## Abstract Complement activation via the alternative pathway by tumor cells was tested by rosette formation of human erythrocytes (HuE). Test cells were treated with C4‐deficient guinea‐pig serum (C4DS) in the presence of Mg^++^ and absence of Ca^++^, following which 10–30% of lymphoma cells and 1
Induction of leukemia in balb mice by allogeneic AKR leukemic cells
✍ Scribed by Christiane Dosne Pasqualini; Fortuna Saal; R. C. Braylan; S. L. Rabasa
- Publisher
- John Wiley and Sons
- Year
- 1970
- Tongue
- French
- Weight
- 620 KB
- Volume
- 5
- Category
- Article
- ISSN
- 0020-7136
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
The intrasplenic inoculation of AKR lymphoma cells into 1‐month‐old BALB mice, followed by a syngeneic intraperitoneal passage, led to the development of short‐latency leukemia of host origin within 24 days; the incidence of leukemia averaged 83% in 88 mice. Electron microscopic studies revealed the presence of intracisternal A and extracellular C‐type viral particles in leukemic lymph nodes. These results were obtained with eight AKR lymphoma inocula out of 107 trials and were never observed in BALB controls and with normal AKR spleen inoculum, except in one animal. In the surviving groups, the incidence of long‐latency leukemia, averaging 19 months, was significantly increased to 45% in the 541 mice which had received AKR lymphoma inocula, as compared to 30% in those receiving normal AKR spleen inocula; the latter value was also significantly higher than the 15% spontaneous incidence of the BALB strain. A number of tumors were observed in the experimental groups. Antigenic studies, using the indirect cytotoxic test, demonstrated the presence of the G (Gross) antigen, in both short‐ and long‐latency leukemias.
📜 SIMILAR VOLUMES
## Abstract Newborn C3H mice were injected with viable or __in vitro__ X‐irradiated cell suspensions from lymph node and spleen mixtures obtained from healthy AKR donors aged 12 to 18 months. Of the group injected with normal intact cells, 30% developed a lymphocytic leukemia, whereas none of the r
demonstration of the induction T of rodent leukemia in mature mice by cell-free materials was reported by Schwartz and coworkers.11 I n the original experiment,ll a n acceleration of the development of leukemia in the high leukemic incidence strain of AKR mice was demonstrated by inoculation of mice