Tobias Schindler
Swiss Tropical and Public Health Institute
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Featured researches published by Tobias Schindler.
American Journal of Tropical Medicine and Hygiene | 2014
Seif Shekalaghe; Mastidia Rutaihwa; Peter F. Billingsley; Mwajuma Chemba; Claudia Daubenberger; Eric R. James; Maximillian Mpina; Omar Juma; Tobias Schindler; Eric Huber; Anusha Gunasekera; Anita Manoj; Beatus Simon; Elizabeth Saverino; L. W. Preston Church; Cornelus C. Hermsen; Robert W. Sauerwein; Christopher V. Plowe; Meera Venkatesan; Philip Sasi; Omar Lweno; Paul Mutani; Ali Hamad; Ali Mohammed; Alwisa Urassa; Tutu Mzee; Debbie Padilla; Adam Ruben; B. Kim Lee Sim; Marcel Tanner
Controlled human malaria infection (CHMI) by mosquito bite has been used to assess anti-malaria interventions in > 1,500 volunteers since development of methods for infecting mosquitoes by feeding on Plasmodium falciparum (Pf) gametocyte cultures. Such CHMIs have never been used in Africa. Aseptic, purified, cryopreserved Pf sporozoites, PfSPZ Challenge, were used to infect Dutch volunteers by intradermal injection. We conducted a double-blind, placebo-controlled trial to assess safety and infectivity of PfSPZ Challenge in adult male Tanzanians. Volunteers were injected intradermally with 10,000 (N = 12) or 25,000 (N = 12) PfSPZ or normal saline (N = 6). PfSPZ Challenge was well tolerated and safe. Eleven of 12 and 10 of 11 subjects, who received 10,000 and 25,000 PfSPZ respectively, developed parasitemia. In 10,000 versus 25,000 PfSPZ groups geometric mean days from injection to Pf positivity by thick blood film was 15.4 versus 13.5 (P = 0.023). Alpha-thalassemia heterozygosity had no apparent effect on infectivity. PfSPZ Challenge was safe, well tolerated, and infectious.
American Journal of Tropical Medicine and Hygiene | 2014
Stefanie Knopp; Nahya Salim; Tobias Schindler; Dimitrios A. Karagiannis Voules; Julian Rothen; Omar Lweno; Alisa S. Mohammed; Raymond Singo; Myrna Benninghoff; Anthony A. Nsojo; Blaise Genton; Claudia Daubenberger
Sensitive diagnostic tools are crucial for an accurate assessment of helminth infections in low-endemicity areas. We examined stool samples from Tanzanian individuals and compared the diagnostic accuracy of a real-time polymerase chain reaction (PCR) with the FLOTAC technique and the Kato–Katz method for hookworm and the Baermann method for Strongyloides stercoralis detection. Only FLOTAC had a higher sensitivity than the Kato–Katz method for hookworm diagnosis; the sensitivities of PCR and the Kato–Katz method were equal. PCR had a very low sensitivity for S. stercoralis detection. The cycle threshold values of the PCR were negatively correlated with the logarithm of hookworm egg and S. stercoralis larvae counts. The median larvae count was significantly lower in PCR false negatives than true positives. All methods failed to detect very low-intensity infections. New diagnostic approaches are needed for monitoring of progressing helminth control programs, confirmation of elimination, or surveillance of disease recrudescence.
