114 research outputs found

    Determination of dilution and quality control of total and anti-measles immunoglobulin G antibody assays

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    Objective: To determine the correct dilution and Quality control commercial ELISA of total and anti-measles antibodies for HIV infected pregnant women.Design: A laboratory based studySetting: The University of Nairobi, Department of Paediatrics laboratory.Subjects: HIV infected pregnant women enrolled and exposed to different ARVs depending on their degree of immunosuppression for prevention of mother-child transmission of HIV-1.Results: The dilution used in this study, was 1:400000. Tight error bars of +/-0.1 were produced hence testing was done in singles not in duplicates as recommended. Validation steps did not pass for measles ELISA.Conclusion: Despite the recommendations of the manufacture each laboratory should always optimize an assay before performing tests and reporting the result. Every laboratory should determine the best dilution to use for quantitative TIgG assays and should perform internal and external quality control before reporting the results. These results will give insight on good laboratory practice during trouble shooting while assays are failing

    Propagating uncertainty to estimates of above-ground biomass for Kenyan mangroves: a scaling procedure from tree to landscape level

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    Mangroves are globally important carbon stores and as such have potential for inclusion in future forest-based climate change mitigation strategies such as Reduced Emissions from Deforestation and Degradation (REDD+). Participation in REDD+ will require developing countries to produce robust estimates of forest above-ground biomass (AGB) accompanied by an appropriate measure of uncertainty. Final estimates of AGB should account for known sources of uncertainty (measurement and predictive) particularly when estimating AGB at large spatial scales. In this study, mixed-effects models were used to account for variability in the allometric relationship of Kenyan mangroves due to species and site effects. A generic biomass equation for Kenyan mangroves was produced in addition to a set of species-site specific equations. The generic equation has potential for broad application as it can be used to predict the AGB of new trees where there is no pre-existing knowledge of the specific species-site allometric relationship: the most commonly encountered scenario in practical biomass studies. Predictions of AGB using the mixed-effects model showed good correspondence with the original observed values of AGB although displayed a poorer fit at higher AGB values, suggesting caution in extrapolation. A strong relationship was found between the observed and predicted values of AGB using an independent validation dataset from the Zambezi Delta, Mozambique (R2 = 0.96, p = < 0.001). The simulation based approach to uncertainty propagation employed in the current study produced estimates of AGB at different spatial scales (tree – landscape level) accompanied by a realistic measure of the total uncertainty. Estimates of mangrove AGB in Kenya are presented at the plot, regional and landscape level accompanied by 95% prediction intervals. The 95% prediction intervals for landscape level estimates of total AGB stocks suggest that between 5.4 and 7.2 megatonnes of AGB is currently held in Kenyan mangrove forests

    Human papillomavirus and abnormal cervical lesions among HIV-infected women in HIV-discordant couples from Kenya

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    Objective HIV infection increases the risk of high-grade cervical neoplasia and invasive cervical carcinoma. The study addresses the limited data describing human papillomavirus (HPV) infection and cervical neoplasia among HIV-infected women in HIV-discordant relationships in sub-Saharan Africa, which is needed to inform screening strategies. Methods A cross-sectional study of HIV-infected women with HIV-uninfected partners was conducted to determine the distribution of type-specific HPV infection and cervical cytology. This study was nested in a prospective cohort recruited between September 2007 and December 2009 in Nairobi, Kenya. Cervical cells for HPV DNA testing and conventional cervical cytology were collected. HPV types were detected and genotyped by Roche Linear Array PCR assay. Results Among 283 women, the overall HPV prevalence was 62%, and 132 (47%) had ≥1 high-risk (HR)-HPV genotype. Of 268 women with cervical cytology results, 18 (7%) had high-grade cervical lesions or more severe by cytology, of whom 16 (89%) were HR-HPV-positive compared with 82 (41%) of 199 women with normal cytology (p<0.001). The most common HR-HPV types in women with a high-grade lesion or more severe by cytology were HPV-52 (44%), HPV-31 (22%), HPV-35 (22%), HPV-51 (22%) and HPV-58 (22%). HR-HPV genotypes HPV-16 or HPV-18 were found in 17% of women with high-grade lesions or more severe. HR-HPV screening applied in this population would detect 89% of those with a high-grade lesion or more severe, while 44% of women with normal or low-grade cytology would screen positive. Conclusion HR-HPV prevalence was high in this population of HIV-infected women with an uninfected partner. Choice of screening for all HR genotypes versus a subset of HR genotypes in these HIV-infected women will strongly affect the performance of an HPV screening strategy relative to cytological screening. Regional and subpopulation differences in HR-HPV genotype distributions could affect screening test performance

