Network


Latest external collaboration on country level. Dive into details by clicking on the dots.

Hotspot


Dive into the research topics where Johan Vekemans is active.

Publication


Featured researches published by Johan Vekemans.


Clinical Infectious Diseases | 2017

Estimates of the Burden of Group B Streptococcal Disease Worldwide for Pregnant Women, Stillbirths, and Children

Anna C Seale; Fiorella Bianchi-Jassir; Neal J Russell; Maya Kohli-Lynch; Cally J Tann; Jenny Hall; Lola Madrid; Hannah Blencowe; Simon Cousens; Carol J. Baker; Linda Bartlett; Clare L. Cutland; Michael G. Gravett; Paul T Heath; Margaret Ip; Kirsty Le Doare; Shabir A. Madhi; Craig E. Rubens; Samir K. Saha; Stephanie J. Schrag; Ajoke Sobanjo-ter Meulen; Johan Vekemans; Joy E Lawn

Group B Streptococcus is an important cause of disease in pregnant women, stillbirth, and infants. These first estimates show the magnitude and the potential impact of maternal vaccination.


F1000Research | 2016

Group B Streptococcus vaccine development: present status and future considerations, with emphasis on perspectives for low and middle income countries

Miwako Kobayashi; Johan Vekemans; Carol J. Baker; Adam J. Ratner; Kirsty Le Doare; Stephanie J. Schrag

Globally, group B Streptococcus (GBS) remains the leading cause of sepsis and meningitis in young infants, with its greatest burden in the first 90 days of life. Intrapartum antibiotic prophylaxis (IAP) for women at risk of transmitting GBS to their newborns has been effective in reducing, but not eliminating, the young infant GBS disease burden in many high income countries. However, identification of women at risk and administration of IAP is very difficult in many low and middle income country (LMIC) settings, and is not possible for home deliveries. Immunization of pregnant women with a GBS vaccine represents an alternate pathway to protecting newborns from GBS disease, through the transplacental antibody transfer to the fetus in utero. This approach to prevent GBS disease in young infants is currently under development, and is approaching late stage clinical evaluation. This manuscript includes a review of the natural history of the disease, global disease burden estimates, diagnosis and existing control options in different settings, the biological rationale for a vaccine including previous supportive studies, analysis of current candidates in development, possible correlates of protection and current status of immunogenicity assays. Future potential vaccine development pathways to licensure and use in LMICs, trial design and implementation options are discussed, with the objective to provide a basis for reflection, rather than recommendations.


Clinical Infectious Diseases | 2017

Maternal Colonization With Group B Streptococcus and Serotype Distribution Worldwide: Systematic Review and Meta-analyses

Jennifer Hall; Nadine Hack Adams; Linda Bartlett; Anna C Seale; Theresa Lamagni; Fiorella Bianchi-Jassir; Joy E Lawn; Carol J. Baker; Clare L. Cutland; Paul T Heath; Margaret Ip; Kirsty Le Doare; Shabir A. Madhi; Craig E. Rubens; Samir K. Saha; Stephanie J. Schrag; Ajoke Sobanjo-ter Meulen; Johan Vekemans; Michael G. Gravett

Abstract Background Maternal rectovaginal colonization with group B Streptococcus (GBS) is the most common pathway for GBS disease in mother, fetus, and newborn. This article, the second in a series estimating the burden of GBS, aims to determine the prevalence and serotype distribution of GBS colonizing pregnant women worldwide. Methods We conducted systematic literature reviews (PubMed/Medline, Embase, Latin American and Caribbean Health Sciences Literature [LILACS], World Health Organization Library Information System [WHOLIS], and Scopus), organized Chinese language searches, and sought unpublished data from investigator groups. We applied broad inclusion criteria to maximize data inputs, particularly from low- and middle-income contexts, and then applied new meta-analyses to adjust for studies with less-sensitive sampling and laboratory techniques. We undertook meta-analyses to derive pooled estimates of maternal GBS colonization prevalence at national and regional levels. Results The dataset regarding colonization included 390 articles, 85 countries, and a total of 299924 pregnant women. Our adjusted estimate for maternal GBS colonization worldwide was 18% (95% confidence interval [CI], 17%–19%), with regional variation (11%–35%), and lower prevalence in Southern Asia (12.5% [95% CI, 10%–15%]) and Eastern Asia (11% [95% CI, 10%–12%]). Bacterial serotypes I–V account for 98% of identified colonizing GBS isolates worldwide. Serotype III, associated with invasive disease, accounts for 25% (95% CI, 23%–28%), but is less frequent in some South American and Asian countries. Serotypes VI–IX are more common in Asia. Conclusions GBS colonizes pregnant women worldwide, but prevalence and serotype distribution vary, even after adjusting for laboratory methods. Lower GBS maternal colonization prevalence, with less serotype III, may help to explain lower GBS disease incidence in regions such as Asia. High prevalence worldwide, and more serotype data, are relevant to prevention efforts.


