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Valeria Tosello

Researcher at Columbia University

Publications -  42
Citations -  2996

Valeria Tosello is an academic researcher from Columbia University. The author has contributed to research in topics: T cell & Leukemia. The author has an hindex of 21, co-authored 41 publications receiving 2734 citations.

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Differential expression of CCR7 defines two distinct subsets of human memory CD4+CD25+ Tregs

TL;DR: The data suggest that a division of labor between CM and EM Tregs ensures tolerance at lymphoid and peripheral locations including tumor sites, and is the main Treg subset found in ovarian tumors.
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Chemokine receptor expression in EBV-associated lymphoproliferation in hu/SCID mice: implications for CXCL12/CXCR4 axis in lymphoma generation.

TL;DR: It is demonstrated that CXCL12 expression may be associated with EBV infection and suggested that the CXCR4/CXCL 12 axis may participate in the EBV-associated lymphomagenesis process in immunodeficient hosts and demonstrated that antagonizing the CxCL12/CxCR4 axis in vivo strongly counteracted lymphoma development.
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Differential regulation of hypoxia-induced CXCR4 triggering during B-cell development and lymphomagenesis.

TL;DR: It is shown that hypoxia is associated with up-regulation of CXCR4 expression in human normal and malignant B cells, through both transcriptional and posttranslational mechanisms.
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The cytotoxic T-lymphocyte response against a poorly immunogenic mammary adenocarcinoma is focused on a single immunodominant class I epitope derived from the gp70 Env product of an endogenous retrovirus.

TL;DR: In a Cold Target Inhibition assay, lytic activity of a mixed leukocyte-tumor culture was inhibited in an overlapping fashion by both the TS/A line used for restimulation and 293L(d) cells loaded with gp70(423-431) peptide, thus demonstrating that all or most of the cytotoxic activity was directed exclusively against this antigenic epitope.
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Large and Dissimilar Repertoire of Melan-A/MART-1-Specific CTL in Metastatic Lesions and Blood of a Melanoma Patient

TL;DR: Compared the TCR usage of Melan-A-specific T cells from different compartments of a single melanoma patient to evaluate possible clonotype expansion or preferential homing over a 4-mo follow-up period buttress the notion that the CTLs recognizing the immunodominant Ag of Mela-A comprise a high number of different clonotypic TCR.