PLOS Neglected Tropical Diseases | 2015
Nahya Salim; Stefanie Knopp; Omar Lweno; Ummi Abdul; Ali Mohamed; Tobias Schindler; Julian Rothen; John Masimba; Denis Kwaba; Alisa S. Mohammed; Fabrice Althaus; Salim Abdulla; Marcel Tanner; Claudia Daubenberger; Blaise Genton
Background Plasmodium and soil transmitted helminth infections (STH) are a major public health problem, particularly among children. There are conflicting findings on potential association between these two parasites. This study investigated the Plasmodium and helminth co-infections among children aged 2 months to 9 years living in Bagamoyo district, coastal region of Tanzania. Methods A community-based cross-sectional survey was conducted among 1033 children. Stool, urine and blood samples were examined using a broad set of quality controlled diagnostic methods for common STH (Ascaris lumbricoides, hookworm, Strongyloides stercoralis, Enterobius vermicularis, Trichuris trichura), schistosoma species and Wuchereria bancrofti. Blood slides and malaria rapid diagnostic tests (mRDTs) were utilized for Plasmodium diagnosis. Results Out of 992 children analyzed, the prevalence of Plasmodium infection was 13% (130/992), helminth 28.5% (283/992); 5% (50/992) had co-infection with Plasmodium and helminth. The prevalence rate of Plasmodium, specific STH and co-infections increased significantly with age (p < 0.001), with older children mostly affected except for S. stercoralis monoinfection and co-infections. Spatial variations of co-infection prevalence were observed between and within villages. There was a trend for STH infections to be associated with Plasmodium infection [OR adjusted for age group 1.4, 95% CI (1.0–2.1)], which was more marked for S. stercoralis (OR = 2.2, 95% CI (1.1–4.3). Age and not schooling were risk factors for Plasmodium and STH co-infection. Conclusion The findings suggest that STH and Plasmodium infections tend to occur in the same children, with increasing prevalence of co-infection with age. This calls for an integrated approach such as using mass chemotherapy with dual effect (e.g., ivermectin) coupled with improved housing, sanitation and hygiene for the control of both parasitic infections.
American Journal of Tropical Medicine and Hygiene | 2017
Ali Hamad; Dolores O. Mandumbi; Ally Olotu; Luis Segura; Sumana Chakravarty; B. Kim Lee Sim; Oscar M. Embon; Mitoha O. Ayekaba; Thomas L. Richie; Dianna Hergott; Mwajuma Chemba; Elizabeth Nyakarungu; Vicente Urbano; Esther Eburi; Stephen L. Hoffman; Elizabeth Saverino; Chris Schwabe; Matilde Riloha Rivas; Anita Manoj; Yonas Abebe; Tobias Schindler; Carl D. Maas; Eric R. James; Marcel Tanner; Martin Eka; José Raso; Claudia Daubenberger; Minglin Li; Salim Abdulla; Adam Ruben
Abstract. Equatorial Guinea (EG) has implemented a successful malaria control program on Bioko Island. A highly effective vaccine would be an ideal complement to this effort and could lead to halting transmission and eliminating malaria. Sanaria® PfSPZ Vaccine (Plasmodium falciparum sporozoite Vaccine) is being developed for this purpose. To begin the process of establishing the efficacy of and implementing a PfSPZ Vaccine mass vaccination program in EG, we decided to conduct a series of clinical trials of PfSPZ Vaccine on Bioko Island. Because no clinical trial had ever been conducted in EG, we first successfully established the ethical, regulatory, quality, and clinical foundation for conducting trials. We now report the safety, tolerability, and immunogenicity results of the first clinical trial in the history of the country. Thirty adult males were randomized in the ratio 2:1 to receive three doses of 2.7 × 105 PfSPZ of PfSPZ Vaccine (N = 20) or normal saline placebo (N = 10) by direct venous inoculation at 8-week intervals. The vaccine was safe and well tolerated. Seventy percent, 65%, and 45% of vaccinees developed antibodies to Plasmodium falciparum (Pf) circumsporozoite protein (PfCSP) by enzyme-linked immunosorbent assay, PfSPZ by automated immunofluorescence assay, and PfSPZ by inhibition of sporozoite invasion assay, respectively. Antibody responses were significantly lower than responses in U.S. adults who received the same dosage regimen, but not significantly different than responses in young adult Malians. Based on these results, a clinical trial enrolling 135 subjects aged 6 months to 65 years has been initiated in EG; it includes PfSPZ Vaccine and first assessment in Africa of PfSPZ-CVac. ClinicalTrials.gov identifier: NCT02418962.
