ライフサイエンスコーパス: lymphocyte subset

1 cytic infections that are controlled by this lymphocyte subset.

2 ontinuous activation/proliferation of this T-lymphocyte subset.

3 id recovery in lymphocyte populations across lymphocyte subsets.

4 phils, inflammatory monocytes, and different lymphocyte subsets.

5 SOCE and defects in the function of several lymphocyte subsets.

6 s involved in the homing of pDCs and certain lymphocyte subsets.

7 NHL does not cause prolonged suppression of lymphocyte subsets.

8 trating CD4 and CD8 lymphocytes and CXCR3+ T-lymphocyte subsets.

9 cytotoxicity and to enumerate and phenotype lymphocyte subsets.

10 n, but with different kinetics, in different lymphocyte subsets.

11 f pro- and anti-inflammatory cytokines and T-lymphocyte subsets.

12 s of trafficking and proliferation for these lymphocyte subsets.

13 cantly higher frequencies than on peripheral lymphocyte subsets.

14 tion and hyperactivation of specific splenic lymphocyte subsets.

15 load and had no effect on CD4(+)- or CD8(+)-lymphocyte subsets.

16 tissue architecture and the distribution of lymphocyte subsets.

17 lso in the activation and differentiation of lymphocyte subsets.

18 ndothelial cells, myeloid cells, and certain lymphocyte subsets.

19 C attracts eosinophils in addition to memory lymphocyte subsets.

20 d in CD4(+), CD8(+), CD20(+), and CD16/56(+) lymphocyte subsets.

21 ir expression is differentially regulated in lymphocyte subsets.

22 factors known to define innate and adaptive lymphocyte subsets.

23 els of this receptor in different functional lymphocyte subsets.

24 ns include immunophenotyping of alloreactive lymphocyte subsets.

25 localized predominately in CD4(+) and CD8(+) lymphocyte subsets.

26 and blood was drawn to test for viruses and lymphocyte subsets.

27 ells, indicating an efficient priming of all lymphocyte subsets.

28 that share the ability to activate specific lymphocyte subsets.

29 vitamin A on birth outcomes and counts of T lymphocyte subsets.

30 sitive EBV serologies. and markedly abnormal lymphocyte subsets.

31 MV associates with phenotypic alterations in lymphocyte subsets.

32 cs of innate leukocytes and naive and memory lymphocyte subsets.

33 kine-release syndrome and no impact on blood lymphocyte subsets.

34 robust generation of functionally diverse T lymphocyte subsets.

35 o be pivotal in shaping the programs of both lymphocyte subsets.

36 ry to detect DOCK8 protein expression within lymphocyte subsets.

37 ates immune homeostasis and the fate of many lymphocyte subsets.

38 -stimulated genes, natural killer cells, and lymphocyte subsets.

39 ase was significant for several intrahepatic lymphocytes subsets.

40 unologic response to therapy, as measured by lymphocyte subsets, 3-color flow cytometric measures, an

41 and other innate immune cells are important lymphocyte subsets able both to produce cytokines includ

42 clusion, we show that SCARF-1 contributes to lymphocyte subset adhesion to primary human HSEC and cou

43 ns, NK cells compose the third most abundant lymphocyte subset after T cells and B cells.

44 lions diagnosed with LLV infection displayed lymphocyte subset alterations and progressive behavioral

45 As compared to unrelated healthy controls, lymphocyte subset alterations were greatest in the proba

46 The association of neuropathy and lymphocyte subset alterations with chronic LLV infection

47 We compared T lymphocyte subsets among HIV-HHV-8+ and HIV-HHV-8- infec

48 Tabulated data from T- and B-lymphocyte subset analysis and antidrug antibody respons

49 Lymphocyte subset analysis demonstrated that HIV-positiv

50 Lymphocyte subset analysis performed in 20 patients avai

51 d in HG patients compared to controls in all lymphocyte subsets analyzed.