    Opportunities and Challenges to Emergency Department-Based HIV Testing Services and Self-Testing Programs: A Qualitative Study of Healthcare Providers and Patients in Kenya

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    BACKGROUND: Young people in Sub-Saharan Africa, especially males, have been insufficiently engaged through HIV Testing Services (HTS). In Kenya, younger persons are often treated in emergency departments (EDs) for injuries, an interaction where HTS and HIV self-testing (HIVST) can be leveraged. Data from stakeholders on ED-HTS and HIVST is lacking and needed to understand opportunities and barriers for HIV testing and care, and inform program implementation. METHODS: Between December 2021 and March 2022, 32 in-depth interviews (IDIs) were conducted with 16 male and 16 female patients who had been treated in the Kenyatta National Hospital (KNH) ED, half of whom had been HIV-tested. Six focus-group discussions (FGDs) were also conducted with 50 nurses, doctors, HIV testing counselors, and administrators working in the ED. All transcripts were double-coded and thematically analyzed using Dedoose software and a parallel inductive and deductive coding approach which allowed for capture of both a priori and emergent themes. RESULTS: Patients and providers agreed that ED-HTS are facilitated by friendly staff, patient education, high perceived HIV risk, and confidentiality. However, ED-HTS is limited by burdens on staff, resources, time, and space, as well as severity of patient injuries limiting ability to consent to or prioritize HIV testing. These limitations provide opportunities for ED-HIVST: particularly the ability to test at a comfortable time and place, especially when provided alongside sufficient HIV and testing education, contact with healthcare providers, and psychosocial support. Barriers for ED-HIVST where identified and as patients’ concerns about HIVST accuracy and mental health impacts of a positive test, as well providers’ identified barriers on their concerns for loss to follow up and inability to complete confirmatory testing. COM-B Model [Figure: see text] Application of the COM-B Model of Behavior Change to ED-HIVST Acceptability in Kenya CONCLUSION: ED stakeholders are receptive to HTS and HIVST, and patients desire the opportunity to use HIVST. Potential challenges—such as psychological effects of testing positive, worries about access to follow-up care, and confusion about how to self-administer testing, may be addressed through programming designed to promote education, access and ensure follow-up mechanisms. DISCLOSURES: All Authors: No reported disclosures

    The Magnitude and Kinetics of the Mucosal HIV-Specific CD8+ T Lymphocyte Response and Virus RNA Load in Breast Milk

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    BACKGROUND: The risk of postnatal HIV transmission is associated with the magnitude of the milk virus load. While HIV-specific cellular immune responses control systemic virus load and are detectable in milk, the contribution of these responses to the control of virus load in milk is unknown. METHODS: We assessed the magnitude of the immunodominant GagRY11 and subdominant EnvKY9-specific CD8+ T lymphocyte response in blood and milk of 10 A*3002+, HIV-infected Malawian women throughout the period of lactation and correlated this response to milk virus RNA load and markers of breast inflammation. RESULTS: The magnitude and kinetics of the HIV-specific CD8+ T lymphocyte responses were discordant in blood and milk of the right and left breast, indicating independent regulation of these responses in each breast. However, there was no correlation between the magnitude of the HIV-specific CD8+ T lymphocyte response and the milk virus RNA load. Further, there was no correlation between the magnitude of this response and markers of breast inflammation. CONCLUSIONS: The magnitude of the HIV-specific CD8+ T lymphocyte response in milk does not appear to be solely determined by the milk virus RNA load and is likely only one of the factors contributing to maintenance of low virus load in milk
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