American Journal of Tropical Medicine and Hygiene | 2018
Jongo Sa; Shekalage Sa; Church Lwp; Ruben Aj; Tobias Schindler; Zenklusen I; Rutishauser T; Julian Rothen; Tumbo A; Mkindi C; Maximillian Mpina; Mtoro At; Ishizuka As; Ramadhani Kk; Milando Fa; Qassim M; Omar Juma; Mwakasungula S; Simon B; James Er; Abebe Y; Chakravarty S; Saverino E; Bakari Bm; Billingsley Pf; Seder Ra; Claudia Daubenberger; Sim Bkl; Richie Tl; Marcel Tanner
Abstract. We are using controlled human malaria infection (CHMI) by direct venous inoculation (DVI) of cryopreserved, infectious Plasmodium falciparum (Pf) sporozoites (SPZ) (PfSPZ Challenge) to try to reduce time and costs of developing PfSPZ Vaccine to prevent malaria in Africa. Immunization with five doses at 0, 4, 8, 12, and 20 weeks of 2.7 × 105 PfSPZ of PfSPZ Vaccine gave 65% vaccine efficacy (VE) at 24 weeks against mosquito bite CHMI in U.S. adults and 52% (time to event) or 29% (proportional) VE over 24 weeks against naturally transmitted Pf in Malian adults. We assessed the identical regimen in Tanzanians for VE against PfSPZ Challenge. Twenty- to thirty-year-old men were randomized to receive five doses normal saline or PfSPZ Vaccine in a double-blind trial. Vaccine efficacy was assessed 3 and 24 weeks later. Adverse events were similar in vaccinees and controls. Antibody responses to Pf circumsporozoite protein were significantly lower than in malaria-naïve Americans, but significantly higher than in Malians. All 18 controls developed Pf parasitemia after CHMI. Four of 20 (20%) vaccinees remained uninfected after 3 week CHMI (P = 0.015 by time to event, P = 0.543 by proportional analysis) and all four (100%) were uninfected after repeat 24 week CHMI (P = 0.005 by proportional, P = 0.004 by time to event analysis). Plasmodium falciparum SPZ Vaccine was safe, well tolerated, and induced durable VE in four subjects. Controlled human malaria infection by DVI of PfSPZ Challenge appeared more stringent over 24 weeks than mosquito bite CHMI in United States or natural exposure in Malian adults, thereby providing a rigorous test of VE in Africa.
Genome Announcements | 2017
Julian Rothen; Tobias Schindler; Joël F. Pothier; Mario Younan; Ulrich Certa; Claudia Daubenberger; Valentin Pflüger; Joerg Jores
ABSTRACT We present draft whole-genome sequences of seven Streptococcus agalactiae strains isolated from Camelus dromedarius in Kenya and Somalia. These data are an extension to the group B Streptococcus (GBS) pangenome and might provide more insight into the underlying mechanisms of pathogenicity and antibiotic resistance of camel GBS.
BMC Infectious Diseases | 2014
Nahya Salim; Tobias Schindler; Ummi Abdul; Julian Rothen; Blaise Genton; Omar Lweno; Alisa S. Mohammed; John Masimba; Denis Kwaba; Salim Abdulla; Marcel Tanner; Claudia Daubenberger; Stefanie Knopp
International journal of molecular epidemiology and genetics | 2014
Solomon Mwakasungula; Tobias Schindler; Said Jongo; Elena Moreno; Kasimu Kamaka; Mgeni Mohammed; Selina Joseph; Ramla Rashid; Thabit Athuman; Anneth Tumbo; Ali Hamad; Omar Lweno; Marcel Tanner; Seif Shekalaghe; Claudia Daubenberger
Archive | 2016
Said Jongo; Seif Shekalaghe; Thomas L. Richie; Claudia Daubenberger; Peter F. Billingsley; Robert W. Sauerwein; Maximillian Mpina; Kamaka Kassimu; Tobias Schindler; Isabelle Zenklusen; Kim Lee Sim; Florence A. Milando; Hussein S. Mbarak; Anneth Tumbo; Thabit Athuman; Ummi Abdul; Hajirani Msuya; Ramla Rashid; Selina Aloyce; Elena Moreno; Theresia Ngonyani; Omar Juma; Omar Lweno; Ali Hamad; Mgeni Mohamed; Bakary Mwalim; William Kato; Conrad Gwandu; Beatus Bongole; Sumana Chakravarty
Archive | 2014
Seif Shekalaghe; Mastidia Rutaihwa; Peter F. Billingsley; Mwajuma Chemba; Eric R. James; Maximillian Mpina; Omar Juma; Tobias Schindler; Eric Huber; Anusha Gunasekera; Anita Manoj; Beatus Simon; Elizabeth Savarino; L. W. Preston Church; Cornelus C. Hermsen; Robert W. Sauerwein; Christopher V. Plowe; Meera Venkatesan; Omar Lweno; Paul Mutani; Ali Hamad; Ali Mohammed; Alwisa Urassa; Tutu Mzee; Debbie Padilla; Adam Ruben; B. Kim; Lee Sim; Marcel Tanner; Salim Abdullah