52 ines and their receptors; (4) expansion of B lymphocyte subset and myosin heavy chain class II-expres

53 luster of differentiation (CD)8alpha/beta+ T lymphocyte subset and the percentage of CD8alpha/beta+ T

54 f rat IL-10 (rIL-10) to assess its impact on lymphocyte subsets and activation of hepatic stellate ce

55 th TNBC, although the relative importance of lymphocyte subsets and associated protein expression is

56 lar integrity and function, we evaluated how lymphocyte subsets and complement specifically affect mi

57 uation, whole blood flow cytometry to assess lymphocyte subsets and eosinophil activation, and serum

58 mined using immunohistochemical staining for lymphocyte subsets and for the cytokines interleukin-10

59 before and after ART initiation, examining T-lymphocyte subsets and inflammatory biomarkers in periph

60 n were associated with maintenance of normal lymphocyte subsets and intact lymphoid architecture (n =

61 d immunological parameters included standard lymphocyte subsets and lymphocyte surface markers of mat

62 on allows the detection of discrete CD8(+) T lymphocyte subsets and may be useful for assessing the i

63 In addition, we generated information on lymphocyte subsets and mitogen-mediated proliferation of

64 ophil activation and induction of regulatory lymphocyte subsets and of blocking antibodies have been

65 Their lymphocyte subsets and plasma HIV viral loads were measu

66 ly viremia are mediated by multiple effector lymphocyte subsets and serum antibodies.

67 Absolute numbers of lymphocyte subsets and serum immunoglobulin levels were

68 d numbers of human CD4(+) naive and memory T lymphocyte subsets and skin- and gut-homing memory T cel

69 ant expression of granzymes A and B in human lymphocyte subsets and T regulatory cells, which suggest

70 s remitter) to determine absolute numbers of lymphocyte subsets and the proportion of glycosylphospha

71 may involve antagonism between T helper (TH) lymphocyte subsets and their cytokines.

72 t of A-T and age on the proportions of major lymphocyte subsets and their pattern of CD95 expression

73 ssion, such as markers of epithelial injury, lymphocyte subsets, and circulating fibrocytes, will be

74 r lung leukocytes, including eosinophils and lymphocyte subsets, and depletion of neutrophils in sens

75 Plasma interleukin (IL)-6, lymphocyte subsets, and DNA binding of nuclear factor (N

76 mCD40-LMP1tg mice had normal lymphocyte subsets, and immunization elicited an antibod

77 ments, Clinically, we assessed EBV serology, lymphocyte subsets, and the efficacy of interferon-alpha

78 tokine stimulation in human memory and naive lymphocyte subsets as identified by five differentiation

79 ed increase in the total number of activated lymphocyte subsets as indicated by CD69 upregulation.

80 In parallel, T lymphocyte subsets, as key constituents of the adaptive

81 terations in the receptor populations within lymphocyte subsets, as well as in repertoires responding

82 d peripheral blood complete blood counts and lymphocyte subsets assayed in a single flow cytometry la

83 with monoclonal antibodies that deplete each lymphocyte subset at the time of virus inoculation.

84 (+), central memory CD4(+), and regulatory T-lymphocyte subsets at enrollment was not associated with

85 The evolutionary conservation of T lymphocyte subsets bearing alphabeta TCRs using invarian

86 irmed by antibody-mediated depletion of this lymphocyte subset before a third infection.

87 to reduced fibrosis and alterations in liver lymphocyte subsets both in untreated liver and following

88 CD1-deficient mice were found to lack this lymphocyte subset, but they could nevertheless mount a p

89 l marker for discriminating normal B lineage lymphocyte subsets, but our results suggest new ways for

90 led immunophenotyping of blood leukocyte and lymphocyte subsets by flow cytometry.