Clinical Infectious Diseases | 2017

Infant Group B Streptococcal Disease Incidence and Serotypes Worldwide: Systematic Review and Meta-analyses

Lola Madrid; Anna C Seale; Maya Kohli-Lynch; Karen Edmond; Joy E Lawn; Paul T. Heath; Shabir A. Madhi; Carol J. Baker; Linda Bartlett; Clare L. Cutland; Michael G. Gravett; Margaret Ip; Kirsty Le Doare; Craig E. Rubens; Samir K. Saha; Ajoke Sobanjo-ter Meulen; Johan Vekemans; Stephanie J. Schrag

Abstract Background Group B Streptococcus (GBS) remains a leading cause of neonatal sepsis in high-income contexts, despite declines due to intrapartum antibiotic prophylaxis (IAP). Recent evidence suggests higher incidence in Africa, where IAP is rare. We investigated the global incidence of infant invasive GBS disease and the associated serotypes, updating previous estimates. Methods We conducted systematic literature reviews (PubMed/Medline, Embase, Latin American and Caribbean Health Sciences Literature [LILACS], World Health Organization Library Information System [WHOLIS], and Scopus) and sought unpublished data regarding invasive GBS disease in infants aged 0–89 days. We conducted random-effects meta-analyses of incidence, case fatality risk (CFR), and serotype prevalence. Results We identified 135 studies with data on incidence (n = 90), CFR (n = 64), or serotype (n = 45). The pooled incidence of invasive GBS disease in infants was 0.49 per 1000 live births (95% confidence interval [CI], .43–.56), and was highest in Africa (1.12) and lowest in Asia (0.30). Early-onset disease incidence was 0.41 (95% CI, .36–.47); late-onset disease incidence was 0.26 (95% CI, .21–.30). CFR was 8.4% (95% CI, 6.6%–10.2%). Serotype III (61.5%) dominated, with 97% of cases caused by serotypes Ia, Ib, II, III, and V. Conclusions The incidence of infant GBS disease remains high in some regions, particularly Africa. We likely underestimated incidence in some contexts, due to limitations in case ascertainment and specimen collection and processing. Burden in Asia requires further investigation.


Vaccine | 2016

WHO consultation on group B Streptococcus vaccine development: Report from a meeting held on 27-28 April 2016.

Miwako Kobayashi; Stephanie J. Schrag; Mark Alderson; Shabir A. Madhi; Carol J. Baker; Ajoke Sobanjo-ter Meulen; David C. Kaslow; Peter G. Smith; Vasee S. Moorthy; Johan Vekemans

Globally, group B Streptococcus (GBS) remains a leading cause of sepsis and meningitis in infants in the first 90 days of life. Intrapartum antibiotic prophylaxis (IAP) for women at increased risk of transmitting GBS to their newborns has been effective in reducing part, but not all, of the GBS disease burden in many high income countries (HICs). In low- and middle-income countries (LMICs), IAP use is low. Immunization of pregnant women with a GBS vaccine represents an alternative strategy to protecting newborns and young infants, through transplacental antibody transfer and potentially by reducing new vaginal colonization. This vaccination strategy was first suggested in the 1970s and several potential GBS vaccines have completed phase I/II clinical trials. During the 2015 WHO Product Development for Vaccines Advisory Committee meeting, GBS was identified as a high priority for the development of a vaccine for maternal immunization because of the major public health burden posed by GBS in LMICs, and the high technical feasibility for successful development. Following this meeting, the first WHO technical consultation on GBS vaccines was held on the 27th and 28th of April 2016, to consider development pathways for such vaccines, focused on their potential role in reducing newborn and young infant deaths and possibly stillbirths in LMICs. Discussion topics included: (1) pathophysiology of disease; (2) current gaps in the knowledge of global disease burden and serotype distribution; (3) vaccine candidates under development; (4) design considerations for phase III trials; and (5) pathways to licensure, policy recommendations and use. Efforts to address gaps identified in each of these areas are needed to establish the public health need for, the development and deployment of, efficacious GBS vaccines. In particular, more work is required to understand the global disease burden of GBS-associated stillbirths, and to develop quality-assured standardized antibody assays to identify correlates of protection.


Clinical Infectious Diseases | 2017

Group B Streptococcal Disease Worldwide for Pregnant Women, Stillbirths, and Children: Why, What, and How to Undertake Estimates?

