Impairment of in vitro generation of cytotoxic or T suppressor lymphocytes by friend leukemia virus infection in mice
✍ Scribed by Prof. E. Garaci; G. Migliorati; T. Jezzi; A. Bartocci; L. Gioia; C. Rinaldi; E. Bonmassar
- Publisher
- John Wiley and Sons
- Year
- 1981
- Tongue
- French
- Weight
- 705 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0020-7136
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Spleen cells collected from DBA/2 (H‐2~d~) mice inoculated with the polycythemic variant of Friend‐Leukemia Virus Complex (FLV‐P) were tested for T‐dependent immune functions, such as the in vitro generation of cytotoxic T lymphocytes (CTL) and of non‐specific T suppressor lymphocytes (STL). CTL were generated against H‐2~b~ splenocytes, and STL were obtained following a 5‐day lymphocyte culture without stimulator cells. A progressive and severe impairment of the generation of both CLT and STL was found from 2 weeks onward after infection, being almost totally abolished 3–4 weeks after virus challenge. Suppressor cells (SC) capable of inhibiting CTL generation was detected in FLV‐P bearing mice. Suppressor activity was unaffected by anti‐Thy 1.2 serum and complement but was removed following iron‐magnet depletion or passage through nylon‐wool column. Moreover complete recovery of the competence of CTL generation was attained when FLV‐P infected splenocytes were passed through nylon‐wool column. It is concluded that FLV‐P infection depresses T‐dependent cytotoxic and suppressor responses in mice, by the appearance of non‐T adherent phagocytic cells, capable of impairing CTL generation in vitro.
📜 SIMILAR VOLUMES
## Abstract Lymphoid tissues of mice infected with murine leukemia virus (Friend) (MuLV‐F) were examined for the presence of cellular markers of MuLV‐F infection. The Friend virus‐associated cell membrane antigen (FVMA) and the virus group‐specific antigen (GSA) were detectable on cells from the sp
## Abstract The infection of isolated B and T cells by a murine leukemia virus (Friend) (MuLV‐F) was studied both __in vitro__ and __in vitro__ with an implanted diffusion chamber system. Lymphocytes were obtained from pools of normal spleen cells by filtration of the cell suspension through a nylo
## Abstract It has previously been shown that DBA/2 mice protected against the development of Friend leukemia virus (FLV)^4^‐induced disease by the passive administration of heterologous antisera directed against disrupted virions or the major viral envelope glycoprotein (gp71) fail to undergo the