91 e performed comprehensive phenotyping of 120 lymphocyte subsets by high dimensional flow cytometry, a

92 Mean lymphocyte subset (CD4+/CD8+) ratios were significantly

93 data describing the effect of alemtuzumab on lymphocyte subsets collected during the phase 3 trial pr

94 opment innate lymphoid cells and specialized lymphocyte subsets colonize peripheral tissues, where th

95 In this review, we summarize the main lymphocyte subsets controlling immune responsiveness in

96 hnicity were not significant determinants of lymphocyte subset counts in this population.

97 sion, blood stem cell recipients have higher lymphocyte-subset counts and this appears to result in f

98 Immune variables included lymphocyte subsets, cytokine production, and markers of

99 Examination of lymphocyte subsets demonstrated that phenotypically naiv

100 mplete protection, and transfers of purified lymphocyte subsets demonstrated that this effect require

101 In vivo lymphocyte subset depletions established that both T- an

102 ively demonstrate that the predominance of a lymphocyte subset determines the functional consequences

103 Other lymphocyte subsets develop normally but produce low leve

104 w-derived or parenchymal cells for mediating lymphocyte subset development.

105 Plasma viral load, lymphocyte subsets, diagnostic evaluation (including cul

106 We investigated whether CD4 and CD8 lymphocyte subsets differed in IL-7Ralpha expression and

107 ce markers could be used directly to monitor lymphocyte subset distribution in human diseases.

108 h of the remaining IL-5- or IL-17A-producing lymphocyte subsets dominated the neutrophil or eosinophi

109 reg population increased more than any other lymphocyte subset during HD IL-2 therapy and had an acti

110 y a unique dual role of attracting activated lymphocyte subsets during inflammation as well as facili

111 T cells were the predominant lymphocyte subset entering PLN, MLN, Peyer's patches, an

112 ined that proliferating cells, regardless of lymphocyte subset, exhibited increased expression of CD2

113 lls affecting both memory and naive CD4(+) T lymphocyte subsets following administration by either ro

114 ut mice revealed a requirement for the CD4 T lymphocyte subset for the complete rejection of tumors.

115 nd differential white blood cell counts, and lymphocyte subsets for 301 infants, with serial measurem

116 mal patterns of SH2D1A protein expression in lymphocyte subsets for healthy subjects.

117 revealed a requirement for both CD4 and CD8 lymphocyte subsets for SLC-mediated tumor regression.

118 TS were assessed for immunologic conditions, lymphocyte subsets, forkhead box P3 (FOXP3)(+) Treg cell

119 theta), a key signaling molecule in multiple lymphocyte subsets, formed microclusters in activated NK

120 We measured lymphocyte subset frequency and memory T-cell gamma inte

121 equential and traceless isolation of desired lymphocyte subsets from a single system.

122 rmine F-ara-A-induced apoptosis in different lymphocyte subsets from CLL patients and normal controls

123 vals were generated for absolute numbers and lymphocyte subsets from infants with effective GAs of 22

124 characteristics of B, CD4(+) T and CD8(+) T-lymphocyte subsets from monozygotic twins, we quantify t

125 telomerase activity are impaired in primary lymphocyte subsets from patients with CHH.

126 a), and expression of GCR were determined in lymphocytes subsets from cultured blood using flow cytom

127 ha) and expression of GCR were determined in lymphocytes subsets from cultured blood using flow cytom

128 CMV defense, revealing that these two innate lymphocyte subsets function together to fine-tune antivi

129 file of cord and adult blood lymphocytes and lymphocyte subsets has been assessed at the single-cell

130 ough the effect of fingolimod on circulating lymphocyte subsets has been established, its effect on c

131 Therefore, cytotoxic lymphocyte subsets have similar requirements for Munc13-

132 on, JSY3 provirus was found only in the CD4+ lymphocyte subset; however, by 14 weeks p.i., the greate

133 mune reconstitution included measurements of lymphocyte subsets, immunoglobulins, and response to vac

134 random to evaluate the distribution of BALT lymphocyte subsets immunohistochemically.

