Abstract
Macrophages, given keyhole limpet hemocyanin in vitro, for normal mice initiate in culture antigen-specific T cell-mediated immune reactions. On the other hand, macrophages from nude, from adult-thymectomized, or from neonatal-thymectomized mice are impaired with respect to their capacity to signal such an antigen-specific T cell reaction. Thymocytes from hydrocortisone-treated donors, added in culture to such impaired macrophages, rendered them immunologically potent. The capacity of macrophages from adult-thymectomized mice to promote the activation of antigen-specific 'helper' T cells which, cooperating with B lymphocytes, would lead to antibody production, was also impaired. Thus, it appears that short-lived T lymphocytes control the maturation of macrophages up to a stage at which they can present antigen-specific T cells with antigen in an immunogenic form. We found that such T lymphocytes also control the phagocytic properties of macrophages, yet the impairment of their immunogenic properties does not seem to be derived from decreased phagocytosis.
| Original language | English |
|---|---|
| Pages (from-to) | 4056-4060 |
| Number of pages | 5 |
| Journal | Proceedings of the National Academy of Sciences of the United States of America |
| Volume | 76 |
| Issue number | 8 |
| DOIs | |
| State | Published - 1 Jan 1979 |
| Externally published | Yes |
ASJC Scopus subject areas
- General