BY55/CD160 cannot be considered a cytotoxic marker in cytomegalovirus‐specific human CD8 + T cells
Author(s) -
Merino J.,
Ramírez N.,
Moreno C.,
Toledo E.,
Fernández M.,
SánchezIbarrola A.
Publication year - 2007
Publication title -
clinical & experimental immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.329
H-Index - 135
eISSN - 1365-2249
pISSN - 0009-9104
DOI - 10.1111/j.1365-2249.2007.03387.x
Subject(s) - perforin , cytotoxic t cell , cd8 , immunology , biology , cd28 , interleukin 7 receptor , t cell , jurkat cells , immune system , il 2 receptor , biochemistry , in vitro
Summary CD160/BY55 is a glucosyl‐phosphatidylinositol (GPI)‐anchored cell membrane receptor that is expressed primarily in natural killer (NK) cells. Its presence in CD8 + T lymphocytes is considered to be a marker of cytotoxic activity, although there are few data in this regard. In the present work, we analysed the expression of CD160 in subpopulations of cytomegalovirus (CMV)‐specific CD8 + T cells. Subpopulations were defined by CD28 and CD57 expression and exhibited varying degrees of differentiation and cytotoxic potential, as evaluated by the expression of perforin, interferon (IFN)‐γ and interleukin (IL)‐7Rα/CD127. We included subjects with different intensities of anti‐viral immune response. Results showed that the terminally differentiated CD28 – CD57 + subset displaying the highest level of perforin expressed CD160 at a level similar to that of memory CD28 + CD57 – perforin – cells. A comparison of the expression of perforin in CD160 + cells versus CD160 – cells showed that expression was significantly higher in the absence of CD160. Interestingly, the CMV‐specific CD8 + T cell subset from a patient with ongoing CMV reactivation did not begin to express CD160 until day +92 of the follow‐up period. Taken together, our data show that CD160 cannot be considered a cytotoxic marker in CMV‐specific CD8 + T cells.
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