135 costimulatory molecule CD161 is expressed on lymphocyte subsets implicated in promoting respiratory i

136 Among the various lymphocyte subsets implicated in protection against canc

137 To determine the relative contribution of lymphocyte subsets important for recovery from infection

138 s expressing the Vdelta3 TCR make up a minor lymphocyte subset in blood but are enriched in liver and

139 NK cells are a principal tissue-infiltrating lymphocyte subset in patients with OA and patients with

140 However, they are the most abundant T-lymphocyte subset in some epithelial barriers such as mo

141 the presence of a novel memIgD(+)memIgM(-) B lymphocyte subset in trout that expresses memCCR7 and re

142 unction tests were performed including blood lymphocyte subsets in a random subgroup.

143 e previously observed alterations in splenic lymphocyte subsets in animals with defective migration o

144 ntent and WBC composition changes, including lymphocyte subsets in blood and bone marrow, showed diff

145 ministration markedly altered homeostasis of lymphocyte subsets in blood, with NK cells and gammadelt

146 ing culture was examined independently with lymphocyte subsets in fresh blood, apoptosis was negativ

147 f the ovulatory cycle on HIV-1 RNA level and lymphocyte subsets in HIV-infected women, blood specimen

148 The composition of lymphocyte subsets in hormone-induced lactation breast m

149 Studies on the role of lymphocyte subsets in human diseases have been hampered

150 sed to characterize functional activity of T-lymphocyte subsets in humans infected with T. gondii.

151 the point of rescuing the deficiency of such lymphocyte subsets in IL-15Ralpha(-/-) mice.

152 epresent the first analysis of the role of T lymphocyte subsets in immunity to spotted fever group ri

153 use in therapeutic manipulation of selective lymphocyte subsets in immunological disorders.

154 is, we evaluated circulating IL-7 levels and lymphocyte subsets in multiple clinical cohorts with T-c

155 ceptors and an activation marker on multiple lymphocyte subsets in paired liver biopsy and peripheral

156 ixed hematopoietic chimerism and recovery of lymphocyte subsets in patients receiving a modified CKBM

157 lusion, apoptosis occurs in a broad range of lymphocyte subsets in patients with sepsis and correlate

158 Lymphocyte subsets in peripheral blood, thymus, and sple

159 sought to determine reference intervals for lymphocyte subsets in racially/ethnically diverse preter

160 The role of T-lymphocyte subsets in recovery from foot-and-mouth disea

161 The importance of T-lymphocyte subsets in the control of poxvirus infections

162 To increase our understanding of the role of lymphocyte subsets in the establishment of viral latency

163 iency, characterized by persistently low CD4 lymphocyte subsets in the peripheral blood.

164 We decided to evaluate the role of T lymphocyte subsets in tumor immunity induced by recombin

165 assessed the relative distribution of total lymphocyte subsets in untreated versus anti-LFA-1-treate

166 y reflect its ability to stimulate different lymphocyte subsets in vivo through the activities of rec

167 was associated with increases in circulating lymphocyte subsets including PD-L1E-bearing lymphocytes,

168 because of (a) reduction in CCR5 and CXCR3 T-lymphocyte subset infiltration into the graft, (b) atten

169 efine this population as a distinct memory T-lymphocyte subset, intermediate between naive and centra

170 rthritis is the segregation of CD4 and CD8 T lymphocyte subsets into distinct microdomains within the

171 Migration of lymphocyte subsets into these compartments is essential

172 However, the T-lymphocyte subsets involved in the pathophysiology of hy

173 resentation, processing, immune recognition, lymphocyte subsets involved, and mechanism of cell death

174 Cooperation between these lymphocyte subsets involves recognition of antigens co-p

175 However, function of STAT3 in the B lymphocyte subset is not well understood.

176 Determination of T-lymphocyte subsets is a simple and effective parameter t

177 ducing Th17 cells, but its function in other lymphocyte subsets is not well understood.

