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Four-Gene Pan-African Blood Signature Predicts Progression to Tuberculosis.
Suliman, Sara; Thompson, Ethan G; Sutherland, Jayne; Weiner, January; Ota, Martin O C; Shankar, Smitha; Penn-Nicholson, Adam; Thiel, Bonnie; Erasmus, Mzwandile; Maertzdorf, Jeroen; Duffy, Fergal J; Hill, Philip C; Hughes, E Jane; Stanley, Kim; Downing, Katrina; Fisher, Michelle L; Valvo, Joe; Parida, Shreemanta K; van der Spuy, Gian; Tromp, Gerard; Adetifa, Ifedayo M O; Donkor, Simon; Howe, Rawleigh; Mayanja-Kizza, Harriet; Boom, W Henry; Dockrell, Hazel M; Ottenhoff, Tom H M; Hatherill, Mark; Aderem, Alan; Hanekom, Willem A; Scriba, Thomas J; Kaufmann, Stefan H E; Zak, Daniel E; Walzl, Gerhard.
Afiliação
  • Suliman S; South African Tuberculosis Vaccine Initiative, Institute of Infectious Disease and Molecular Medicine, and.
  • Thompson EG; Division of Immunology, Department of Pathology, University of Cape Town, Cape Town, South Africa.
  • Sutherland J; The Center for Infectious Disease Research, Seattle, Washington.
  • Weiner J; Vaccines and Immunity, Medical Research Council Unit, Fajara, the Gambia.
  • Ota MOC; Max Planck Institute for Infection Biology, Berlin, Germany.
  • Shankar S; Vaccines and Immunity, Medical Research Council Unit, Fajara, the Gambia.
  • Penn-Nicholson A; The Center for Infectious Disease Research, Seattle, Washington.
  • Thiel B; South African Tuberculosis Vaccine Initiative, Institute of Infectious Disease and Molecular Medicine, and.
  • Erasmus M; Division of Immunology, Department of Pathology, University of Cape Town, Cape Town, South Africa.
  • Maertzdorf J; Case Western Reserve University, Cleveland, Ohio.
  • Duffy FJ; South African Tuberculosis Vaccine Initiative, Institute of Infectious Disease and Molecular Medicine, and.
  • Hill PC; Division of Immunology, Department of Pathology, University of Cape Town, Cape Town, South Africa.
  • Hughes EJ; Max Planck Institute for Infection Biology, Berlin, Germany.
  • Stanley K; The Center for Infectious Disease Research, Seattle, Washington.
  • Downing K; Centre for International Health, School of Medicine, University of Otago, Dunedin, New Zealand.
  • Fisher ML; South African Tuberculosis Vaccine Initiative, Institute of Infectious Disease and Molecular Medicine, and.
  • Valvo J; Division of Immunology, Department of Pathology, University of Cape Town, Cape Town, South Africa.
  • Parida SK; Department of Science and Technology/National Research Foundation Centre of Excellence for Biomedical TB Research, and.
  • van der Spuy G; Medical Research Council Centre for TB Research, Division of Molecular Biology and Human Genetics, Faculty of Medicine and Health Sciences, Stellenbosch University, Tygerberg, South Africa.
  • Tromp G; South African Tuberculosis Vaccine Initiative, Institute of Infectious Disease and Molecular Medicine, and.
  • Adetifa IMO; Division of Immunology, Department of Pathology, University of Cape Town, Cape Town, South Africa.
  • Donkor S; South African Tuberculosis Vaccine Initiative, Institute of Infectious Disease and Molecular Medicine, and.
  • Howe R; Division of Immunology, Department of Pathology, University of Cape Town, Cape Town, South Africa.
  • Mayanja-Kizza H; The Center for Infectious Disease Research, Seattle, Washington.
  • Boom WH; Max Planck Institute for Infection Biology, Berlin, Germany.
  • Dockrell HM; Department of Science and Technology/National Research Foundation Centre of Excellence for Biomedical TB Research, and.
  • Ottenhoff THM; Medical Research Council Centre for TB Research, Division of Molecular Biology and Human Genetics, Faculty of Medicine and Health Sciences, Stellenbosch University, Tygerberg, South Africa.
  • Hatherill M; Department of Science and Technology/National Research Foundation Centre of Excellence for Biomedical TB Research, and.
  • Aderem A; Medical Research Council Centre for TB Research, Division of Molecular Biology and Human Genetics, Faculty of Medicine and Health Sciences, Stellenbosch University, Tygerberg, South Africa.
  • Hanekom WA; Vaccines and Immunity, Medical Research Council Unit, Fajara, the Gambia.
  • Scriba TJ; Vaccines and Immunity, Medical Research Council Unit, Fajara, the Gambia.
  • Kaufmann SHE; Immunology Unit, Armauer Hansen Research Institute, Addis Ababa, Ethiopia.
  • Zak DE; Department of Medicine, and.
  • Walzl G; Department of Microbiology, Makerere University, Kampala, Uganda.
Am J Respir Crit Care Med ; 197(9): 1198-1208, 2018 May 01.
Article em En | MEDLINE | ID: mdl-29624071
ABSTRACT
Rationale Contacts of patients with tuberculosis (TB) constitute an important target population for preventive measures because they are at high risk of infection with Mycobacterium tuberculosis and progression to disease.

Objectives:

We investigated biosignatures with predictive ability for incident TB.

Methods:

In a case-control study nested within the Grand Challenges 6-74 longitudinal HIV-negative African cohort of exposed household contacts, we employed RNA sequencing, PCR, and the pair ratio algorithm in a training/test set approach. Overall, 79 progressors who developed TB between 3 and 24 months after diagnosis of index case and 328 matched nonprogressors who remained healthy during 24 months of follow-up were investigated.Measurements and Main

Results:

A four-transcript signature derived from samples in a South African and Gambian training set predicted progression up to two years before onset of disease in blinded test set samples from South Africa, the Gambia, and Ethiopia with little population-associated variability, and it was also validated in an external cohort of South African adolescents with latent M. tuberculosis infection. By contrast, published diagnostic or prognostic TB signatures were predicted in samples from some but not all three countries, indicating site-specific variability. Post hoc meta-analysis identified a single gene pair, C1QC/TRAV27 (complement C1q C-chain / T-cell receptor-α variable gene 27) that would consistently predict TB progression in household contacts from multiple African sites but not in infected adolescents without known recent exposure events.

Conclusions:

Collectively, we developed a simple whole blood-based PCR test to predict TB in recently exposed household contacts from diverse African populations. This test has potential for implementation in national TB contact investigation programs.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: Am J Respir Crit Care Med Assunto da revista: TERAPIA INTENSIVA Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: Am J Respir Crit Care Med Assunto da revista: TERAPIA INTENSIVA Ano de publicação: 2018 Tipo de documento: Article