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1.
Lancet Glob Health ; 12(5): e771-e782, 2024 May.
Article in English | MEDLINE | ID: mdl-38484745

ABSTRACT

BACKGROUND: WHO has proposed elimination of transmission of onchocerciasis (river blindness) by 2030. More than 99% of cases of onchocerciasis are in sub-Saharan Africa. Vector control and mass drug administration of ivermectin have been the main interventions for many years, with varying success. We aimed to identify factors associated with elimination of onchocerciasis transmission in sub-Saharan Africa. METHODS: For this systematic review and meta-analysis we searched for published articles reporting epidemiological or entomological assessments of onchocerciasis transmission status in sub-Saharan Africa, with or without vector control. We searched MEDLINE, PubMed, Web of Science, Embase, Cochrane Central Register of Controlled Trials, African Index Medicus, and Google Scholar databases for all articles published from database inception to Aug 19, 2023, without language restrictions. The search terms used were "onchocerciasis" AND "ivermectin" AND "mass drug administration". The three inclusion criteria were (1) focus or foci located in Africa, (2) reporting of elimination of transmission or at least 10 years of ivermectin mass drug administration in the focus or foci, and (3) inclusion of at least one of the following assessments: microfilarial prevalence, nodule prevalence, Ov16 antibody seroprevalence, and blackfly infectivity prevalence. Epidemiological modelling studies and reviews were excluded. Four reviewers (NM, AJ, AM, and TNK) extracted data in duplicate from the full-text articles using a data extraction tool developed in Excel with columns recording the data of interest to be extracted, and a column where important comments for each study could be highlighted. We did not request any individual-level data from authors. Foci were classified as achieving elimination of transmission, being close to elimination of transmission, or with ongoing transmission. We used mixed-effects meta-regression models to identify factors associated with transmission status. This study is registered in PROSPERO, CRD42022338986. FINDINGS: Of 1525 articles screened after the removal of duplicates, 75 provided 282 records from 238 distinct foci in 19 (70%) of the 27 onchocerciasis-endemic countries in sub-Saharan Africa. Elimination of transmission was reported in 24 (9%) records, being close to elimination of transmission in 86 (30%) records, and ongoing transmission in 172 (61%) records. I2 was 83·3% (95% CI 79·7 to 86·3). Records reporting 10 or more years of continuous mass drug administration with 80% or more therapeutic coverage of the eligible population yielded significantly higher odds of achieving elimination of transmission (log-odds 8·5 [95% CI 3·5 to 13·5]) or elimination and being close to elimination of transmission (42·4 [18·7 to 66·1]) than those with no years achieving 80% coverage or more. Reporting 15-19 years of ivermectin mass drug administration (22·7 [17·2 to 28·2]) and biannual treatment (43·3 [27·2 to 59·3]) were positively associated with elimination and being close to elimination of transmission compared with less than 15 years and no biannual mass drug administration, respectively. Having had vector control without vector elimination (-42·8 [-59·1 to -26·5]) and baseline holoendemicity (-41·97 [-60·6 to -23·2]) were associated with increased risk of ongoing transmission compared with no vector control and hypoendemicity, respectively. Blackfly disappearance due to vector control or environmental change contributed to elimination of transmission. INTERPRETATION: Mass drug administration duration, frequency, and coverage; baseline endemicity; and vector elimination or disappearance are important determinants of elimination of onchocerciasis transmission in sub-Saharan Africa. Our findings underscore the importance of improving and sustaining high therapeutic coverage and increasing treatment frequency if countries are to achieve elimination of onchocerciasis transmission. FUNDING: The Bill & Melinda Gates Foundation and Neglected Tropical Diseases Modelling Consortium, UK Medical Research Council, and Global Health EDCTP3 Joint Undertaking. TRANSLATIONS: For the Swahili, French, Spanish and Portuguese translations of the abstract see Supplementary Materials section.


