High‐frequency and adaptive‐like dynamics of human CD1 self‐reactive T cells

C de Lalla, M Lepore, FM Piccolo… - European journal of …, 2011 - Wiley Online Library
C de Lalla, M Lepore, FM Piccolo, A Rinaldi, A Scelfo, C Garavaglia, L Mori, G De Libero
European journal of immunology, 2011Wiley Online Library
CD1 molecules present lipid antigens to T cells. An intriguing subset of human T cells
recognize CD1‐expressing cells without deliberately added lipids. Frequency, subset
distribution, clonal composition, naïve‐to‐memory dynamic transition of these CD1 self‐
reactive T cells remain largely unknown. By screening libraries of T‐cell clones, generated
from CD4+ or CD4− CD8− double negative (DN) T cells sorted from the same donors, and
by limiting dilution analysis, we find that the frequency of CD1 self‐reactive T cells is …
Abstract
CD1 molecules present lipid antigens to T cells. An intriguing subset of human T cells recognize CD1‐expressing cells without deliberately added lipids. Frequency, subset distribution, clonal composition, naïve‐to‐memory dynamic transition of these CD1 self‐reactive T cells remain largely unknown. By screening libraries of T‐cell clones, generated from CD4+ or CD4CD8 double negative (DN) T cells sorted from the same donors, and by limiting dilution analysis, we find that the frequency of CD1 self‐reactive T cells is unexpectedly high in both T‐cell subsets, in the range of 1/10–1/300 circulating T cells. These T cells predominantly recognize CD1a and CD1c and express diverse TCRs. Frequency comparisons of T‐cell clones from sorted naïve and memory compartments of umbilical cord and adult blood show that CD1 self‐reactive T cells are naïve at birth and undergo an age‐dependent increase in the memory compartment, suggesting a naïve/memory adaptive‐like population dynamics. CD1 self‐reactive clones exhibit mostly Th1 and Th0 functional activities, depending on the subset and on the CD1 isotype restriction. These findings unveil the unanticipated relevance of self‐lipid T‐cell response in humans and clarify the basic parameters of the lipid‐specific T‐cell physiology.
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