## Abstract Susceptibility of mice to viral components present in Friend leukemia virus (FLV) preparation, lymphatic leukemia virus (LLV) and spleen focus‐forming virus (SFFV), was studied by separately determining end point for infection of each component. Mice with __Fv‐1^n^__ genotype were much
In vivo and in vitro recovery of defective friend virus by various leukemia viruses
✍ Scribed by A. Howard Fieldsteel; Peter J. Dawson; Carole Kurahara
- Publisher
- John Wiley and Sons
- Year
- 1971
- Tongue
- French
- Weight
- 450 KB
- Volume
- 8
- Category
- Article
- ISSN
- 0020-7136
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Friend virus‐induced reticulum cell sarcomas afler growth in tissue culture were shown to be free from infectious virus. Retrieval of infectious Friend virus could be accomplished with the aid of Moloney leukemia virus, Graffi leukemia virus, and the lymphatic leukemia virus associated with Friend virus, using both in vivo and in vitro techniques. On initial isolation, the pseudotypes differed from original Friend virus in their markedly reduced ability to induce Friend disease in other than newborn BALB/c mice. It was concluded that, although Friend virus may also exist in a non‐defective form, there was no evidence that the tumors contained other than helper‐dependent virus.
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## Abstract The effector cells from non‐immunized mice capable of lysing ^51^Cr‐labelled FLD‐3 BALB/c Friend virus‐induced erythroleukemia cells __in vitro__ and cells capable of clearing FLD‐3 cells labelled with 5‐iodo‐2′‐deoxyuridine‐^125^I (^125^IdUrd) from the lungs __in vivo__ were characteri
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