Subject(s)
Onchocerciasis, Ocular , Onchocerciasis , Humans , Onchocerciasis/drug therapy , Onchocerciasis/epidemiology , Onchocerciasis/prevention & control , Ivermectin/therapeutic use , Onchocerciasis, Ocular/drug therapy , Onchocerciasis, Ocular/epidemiology , Onchocerciasis, Ocular/prevention & control , Mass Drug Administration , Seroepidemiologic Studies , Africa South of the Sahara/epidemiology
3.
PLoS Negl Trop Dis ; 17(5): e0011320, 2023 May.
Article in English | MEDLINE | ID: mdl-37235598

ABSTRACT

BACKGROUND: Onchocerciasis, also known as "river blindness", is caused by the bite of infected female blackflies (genus Simuliidae) that transmit the parasite Onchocerca volvulus. A high onchocerciasis microfarial load increases the risk to develop epilepsy in children between the ages of 3 and 18 years. In resource-limited settings in Africa where onchocerciasis has been poorly controlled, high numbers of onchocerciasis-associated epilepsy (OAE) are reported. We use mathematical modeling to predict the impact of onchocerciasis control strategies on the incidence and prevalence of OAE. METHODOLOGY: We developed an OAE model within the well-established mathematical modelling framework ONCHOSIM. Using Latin-Hypercube Sampling (LHS), and grid search technique, we quantified transmission and disease parameters using OAE data from Maridi County, an onchocerciasis endemic area, in southern Republic of South Sudan. Using ONCHOSIM, we predicted the impact of ivermectin mass drug administration (MDA) and vector control on the epidemiology of OAE in Maridi. PRINCIPAL FINDINGS: The model estimated an OAE prevalence of 4.1% in Maridi County, close to the 3.7% OAE prevalence reported in field studies. The OAE incidence is expected to rapidly decrease by >50% within the first five years of implementing annual MDA with good coverage (≥70%). With vector control at a high efficacy level (around 80% reduction of blackfly biting rates) as the sole strategy, the reduction is slower, requiring about 10 years to halve the OAE incidence. Increasing the efficacy levels of vector control, and implementing vector control simultaneously with MDA, yielded better results in preventing new cases of OAE. CONCLUSIONS/SIGNIFICANCES: Our modeling study demonstrates that intensifying onchocerciasis eradication efforts could substantially reduce OAE incidence and prevalence in endemic foci. Our model may be useful for optimizing OAE control strategies.


Subject(s)
Epilepsy , Onchocerca volvulus , Onchocerciasis, Ocular , Onchocerciasis , Simuliidae , Child , Animals , Female , Humans , Child, Preschool , Adolescent , Onchocerciasis/complications , Onchocerciasis/drug therapy , Onchocerciasis/epidemiology , South Sudan/epidemiology , Onchocerciasis, Ocular/complications , Onchocerciasis, Ocular/drug therapy , Onchocerciasis, Ocular/epidemiology , Ivermectin/therapeutic use , Epilepsy/epidemiology , Epilepsy/prevention & control , Epilepsy/etiology , Prevalence , Simuliidae/parasitology , Blindness
5.
Parasit Vectors ; 16(1): 46, 2023 Feb 01.
Article in English | MEDLINE | ID: mdl-36726184

ABSTRACT

Onchocerca lupi is an emerging canine ocular pathogen with zoonotic potential. In Europe, known endemic areas are the Iberian Peninsula and Greece, but the parasite has also been found in Romania, Hungary, and Germany. A 5-year-old Irish Wolfhound was presented in August 2021 with ocular discharge. A subconjunctival granulomatous nodule containing several nematode fragments was removed. Molecular analysis of the mitochondrial cytochrome c oxidase subunit I gene confirmed the presence of O. lupi genotype 1. This is the first report of autochthonous O. lupi infection in a dog from Austria.


Subject(s)
Dog Diseases , Filariasis , Onchocerciasis, Ocular , Animals , Dogs , Austria , Dog Diseases/diagnosis , Dog Diseases/parasitology , Onchocerca/genetics , Onchocerciasis, Ocular/diagnosis , Onchocerciasis, Ocular/drug therapy , Onchocerciasis, Ocular/veterinary
6.
PLoS Negl Trop Dis ; 15(7): e0009604, 2021 07.
Article in English | MEDLINE | ID: mdl-34310602

