𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Role of T suppressor cells in the cycling of the immune response against a murine fibrosarcoma

✍ Scribed by Béatrice Payelle; Geneviève Lespinats; Sylvie Tlouzeau


Publisher
John Wiley and Sons
Year
1984
Tongue
French
Weight
587 KB
Volume
34
Category
Article
ISSN
0020-7136

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

Antitumor immunity against a fibrosarcoma in C57BL/6 mice was obtained by means of a semi‐allogenic somatic hybrid cell derived from the fusion of this C57BL/6 fibrosarcoma (MCB6‐1) and A9 cells of C3H origin. In a Winn assay, this immunity could be transferred by T lymphocytes to normal C57BL/6 recipient mice during an early and a late phase after immunization. There appeared to be a transient non‐responsive period during which no immunity could be transferred. Injection of cyclophosphamide (CY) into mice before immunization increased the level of immunity during this period, and reconstitution of animals with normal spleen cells abolished the effect of CY. During the non‐responsive period, suppressor cells were demonstrated in the spleen: the i.v. transfer of these suppressor cells to normal mice significantly inhibited the induction of antitumor immunity; the suppressive effect was transferred by T lymphocytes of the Lyt‐2+ phenotype. No suppressive effect on antitumor protection was observed when suppressor cells were transferred simultaneously with immune T lymphocytes in the Winn assay. From these findings, it appears that T‐suppressor cells regulate the antitumor response, interfering with the afferent (induction) arm of the immune response.


📜 SIMILAR VOLUMES


Abrogation of the in vitro generation of
✍ Dr. Philip Frost; Pamela Prete; Robert Kerbel 📂 Article 📅 1982 🏛 John Wiley and Sons 🌐 French ⚖ 723 KB

## Abstract A reproducible __in vitro__ assay for the effect of suppressor T cells on the generation of an __in vitro__ cytotoxic response to a metastatic murine tumor is described. Suppression in this system is maximal. The model uses splenic T cells from DBA/2 mice bearing the MDAY‐D2 metastatic

Tumor immunity to murine plasma cell tum
✍ B. T. Rouse; M. Röllinghoff; N. L. Warner 📂 Article 📅 1973 🏛 John Wiley and Sons 🌐 English ⚖ 727 KB

## Abstract Spleen cells, thoracic duct lymphocytes and adherent peritoneal exudate cells from mice immunized to syngeneic plasma cell tumors were capable of transferring specific protective immunity to these tumors. Pre‐treatment of these cells with anti‐Θ serum or anti‐lymphocyte serum, but not w