Abstract
ABSTRACTEpstein-Barr virus (EBV) is typically acquired asymptomatically in childhood. In contrast, infection later in life often leads to infectious mononucleosis (IM), a febrile illness characterized by anti-EBV IgM antibody positivity, high loads of circulating latently infected B cells, and a marked lymphocytosis caused by hyperexpansion of EBV-specific CD8+ T cells plus a milder expansion of CD56dim NKG2A+ KIR− natural killer (NK) cells. How the two situations compare is unclear due to the paucity of studies on clinically silent infection. Here we describe five prospectively studied patients with asymptomatic infections identified in a seroepidemiologic survey of university entrants. In each case, the key blood sample had high cell-associated viral loads without a marked CD8 lymphocytosis or NK cell disturbance like those seen in patients during the acute phase of IM. Two of the cases with the highest viral loads showed a coincident expansion of activated EBV-specific CD8+ T cells, but overall CD8+ T cell numbers were either unaffected or only mildly increased. Two cases with slightly lower loads, in whom serology suggests the infection may have been caught earlier in the course of infection, also showed no T or NK cell expansion at the time. Interestingly, in another case with a higher viral load, in which T and NK cell responses were undetectable in the primary blood sample in which infection was detected, EBV-specific T cell responses did not appear until several months later, by which time the viral loads in the blood had already fallen. Thus, some patients with asymptomatic primary infections have very high circulating viral loads similar to those in patients during the acute phase of IM and a cell-mediated immune response that is qualitatively similar to that in IM patients but of a lower magnitude. However, other patients may have quite different immune responses that ultimately could reveal novel mechanisms of host control.IMPORTANCE Epstein-Barr virus (EBV) is transmitted orally, replicates in the throat, and then invades the B lymphocyte pool through a growth-transforming latent infection. While primary infection in childhood is usually asymptomatic, delayed infection is associated with infectious mononucleosis (IM), a febrile illness in which patients have high circulating viral loads and an exaggerated virus-induced immune response involving both CD8+ T cells and natural killer (NK) cells. Here we show that in five cases of asymptomatic infection, viral loads in the blood were as high as those in patients during the acute phase of IM, whereas the cell-mediated responses, even when they resembled those in patients during the acute phase of IM in timing and quality, were never as exaggerated. We infer that IM symptoms arise as a consequence not of the virus infection per se but of the hyperactivated immune response. Interestingly, there were idiosyncratic differences among asymptomatic cases in the relationship between the viral load and the response kinetics, emphasizing how much there is still to learn about primary EBV infection.
Highlights
Epstein-Barr virus (EBV) is typically acquired asymptomatically in childhood
Viral DNA was detected in the majority of but not all seropositive cases (Fig. 1); this reflects the limitation of the assay when applied to DNA from 6 ϫ 105 peripheral blood mononuclear cell (PBMC) [36], since in our hands almost all seropositive individuals are detectably EBV genome positive in the same assay using DNA from 6 ϫ 105 purified peripheral blood B cells [10]
Much is inferred from the study of infectious mononucleosis (IM), a disease which appeared in affluent societies as an unexpected consequence of delayed primary infection and which, in evolutionary terms, is a novelty
Summary
Epstein-Barr virus (EBV) is typically acquired asymptomatically in childhood. In contrast, infection later in life often leads to infectious mononucleosis (IM), a febrile illness characterized by anti-EBV IgM antibody positivity, high loads of circulating latently infected B cells, and a marked lymphocytosis caused by hyperexpansion of EBV-specific CD8ϩ T cells plus a milder expansion of CD56dim NKG2Aϩ KIRϪ natural killer (NK) cells. While primary infection in childhood is usually asymptomatic, delayed infection is associated with infectious mononucleosis (IM), a febrile illness in which patients have high circulating viral loads and an exaggerated virus-induced immune response involving both CD8ϩ T cells and natural killer (NK) cells. While virus shedding in the throat may continue at a high level for several months after IM symptoms have waned [5, 12], the number of latently infected cells in the blood tends to fall quickly during the disease course itself and falls more gradually to reach a stable set point over the following weeks and months [11, 13] These events are coincident with a range of immune responses [14]. The levels of a range of antiviral and/or proinflammatory cytokines and chemokines are reported to be elevated in the plasma of IM patients, including beta interferon (IFN-), IFN-␥, interleukin-1 (IL-1), IL-6, IL-10, Journal of Virology jvi.asm.org 2
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