ABSTRACT

BACKGROUND: Onchocerciasis ("river blindness") can cause severe morbidity, including vision loss and various skin manifestations, and is targeted for elimination using ivermectin mass drug administration (MDA). We calculated the number of people with Onchocerca volvulus infection and onchocercal skin and eye disease as well as disability-adjusted life years (DALYs) lost from 1990 through to 2030 in areas formerly covered by the African Programme for Onchocerciasis Control. METHODS: Per MDA implementation unit, we collated data on the pre-control distribution of microfilariae (mf) prevalence and the history of control. Next, we predicted trends in infection and morbidity over time using the ONCHOSIM simulation model. DALY estimates were calculated using disability weights from the Global Burden of Disease Study. RESULTS: In 1990, prior to MDA implementation, the total population at risk was 79.8 million with 26.0 million (32.5%) mf-positive individuals, of whom 17.5 million (21.9%) had some form of onchocercal skin or eye disease (2.5 million DALYs lost). By 2030, the total population was predicted to increase to 236.1 million, while the number of mf-positive cases (about 6.8 million, 2.9%), people with skin or eye morbidity (4.2 million, 1.8%), and DALYs lost (0.7 million) were predicted to decline. CONCLUSIONS: MDA has had a remarkable impact on the onchocerciasis burden in countries previously under the APOC mandate. In the few countries where we predict continued transmission between now and 2030, intensified MDA could be combined with local vector control efforts, or the introduction of new drugs for mopping up residual cases of infection and morbidity.


Subject(s)
Antiparasitic Agents/therapeutic use , Ivermectin/therapeutic use , Onchocerciasis, Ocular/pathology , Skin Diseases, Parasitic/pathology , Africa South of the Sahara/epidemiology , Antiparasitic Agents/administration & dosage , Humans , Ivermectin/administration & dosage , Mass Drug Administration , Models, Biological , Onchocerciasis, Ocular/drug therapy , Onchocerciasis, Ocular/epidemiology , Risk Factors , Skin Diseases, Parasitic/drug therapy , Skin Diseases, Parasitic/epidemiology
7.
Clin Pharmacol Ther ; 109(4): 867-891, 2021 04.
Article in English | MEDLINE | ID: mdl-33555032

ABSTRACT

Model-informed drug development (MIDD) has a long and rich history in infectious diseases. This review describes foundational principles of translational anti-infective pharmacology, including choice of appropriate measures of exposure and pharmacodynamic (PD) measures, patient subpopulations, and drug-drug interactions. Examples are presented for state-of-the-art, empiric, mechanistic, interdisciplinary, and real-world evidence MIDD applications in the development of antibacterials (review of minimum inhibitory concentration-based models, mechanism-based pharmacokinetic/PD (PK/PD) models, PK/PD models of resistance, and immune response), antifungals, antivirals, drugs for the treatment of global health infectious diseases, and medical countermeasures. The degree of adoption of MIDD practices across the infectious diseases field is also summarized. The future application of MIDD in infectious diseases will progress along two planes; "depth" and "breadth" of MIDD methods. "MIDD depth" refers to deeper incorporation of the specific pathogen biology and intrinsic and acquired-resistance mechanisms; host factors, such as immunologic response and infection site, to enable deeper interrogation of pharmacological impact on pathogen clearance; clinical outcome and emergence of resistance from a pathogen; and patient and population perspective. In particular, improved early assessment of the emergence of resistance potential will become a greater focus in MIDD, as this is poorly mitigated by current development approaches. "MIDD breadth" refers to greater adoption of model-centered approaches to anti-infective development. Specifically, this means how various MIDD approaches and translational tools can be integrated or connected in a systematic way that supports decision making by key stakeholders (sponsors, regulators, and payers) across the entire development pathway.


Subject(s)
Anti-Infective Agents/pharmacology , Drug Development/organization & administration , Models, Biological , United States Food and Drug Administration/organization & administration , Anti-Bacterial Agents/pharmacology , Anti-Infective Agents/pharmacokinetics , Antifungal Agents/pharmacology , Antimalarials/pharmacology , Antitubercular Agents/pharmacology , Antiviral Agents/pharmacology , Body Weight , Dose-Response Relationship, Drug , Drug Approval/organization & administration , Drug Discovery/organization & administration , Drug Resistance, Microbial/drug effects , Drug Resistance, Microbial/physiology , Humans , Immunity/physiology , Ivermectin/therapeutic use , Kidney Function Tests , Liver Function Tests , Microbial Sensitivity Tests , Onchocerciasis, Ocular/drug therapy , Pediatrics , Research Design , United States , United States Food and Drug Administration/standards
8.
PLoS Negl Trop Dis ; 14(11): e0008503, 2020 11.
Article in English | MEDLINE | ID: mdl-33151944

