First administration to humans of a monoclonal antibody cocktail against rabies virus: safety, tolerability, and neutralizing activity

التفاصيل البيبلوغرافية
العنوان: First administration to humans of a monoclonal antibody cocktail against rabies virus: safety, tolerability, and neutralizing activity
المؤلفون: C. Python, E. van Corven, Alexander Berthold Hendrik Bakker, Deborah J. Briggs, C.J. Kissling, Gerrit Jan Weverling, F. Uytdehaag, M.F. Brink, Jaap Goudsmit, Christian Herzog, Charles E. Rupprecht, Willem Egbert Marissen, Fija M. Lagerwerf, Stefan Kostense, S. Worst, R. Grimaldi, Katharina Hartmann, P. Pandya
المساهمون: Amsterdam institute for Infection and Immunity, General Internal Medicine
المصدر: Vaccine, 26(47), 5922-5927. Elsevier BV
سنة النشر: 2008
مصطلحات موضوعية: Adult, Male, Adolescent, Rabies, medicine.medical_treatment, Antibodies, Viral, medicine.disease_cause, Cell Line, Young Adult, Rabies vaccine, Double-Blind Method, Neutralization Tests, medicine, Animals, Humans, Post-exposure prophylaxis, Mononegavirales, Lyssavirus, Aged, General Veterinary, General Immunology and Microbiology, biology, business.industry, Rabies virus, Immunization, Passive, Public Health, Environmental and Occupational Health, Antibodies, Monoclonal, Middle Aged, Rhabdoviridae, biology.organism_classification, medicine.disease, Virology, Vaccination, Treatment Outcome, Infectious Diseases, Rabies Vaccines, Immunology, Molecular Medicine, Female, business, medicine.drug
الوصف: Immediate passive immune prophylaxis as part of rabies post-exposure prophylaxis (PEP) often cannot be provided due to limited availability of human or equine rabies immunoglobulin (HRIG and ERIG, respectively). We report first clinical data from two phase I studies evaluating a monoclonal antibody cocktail CL184 against rabies. The studies included healthy adult subjects in the USA and India and involved two parts. First, subjects received a single intramuscular dose of CL184 or placebo in a double blind, randomized, dose-escalation trial. Second, open-label CL184 (20IU/kg) was co-administered with rabies vaccine. Safety was the primary objective and rabies virus neutralizing activity (RVNA) was investigated as efficacy parameter. Pain at the CL184 injection site was reported by less than 40% of subjects; no fever or local induration, redness or swelling was observed. RVNA was detectable from day 1 to day 21 after a single dose of CL184 20 or 40IU/kg. All subjects had adequate (>0.5IU/mL) RVNA levels from day 14 onwards when combined with rabies vaccine. CL184 appears promising as an alternative to RIG in PEP.
اللغة: English
تدمد: 0264-410X
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::98edecd3817d972b363de9c069d53072Test
https://doi.org/10.1016/j.vaccine.2008.08.050Test
حقوق: OPEN
رقم الانضمام: edsair.doi.dedup.....98edecd3817d972b363de9c069d53072
قاعدة البيانات: OpenAIRE