The perivascular space (PVS) of human thymus increases in volume during agi
ng as thymopoiesis declines. Understanding the composition of the PVS is th
erefore vital to understanding mechanisms of thymic atrophy. We have analyz
ed 87 normal and 31 myasthenia gravis (MG) thymus tissues from patients ran
ging in age from newborn to 78 years, using immunohistologic and molecular
assays. We confirmed that although thymic epithelial space (TES) volume dec
reases progressively with age, thymopoiesis with active T-cell receptor gen
e rearrangement continued normally within the TES into late life. Hematopoi
etic cells present in the adult PVS include T cells, B cells, and monocytes
. Eosinophils are prominent in PVS of infants 2 years of age or younger. In
the normal adult and the MG thymus, the PVS includes mature single-positiv
e (CD1a(-) and CD4(+) or CD8(+))T lymphocytes that express CD45RO, and cont
ains clusters of T cells expressing the TIA-1 cytotoxic granule antigen, su
ggesting a peripheral origin. PBMCs bind in vitro to MECA-79(+) high endoth
elial venules present in the PVS, suggesting a mechanism for the recruitmen
t of peripheral cells to thymic PVS. Therefore, in both normal subjects and
MG patients, thymic PVS may be a compartment of the peripheral immune syst
em that is not directly involved in thymopoiesis.