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1 rognostic factor associated with progressive lymphocytosis.
2 eristic lymphocyte clone and the presence of lymphocytosis.
3 mal blood count and 13.9% (309 of 2228) with lymphocytosis.
4 50% of cases of CD4(+) T-cell large granular lymphocytosis.
5 microl), with 56% of patients experiencing a lymphocytosis.
6 ammation, often granulomatous, and meningeal lymphocytosis.
7 vels with only a few cases developing marked lymphocytosis.
8 okine production by T cells and induction of lymphocytosis.
9 (-/-) mice failed to develop splenomegaly or lymphocytosis.
10 a significant decrease of monoclonal B-cell lymphocytosis.
11 velopment and/or maintenance of persistent B lymphocytosis.
12 1 IWCLL partial response (PR) and 3 PRs with lymphocytosis.
13 e with the preneoplastic syndrome persistent lymphocytosis.
14 phadenopathy or significant peripheral blood lymphocytosis.
15 onse criteria modified for treatment-related lymphocytosis.
16 ymerase chain reaction and leukocytosis with lymphocytosis.
17 68%; 38 (34%) of 111 patients had transient lymphocytosis.
18 who achieved nodal response with persistent lymphocytosis.
19 on samples from nine patients with prolonged lymphocytosis.
20 sulted in the near abolishment of the B cell lymphocytosis.
21 treated patients had a partial response with lymphocytosis.
22 espective groups had a partial response with lymphocytosis.
23 ed by a more benign monoclonal CD5(+) B-cell lymphocytosis.
24 taken into account when considering duodenal lymphocytosis.
25 que family with hereditary polyclonal B cell lymphocytosis.
26 e the CLL precursor lesion monoclonal B cell lymphocytosis.
27 than 50% in 19 of 21 patients with baseline lymphocytosis.
28 romote cell proliferation and does not cause lymphocytosis.
29 g rapid lymph node shrinkage and a transient lymphocytosis.
30 an indolent lymphoma with monoclonal B-cell lymphocytosis.
31 n the preleukemic state of monoclonal B-cell lymphocytosis.
32 RC3 lesions were absent in monoclonal B-cell lymphocytosis (0 of 63) and were rare in CLL at diagnosi
33 pdated criteria of PR with treatment-induced lymphocytosis.(1,2) The median progression-free survival
34 hemotherapy, 13 patients with large granular lymphocytosis, 20 controls who had received renal allogr
36 leucocytosis (64 versus 22%, P: < 0.05), CSF lymphocytosis (64 versus 42%, not significant) and CSF p
37 is (frequency 99.9%, 95% CI 68.5-100.0), CSF lymphocytosis (97.9%, 51.9-100.0), fever (89.8%, 79.8-95
39 f IL-2 administered, and the maximal rebound lymphocytosis after cessation of IL-2 correlated with ac
40 ons after DLI developed a significant B-cell lymphocytosis after treatment, which did not occur in pa
42 had raised CSF protein levels and 73% had a lymphocytosis, although 57% of all submitted samples sho
45 D and correlate with the degree of pulmonary lymphocytosis and clinical measures of disease severity.
47 characterized by chronic cerebrospinal fluid lymphocytosis and elevated levels of the antiviral cytok
50 , the authors discuss the current work-up of lymphocytosis and highlight how to use recently identifi
51 h upon repeated TCR engagement and pulmonary lymphocytosis and hyperinflammation in Mtb-infected mice
52 ) patients with CD4(+) T-cell large granular lymphocytosis and implicate cytomegalovirus as a likely
53 le of cytomegalovirus (CMV) infection in CD8 lymphocytosis and inflammation in ART-treated HIV infect
54 OR1 x TCL1) developed CD5(+)B220(low) B-cell lymphocytosis and leukemia at a significantly younger me
58 account for a significant proportion of the lymphocytosis and provide molecular evidence that these
59 itive group, 17 animals exhibited persistent lymphocytosis, and 100% of these were herpesvirus positi
60 mice deficient in IL-2 exhibit splenomegaly, lymphocytosis, and autoimmunity, suggesting this cytokin
62 nd that medullary carcinoma, intraepithelial lymphocytosis, and poor differentiation were the best di
63 is model, PCI-32765 caused a transient early lymphocytosis, and profoundly inhibited CLL progression,
64 staining included marked tumor infiltrating lymphocytosis, and solid/cribiform or signet ring histol
65 hypergammaglobulinemia, autoimmunity, B-cell lymphocytosis, and the expansion of an unusual populatio
66 ures are associated with cerebrospinal fluid lymphocytosis, and the later features with appearance of
67 expand, suggesting that the profound CD8(+) lymphocytosis associated with acute EBV infection is com
69 evelop an early-onset indolent CD5(+) B-cell lymphocytosis attributed to a defect in secondary V(D)J
70 e shrinkage, along with a transient surge in lymphocytosis, before inducing objective remissions.
72 ting latently infected B cells, and a marked lymphocytosis caused by hyperexpansion of EBV-specific C
73 rcinoma, three (9%) cases of benign reactive lymphocytosis confirmed at open biopsy, and one (3%) cas
74 reduced CD4+ CD45RA+ T cells, and CD8+ CD57+ lymphocytosis, confirming the concept of a subgroup of p
81 ubcutaneous infusion produced a much greater lymphocytosis, elevation in acute-phase reactants, and f
82 umor-bearing animals resulted in a transient lymphocytosis, followed by a clear reduction in tumor in
85 a normal blood count and 2228 subjects with lymphocytosis (>4000 lymphocytes per cubic millimeter) f
87 the general population and in subjects with lymphocytosis have features in common with CLL cells.