178 e function and development of several innate lymphocyte subsets, is also important for the myeloid-de

179 Transfer of specific T lymphocyte subsets isolated from the spleens of healthy

180 om B6.C-H2bm12 mice were transplanted into T lymphocyte subset knockout recipients and T lymphocyte-r

181 expression levels of L-selectin in different lymphocyte subsets, L-selectin-mediated enhancement of c

182 piratory tract, with the depletion of either lymphocyte subset leading to increased titers in the lun

183 In all patients analyzed for lymphocyte subsets, lymphopenia induced by TMZ affected

184 Treatments that increase GCR in these lymphocyte subsets may improve graft survival.

185 Blood was obtained for enumeration of lymphocyte subsets, measurement of serum autoantibody an

186 Lymphocyte subset measurements included total T cells, h

187 ost a complete absence of CD4 T lymphocytes, lymphocyte subset monitoring is useful in identifying de

188 induced expansion of circulating leukocytes, lymphocyte subsets, monocytes and granulocytes.

189 T lymphocyte subsets, monocytes and neutrophils from organ

190 ts peaked around 1 year, whereas most memory lymphocyte subsets more gradually increased during the f

191 t changes in the numbers and distribution of lymphocyte subsets, NK cell receptor expression, or in v

192 rols the differentiation and function of a T lymphocyte subset, NK1+ natural T cells, proposed to reg

193 nd their plasma viral RNA loads, circulating lymphocyte subset numbers, and eventual disease outcomes

194 lso was determined for CD4- and CD8-enriched lymphocyte subsets obtained by antibody and complement d

195 Despite evidence that the particular lymphocyte subset of gammadelta T cells contributes to p

196 ive, unactivated CD26(low) CD45RA+ CD45R0- T lymphocyte subset of peripheral blood lymphocytes.

197 Ly-6C Ag were examined on splenic and thymic lymphocyte subsets of Ly-6.1 and Ly-6.2 strains of mice

198 signals for HHV-8 were demonstrated in the B lymphocyte subsets of PBMCs and/or in spermatozoa and mo

199 No modification of memory T lymphocytes subsets or numbers was observed in the perip

200 ll activation, significant alteration of the lymphocyte subsets, or induce clinically observable auto

201 luences of these core cytokines on precursor lymphocyte subsets overlap during development and are of

202 Groups were compared with respect to lymphocyte subsets, phagocytosis, oxidative burst capaci

203 Adoptive transfer of T lymphocyte subset populations into nude recipients confi

204 We further identified a CD4(+) T lymphocyte subset producing IFN-gamma together with a co

205 Circulating T-lymphocyte subset profiles in conventional HIV- BDD were

206 Both CD4 and CD8 lymphocyte subsets proliferated to pathogenic peptides.

207 )CD28(null) T cells, a functionally aberrant lymphocyte subset rarely seen in individuals younger tha

208 l transplantation because they are the first lymphocyte subset recovering after the allograft.

209 may allow differential, segmental control of lymphocyte subset recruitment into functionally distinct

210 usly shown that gammadeltaT cells, a small T lymphocyte subset, reduce acute inflammatory lung damage

211 PG27 largely normalized splenic T lymphocyte subsets, reduced allospecific cytotoxic T lym

212 Lymphocyte subsets remained unaltered in all monkeys.

213 the DNA methylome and the transcriptome of B-lymphocyte subsets representing stages of the humoral im

214 we review newly discovered roles for BCL6 in lymphocyte subsets residing within and outside of germin

215 Flow cytometric analyses of T lymphocyte subsets revealed that the proportions of Fcep

216 The identification of the lymphocyte subsets secreting interferon (IFN) gamma and

217 , in vivo depletion of either CD4+ or CD8+ T lymphocyte subsets significantly prolonged survival in m

218 er, recent studies have revealed two lamprey lymphocyte subsets so closely resembling B cells and T c

