We use cookies to understand how you use our site and to improve your experience. This includes personalizing content and advertising. To learn more, click here. By continuing to use our site, you accept our use of cookies. Cookie Policy.

Features Partner Sites Information LinkXpress
Sign In
Advertise with Us
INTEGRA BIOSCIENCES AG

Download Mobile App




Events

09 Apr 2024 - 12 Apr 2024
15 Apr 2024 - 17 Apr 2024
23 Apr 2024 - 26 Apr 2024

Molecular Changes Associated with Treating Lymphatic Filariasis

By LabMedica International staff writers
Posted on 09 Oct 2019
Print article
Image: A peripheral blood smear showing Wuchereria bancrofti microfilaria, found in a patient with lymphatic filariasis (Photo courtesy of Medical Chemical Corporation).
Image: A peripheral blood smear showing Wuchereria bancrofti microfilaria, found in a patient with lymphatic filariasis (Photo courtesy of Medical Chemical Corporation).
Lymphatic filariasis (LF) is a disabling neglected tropical disease that is caused by the mosquito-borne filarial parasites Wuchereria bancrofti, Brugia malayi and B. timori. Adult worms live in the human host’s lymphatic system and release larval parasites (microfilariae or Mf) that circulate in the blood.

Although treatment is safe, transient mild to moderate systemic adverse events, such as joint pain, fever, rash, or cough, are common in individuals with circulating microfilariae in the blood. Since these adverse events (AEs) are quite uncommon in uninfected individuals, they are believed to be triggered by host responses to dying filarial worms rather than the drugs themselves.

Tropical Medicine specialists at the Washington University School of Medicine (St. Louis, MO, USA) randomly assigned 89 W. bancrofti-infected adults to one of four treatment arms and all participants had AE assessments performed 24 hours after treatment. The AE study enrolled a subset of 95 treated participants and specific analyses that were performed on samples from each of the 95 individuals. Nine of these participants experienced moderate AEs, 24 had mild AEs, and 62 had no AEs. There was no difference in age or sex distribution between the three AE groups.

The scientists used various methodologies to assess the participants’ reactions to the infection. This included a direct sandwich enzyme immunoassay (EIA) that uses the monoclonal antibody AD12 that binds to a carbohydrate epitope on circulating filarial antigen (CFA); immunoprecipitation and western blots where chemiluminescence was detected by a ChemiDoc imager; immune complex and complement components assays; 27 cytokines were measured with the MAGPIX system with the Bio-Rad Bio-Plex Human 27-Plex Cytokine Panel and Bio-Plex Cytokine Reagent Kit. Molecular analyses of RNA and differential gene expression and overall expression patterns were performed.

The investigators found that levels of filarial antigens increased after treatment in individuals with AEs, and this suggests that AEs are triggered by host responses to dying parasites. AEs were associated with elevations in serum levels of certain immune molecules called cytokines. Moreover, when the team compared patterns of gene expression in white blood cells between people with moderate AEs and those without AEs, they found 744 genes upregulated in people with AEs, including many genes involved in immune signaling.

The authors concluded that their study has provided new insights regarding the pathogenesis of post-treatment AEs in LF-infected individuals. The results are consistent with the hypothesis that a Wolbachia lipoprotein triggers AEs by binding to TLR2-TLR6, but other uncharacterized filarial antigens might also play a role. The study was published on September 26, 2019, in the journal PLOS Neglected Tropical Diseases.

Related Links:
Washington University School of Medicine

Platinum Member
COVID-19 Rapid Test
OSOM COVID-19 Antigen Rapid Test
One Step HbA1c Measuring System
GREENCARE A1c
Complement 3 (C3) Test
GPP-100 C3 Kit
New
Gold Member
TORCH Panel Rapid Test
Rapid TORCH Panel Test

Print article

Channels

Clinical Chemistry

view channel
Image: Reaching speeds up to 6,000 RPM, this centrifuge forms the basis for a new type of inexpensive, POC biomedical test (Photo courtesy of Duke University)

POC Biomedical Test Spins Water Droplet Using Sound Waves for Cancer Detection

Exosomes, tiny cellular bioparticles carrying a specific set of proteins, lipids, and genetic materials, play a crucial role in cell communication and hold promise for non-invasive diagnostics.... Read more

Molecular Diagnostics

view channel
Image: MOF materials efficiently enrich cfDNA and cfRNA in blood through simple operational process (Photo courtesy of Science China Press)

Blood Circulating Nucleic Acid Enrichment Technique Enables Non-Invasive Liver Cancer Diagnosis

The ability to diagnose diseases early can significantly enhance the effectiveness of clinical treatments and improve survival rates. One promising approach for non-invasive early diagnosis is the use... Read more

Hematology

view channel
Image: The low-cost portable device rapidly identifies chemotherapy patients at risk of sepsis (Photo courtesy of 52North Health)

POC Finger-Prick Blood Test Determines Risk of Neutropenic Sepsis in Patients Undergoing Chemotherapy

Neutropenia, a decrease in neutrophils (a type of white blood cell crucial for fighting infections), is a frequent side effect of certain cancer treatments. This condition elevates the risk of infections,... Read more

Pathology

view channel
Image: The OvaCis Rapid Test discriminates benign from malignant epithelial ovarian cysts (Photo courtesy of INEX)

Intra-Operative POC Device Distinguishes Between Benign and Malignant Ovarian Cysts within 15 Minutes

Ovarian cysts represent a significant health issue for women globally, with up to 10% experiencing this condition at some point in their lives. These cysts form when fluid collects within a thin membrane... Read more
Copyright © 2000-2024 Globetech Media. All rights reserved.