3 results match your criteria: "United States Army Medical Component-Armed Forces Research Institute of Medical Sciences (USAMC-AFRIMS)[Affiliation]"
J Acquir Immune Defic Syndr
April 2017
*Hawaii Center for AIDS, University of Hawaii, Honolulu, HI;†Division of Neurology, Department of Medicine, Phramongkutklao Hospital, Bangkok, Thailand;‡Department of Neurology, Memory and Aging Center, University of California, San Francisco, San Francisco, CA;§SEARCH, Thai Red Cross AIDS Research Center, Bangkok, Thailand;‖US Military HIV Research Program, Walter Reed Army Institute of Research, Silver Spring, MD;¶Henry M. Jackson Foundation for the Advancement of Military Medicine, Bethesda, MD;#Biostatistics and Data Management Core, University of Hawaii, Honolulu, HI; and**Department of Retrovirology, US Army Medical Component-Armed Forces Research Institute of Medical Sciences (USAMC-AFRIMS), Bangkok, Thailand.
J Parasitol
October 2014
Division of Experimental Therapeutics, Walter Reed Army Institute of Research, Silver Spring, Maryland 20910; * Department of Veterinary Medicine, United States Army Medical Component-Armed Forces Research Institute of Medical Sciences (USAMC-AFRIMS), Bangkok, Thailand 10400. Correspondence should be sent to:
Since the 1940s, the large animal model to assess novel causal prophylactic antimalarial agents has been the Plasmodium cynomolgi sporozoite-infected Indian-origin rhesus monkey. In 2009 the model was reassessed with 3 clinical standards: primaquine (PQ), tafenoquine (TQ), and atovaquone-proguanil. Both control monkeys were parasitemic on day 8 post-sporozoite inoculation on day 0.
View Article and Find Full Text PDFVaccine
August 2011
Department of Veterinary Medicine, United States Army Medical Component-Armed Forces Research Institute of Medical Sciences (USAMC-AFRIMS), Bangkok, Thailand.
Immune sera from volunteers vaccinated in a blinded Phase 3 clinical trial with JE-VAX(®) and a new Japanese encephalitis virus (JEV) vaccine (IC51 or IXIARO), were tested for the ability to protect mice against lethal JEV challenge. Sera from IXIARO vaccinated subjects were pooled into four batches based on neutralizing antibody measured by plaque reduction neutralization test (PRNT(50) titer): high (∼200), medium (∼40-50), low (∼20) and negative (<10). Pooled sera from JE-VAX(®) vaccinated subjects (PRNT(50) titer∼55) and pooled JEV antibody negative pre-vaccination sera were used as controls.
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