219 These specialized tissue-resident lymphocyte subsets span the innate-adaptive continuum an

220 Whether L-selectin also regulates lymphocyte subset-specific migration into specific lymph

221 ells function via provision of help to other lymphocyte subsets, such as B cells and CD8 T cells, or

222 ted role in facilitating activation of other lymphocyte subsets, such as invariant natural killer T (

223 rtant new frontier is the role of regulatory lymphocyte subsets, such as regulatory T cells, gammadel

224 l differences in CD44 function between these lymphocyte subsets suggest an important biological role

225 Recently, the T lymphocyte subset T(H)17 was shown to play a role in reg

226 increases in the frequency of CD4 and CD8 T lymphocyte subsets, T cell activation markers CXCR3, CD6

227 We compare changes in lymphocyte subsets, T cell proliferative responses to di

228 show that NFATx mRNA was expressed in all T lymphocyte subsets tested and was highest in CD4+CD8+ do

229 onocyte), consistent with a progenitor/pre-B lymphocyte subset that does not express cytoplasmic mu-c

230 ts for a possible role for CD8(+) T cells, a lymphocyte subset that has long been underrated in multi

231 emonstrate that CD4+ T cells are the primary lymphocyte subset that mediates cellular infiltration, l

232 marginal zone (MZ) B cells, a pre-activated lymphocyte subset that mounts antibody responses to T-ce

233 ing; however, the mechanism of death and the lymphocyte subsets that are targeted remain unknown.

234 ggest that fetal thymi contain several novel lymphocyte subsets that can be induced to overgrow the n

235 in signaling pathways were seen in all SLE B lymphocyte subsets that manifested phenotypic features o

236 , and to shed light on the specialization of lymphocyte subsets that mediate inflammation and immune

237 vances in the understanding of the diverse T lymphocyte subsets that provide acute and long-term prot

238 he differentiation and function of several T lymphocyte subsets that provide immunity to infection, m

239 aining was significantly reduced on CD8(+) T lymphocyte subsets that showed immunophenotypic evidence

240 his study, we used a murine model to examine lymphocyte subsets that ultimately drive the eosinophil

241 fectivity assays, using live sorted CD4(+) T lymphocyte subsets, that 30-90% of circulating naive cel

242 ow that the ObR is expressed on normal mouse lymphocyte subsets, that leptin plays a role in lymphocy

243 Normal animals contain an autoreactive B lymphocyte subset, the B-1 subset, which is controlled b

244 seropositivity modulated the distribution of lymphocyte subsets, the functional defects were present

245 Although statistically significant for both lymphocyte subsets, this relationship was more pronounce

246 eptors and their ligands in the migration of lymphocyte subsets through lymphoid and nonlymphoid tiss

247 integrin/VCAM-1, and LFA-1, targets specific lymphocyte subsets to BALT.

248 The precise role and contributions of T lymphocyte subsets to CAV development remains unknown.

249 ytes, granulocytes, lymphocytes, and several lymphocyte subsets to confirm the diagnosis of DC, disti

250 gy, we evaluated the regional recruitment of lymphocyte subsets to different areas of the female geni

251 investigate the ability of distinct CD4(+) T lymphocyte subsets to enter and persist in non-lymphoid,

252 e so as to dissect the contribution of these lymphocyte subsets to HLH-like disease severity after ly

253 The relative contributions of T-lymphocyte subsets to host defense in cattle infected wi

254 ities correlate with functional migration of lymphocyte subsets to known CCR7 ligands.

255 Thus, the differential migration of T and B lymphocyte subsets to lymphoid tissues is regulated in p

256 d us to investigate the ability of different lymphocyte subsets to produce this dichotomous eosinophi

257 isperses the immunologic repertoire, directs lymphocyte subsets to the specialized microenvironments

258 mbers over time, between tissues, and across lymphocyte subsets; to detect clonal expansion; and to d

259 there were no differences in the profiles of lymphocyte subsets [total T cells (CD3+), T helper cells

260 Thus, chemokines can regulate the arrest of lymphocyte subsets under flowing conditions, which may a

261 ontained a higher percentage of Tregs in the lymphocyte subset versus regressor tumors.

