Immunophenotypic analysis of peripheral mononuclear cells was performed by FACS to detect total number of NK cells, subtypes and intracellular IFN gamma and TNF production by NK cells in the different patient groups.\n\nResults: The total mean CD56(+)/CD3(-) NK cell proportions in acute and severe malaria subjects were 9.14% (7.15% CD56(dim), 2.01%CD56(bright)) and 19.62% (16.05%CD56(dim), 3.58%CD56(bright)), EVP4593 respectively, in contrast to healthy controls from endemic (total

mean CD56(+)/CD3(-) 1.2%) and non-endemic area (total mean CD56(+)/CD3(-) 0.67%). Analysis of basal IFN gamma and TNF levels confirmed the CD56(bright) NK population as the main cytokine producer (p < 0.0001) in the groups affected with malaria, with the CD56(dim) NK cell exhibiting the highest potential of TNF production after stimulus in the acute malaria group.\n\nConclusions: The results confirm the important role of not only CD56(bright) but also of CD56(dim) NK cell populations as producers of the two cytokines in malaria KPT-8602 concentration patients in Colombia.”
“BackgroundCD36 is a multifunctional membrane receptor and is expressed in 3 several cell lines. Individuals

who lack platelet (PLT) CD36 are at risk for immunization against this antigen, leading to several clinical syndromes. This study aimed to investigate the frequency and molecular basis of CD36 deficiency in Shanghai. Study Design and MethodsWhole blood samples were collected from healthy blood donors, and the PLTs and monocytes were analyzed FG-4592 in vitro using flow cytometry to determine CD36 deficiency type. After genomic DNA was extracted, Exons 3 to 14 of CD36 gene including a part of relevant flanking introns were amplified. Direct nucleotide sequencing and sequence alignment were performed. The samples that showed mutations were confirmed by clonal sequencing. ResultsOf the 1022 healthy blood donors analyzed, 22 individuals failed to express CD36 on PLTs; two of them expressed no CD36 on their monocytes either. These results demonstrated that the frequencies of Type I

(lacking CD36 expression on PLTs and monocytes) and Type II (lacking CD36 expression on PLTs only) CD36 deficiency among the study population were 0.2 and 2.0%, respectively. Nucleotide sequencing analysis revealed nine different mutations including six mutations that were not yet reported. The most frequent mutations among the study population were 329-330delAC and 1228-1239delATTGTGCCTATT. ConclusionThe study findings have confirmed the fact that the frequency of CD36 deficiency in the Chinese population is slightly lower than that in other Asian countries. The identification of several new mutation types indicated the polymorphism of CD36 gene in the Shanghai population.”
“Correct mitochondrial dynamics are essential to neuronal function.