89 only to subcutaneous and/or cutaneous sites, lymphocytosis immediately after treatment, and long-term
92 rheumatoid factor at onset of lung disease, lymphocytosis in bronchoalveolar lavage fluid (BALF), an
93 ported by positive precipitating antibodies, lymphocytosis in bronchoalveolar lavage fluid, and chara
97 granulomatous lung lesions, peribronchiolar lymphocytosis, increased cell concentrations in lavage,
98 mmune activation was induced, as measured by lymphocytosis, increased peripheral-blood natural killer
99 cella antibodies in CSF; (3) the presence of lymphocytosis, increased protein, and decreased glucose
100 alatine petechiae, splenomegaly, or atypical lymphocytosis is associated with an increased likelihood
101 vine leukemia virus (BLV)-induced persistent lymphocytosis is characterized by a polyclonal expansion
103 ion characteristic of BLV-induced persistent lymphocytosis is IL-2 dependent and antigen dependent.
105 ymphoma cells associated with redistribution lymphocytosis, leading to more potent antitumour activit
106 ction, including oral transmission, atypical lymphocytosis, lymphadenopathy, activation of CD23(+) pe
108 logic entity usually characterized by marked lymphocytosis, massive splenomegaly, an aggressive cours
109 ria to distinguish between monoclonal B-cell lymphocytosis (MBL) and CLL could minimize patient distr
115 cytic leukemia (CLL) -like monoclonal B-cell lymphocytosis (MBL) shares common immunophenotype and cy
116 ved in the transition from monoclonal B-cell lymphocytosis (MBL) to CLL and tested miR-15a/16-1 clust
121 ated genes in CLL (5.3%) and in monoclonal B lymphocytosis (MBL, 7%), a B-cell expansion that can evo
122 t(14;18) translocation and monoclonal B-cell lymphocytosis, no clear link between the presence of abe
123 s presenting with lymphocytosis, progressive lymphocytosis occurred in 51 (28%), progressive CLL deve
128 D8+ T-lymphocyte ratio, and marked pulmonary lymphocytosis on histologic examination when compared wi
129 -associated viral loads without a marked CD8 lymphocytosis or NK cell disturbance like those seen in
130 ontrary, eosinophilia (OR, 1.6; P = 0.0002), lymphocytosis (OR, 1.84; P = 0.0002), increased erythroc
133 disease categories such as monoclonal B-cell lymphocytosis (peripheral blood clonal lymphocytosis tha
136 e mechanism of leukemogenesis and persistent lymphocytosis (PL; benign expansion of B lymphocytes) in
137 patients are preceded by a monoclonal B-cell lymphocytosis precursor state, patterns of immune defect
138 antly higher prevalence of monoclonal B cell lymphocytosis, premalignant condition poorly described i
145 hepatitis C infection, including sinusoidal lymphocytosis, steatosis, portal lymphoid aggregates/fol
146 btained from patients with monoclonal B-cell lymphocytosis, suggesting a role for LEF-1 early in CLL
147 sponse to HIV-1, termed diffuse infiltrative lymphocytosis syndrome (DILS), which resembles autoimmun
148 f spondyloarthritis and Diffuse Infiltrative Lymphocytosis Syndrome has decreased, whereas the muscul
149 V-infected persons with diffuse infiltrative lymphocytosis syndrome, a disease in which host immunoge
150 er manifestation of the diffuse infiltrative lymphocytosis syndrome, usually associated with a milder
152 ay marked lymphadenopathy, splenomegaly, and lymphocytosis, TDAG51-/- mice had no apparent defects in
154 -cell lymphocytosis (peripheral blood clonal lymphocytosis that does not meet other criteria for CLL)
155 e, many studies have attempted to define the lymphocytosis that occurs during acute EBV infection in
157 This illness is characterized by a striking lymphocytosis, the nature of which has been controversia
158 esponse and 10% with a partial response with lymphocytosis; the remaining 5% of patients had stable d
159 sponse and six (40%) a partial response with lymphocytosis; the remaining three (20%) patients had st
161 Cell mobilization studies revealed that the lymphocytosis was attributable to a combination of block
164 s with late-stage disease, termed persistent lymphocytosis, was significantly decreased compared to t
165 D4/CD8 ratio, increased blood CD8 count, and lymphocytosis were additional biomarkers highly correlat
166 t of 185 subjects with CLL-phenotype MBL and lymphocytosis were monitored for a median of 6.7 years (
167 etermined significance and monoclonal B-cell lymphocytosis, which are precursor states for hematologi
168 egories: chronic T-cell leukemia and NK-cell lymphocytosis, which are similarly indolent diseases cha
169 of lymphadenopathy accompanied by transient lymphocytosis, which is reversible upon temporary drug d
171 and clinical significance of a clonal B-cell lymphocytosis with an immunophenotype consistent with ma
173 ow cytometry showed that BIV causes a B-cell lymphocytosis with no consistent, significant changes in
175 (KO) mice develop a progressive nonlethal B lymphocytosis, with expansion of B220(+) cells in the bo
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