ABSTRACT

Onchocerciasis also known as river blindness is a neglected tropical disease and the world's second-leading infectious cause of blindness in humans; it is caused by Onchocerca volvulus. Current treatment with ivermectin targets microfilariae and transmission and does not kill the adult parasites, which reside within subcutaneous nodules. To support the development of macrofilaricidal drugs that target the adult worm to further support the elimination of onchocerciasis, an in-depth understanding of O. volvulus biology especially the factors that support the longevity of these worms in the human host (>10 years) is required. However, research is hampered by a lack of access to adult worms. O. volvulus is an obligatory human parasite and no small animal models that can propagate this parasite were successfully developed. The current optimized 2-dimensional (2-D) in vitro culturing method starting with O. volvulus infective larvae does not yet support the development of mature adult worms. To overcome these limitations, we have developed and applied 3-dimensional (3-D) culture systems with O. volvulus larvae that simulate the human in vivo niche using in vitro engineered skin and adipose tissue. Our proof of concept studies have shown that an optimized indirect co-culture of in vitro skin tissue supported a significant increase in growth of the fourth-stage larvae to the pre-adult stage with a median length of 816-831 µm as compared to 767 µm of 2-D cultured larvae. Notably, when larvae were co-cultured directly with adipose tissue models, a significant improvement for larval motility and thus fitness was observed; 95% compared to 26% in the 2-D system. These promising co-culture concepts are a first step to further optimize the culturing conditions and improve the long-term development of adult worms in vitro. Ultimately, it could provide the filarial research community with a valuable source of O. volvulus worms at various developmental stages, which may accelerate innovative unsolved biomedical inquiries into the parasite's biology.


Subject(s)
Antiparasitic Agents/therapeutic use , Bioartificial Organs/parasitology , Drug Development/methods , Onchocerca volvulus/growth & development , Onchocerciasis, Ocular/drug therapy , Skin/parasitology , Africa , Animals , Humans , Ivermectin/therapeutic use , Microfilariae/drug effects , Onchocerca volvulus/drug effects , Onchocerciasis, Ocular/pathology , Organ Culture Techniques , Proof of Concept Study
10.
Int J Dermatol ; 59(9): 1065-1070, 2020 Sep.
Article in English | MEDLINE | ID: mdl-31513297

ABSTRACT

Onchocerciasis is a leading cause of blindness in the world. It may be seen in temperate climates of the United States and Europe in immigrants and travelers from endemic regions, often linked to poverty and war. One should be aware of an incubation period that can be up to 15 months. In its early stage and throughout its course, onchocerciasis has noteworthy skin findings, facilitating diagnosis, as onchodermatitis resembles common eczema with variable degrees of papular, lichenoid, atrophic, and pigmentary alterations, features not suggestive if one is unaware of an individual's immigration and travel history. The same concept applies for the encysted worms (onchocercomas), as they tend to appear as common skin cysts and benign neoplasms. New methods can be employed to increase diagnostic sensitivity and specificity. Ivermectin is the gold standard of therapy, the use of which has almost miraculously eliminated this disease from large areas of the earth. However, its effect remains isolated to microfilariae and can be devastating in those coinfected with Loa loa. Recently, the symbiotic relationship between adult worms and Wolbachia bacteria has been discovered and, with it, the possibility of adding doxycycline as a treatment option. We also discuss coinfection with HIV and other diseases.


Subject(s)
Eczema , Onchocerciasis, Ocular , Onchocerciasis , Animals , Europe , Ivermectin/therapeutic use , Larva , North America , Onchocerciasis/complications , Onchocerciasis/diagnosis , Onchocerciasis/drug therapy , Onchocerciasis, Ocular/diagnosis , Onchocerciasis, Ocular/drug therapy , Onchocerciasis, Ocular/epidemiology
11.
ACS Infect Dis ; 6(2): 180-185, 2020 02 14.
Article in English | MEDLINE | ID: mdl-31876143

ABSTRACT

The optimization of a series of benzimidazole-benzoxaborole hybrid molecules linked via a ketone that exhibit good activity against Onchocerca volvulus, a filarial nematode responsible for the disease onchocerciasis, also known as river blindness, is described. The lead identified in this series, 21 (AN15470), was found to have acceptable pharmacokinetic properties to enable an evaluation following oral dosing in an animal model of onchocerciasis. Compound 21was effective in killing worms implanted in Mongolian gerbils when dosed orally as a suspension at 100 mg/kg/day for 14 days but not when dosed orally at 100 mg/kg/day for 7 days.


Subject(s)
Benzimidazoles/therapeutic use , Boron Compounds/therapeutic use , Ketones/chemistry , Onchocerciasis, Ocular/drug therapy , Administration, Oral , Animals , Benzimidazoles/pharmacokinetics , Boron Compounds/pharmacokinetics , Disease Models, Animal , Female , Filaricides/pharmacokinetics , Filaricides/therapeutic use , Gerbillinae , Male
14.
Folia Med (Plovdiv) ; 60(4): 580-593, 2018 Dec 01.
Article in English | MEDLINE | ID: mdl-31188767

ABSTRACT

BACKGROUND: The suggested dose of ivermectin is 300 µG/kg/day for onchocerciasis but it has low water solubility and poor oral bioavailability. AIM: To prepare and evaluate a solid lipid-based self-emulsifying drug delivery system of ivermectin. MATERIALS AND METHODS: Based on supersaturated solubility study, oil, surfactant, and co-surfactant were selected. On the basis of ternary phase diagrams and simplex-lattice design, self-emulsifying, drug delivery formulations had been developed and optimized. Ivermectin-excipients compatibility studies were performed using differential scanning calorimetry and Fourier transform infrared spectroscopy. Solid self-emulsifying drug delivery formulation was formulated from the optimized batch by surface assimilation method and filled into hard gelatin capsules. In vitro release rate and in vivo pharmacokinetic parameters of ivermectin from the capsules were determined. Two-tailed paired t-test/Dunnett multiple comparison tests were performed for in vivo pharmacokinetic parameter at 95 % of confidence level. RESULTS: Soybeans oil, tween 80, and span 80 were selected as oil, surfactant, and co-surfactant respectively. The ternary diagrams were shown the maximum area for emulsion in 1:2 surfactant/co-surfactant ratio. The optimized batch had found with 30 mg ivermectin, 6.17 g soybeans oil, 0.30 g tween 80, and 3.50 g span 80. All differential scanning calorimetry and Fourier transform infrared characteristic peaks of the optimized formulation were identical with that of pure ivermectin. The area under the curve of ivermectin from the capsule was about two-fold higher than that of ivermectin suspension. CONCLUSIONS: Solid self-emulsifying drug delivery system was an effective oral solid dosage form to improve the oral bioavailability of ivermectin.


Subject(s)
Antiparasitic Agents/administration & dosage , Drug Delivery Systems , Ivermectin/administration & dosage , Administration, Oral , Animals , Antiparasitic Agents/blood , Antiparasitic Agents/pharmacokinetics , Biological Availability , Dosage Forms , Drug Compounding , Emulsions , Hexoses , Humans , In Vitro Techniques , Ivermectin/blood , Ivermectin/pharmacokinetics , Male , Onchocerciasis, Ocular/blood , Onchocerciasis, Ocular/drug therapy , Polysorbates , Rats , Rats, Wistar , Solubility , Soybean Oil , Surface-Active Agents
15.
Trends Parasitol ; 34(1): 64-79, 2018 01.
Article in English | MEDLINE | ID: mdl-28958602

ABSTRACT

Human onchocerciasis - commonly known as river blindness - is one of the most devastating yet neglected tropical diseases, leaving many millions in sub-Saharan Africa blind and/or with chronic disabilities. Attempts to eliminate onchocerciasis, primarily through the mass drug administration of ivermectin, remains challenging and has been heightened by the recent news that drug-resistant parasites are developing in some populations after years of drug treatment. Needed, and needed now, in the fight to eliminate onchocerciasis are new tools, such as preventive and therapeutic vaccines. This review summarizes the progress made to advance the onchocerciasis vaccine from the research laboratory into the clinic.


