Infection-associated Immune Perturbations Resolve 1 Year Following Treatment for Loa loa.
Jesica A Herrick, Michelle A Makiya, Nicole Holland-Thomas...
https://pubmed.ncbi.nlm.nih.gov/32055862/Actively Recruiting
Led by National Institute of Allergy and Infectious Diseases (NIAID) · Updated on 2026-08-12
500
Participants Needed
1
Research Sites
N/A
Total Duration
This research focuses on patients with filarial infections, which are caused by parasitic worms transmitted through mosquito bites. The study aims to explore the immune systems response to these infections, including how people become susceptible, develop disease, and respond to treatment. The study includes patients diagnosed with or suspected of having infections such as Wuchereria bancrofti, Brugia malayi, Onchocerca volvulus, and Loa loa, among others. The research is observational and involves standard medical care without experimental diagnostics or treatments. Participants receive standard treatments like diethylcarbamazine or ivermectin depending on the infection type. Diagnostic tests include routine evaluations and may involve lung, skin, or heart assessments. Some patients might undergo skin biopsies or bronchoalveolar lavage if medically necessary. Additional research procedures include extra blood draws to study immune cells, urine collections, skin allergy tests, and leukapheresis to collect white blood cells in adults. During the study, participants undergo frequent and detailed follow-up evaluations including physical exams and blood tests. Researchers monitor immune responses and clinical outcomes over time, collecting blood and serum samples for laboratory studies. The main goal is to identify markers of infection, treatment responses, and immune regulation over a 10-year period. This long-term observation helps understand disease progression and treatment effects while ensuring patients receive optimal clinical care.
CONDITIONS
Host Response to Infection and Treatment in Filarial Diseases
L
Lori A Penrod, R.N.
T
Thomas B Nutman, M.D.
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National Institute of Allergy and Infectious Diseases (NIAID)
Lead Sponsor
You may qualify if you...
You will not qualify if you...
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Up to 10 years
Participants receive routine medical evaluations to diagnose and monitor filarial infections, including blood tests, urine collections, skin tests, and possibly biopsies or lung procedures if needed. Standard treatment with approved medications is provided based on infection type.
Regular follow-up visits for clinical and immune assessments
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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Lead Sponsor