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Virginia Polytechnic Institute and State University

Glucocorticosteroid modification of lymphocyte blastogenesis in fibrosarcoma-bearing mice

Abstract

dc:description.abstract

Glucocorticosteroids are drugs commonly used to suppress immune or inflammatory responses. The present study was done to evaluate the influence of glucocorticoids on immunity in fibrosarcoma-bearing mice. Effects of hydrocortisone-21-sodium succinate (HCS) on mitogen-induced lymphocyte proliferation were assessed. T cells from nontumor-bearing mice showed a 2-fold suppression of phytohemagglutinin (PHA) responsiveness with the addition of 0.1 µg HCS. However, T cells from mice with 3-4 week tumors did not demonstrate as great a suppression, if any. Kinetic studies during tumor growth demonstrated a decrease in HCS suppression of mitogen-induced DNA synthesis at 8-10 days post-tumor cell inoculation. RCS-treated cells from mice with 3-4 week tumors had a 2- fold increase in blastogenesis over untreated PHA controls. The role of macrophages and their involvement in the steroid sensitivity of the PHA response is unclear. Evidence reported here indicated that macrophages may be involved as mediators of steroid sensitivity and may therefore limit the extent of their suppressive and/or enhancing activity. In vivo administration of methylprednisolone acetate (MPA) demonstrated that steroids can interfere with the growth and progression of fibrosarcomas in their syngenic BALB/c hosts. The strongest delay in tumor appearance was observed when the steroid was administered 4-7 days post-tumor cell inoculation. It is assumed that after tumor cell inoculation, precursor cells of both suppressor and cytotoxic lymphocytes were entering a proliferative stage to form mature cells. These studies indicated that steroid suppression was directed against a suppressor T cell and possibly acts by preventing its differentiation. It is thought that this suppressor cell acts by inhibiting the lytic function of effector T cells. Thus, by eliminating suppressor T cells, the immune response is capable of eliciting strong anti-tumor immunity.

Degree

thesis:*
Name thesis:degree_name
M.S.
Level thesis:degree_level
masters
Discipline thesis:degree_discipline
Microbiology
Department dc:contributor.department
Microbiology
Grantor dc:publisher
Virginia Polytechnic Institute and State University
Year dc:date.issued
1978

Author and committee

dc:creator, dc:contributor.*
Author dc:creator
  • Willard, Karen Elizabeth

Rights

dc:rights
Statement dc:rights
  • In Copyright
Language dc:language.iso
en

Identifiers

dc:identifier.*
Handle dc:identifier.uri
http://hdl.handle.net/10919/114399
OAI identifier oai:identifier
oai:vtechworks.lib.vt.edu:10919/114399

Chain of custody

source
Harvested from
Virginia Tech
Base URL
vtechworks.lib.vt.edu/oai/request
Last updated
2026-07-22
Source record
OAI-PMH GetRecord
related terms
citation

Willard, Karen Elizabeth. Glucocorticosteroid modification of lymphocyte blastogenesis in fibrosarcoma-bearing mice. masters thesis, Virginia Polytechnic Institute and State University, 1978. http://hdl.handle.net/10919/114399