Subject(s)
Onchocerciasis, Ocular/prevention & control , Vaccines , Animals , Antiparasitic Agents/pharmacology , Antiparasitic Agents/standards , Antiparasitic Agents/therapeutic use , Drug Resistance , Humans , Onchocerca volvulus/drug effects , Onchocerciasis, Ocular/drug therapy , Onchocerciasis, Ocular/immunology , Onchocerciasis, Ocular/transmission
16.
Clin Infect Dis ; 65(12): 2026-2034, 2017 Nov 29.
Article in English | MEDLINE | ID: mdl-29020189

ABSTRACT

BACKGROUND: Mass drug administration (MDA) with ivermectin is the cornerstone of efforts to eliminate human onchocerciasis by 2020 or 2025. The feasibility of elimination crucially depends on the effects of multiple ivermectin doses on Onchocerca volvulus. A single ivermectin (standard) dose clears the skin-dwelling microfilarial progeny of adult worms (macrofilariae) and temporarily impedes the release of such progeny by female macrofilariae, but a macrofilaricidal effect has been deemed minimal. Multiple doses of ivermectin may cumulatively and permanently reduce the fertility and shorten the lifespan of adult females. However, rigorous quantification of these effects necessitates interrogating longitudinal data on macrofilariae with suitably powerful analytical techniques. METHODS: Using a novel mathematical modeling approach, we analyzed, at an individual participant level, longitudinal data on viability and fertility of female worms from the single most comprehensive multiple-dose clinical trial of ivermectin, comparing 3-monthly with annual treatments administered for 3 years in Cameroon. RESULTS: Multiple doses of ivermectin have a partial macrofilaricidal and a modest permanent sterilizing effect after 4 or more consecutive treatments, even at routine MDA doses (150 µg/kg) and frequencies (annual). The life expectancy of adult O. volvulus is reduced by approximately 50% and 70% after 3 years of annual or 3-monthly (quarterly) exposures to ivermectin. CONCLUSIONS: Our quantification of macrofilaricidal and sterilizing effects of ivermectin should be incorporated into transmission models to inform onchocerciasis elimination efforts in Africa and residual foci in Latin America. It also provides a framework to assess macrofilaricidal candidate drugs currently under development.


Subject(s)
Dose-Response Relationship, Drug , Filaricides/therapeutic use , Ivermectin/therapeutic use , Onchocerca volvulus/drug effects , Onchocerciasis, Ocular/drug therapy , Adolescent , Adult , Animals , Cameroon/epidemiology , Disease Eradication/methods , Filaricides/administration & dosage , Humans , Ivermectin/administration & dosage , Longitudinal Studies , Male , Middle Aged , Models, Theoretical , Onchocerca volvulus/physiology , Onchocerciasis, Ocular/epidemiology , Onchocerciasis, Ocular/parasitology , Young Adult
17.
Parasitol Res ; 116(3): 1013-1022, 2017 Mar.
Article in English | MEDLINE | ID: mdl-28111713

ABSTRACT

River blindness, caused by infection with the filarial nematode Onchocerca volvulus, is a neglected tropical disease affecting millions of people. There is a clear need for diagnostic tools capable of identifying infected patients, but that can also be used for monitoring disease progression and treatment efficacy. Plasma-derived parasitic microRNAs have been suggested as potential candidates for such diagnostic tools. We have investigated whether these parasitic microRNAs are present in sufficient quantity in plasma of Onchocerca-infected patients to be used as a diagnostic biomarker for detection of O. volvulus infection or treatment monitoring. Plasma samples were collected from different sources (23 nodule-positive individuals and 20 microfilaridermic individuals), microRNAs (miRNAs) were extracted using Qiagen miRNeasy kit, and a set of 17 parasitic miRNAs was evaluated on these miRNA extracts using miRCURY Locked Nucleic Acid (LNA) Universal RT microRNA PCR system. Of the 17 miRNAs evaluated, only 7 miRNAs were found to show detectable signal in a number of samples: bma-miR-236-1, bma-miR-71, ov-miR71-22nt, ov-miR-71-23nt, ov-miR-100d, ov-bantam-a, and ov-miR-87-3p. Subsequent melting curve analysis, however, indicated that the signals observed for ov-miR-71 variants and ov-miR-87-3p are non-specific. The other miRNAs only showed positive signal in one or few samples with Cq values just below the cutoff. Our data indicate that parasitic miRNAs are not present in circulation at a sufficiently high level to be used as biomarker for O. volvulus infection or treatment monitoring using LNA-based RT-qPCR analysis.


