LYMPHOKINE-ACTIVATED KILLER ACTIVITY IN LONG-TERM CULTURES WITH ANTI-CD3 PLUS INTERLEUKIN-2 - IDENTIFICATION AND ISOLATION OF EFFECTOR SUBSETS
- 15 February 1989
- journal article
- research article
- Vol. 49 (4) , 963-968
Abstract
Peripheral blood lymphocytes cultured in recombinant interleukin 2 during 3 to 5 days (short-term cultures) develop the ability to lyse natural killer-resistant tumor lines and fresh tumor cells, i.e., express lymphokine-activated killer (LAK) function. Phenotypic analysis has shown these cells to be natural killer cells, i.e., CD16+ and/or Leu 19+ cells. CD3+, CD16- T-cells, instead, develop very low LAK function in these cultures. We recently reported the development of long-term (up to 21 days) cultured cells with LAK activity by stimulation with OKT3+ interleukin 2 (IL2). These culture conditions repeatedly resulted in a several hundred-fold expansion in cell number. Specific LAK activity on Day 14 of culture was comparable to that of 3-day LAK cultures and could be further enhanced by the addition of interleukin 1.beta., .beta.-, or .gamma.-interferon. Total LAK activity was greatly increased in OKT3 + IL2 cultures over that found in short-term cultures. Isolation of effectors mediating LAK function in long-term cultures stimulated with OKT3 + IL2 showed that both CD3+, CD16- cells and CD16+,CD3- cells tested on Day 14 of culture expressed equivalent levels of LAK activity as shown by lysis of natural killer-resistant targets, HL60 and Daudi. Further dissection of the subpopulations developing LAK activity demonstrated that, in addition to CD16+,CD3- cells, CD3+, CD4-,CD8- cells and Leu 19+,CD3-,CD16-, cells also developed high LAK activity in long-term cultures with OKT3 + IL2. Furthes, long term culture with OKT3 + IL2 induced increase in the numbers not only of CD3+,CD4-,CD8- cells but also of CD16+,CD3- and Leu19+,CD3-,CD16- cells. Although there is a significant increase in the number of CD3+,CD8+ cells, neither these, nor the CD3+,CD4+ cells, mediate LAK activity to the same extent as the populations mentioned above.This publication has 0 references indexed in Scilit: