium research and diagnosis
  • HIV/AIDS drug development and treatment
  • Viral Infections and Vectors
  • Liver Disease Diagnosis and Treatment
  • HIV, Drug Use, Sexual Risk
  • Pneumocystis jirovecii pneumonia detection and treatment
  • Immune Cell Function and Interaction
  • Viral Infections and Outbreaks Research
  • Infectious Diseases and Tuberculosis
  • Pharmaceutical Economics and Policy
  • T-cell and B-cell Immunology
  • Immunodeficiency and Autoimmune Disorders
  • Hepatitis Viruses Studies and Epidemiology
  • Nutrition and Health in Aging
  • Burkholderia infections and melioidosis
  • Diagnosis and treatment of tuberculosis
  • SARS-CoV-2 detection and testing
  • Respiratory viral infections research
  • Reproductive tract infections research

Global Antibiotic Research & Development Partnership
2024

Stellenbosch University
2005-2023

International AIDS Society
2020-2022

South African Medical Research Council
2020

Médecins Sans Frontières
2012-2020

Médecins Sans Frontières
2019

Foundation for Innovative New Diagnostics
2017

Médecins Sans Frontières‎
2014-2017

Médecins Sans Frontières
2012

University of Cape Town
2010

Sara Suliman Ethan Thompson Jayne S. Sutherland January Weiner Martin O. C. Ota and 95 more Steven G. Smith Adam Penn‐Nicholson Bonnie Thiel Mzwandile Erasmus Jeroen Maertzdorf Fergal J. Duffy Philip C. Hill E. Jane Hughes Kim Stanley Katrina Downing Michelle Fisher Joe Valvo Shreemanta K. Parida Gian van der Spuy Gerard Tromp Ifedayo Adetifa Simon Donkor Rawleigh Howe Harriet Mayanja‐Kizza W. Henry Boom Hazel M. Dockrell Tom H. M. Ottenhoff Mark Hatherill Alan Aderem Willem A. Hanekom Thomas J. Scriba Stefan H. E. Kaufmann Daniel E. Zak Gerhard Walzl Gerhard Walzl Gillian F. Black Gian van der Spuy Kim Stanley Magdalena Kriel Nelita du Plessis Nonhlanhla Nene Teri Roberts Léanie Kleynhans Andrea Gutschmidt Bronwyn Smith Nonhlanhla Nene André G. Loxton Novel N. Chegou Gerard Tromp David L. Tabb Tom H. M. Ottenhoff Michèl R. Klein Mariëlle C. Haks Kees L. M. C. Franken Annemieke Geluk Krista E. van Meijgaarden Simone A. Joosten W. Henry Boom Bonnie Thiel Harriet Mayanja‐Kizza Moses Joloba Sarah Zalwango Mary Nsereko Brenda Okwera Hussein Kisingo Stefan H. E. Kaufmann Shreemanta K. Parida Robert Golinski Jeroen Maertzdorf January Weiner Mark Z. Jacobson Hazel M. Dockrell Steven G. Smith Patricia Gorak‐Stolinska Yun‐Gyoung Hur Maeve K. Lalor Ji‐Sook Lee Amelia C. Crampin Neil French Bagrey Ngwira Anne Ben‐Smith Kate E. Watkins Lyn Ambrose Felanji Simukonda Hazzie Mvula Femia Chilongo Jacky Saul Keith Branson Sara Suliman Thomas J. Scriba Hassan Mahomed E. Jane Hughes Nicole Bilek Mzwandile Erasmus Onke Xasa Ashley Veldsman Katrina Downing Michelle Fisher Adam Penn‐Nicholson Humphrey Mulenga

Rationale: Contacts of patients with tuberculosis (TB) constitute an important target population for preventive measures because they are at high risk infection Mycobacterium and progression to disease.Objectives: We investigated biosignatures predictive ability incident TB.Methods: In a case–control study nested within the Grand Challenges 6-74 longitudinal HIV-negative African cohort exposed household contacts, we employed RNA sequencing, PCR, pair ratio algorithm in training/test set...

10.1164/rccm.201711-2340oc article EN American Journal of Respiratory and Critical Care Medicine 2018-04-06

Despite immense progress in antiretroviral therapy (ART) scale-up, many people still lack access to basic standards of care, with our ability meet the Joint United Nations Programme on HIV/AIDS 90-90-90 treatment targets for dependent dramatic improvements diagnostics. The World Health Organization recommends routine monitoring ART effectiveness using viral load (VL) testing at 6 months and every 12 months, monitor adherence minimize failure, will publish its VL toolkit later this year....

10.1093/cid/ciw001 article EN cc-by-nc-nd Clinical Infectious Diseases 2016-01-06
Munyaradzi Musvosvi Huang Huang Chunlin Wang Qiong Xia Virginie Rozot and 95 more Akshaya Krishnan Péter Ács Abhilasha Cheruku Gerlinde Obermoser Alasdair Leslie Samuel M. Behar Willem A. Hanekom Nicole Bilek Michelle Fisher Stefan H. E. Kaufmann Gerhard Walzl Mark Hatherill Mark M. Davis Thomas J. Scriba Fazlin Kafaar Leslie Workman Humphrey Mulenga Thomas J. Scriba E. Jane Hughes Nicole Bilek Mzwandile Erasmus Onke Nombida Ashley Veldsman Yolundi Cloete Deborah Abrahams Sizulu Moyo Sebastian Gelderbloem Michèle Tameris Hennie Geldenhuys Willem A. Hanekom Gregory Hussey Rodney Ehrlich Suzanne Verver Larry Geiter Gerhard Walzl Gillian F. Black Gian van der Spuy Kim Stanley Magdalena Kriel Nelita du Plessis Nonhlanhla Nene Teri Roberts Léanie Kleynhans Andrea Gutschmidt Bronwyn Smith André G. Loxton Novel N. Chegou Gerard Tromp David L. Tabb Tom H. M. Ottenhoff Michèl R. Klein Mariëlle C. Haks Kees L. M. C. Franken Annemieke Geluk Krista E. van Meijgaarden Simone A. Joosten W. Henry Boom Bonnie Thiel Harriet Mayanja‐Kizza Moses Joloba Sarah Zalwango Mary Nsereko Brenda Okwera Hussein Kisingo Stefan H. E. Kaufmann Shreemanta K. Parida Robert Golinski Jeroen Maertzdorf January Weiner Mark Z. Jacobson Hazel M. Dockrell Maeve K. Lalor Steven G. Smith Patricia Gorak‐Stolinska Yun‐Gyoung Hur Ji‐Sook Lee Amelia C. Crampin Neil French Bagrey Ngwira Anne Ben‐Smith Kate E. Watkins Lyn Ambrose Felanji Simukonda Hazzie Mvula Femia Chilongo Jacky Saul Keith Branson Sara Suliman Thomas J. Scriba Hassan Mahomed E. Jane Hughes Nicole Bilek Mzwandile Erasmus Onke Nombida Ashley Veldsman

Abstract Antigen-specific, MHC-restricted αβ T cells are necessary for protective immunity against Mycobacterium tuberculosis , but the ability to broadly study these responses has been limited. In present study, we used single-cell and bulk cell receptor (TCR) sequencing GLIPH2 algorithm analyze M. -specific sequences in two longitudinal cohorts, comprising 166 individuals with infection who progressed either ( n = 48) or controlled 118). We found 24 groups similar TCR-β sequences,...

10.1038/s41591-022-02110-9 article EN cc-by Nature Medicine 2023-01-01

The recent introduction of fluorescent bead-based technology, allowing the measurement multiples analytes in a single 25–50 µl sample has revolutionized study cytokine responses. However, such multiplex approaches may compromise ability these assays to accurately measure actual levels. This evaluates performance three commercially available immunoassays (Bio-Rad's Cytokine 17-plex kit; LINCO Inc's 29-plex and RnD System's Fluorokine-Multi Analyte Profiling (MAP) base kit A B). Inc was found...

10.1371/journal.pone.0002535 article EN cc-by PLoS ONE 2008-07-01

There are inefficiencies in current approaches to monitoring patients on antiretroviral therapy sub-Saharan Africa. Patients typically attend clinics every 1 3 months for clinical assessment. The clinic costs comparable with the of drugs themselves and CD4 counts measured 6 months, but rarely switched second-line therapies. To ensure sustainability treatment programmes, a transition more cost-effective delivery is needed. In contrast count, measurement level HIV RNA plasma (the viral load)...

10.1038/nature16046 article EN cc-by Nature 2015-12-01

Background The accurate diagnosis of TB in HIV-infected patients, particularly with advanced immunosuppression, is difficult. Recent studies indicate that a lipoarabinomannan (LAM) assay (Clearview-TB®-ELISA) may have some utility for the patients; however, precise subgroup benefit from this technology requires clarification. LAM sputum samples has, hitherto, not been evaluated. Methods was measured and urine obtained 500 consecutively recruited ambulant suspected TB, 2 primary care clinics...

10.1371/journal.pone.0009848 article EN cc-by PLoS ONE 2010-03-23
Adam Penn‐Nicholson Stanley Kimbung Mbandi Ethan Thompson Simon C. Mendelsohn Sara Suliman and 95 more Novel N. Chegou Stephanus T. Malherbe Fatoumatta Darboe Mzwandile Erasmus Willem A. Hanekom Nicole Bilek Michelle Fisher Stefan H. E. Kaufmann Jill Winter Melissa Murphy Robin Wood Carl Morrow Ildiko Van Rhijn Branch Moody Megan Murray Bruno B. Andrade Timothy R. Sterling Jayne S. Sutherland Kogieleum Naidoo Nesri Padayatchi Gerhard Walzl Mark Hatherill Daniel E. Zak Thomas J. Scriba Fazlin Kafaar Leslie Workman Humphrey Mulenga E. Jane Hughes Onke Xasa Ashley Veldsman Yolundi Cloete Deborah Abrahams Sizulu Moyo Sebastian Gelderbloem Michèle Tameris Hennie Geldenhuys Rodney Ehrlich Suzanne Verver Larry Geiter Gillian F. Black Gian van der Spuy Kim Stanley Magdalena Kriel Nelita du Plessis Nonhlanhla Nene Teri Roberts Léanie Kleynhans Andrea Gutschmidt Bronwyn Smith André G. Loxton Gerard Tromp David L. Tabb Tom H. M. Ottenhoff Michèl R. Klein Mariëlle C. Haks Kees L. M. C. Franken Annemieke Geluk Krista E. van Meijgaarden Simone A. Joosten W. Henry Boom Bonnie Thiel Harriet Mayanja‐Kizza Moses Joloba Sarah Zalwango Mary Nsereko Brenda Okwera Hussein Kisingo Shreemanta K. Parida Robert Golinski Jeroen Maertzdorf January Weiner Mark Z. Jacobson Hazel M. Dockrell Steven G. Smith Patricia Gorak‐Stolinska Yun‐Gyoung Hur Maeve K. Lalor Ji‐Sook Lee Amelia C. Crampin Neil French Bagrey Ngwira Anne Ben‐Smith Kate E. Watkins Lyn Ambrose Felanji Simukonda Hazzie Mvula Femia Chilongo Jacky Saul Keith Branson Hassan Mahomed E. Jane Hughes Onke Xasa Ashley Veldsman Katrina Downing Humphrey Mulenga

Abstract Improved tuberculosis diagnostics and tools for monitoring treatment response are urgently needed. We developed a robust simple, PCR-based host-blood transcriptomic signature, RISK6, multiple applications: identifying individuals at risk of incident disease, as screening test subclinical or clinical tuberculosis, treatment. RISK6 utility was validated by blind prediction using quantitative real-time (qRT) PCR in seven independent cohorts. Prognostic performance significantly...

10.1038/s41598-020-65043-8 article EN cc-by Scientific Reports 2020-05-25

The balance between effector and regulatory responses after Mycobacterium tuberculosis infection may dictate outcome progression to active disease. We investigated T cell in bacille Calmette-Guerin (BCG)-stimulated peripheral blood mononuclear cells whole cultures from persons with (TB), TB at the end of 6 months treatment, healthy control subjects latent infection. All 3 groups displayed BCG-induced increases phenotypes as defined by CD4(+)CD25(lo) CD4(+)CD25(hi) cells, respectively. In...

10.1086/511277 article EN The Journal of Infectious Diseases 2007-02-14

The inflammatory response to Mycobacterium tuberculosis (M.tb) at the site of disease is Th1 driven. Whether Th17 cytokines, IL-17 and IL-22, contribute this in humans unknown. We hypothesized that IL-22 pleural pericardial sites human (TB). studied effusions, established TB sites, from HIV-uninfected patients. Levels soluble cytokines were measured by ELISA MMP-9 luminex. Bronchoalveolar lavage or mycobacteria-specific T cell cytokine expression was analyzed intracellular staining. not...

10.1016/j.tube.2011.06.009 article EN cc-by Tuberculosis 2011-07-24

We aimed to determine whether shotgun proteomic approaches could be used identify tuberculosis (TB)-specific biomarkers in the urine of well-characterised patients with active TB versus no TB. Patients suspected (n=63) were classified as: definite ( Mycobacterium positive culture, n=21); presumed latent-TB infection (LTBI) M. negative radiological features TB, a QuantiFERON-TB Gold In-Tube (QFT-IT) test and T-SPOT.TB test, n=24); non-TB/non-LTBI QFT-IT n=18). Urine proteins, range 3–50 kDa,...

10.1183/09031936.00175113 article EN European Respiratory Journal 2014-04-17

There have been few reports on programmatic experience of viral hepatitis testing and treatment in resource-limited settings. To inform the development 2017 World Health Organization (WHO) guidance particular feasibility proposed recommendations, we undertook a survey across range organisations engaged with low- middle-income countries (LMICs). Our objective was to describe current B C practices settings different countries, as well key barriers or challenges encountered solutions promote...

10.1186/s12879-017-2767-0 article EN cc-by BMC Infectious Diseases 2017-11-01

The current low access to virological testing confirm chronic viraemic HCV infection in low- and middle-income countries (LMIC) is limiting the rollout of hepatitis C (HCV) care. Existing tests are complex, costly require sophisticated laboratory infrastructure. Diagnostic manufacturers need guidance on optimal characteristics a test needs have ensure greatest impact diagnosis treatment LMIC. Our objective was develop target product profile (TPP) for viraemia using global stakeholder...

10.1186/s12879-017-2770-5 article EN cc-by BMC Infectious Diseases 2017-11-01
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