Subject(s)
DNA, Helminth/genetics , MicroRNAs/genetics , Oligonucleotides/genetics , Onchocerca volvulus/isolation & purification , Onchocerciasis, Ocular/parasitology , Real-Time Polymerase Chain Reaction/methods , Adolescent , Adult , Aged , Aged, 80 and over , Animals , Anthelmintics/therapeutic use , Biomarkers/blood , DNA, Helminth/blood , DNA, Helminth/metabolism , Female , Humans , Male , MicroRNAs/blood , MicroRNAs/metabolism , Middle Aged , Oligonucleotides/metabolism , Onchocerca volvulus/genetics , Onchocerca volvulus/metabolism , Onchocerciasis, Ocular/blood , Onchocerciasis, Ocular/diagnosis , Onchocerciasis, Ocular/drug therapy , Treatment Outcome , Young Adult
18.
Vet Ophthalmol ; 20(4): 349-356, 2017 Jul.
Article in English | MEDLINE | ID: mdl-27624855

ABSTRACT

OBJECTIVE: To describe the clinical exam findings, treatment and outcomes of 16 dogs diagnosed with ocular onchocerciasis in New Mexico. MATERIALS AND METHODS: Records of dogs diagnosed by the primary author were reviewed (2011-2015). Records that were accessible and included a diagnosis of Onchocerca lupi by histopathologic or molecular identification of the nematode were included. RESULTS: Sixteen cases were included. 3/16 dogs were treated with year-round heartworm prophylaxis prior to infection. Clinical exam findings included conjunctival hyperemia and/or episcleral injection (16/16), focal subconjunctival mass(es) (14/16), retinal detachment (7/16), corneal edema (4/16), chemosis (3/16), corneal opacity (2/16), exophthalmia (1/16), glaucoma (1/16), strabismus (1/16), blepharospasm (1/16), and vitreal degeneration (1/16). Ocular involvement was unilateral in 7/16 dogs and bilateral in 9/16 dogs. The diagnosis was confirmed via histologic identification of the nematodes and/or PCR. Treatment consisted of medical management or a combination medical and surgical management. Known or suspected recurrence of disease was documented in 10 dogs. CONCLUSIONS: Canine ocular onchocerciasis is endemic in New Mexico. Histopathology and molecular identification are useful diagnostic tools. Medical management alone was successful in many cases.


Subject(s)
Dog Diseases/diagnosis , Dog Diseases/drug therapy , Onchocerciasis, Ocular/drug therapy , Onchocerciasis, Ocular/veterinary , Animals , Dog Diseases/parasitology , Dogs , Female , Male , New Mexico , Onchocerca/isolation & purification , Onchocerciasis, Ocular/diagnosis , Retrospective Studies
19.
Adv Parasitol ; 94: 247-341, 2016.
Article in English | MEDLINE | ID: mdl-27756456

ABSTRACT

Human onchocerciasis (river blindness) is one of the few neglected tropical diseases (NTDs) whose control strategies have been informed by mathematical modelling. With the change in focus from elimination of the disease burden to elimination of Onchocerca volvulus, much remains to be done to refine, calibrate and validate existing models. Under the impetus of the NTD Modelling Consortium, the teams that developed EPIONCHO and ONCHOSIM have joined forces to compare and improve these frameworks to better assist ongoing elimination efforts. We review their current versions and describe how they are being used to address two key questions: (1) where can onchocerciasis be eliminated with current intervention strategies by 2020/2025? and (2) what alternative/complementary strategies could help to accelerate elimination where (1) cannot be achieved? The control and elimination of onchocerciasis from the African continent is at a crucial crossroad. The African Programme for Onchocerciasis Control closed at the end of 2015, and although a new platform for support and integration of NTD control has been launched, the disease will have to compete with a myriad of other national health priorities at a pivotal time in the road to elimination. However, never before had onchocerciasis control a better arsenal of intervention strategies as well as diagnostics. It is, therefore, timely to present two models of different geneses and modelling traditions as they come together to produce robust decision-support tools. We start by describing the structural and parametric assumptions of EPIONCHO and ONCHOSIM; we continue by summarizing the modelling of current treatment strategies with annual (or biannual) mass ivermectin distribution and introduce a number of alternative strategies, including other microfilaricidal therapies (such as moxidectin), macrofilaricidal (anti-wolbachial) treatments, focal vector control and the possibility of an onchocerciasis vaccine. We conclude by discussing challenges, opportunities and future directions.