Joy E Lawn; Fiorella Bianchi-Jassir; Neal J Russell; Maya Kohli-Lynch; Cally J Tann; Jennifer Hall; Lola Madrid; Carol J. Baker; Linda Bartlett; Clare L. Cutland; Michael G. Gravett; Paul T Heath; Margaret Ip; Kirsty Le Doare; Shabir A. Madhi; Craig E. Rubens; Samir K. Saha; Stephanie J. Schrag; Ajoke Sobanjo-ter Meulen; Johan Vekemans; Anna C Seale

Group B Streptococcus is associated with multiple adverse pregnancy outcomes, yet previous epidemiology and interventions have mainly focused on neonatal invasive disease in high-income settings. We describe the rationale and approach for the first worldwide estimates of all relevant outcomes.


Clinical Infectious Diseases | 2017

Intrapartum Antibiotic Chemoprophylaxis Policies for the Prevention of Group B Streptococcal Disease Worldwide: Systematic Review

K Le Doare; M O'Driscoll; K Turner; F Seedat; Neal J Russell; Anna C Seale; Paul T Heath; Joy E Lawn; Carol J. Baker; Linda Bartlett; Clare L. Cutland; Michael G. Gravett; Margaret Ip; Shabir A. Madhi; Craig E. Rubens; Samir K. Saha; Stephanie J. Schrag; A Sobanjo-Ter Meulen; Johan Vekemans; Beate Kampmann; A Ramoni; Rb Helmig; K Makikallio; T Asatiani; M Fisher; M Feinstein; Y Oz; Me Suzin; Eisenberg; A Berardi

There is heterogeneity in intrapartum antibiotic use and implementation of policy varies widely. Global strategies to enhance the prevention of group B streptococcal disease that may include maternal vaccination are needed.


Clinical Infectious Diseases | 2017

Neurodevelopmental Impairment in Children After Group B Streptococcal Disease Worldwide: Systematic Review and Meta-analyses

Maya Kohli-Lynch; Neal J Russell; Anna C Seale; Cally J Tann; Carol J. Baker; Linda Bartlett; Clare L. Cutland; Michael G. Gravett; Paul T Heath; Margaret Ip; K Le Doare; Shabir A. Madhi; Craig E. Rubens; Samir K. Saha; Stephanie J. Schrag; A Sobanjo-Ter Meulen; Johan Vekemans; C O'Sullivan; F Nakwa; H Ben Hamouda; H. Soua; K Giorgakoudi; Shamez Ladhani; Theresa Lamagni; H Rattue; Caroline L. Trotter; Joy E Lawn

Group B Streptococcus (GBS) is a leading cause of invasive disease in infants, causing mortality and neurodevelopmental impairment (NDI) in survivors. This article estimates the percentage of survivors of infant GBS disease with NDI.


Clinical Infectious Diseases | 2017

Preterm Birth Associated With Group B Streptococcus Maternal Colonization Worldwide: Systematic Review and Meta-analyses

Fiorella Bianchi-Jassir; Anna C Seale; Maya Kohli-Lynch; Joy E Lawn; Carol J. Baker; Linda Bartlett; Clare L. Cutland; Michael G. Gravett; Paul T Heath; Margaret Ip; Kirsty Le Doare; Shabir A. Madhi; Samir K. Saha; Stephanie J. Schrag; Ajoke Sobanjo-ter Meulen; Johan Vekemans; Craig E. Rubens

Complications of preterm birth are the leading cause of deaths in children aged <5 years. Group B Streptococcus may be a preventable and important contributor to this burden.


Clinical Infectious Diseases | 2017

Stillbirth with Group B Streptococcus Disease Worldwide: Systematic Review and Meta-analyses

Anna C Seale; Hannah Blencowe; Fiorella Bianchi-Jassir; Nicholas D. Embleton; Quique Bassat; Jaume Ordi; Clara Menéndez; Clare L. Cutland; Carmen Briner; James A. Berkley; Joy E Lawn; Carol J. Baker; Linda Bartlett; Michael G. Gravett; Paul T Heath; Margaret Ip; Kirsty Le Doare; Craig E. Rubens; Samir K. Saha; Stephanie J. Schrag; Ajoke Sobanjo-ter Meulen; Johan Vekemans; Shabir A. Madhi

Group B Streptococcus (GBS) is associated with invasive disease in utero and stillbirth. We estimated that 1% of all stillbirths in developed countries and 4% in Africa were associated with GBS.

Collaboration


Dive into the Johan Vekemans's collaboration.

Top Co-Authors

Avatar

Carol J. Baker

Baylor College of Medicine

View shared research outputs
Top Co-Authors

Avatar

Stephanie J. Schrag

National Center for Immunization and Respiratory Diseases

View shared research outputs
Top Co-Authors

Avatar

Shabir A. Madhi

University of the Witwatersrand

View shared research outputs
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar

Clare L. Cutland

University of the Witwatersrand

View shared research outputs
Top Co-Authors

Avatar

Linda Bartlett

Johns Hopkins University

View shared research outputs
Top Co-Authors

Avatar
Researchain Logo
Decentralizing Knowledge