scholarly journals A Case of Fatal Strongyloidiasis in a Patient with Chronic Lymphocytic Leukemia and Molecular Characterization of the Isolate

2008 ◽  
Vol 46 (4) ◽  
pp. 261 ◽  
Author(s):  
Eshrat Beigom Kia ◽  
Hamid Reza Rahimi ◽  
Hossein Mirhendi ◽  
Mohammad Reza Nilforoushan ◽  
Ardeshir Talebi ◽  
...  
2021 ◽  
pp. 1-11
Author(s):  
Rashmi Kanagal-Shamanna ◽  
Haiyan Bao ◽  
Hutton Kearney ◽  
Stephanie Smoley ◽  
Zhenya Tang ◽  
...  

PLoS ONE ◽  
2012 ◽  
Vol 7 (11) ◽  
pp. e48485 ◽  
Author(s):  
Ana Eugenia Rodríguez ◽  
Jose Ángel Hernández ◽  
Rocío Benito ◽  
Norma C. Gutiérrez ◽  
Juan Luis García ◽  
...  

2013 ◽  
Vol 54 (8) ◽  
pp. 1769-1779 ◽  
Author(s):  
Anna Lanemo Myhrinder ◽  
Eva Hellqvist ◽  
Ann-Charlotte Bergh ◽  
Mattias Jansson ◽  
Kenneth Nilsson ◽  
...  

2020 ◽  
Vol 11 (1) ◽  
Author(s):  
Alison D. Tang ◽  
Cameron M. Soulette ◽  
Marijke J. van Baren ◽  
Kevyn Hart ◽  
Eva Hrabeta-Robinson ◽  
...  

Blood ◽  
1981 ◽  
Vol 58 (5) ◽  
pp. 1053-1055 ◽  
Author(s):  
S Davis

Abstract Peripheral blood lymphocytes from normal donors and patients with chronic lymphocytic leukemia, B-cell type, were purified into T, helper T, and suppressor T lymphocytes by fluorescence-activated cell sorting using OKT3, OKT4, and OKT8 monoclonal antibodies. The maximum response of the purified subpopulations to stimulation by phytohemagglutinin (PHA) was determined by measuring the production of colonies when the stimulated cells were grown on agar. The helper T cells in normal and CLL patients were the most responsive to PHA stimulation, although the responsiveness of helper T cells to PHA was decreased in CLL. Purified CLL B cells responded minimally to PHA stimulation, but normal B lymphocytes did not. The abnormal response of CLL lymphocytes to PHA appears to be due abnormal helper T cells, and, to a smaller extent, to the ability of CLL B lymphocytes to respond.


Blood ◽  
2006 ◽  
Vol 109 (7) ◽  
pp. 2989-2998 ◽  
Author(s):  
Riccardo Bomben ◽  
Michele Dal Bo ◽  
Daniela Capello ◽  
Dania Benedetti ◽  
Daniela Marconi ◽  
...  

Abstract IGHV3-21–using chronic lymphocytic leukemia (CLL) is a distinct entity with restricted immunoglobulin gene features and poor prognosis and is more frequently encountered in Northern than Southern Europe. To further investigate this subset and its geographic distribution in the context of a country (Italy) with both continental and Mediterranean areas, 37 IGHV3-21 CLLs were collected out of 1076 cases enrolled by different institutions from Northern or Central Southern Italy. Of the 37 cases, 18 were identified as homologous (hom)HCDR3–IGHV3-21 CLLs and were found almost exclusively (16 of 18) in Northern Italy; in contrast, 19 nonhomHCDR3–IGHV3-21 cases were evenly distributed throughout Italy. Clinically, poor survivals were documented for IGHV3-21 CLLs as well as for subgroups of mutated and homHCDR3–IGHV3-21 CLLs. Negative prognosticators CD38, ZAP-70, CD49d, and CD79b were expressed at higher levels in homHCDR3 than nonhomHCDR3–IGHV3-21 cases. Differential gene expression profiling (GEP) of 13 IGHV3-21 versus 52 non–IGHV3-21 CLLs identified, among 122 best-correlated genes, TGFB2 and VIPR1 as down- and up-regulated in IGHV3-21 CLL cases, respectively. Moreover, GEP of 7 homHCDR3 versus 6 nonhomHCDR3–IGHV3-21 CLLs yielded 20 differentially expressed genes, with WNT-16 being that expressed at the highest levels in homHCDR3–IGHV3-21 CLLs. Altogether, IGHV3-21 CLLs, including those with homHCDR3, had a peculiar global phenotype in part explaining their worse clinical outcome.


Sign in / Sign up

Export Citation Format

Share Document