C57BU6J mice immunized with devitalized Ehrlich tumor (ET) cells produce high serum levels of IgM antibodies to E l cell-surface carbohydrates that are critical in the observed resistance against this tumor. However, this response is not found in El-bearing mice at any stage of tumor development. Si
Development of splenic natural suppressor (NS) cells in ehrlich tumor-bearing mice
โ Scribed by Jose L. Subiza; Juan E. Vinuela; Rosa Rodriguez; Juana Gil; M. Angeles Figueredo; Emilio G. de la Concha
- Publisher
- John Wiley and Sons
- Year
- 1989
- Tongue
- French
- Weight
- 873 KB
- Volume
- 44
- Category
- Article
- ISSN
- 0020-7136
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โฆ Synopsis
Spleen cells from C57BU6J mice bearing Ehrlich carcinoma growing as a solid tumor show progressive unresponsiveness to concanavalin A (Con A) and lipopolysaccharide (LPS) mitogens. This is accompanied by striking spleen enlargement with marked hematopoietic activity. Lymphoproliferative assays of normal spleen cells in co-culture with tumor-bearing spleen cells (TBSC) show that: (a) TBSC contain non-specific suppressor cells able to abrogate both Con A and LPS responses, or mixed lymphocyte reaction, of normal spleen cells and (b) suppression by TBSC is MHC-unrestricted, nonprostaglandin-mediated and greatly enhanced by Con A supernatants. Suppressor cells associated with TBSC are large, low-density cells without markers of mature B or T lymphocytes or of the mononuclear phagocyte system. Most appear to be asialo-GM,-negative, as suppression was only partially inhibited by treatment with anti-asialo-GM, and complement. Since NK activity is lacking in TBSC, our data strongly suggest that these "null" suppressor cells are related to the natural suppressor (NS) cells found described in normal bonemarrow and neonatal spleens, or induced in adult spleens by total lymphoid irradiation, graft-vs.-host disease, or cyclophosphamide treatment.
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## Abstract The activity of systemic and __in situ__ natural killer (NK) cells was measured in 3โ to 5โweekโold CBA mice with progressively growing murine sarcoma virus (MSV)โinduced tumors. Splenic NK activity was depressed in tumorโbearing mice. NK activity was quite low or not detectable in unfr