262 We evaluated mucosal T lymphocyte subsets, virus-specific cellular responses, g

263 However, when either lymphocyte subset was donated by the aged mice, the muta

264 cytometric techniques we found that the CD4 lymphocyte subset was preferentially recruited to the up

265 amma, TNFalpha, and a loss of GCR from these lymphocyte subsets was also found in BOS.

266 gamma, TNFalpha and a loss of GCR from these lymphocyte subsets was also found in BOS.

267 Also, infection of both CD4(+) and CD8(+) lymphocyte subsets was associated with higher virus load

268 cytometry and expression profiling of sorted lymphocyte subsets, we unequivocally demonstrate the exi

269 eived placebo in terms of sequential data on lymphocyte subsets; weight, height, and head circumferen

270 Lymphocyte subsets were abnormal in all patients; the mo

271 Peripheral blood lymphocyte subsets were analyzed by flow cytometry.

272 Multilineage chimerism, clonal deletion, and lymphocyte subsets were analyzed by flow cytometry.

273 scores, pulmonary function test results, and lymphocyte subsets were analyzed.

274 Humoral immune responses and CD4+ lymphocyte subsets were compared in 5 HIV-uninfected vac

275 depletion indicated that both CD4+ and CD8+ lymphocyte subsets were decreased.

276 d by enzyme-linked immunosorbent assay kits, lymphocyte subsets were determined using four-color fluo

277 Lymphocyte subsets were enumerated by flow cytometry.

278 Concurrent BALF lymphocyte subsets were examined by flow cytometry, incl

279 nd 365 after transplantation, counts of most lymphocyte subsets were higher in the blood stem cell re

280 To address which lymphocyte subsets were impaired in the LTalpha-/- mice,

281 rmine if distinct alphabeta and gammadelta T-lymphocyte subsets were involved in the response of the

282 No obvious differences in lymphocyte subsets were observed.

283 determine the source of IL-10, CD4+ and CD8+ lymphocyte subsets were obtained by selective depletion

284 The three T-lymphocyte subsets were positively correlated with CD4 T

285 eta(+) gammadelta T cells constitute a novel lymphocyte subset, which is strongly enriched within the

286 Thymic NK1.1+ cells are a recently described lymphocyte subset whose biologic function is not well de

287 Natural killer (NK) T cells are a lymphocyte subset with a distinct surface phenotype, an

288 role during the development of NKT cells, a lymphocyte subset with immunoregulatory functions in res

289 Type I NKT cells are a lymphocyte subset with important roles in regulating imm

290 Regulatory T cells (Tregs) are a lymphocyte subset with intrinsic immunosuppressive prope

291 porally controlled fate mapping of an innate lymphocyte subset with notable nuances as compared to ti

292 T(SCM) constitute a recently identified lymphocyte subset with stem cell-like qualities, includi

293 other measures of blood tumor burden, i.e., lymphocyte subsets with a CD4+CD7- and CD4+CD26- phenoty

294 or identification of peripheral blood memory lymphocyte subsets with distinct tissue and microenviron

295 The identification of lymphocyte subsets with non-overlapping effector functio

296 it large numbers of naive T cells and harbor lymphocyte subsets with opposing activities, including C

297 constituted different quantities of CD4(+) T lymphocyte subsets with preferential expansion of CXCR3(

298 ene expression profiles and peripheral blood lymphocyte subsets with those of subjects with stable gr

299 lymphoid cells encompass a diverse array of lymphocyte subsets with unique phenotype that initiate i

300 We analyzed the kinetics of T-lymphocyte subsets within the first 8 months posttranspl