Publications by authors named "Maria Encarnita Mariotti-Ferrandiz"

Article Synopsis
  • T and B cell repertoires are groups of lymphocytes defined by their specific receptors, and this text reviews tools and strategies used to analyze their diversity.
  • It highlights both classical methods, like flow cytometry and specatyping, as well as recent advancements in next-generation sequencing (NGS) that enable comprehensive and rapid analysis of these repertoires.
  • The discussion also covers standardized nomenclature, statistical modeling approaches, and the ongoing developments in mathematical strategies which represent the future of repertoire analysis.
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Recombination activating gene (RAG)-deficient TCR (T Cell Receptor) Tg (transgenic) mice are routinely used as sources of monoclonal T cells. We found that after the transfer of T cells from a RAG-2-deficient 5CC7 TCR Tg mice into allogeneic hosts we recovered a population of T cells expressing diverse alphabeta-TCRs. In fact, in the thymus and spleen of the 5CC7 RAG-2-deficient donor mice, we detected rare T cells expressing non-Tg TCR chains.

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Natural regulatory T cells (T(reg)) represent a distinct lineage of T lymphocytes committed to suppressive functions, and expression of the transcription factor Foxp3 is thought to identify this lineage specifically. Here we report that, whereas the majority of natural CD4(+)Foxp3(+) T cells maintain stable Foxp3 expression after adoptive transfer to lymphopenic or lymphoreplete recipients, a minor fraction enriched within the CD25(-) subset actually lose it. Some of those Foxp3(-) T cells adopt effector helper T cell (T(h)) functions, whereas some retain "memory" of previous Foxp3 expression, reacquiring Foxp3 upon activation.

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