Selective attrition of non-recirculating T cells during normal passage through the lung vascular bed.

Transient arrest of T lymphocytes in the lung vascular bed following infusion of cells subjected to in vitro manipulations has been recognized for many years as a troublesome 'artefact', and has generally been attributed to trauma-induced changes in lymphocyte surface membranes. However, a number of laboratories have reported that the trapping process also occurs under situations where lymphocyte surface damage is minimal or absent, suggesting that the phenomenon may represent an intrinsic component of normal lymphocyte circulation. Consistent with these suggestions, recent studies from our laboratory have demonstrated the presence of large numbers of T cells in collagenase digests of normal peripheral lung tissue, which cannot be removed by broncho-alveolar lavage or perfusion of the tissue vascular bed. In the present experiments we have characterized these lung T cells in SPF rats. The properties common to this population include hydroxyurea sensitivity, high CD8:CD4 ratio and high frequency of cells recently derived from the thymus, and saturation thymidine-labelling studies indicated that greater than 90% of the lung T cells had divided within a 14-day test period. Additionally, cloning studies under conditions of limiting dilution indicate markedly reduced capacity for proliferation, relative to T cells in blood or spleen. We interpret these data to indicate that selective trapping and subsequent down-regulation of non-recirculating T cells is a normal consequence of passage through the lung vascular bed.