Impaired T-cell differentiation in the thymus at the early stages of acute pathogenic chimeric simian–human immunodeficiency virus (SHIV) infection in contrast to less pathogenic SHIV infection

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One of the mechanisms by which HIV infection induces the depletion of CD4 + T cells has been suggested to be impairment of T-cell development in the thymus, although there is no direct evidence that this occurs. To examine this possibility, we compared T-cell maturation in the intrathymic progenitors between macaques infected with an acute pathogenic chimeric simian–human immunodeficiency virus (SHIV), which causes profound and irreversible CD4 + T-cell depletion, and macaques infected with a less pathogenic SHIV, which causes only a transient CD4 + T-cell decline. Within 27 days post-inoculation (dpi), the two virus infections caused similar increases in plasma viral loads and similar decreases in CD4 + T-cell counts. However, in the thymus, the acute pathogenic SHIV resulted in increased thymic involution, atrophy and the depletion of immature T cells including CD4 +CD8 + double-positive (DP) cells, whereas the less pathogenic SHIV did not have these effects. Ex vivo differentiation of CD3 −CD4 −CD8 − triple-negative (TN) intrathymic progenitors to DP cells was assessed by a monkey–mouse xenogenic fetal thymus organ culture system. Differentiation was impaired in the TN intrathymic progenitors of the acute pathogenic SHIV-infected monkeys, while differentiation was not impaired in the TN intrathymic progenitors of the less pathogenic SHIV-infected monkeys. These differences suggest that dysfunction of thymic maturation makes an important contribution to the irreversible depletion of circulating CD4 + T cells in vivo.