Subject(s)
Antiparasitic Agents/administration & dosage , Models, Theoretical , Onchocerca volvulus/drug effects , Onchocerciasis, Ocular/prevention & control , Animals , Disease Eradication , Humans , Ivermectin/administration & dosage , Macrolides/administration & dosage , Microfilariae , Onchocerca volvulus/immunology , Onchocerca volvulus/physiology , Onchocerciasis, Ocular/drug therapy , Onchocerciasis, Ocular/parasitology , Vaccines
20.
Parasit Vectors ; 9(1): 509, 2016 09 20.
Article in English | MEDLINE | ID: mdl-27645887

ABSTRACT

BACKGROUND: Onchocerciasis or "river blindness" is a chronic parasitic disease caused by the filarial worm Onchocerca volvulus, transmitted through infected blackflies (Simulium spp.). Bioko Island (Equatorial Guinea) used to show a high endemicity for onchocerciasis. During the last years, the disease control programmes using different larvicides and ivermectin administration have considerably reduced the prevalence and intensity of infection. Based on this new epidemiological scenario, in the present work we aimed to assess the impact of the strategies applied against onchocerciasis in Bioko Island by an evaluation of IgG4 antibodies specific for recombinant Ov-16 in ELISA. METHODS: A cross-sectional study was conducted in Bioko Island from mid-January to mid-February, 2014. Twenty communities were randomly selected from rural and urban settings. A total of 140 households were chosen. In every selected household, all individuals aged 5 years and above were recruited; 544 study participants agreed to be part of this work. No previous data on onchocerciasis seroprevalence in the selected communities were available. Blood samples were collected and used in an "ELISA in-house" prepared with recombinant Ov-16, expressed and further purified. IgG4 antibodies specific for recombinant Ov-16 were evaluated by ELISA in all of the participants. RESULTS: Based on the Ov-16 ELISA, the onchocerciasis seroprevalence was 7.9 %, mainly concentrated in rural settings; samples from community Catedral Ela Nguema (# 16) were missed during the field work. Among the rural setups, communities Inasa Maule (# 7), Ruiché (# 20) and Barrios Adyacentes Riaba (# 14), had the highest seropositivity percentages (29.2, 26.9 and 23.8 %, respectively). With respect to the urban settings, we did not find any positive case in communities Manzana Casa Bola (# 3), Colas Sesgas (# 6), Getesa (# 8), Moka Bioko (# 9), Impecsa (# 10), Baney Zona Baja (# 12) and Santo Tomás de Aquino (# 1). No onchocerciasis seropositive samples were found in 10-year-old individuals or younger. The IgG4 positive titles increased in older participants. CONCLUSIONS: A significant decline in onchocerciasis prevalence was observed in Bioko Island after years of disease-vector control and CDTI strategy. The seroprevalence increased with age, mainly in rural settings that could be due to previous exposure of population to the filarial parasite, eliminated by the control programmes introduced against onchocerciasis. A new Ov-16 serological evaluation with a larger sample size of children below 10 years of age is required to demonstrate the interruption of transmission of O. volvulus in the human population of Bioko Island (Equatorial Guinea) according to the WHO criteria.


Subject(s)
Antibodies, Helminth/blood , Immunoglobulin G/blood , Onchocerca volvulus/immunology , Onchocerciasis, Ocular/epidemiology , Onchocerciasis/epidemiology , Seroepidemiologic Studies , Adolescent , Adult , Animals , Antigens, Helminth/immunology , Child , Child, Preschool , Cross-Sectional Studies , Enzyme-Linked Immunosorbent Assay , Equatorial Guinea/epidemiology , Family Characteristics , Female , Humans , Insect Vectors/parasitology , Ivermectin/therapeutic use , Male , Middle Aged , Onchocerca volvulus/isolation & purification , Onchocerciasis/drug therapy , Onchocerciasis/immunology , Onchocerciasis, Ocular/drug therapy , Onchocerciasis, Ocular/immunology , Onchocerciasis, Ocular/parasitology , Prevalence , Simuliidae/parasitology , Young Adult
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