TY - JOUR
T1 - Intrathymic effect of acute pathogenic SHIV infection on T-lineage cells in newborn macaques
AU - Suzuki, Hajime
AU - Motohara, Makiko
AU - Miyake, Ariko
AU - Ibuki, Kentaro
AU - Fukazawa, Yoshinori
AU - Inaba, Katsuhisa
AU - Masuda, Kyoko
AU - Minato, Nagahiro
AU - Kawamoto, Hiroshi
AU - Hayami, Masanori
AU - Miura, Tomoyuki
PY - 2005
Y1 - 2005
N2 - We intrarectally infected newborn macaques with a pathogenic simian/human immunodeficiency virus (SHIV) that induced rapid and profound CD4+ T cell depletion, and examined the early effects of this SHIV on the thymus. After intrarectal infection, viral loads were much higher in the thymus than in other lymphoid tissues in newborns. In contrast, no clear difference was seen in the viral loads of different tissues in adults. Histological and immunohistochemical observations showed severe thymic involution. Depletion of CD4+ thymocytes began in the medulla at 2 weeks post infection and spread over the whole thymus. After in vivo infection, the CD2+ subpopulation, which represents a relatively later stage of T cell progenitors, was selectively reduced and development of thymocytes from CD3-CD4 -CD8- cells to CD4+CD8+ cells was impaired. These results suggest that profound and irreversible loss of CD4 + cells that are observed in the peripheral blood of SHIV-infected monkeys are due to destruction of the thymus and impaired thymopoiesis as a result of SHIV infection in the thymus.
AB - We intrarectally infected newborn macaques with a pathogenic simian/human immunodeficiency virus (SHIV) that induced rapid and profound CD4+ T cell depletion, and examined the early effects of this SHIV on the thymus. After intrarectal infection, viral loads were much higher in the thymus than in other lymphoid tissues in newborns. In contrast, no clear difference was seen in the viral loads of different tissues in adults. Histological and immunohistochemical observations showed severe thymic involution. Depletion of CD4+ thymocytes began in the medulla at 2 weeks post infection and spread over the whole thymus. After in vivo infection, the CD2+ subpopulation, which represents a relatively later stage of T cell progenitors, was selectively reduced and development of thymocytes from CD3-CD4 -CD8- cells to CD4+CD8+ cells was impaired. These results suggest that profound and irreversible loss of CD4 + cells that are observed in the peripheral blood of SHIV-infected monkeys are due to destruction of the thymus and impaired thymopoiesis as a result of SHIV infection in the thymus.
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U2 - 10.1111/j.1348-0421.2005.tb03646.x
DO - 10.1111/j.1348-0421.2005.tb03646.x
M3 - Article
C2 - 16034211
AN - SCOPUS:24744457513
SN - 0385-5600
VL - 49
SP - 667
EP - 679
JO - MICROBIOLOGY and IMMUNOLOGY
JF - MICROBIOLOGY and IMMUNOLOGY
IS - 7
ER -