Characterization of the expanded T cell population in infectious mononucleosis: apoptosis, expression of apoptosis-related genes, and Epstein-Barr virus (EBV) status
Cs. Verbeke et al., Characterization of the expanded T cell population in infectious mononucleosis: apoptosis, expression of apoptosis-related genes, and Epstein-Barr virus (EBV) status, CLIN EXP IM, 120(2), 2000, pp. 294-300
Infectious mononucleosis (IM), a manifestation of primary infection with EB
V, is characterized by a massive expansion of the T cell population. In thi
s study we examined this expanded T cell population regarding its EBV statu
s, its proliferative and apoptotic activity, and its expression of apoptosi
s-related genes. Whereas previous studies were performed on ex vivo culture
s or on peripheral blood, our investigations included in vivo analysis of I
M tonsillectomy specimens (14 cases) by in situ hybridization for viral RNA
(EBERs) combined with immunohistochemistry (IHC; CD3, CD45RO, CD20, CD79a,
Ki-67, Bcl-2, Bax, Fas, FasL) and the TUNEL method. Of the EBER+ cells 50-
70% showed expression of the B cell markers CD20/CD79a. The remainder of th
e EBER+ cells expressed neither B nor T cell antigens. No co-expression of
EBERs and T cell antigens was detected in any of the specimens. In accordan
ce with a high rate of apoptosis (up to 2.37%) within the expanded T cell p
opulation, Bcl-2 expression was drastically reduced and FasL expression rem
arkably increased. The levels of Bax and Fas expression showed no or modera
te up-regulation. In conclusion, the massive expansion of IM T cells is not
caused by EBV infection of these cells but merely represents an intense im
mune reaction. Through altered expression of Bcl-2/Bax and Fas/FasL, the ac
tivated T cells are subject to enhanced apoptosis while residing within the
lymphoid tissue, which eventually allows the efficient silencing of this p
otentially damaging T cell response.