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1.
Lancet Infect Dis ; 24(2): 150-160, 2024 Feb.
Article in English | MEDLINE | ID: mdl-37776876

ABSTRACT

BACKGROUND: Morbidity and mortality from dengue virus (DENV) is rapidly growing in the large populations of south Asia. Few formal evaluations of candidate dengue vaccine candidates have been undertaken in India, Pakistan, or Bangladesh. Tetravalent vaccines must be tested for safety and immunogenicity in all age groups and in those previously exposed and naive to DENV infections. TV005 is a live, attenuated tetravalent dengue vaccine. We evaluated the safety and immunogenicity of a single dose of TV005 across age groups in dengue-endemic Bangladesh. METHODS: We performed a randomised, placebo-controlled age de-escalating clinical trial of TV005 at a single clinical site in dengue-endemic Dhaka, Bangladesh, following a technology transfer from the USA. Healthy (as determined by history, clinical examination, and safety laboratory test results) volunteers aged 1-50 years were randomly assigned 3:1 (stratified by four age groups) to receive a single dose of TV005 vaccine or placebo. Participants were followed up for 3 years. The study was double blind and was unmasked at day 180; outcome assessors, clinic staff, and volunteers remained blind throughout. Primary outcomes were safety, evaluated per-protocol as proportion of volunteers with solicited related adverse events of any severity through 28 days post dosing, and post-vaccination seropositivity by day 180 using serotype-specific neutralising antibodies (PRNT50 ≥10). Secondary outcomes included viremia, impact of past dengue exposure, and durability of antibody responses. This study is registered with Clinicaltrials.gov, NCT02678455, and is complete. FINDINGS: Between March 13, 2016, and Feb 14, 2017, 192 volunteers were enrolled into four age groups (adults [18-50 years; 20 male and 28 female], adolescents [11-17 years; 27 male and 21 female], children [5-10 years; 15 male and 33 female], and young children [1-4 years; 29 male and 19 female]) with 48 participant per group. All participants were Bangladeshi. Vaccination was well tolerated and most adverse events were mild. Rash was the most common vaccine-associated solicited adverse event, in 37 (26%) of 144 vaccine recipients versus six (12%) of 48 placebo recipients; followed by fever in seven (5% of 144) and arthralgias in seven (6% of 108), which were only observed in vaccine recipients. Post-vaccine, volunteers of all ages (n=142) were seropositive to most serotypes with 118 (83%) seropositive to DENV 1, 141 (99%) to DENV 2, 137 (96%) to DENV 3, and 124 (87%) to DENV 4, overall by day 180. Post-vaccination, viraemia was not consistently found and antibody titres were higher (10-15-fold for DENV 1-3 and 1·6-fold for DENV 4) in individuals with past dengue exposure compared with the dengue-naive participants (DENV 1 mean 480 [SD 4·0] vs 32 [2·4], DENV 2 1042 [3·2] vs 105 [3·1], DENV 3 1406 [2·8] vs 129 [4·7], and DENV 4 105 [3·3] vs 65 [3·1], respectively). Antibody titres to all serotypes remained stable in most adults (63-86%) after 3 years of follow-up. However, as expected for individuals without past exposure to dengue, titres for DENV 1, 3, and 4 waned by 3 years in the youngest (1-4 year old) cohort (69% seropositive for DENV 2 and 22-28% seropositive for DENV 1, 3, and 4). INTERPRETATION: With 3 years of follow-up, the single-dose tetravalent dengue vaccine, TV005, was well tolerated and immunogenic for all four serotypes in young children to adults, including individuals with no previous dengue exposure. FUNDING: National Institutes of Health-National Institute of Allergy and Infectious Diseases Intramural Research Program and Johns Hopkins University. TRANSLATION: For the Bangla translation of the abstract see Supplementary Materials section.


Subject(s)
Dengue Vaccines , Dengue Virus , Dengue , Adult , Child , Adolescent , Humans , Male , Female , Child, Preschool , Infant , Serogroup , Bangladesh , Vaccines, Attenuated , Double-Blind Method , Viremia , Immunogenicity, Vaccine , Antibodies, Viral
2.
Trends Parasitol ; 39(9): 760-773, 2023 09.
Article in English | MEDLINE | ID: mdl-37500334

ABSTRACT

Bangladesh has dramatically reduced malaria by 93% from 2008 to 2020. The strategy has been district-wise, phased elimination; however, the last districts targeted for elimination include remote, forested regions which present several challenges for prevention, detection, and treatment of malaria. These districts border Myanmar which harbors Plasmodium falciparum malaria parasites resistant to artemisinins, key drugs used in artemisinin-based combination therapies (ACTs) that have been vital for control programs. Challenges in monitoring emergence of artemisinin resistance (AR), tracking parasite reservoirs, changes in vector behavior and responses to insecticides, as well as other environmental and host factors (including the migration of Forcibly Displaced Myanmar Nationals; FDMNs) may pose added hazards in the final phase of eliminating malaria in Bangladesh.


Subject(s)
Antimalarials , Malaria, Falciparum , Malaria , Humans , Plasmodium falciparum , Bangladesh/epidemiology , Drug Resistance , Malaria/drug therapy , Malaria/prevention & control , Malaria/parasitology , Malaria, Falciparum/drug therapy , Malaria, Falciparum/prevention & control , Malaria, Falciparum/parasitology , Antimalarials/pharmacology , Antimalarials/therapeutic use
3.
Sci Total Environ ; 814: 151952, 2022 Mar 25.
Article in English | MEDLINE | ID: mdl-34843766

ABSTRACT

Nocturnal water losses were for long considered negligible, but it is now known that incomplete stomatal closure during the night leads to significant water losses at leaf, plant and ecosystem scales. However, only daytime transpiration is currently accounted for in evapotranspiration studies. Important uncertainties on the drivers of nocturnal water fluxes hinder its incorporation within modelling frameworks because some studies indicate that night-time stomatal drivers may differ from day-time responses. Here, we synthesise the studies on nocturnal stomatal conductance (gn) to determine underlying drivers through a systematic literature review and, whenever possible, meta-analytical techniques. Similar to daytime responses, we found negative effects of vapour pressure deficit, predawn water potential, air temperature, and salinity on gn across the plant species. However, the most apparent trend was an increase of gn from the beginning until the end of the night, indicating significant and widespread endogenous regulation by the circadian clock. We further observed how neither elevated CO2 nor nutrient status affected gn significantly across species. We also did not find any significant associations between gn and elevated ozone or increasing plant age. There was a paucity of studies on climatic extremes such heat waves and also few studies connected gn with anatomical features such as leaf specific area or stomatal density. Further studies are also needed to address the effects of plant sex, abscisic acid concentrations and genotypic variations on gn. Our findings solve the long-term conundrum on whether stomatal responses to daytime drivers are the same as those that during the nighttime.


Subject(s)
Plant Stomata , Plant Transpiration , Ecosystem , Plant Leaves , Plants , Water
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