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. 2003 Dec;163(6):2179-84.
doi: 10.1016/S0002-9440(10)63575-4.

Latent herpesvirus infection in human trigeminal ganglia causes chronic immune response

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Latent herpesvirus infection in human trigeminal ganglia causes chronic immune response

Diethilde Theil et al. Am J Pathol. 2003 Dec.

Abstract

The majority of trigeminal ganglia (TGs) are latently infected with alpha-herpesviruses [herpes simplex virus type-1 (HSV-1) and varicella-zoster virus (VZV)]. Whereas HSV-1 periodically reactivates in the TGs, VZV reactivates very rarely. The goal of this study was to determine whether herpesvirus latency is linked to a local immune cell infiltration in human TGs. T cells positive for the CD3 and CD8 markers, and CD68-positive macrophages were found in 30 of 42 examined TGs from 21 healthy individuals. The presence of immune cells correlated constantly with the occurrence of the HSV-1 latency-associated transcript (LAT) and only irregularly with the presence of latent VZV protein. In contrast, uninfected TGs showed no immune cell infiltration. Quantitative RT-PCR revealed that CD8, interferon-gamma, tumor necrosis factor-alpha, IP-10, and RANTES transcripts were significantly induced in TGs latently infected with HSV-1 but not in uninfected TGs. The persisting lymphocytic cell infiltration and the elevated CD8 and cytokine/chemokine expression in the TGs demonstrate for the first time that latent herpesviral infection in humans is accompanied by a chronic inflammatory process at an immunoprivileged site but without any neuronal destruction. The chronic immune response seems to maintain viral latency and influence viral reactivation.

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Figures

Figure 1.
Figure 1.
Representative photomicrographs of tissue sections from human TGs latently infected with HSV-1 and/or VZV, which were stained by IHC with anti-CD3, anti-CD8, and anti-CD68 antibodies. Neuron encircled by several rows of CD3-positive T cells (arrow, a) and clusters of CD3-positive T cells among ganglionic neurons (arrow, b). Infiltrating T cells stained positive with anti-CD8 antibodies. The pattern of staining was similar to that of CD3-positive T cells. CD8-positive T cells surrounding single neurons (arrow, c; encircled, d). Only a few T cells stained positive with anti-CD4 antibodies (encircled, e; arrowheads point to CD4-positive cells scattered among the ganglionic neurons). T cells were also present as clusters among nerve fibers: CD3-positive cells in a sagittal section (encircled, f) and CD8-positive cells in a transverse section of nerve fibers (encircled, g). When LAT ISH was combined with IHC (h) some CD3-positive T cells (arrowheads) were found occasionally around LAT-positive neurons (arrows). Single cells or clusters of cells among the neurons showed CD68 positivity (encircled, i). Small clusters of CD68-positive macrophages (encircled, j) were found in the vicinity of LAT-positive neurons (arrows). Neurons positive for VZV-protein 62 (k, arrowheads) from a child who died of sudden infant death and who showed no HSV-1 and no T-cell infiltration. Neurons positive for VZV-protein 62 (l, filled arrowheads) from a young man who was latently infected with HSV-1 and showed T-cell infiltrates (arrows, l) around VZV-free neurons. Some neurons showed brown lipofuscin granules near the plasma membrane (open arrowheads, l) distinguishable from the VZV protein that usually fills up the whole cytoplasm. Photomicrographs of a to c, f, and h to l were taken from paraffin and photomicrographs of d, e, g from frozen tissue sections. Magnification, ×400. Tissue sections from a, b, d, e, g, k, and l were slightly counterstained with hematoxylin.
Figure 2.
Figure 2.
Quantification of CD8, cytokine, and chemokine mRNA expression by real-time RT-PCR. Each diagram shows the comparison of 12 HSV-1 negative TGs (neg) with 15 HSV-1 positive TGs (pos). The y axis represents the relative transcript number of the gene of interest compared to the housekeeping gene. Dots represent mean values, boxes represent SEM, and whiskers represent 1.96 × SEM.

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References

    1. Croen DK, Ostrove JM, Dragovic LJ, Smialek JE, Straus SE: Latent herpes simplex virus in human trigeminal ganglia: detection of an immediate early gene ’antisense’ transcript by in situ hybridisation. N Engl J Med 1987, 317:1427-1432 - PubMed
    1. Furuta Y, Takasu T, Sato KC, Fukuda S, Inuyama Y, Nagashima K: Latent herpes virus type 1 in human geniculate ganglia. Acta Neuropathol (Berl) 1992, 84:39-44 - PubMed
    1. Theil D, Arbusow V, Derfuss T, Strupp M, Pfeiffer M, Mascolo A, Brandt T: Prevalence of HSV-1 LAT in human trigeminal, geniculate, and vestibular ganglia and its implication for cranial nerve syndromes. Brain Pathol 2001, 11:408-413 - PMC - PubMed
    1. Simmons A, Tscharke D, Speck P: The role of immune mechanisms in control of herpes simplex virus infection of the peripheral nervous system. Curr Top Microbiol Immunol 1992, 179:31-56 - PubMed
    1. Mester JC, Rouse BT: The mouse model and understanding immunity to herpes simplex virus. Rev Infect Dis 1991, 13:935-945 - PubMed

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